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Search Results (127,988)

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13 pages, 278 KiB  
Article
A Study of Factors Contributing to the Nutritional Status of Elderly People Receiving Home Care
by Eirini Stratidaki, Enkeleint A. Mechili, Christina Ouzouni, Athina E. Patelarou, Konstantinos Giakoumidakis, Aggelos Laliotis and Evridiki Patelarou
Nutrients 2024, 16(18), 3135; https://doi.org/10.3390/nu16183135 (registering DOI) - 17 Sep 2024
Abstract
(1) Background: Nutrition is a critical aspect of health and well-being in the elderly population, as physiological changes associated with aging can impact nutrient utilization and dietary needs. The aim of this study was the assessment of nutritional screening and associated factors among [...] Read more.
(1) Background: Nutrition is a critical aspect of health and well-being in the elderly population, as physiological changes associated with aging can impact nutrient utilization and dietary needs. The aim of this study was the assessment of nutritional screening and associated factors among community-dwelling elderly people. (2) Methods: This study is the first phase of an intervention trial of people aged 65 years and over who received primary health services and resided in the municipality of Archanes Asterousia in Crete, Greece. Nutritional risk was assessed using the Mini Nutritional Assessment. Diet-related factors were analyzed, including health status (oral hygiene, depression, cognitive decline, impaired functioning, quality of life), social factors (educational attainment, marital status, type of work before 60 years), and lifestyle factors (smoking, drinking, diet). (3) Results: A total of 730 elderly people were evaluated (males, 31.5%), with an average age (±SD) of 76.83 (±6.68) years. MNA was found to have a statistically significant connection with assessment of oral hygiene, mental state, Charlson comorbidity, functional independence (assessed with the Barthel scale), and quality of life. The exception was geriatric depression (GDS), with which no statistically significant association was found (p > 0.05). Nutritional risk analysis revealed 379 participants (51.9%) to be adequately nourished, 205 (28.1%) to be at risk of malnutrition, and 146 (20.0%) to be malnourished. (4) Conclusions: These results clearly demonstrated the key factors that contribute to the nutritional screening of elderly people and need to be addressed by health authorities and social services. Full article
18 pages, 2109 KiB  
Article
Tear Proteomics in Children and Adolescents with Type 1 Diabetes: A Promising Approach to Biomarker Identification of Diabetes Pathogenesis and Complications
by Eleni Angelopoulou, Rosa-Anna Kitani, Rafael Stroggilos, Vasiliki Lygirou, Ioannis-Anargyros Vasilakis, Konstantina Letsou, Antonia Vlahou, Jerome Zoidakis, Martina Samiotaki, Christina Kanaka-Gantenbein and Nicolas C. Nicolaides
Int. J. Mol. Sci. 2024, 25(18), 9994; https://doi.org/10.3390/ijms25189994 (registering DOI) - 17 Sep 2024
Abstract
The aim of the current study was to investigate the tear proteome in children and adolescents with type 1 diabetes (T1D) compared to healthy controls, and to identify differences in the tear proteome of children with T1D depending on different characteristics of the [...] Read more.
The aim of the current study was to investigate the tear proteome in children and adolescents with type 1 diabetes (T1D) compared to healthy controls, and to identify differences in the tear proteome of children with T1D depending on different characteristics of the disease. Fifty-six children with T1D at least one year after diagnosis, aged 6–17 years old, and fifty-six healthy age- and sex-matched controls were enrolled in this cross-sectional study. The proteomic analysis was based on liquid chromatography tandem mass spectrometry (LC-MS/MS) enabling the identification and quantification of the protein content via Data-Independent Acquisition by Neural Networks (DIA-NN). Data are available via ProteomeXchange with the identifier PXD052994. In total, 3302 proteins were identified from tear samples. Two hundred thirty-nine tear proteins were differentially expressed in children with T1D compared to healthy controls. Most of them were involved in the immune response, tissue homeostasis and inflammation. The presence of diabetic ketoacidosis at diagnosis and the level of glycemic control of children with T1D influenced the tear proteome. Tear proteomics analysis revealed a different proteome pattern in children with T1D compared to healthy controls offering insights on deregulated biological processes underlying the pathogenesis of T1D. Differences within the T1D group could unravel biomarkers for early detection of long-term complications of T1D. Full article
(This article belongs to the Section Molecular Pathology, Diagnostics, and Therapeutics)
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<p>Heatmap with the expression of markers of exosomes in tear samples (Mann–Whitney test, <span class="html-italic">p</span>-value &lt; 0.05). Black color denotes a missing value.</p>
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<p>Heatmap of the deregulated biological pathways in children with type 1 diabetes compared to healthy controls (Mann–Whitney test, <span class="html-italic">p</span>-value &lt; 0.05).</p>
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<p>Volcano plot demonstrating the proteins involved in the adaptive immune response that were found to be statistically differentially expressed between the type 1 diabetes group and the HC group (Mann–Whitney test, <span class="html-italic">p</span>-value &lt; 0.05).</p>
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<p>Heatmap of the deregulated biological pathways in children with type 1 diabetes with poor glycemic control [HbA1c &gt; 56 mmol/mol (7.3%)] compared to those with good glycemic control [HbA1c ≤ 56 mmol/mol (7.3%)] (Mann–Whitney test, <span class="html-italic">p</span>-value &lt; 0.05).</p>
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16 pages, 1182 KiB  
Review
The Effect of Dietary Types on Gut Microbiota Composition and Development of Non-Communicable Diseases: A Narrative Review
by Martin Soldán, Ľubica Argalášová, Lucia Hadvinová, Bonzel Galileo and Jana Babjaková
Nutrients 2024, 16(18), 3134; https://doi.org/10.3390/nu16183134 (registering DOI) - 17 Sep 2024
Abstract
Introduction: The importance of diet in shaping the gut microbiota is well established and may help improve an individual’s overall health. Many other factors, such as genetics, age, exercise, antibiotic therapy, or tobacco use, also play a role in influencing gut microbiota. Aim: [...] Read more.
Introduction: The importance of diet in shaping the gut microbiota is well established and may help improve an individual’s overall health. Many other factors, such as genetics, age, exercise, antibiotic therapy, or tobacco use, also play a role in influencing gut microbiota. Aim: This narrative review summarizes how three distinct dietary types (plant-based, Mediterranean, and Western) affect the composition of gut microbiota and the development of non-communicable diseases (NCDs). Methods: A comprehensive literature search was conducted using the PubMed, Web of Science, and Scopus databases, focusing on the keywords “dietary pattern”, “gut microbiota” and “dysbiosis”. Results: Both plant-based and Mediterranean diets have been shown to promote the production of beneficial bacterial metabolites, such as short-chain fatty acids (SCFAs), while simultaneously lowering concentrations of trimethylamine-N-oxide (TMAO), a molecule associated with negative health outcomes. Additionally, they have a positive impact on microbial diversity and therefore are generally considered healthy dietary types. On the other hand, the Western diet is a typical example of an unhealthy nutritional approach leading to an overgrowth of pathogenic bacteria, where TMAO levels rise and SCFA production drops due to gut dysbiosis. Conclusion: The current scientific literature consistently highlights the superiority of plant-based and Mediterranean dietary types over the Western diet in promoting gut health and preventing NCDs. Understanding the influence of diet on gut microbiota modulation may pave the way for novel therapeutic strategies. Full article
(This article belongs to the Special Issue The Role of Preventive Nutrition in Cardio-Metabolic Disease)
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<p>Characteristics of three distinct dietary types. Abbreviations: SCFAs—short-chain fatty acids, TMAO—trimethylamine-N-oxide, CRC—colorectal cancer, PUFAs—polyunsaturated fatty acids, EVOO—extra virgin olive oil. Created in BioRender. Soldán, M. (2024) <a href="http://BioRender.com/a05r617" target="_blank">BioRender.com/a05r617</a> (accessed on 8 September 2024).</p>
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30 pages, 8586 KiB  
Review
Unraveling the Dynamic Properties of New-Age Energy Materials Chemistry Using Advanced In Situ Transmission Electron Microscopy
by Subramaniyan Ramasundaram, Sampathkumar Jeevanandham, Natarajan Vijay, Sivasubramani Divya, Peter Jerome and Tae Hwan Oh
Molecules 2024, 29(18), 4411; https://doi.org/10.3390/molecules29184411 (registering DOI) - 17 Sep 2024
Abstract
The field of energy storage and conversion materials has witnessed transformative advancements owing to the integration of advanced in situ characterization techniques. Among them, numerous real-time characterization techniques, especially in situ transmission electron microscopy (TEM)/scanning TEM (STEM) have tremendously increased the atomic-level understanding [...] Read more.
The field of energy storage and conversion materials has witnessed transformative advancements owing to the integration of advanced in situ characterization techniques. Among them, numerous real-time characterization techniques, especially in situ transmission electron microscopy (TEM)/scanning TEM (STEM) have tremendously increased the atomic-level understanding of the minute transition states in energy materials during electrochemical processes. Advanced forms of in situ/operando TEM and STEM microscopic techniques also provide incredible insights into material phenomena at the finest scale and aid to monitor phase transformations and degradation mechanisms in lithium-ion batteries. Notably, the solid–electrolyte interface (SEI) is one the most significant factors that associated with the performance of rechargeable batteries. The SEI critically controls the electrochemical reactions occur at the electrode–electrolyte interface. Intricate chemical reactions in energy materials interfaces can be effectively monitored using temperature-sensitive in situ STEM techniques, deciphering the reaction mechanisms prevailing in the degradation pathways of energy materials with nano- to micrometer-scale spatial resolution. Further, the advent of cryogenic (Cryo)-TEM has enhanced these studies by preserving the native state of sensitive materials. Cryo-TEM also allows the observation of metastable phases and reaction intermediates that are otherwise challenging to capture. Along with these sophisticated techniques, Focused ion beam (FIB) induction has also been instrumental in preparing site-specific cross-sectional samples, facilitating the high-resolution analysis of interfaces and layers within energy devices. The holistic integration of these advanced characterization techniques provides a comprehensive understanding of the dynamic changes in energy materials. This review highlights the recent progress in employing state-of-the-art characterization techniques such as in situ TEM, STEM, Cryo-TEM, and FIB for detailed investigation into the structural and chemical dynamics of energy storage and conversion materials. Full article
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<p>In situ solid-state/electrochemical biasing TEM characterization for energy materials. (<b>A</b>) Single-particle-level characterization of (<b>a</b>) graphene cage-like layer covering connected with the electrical circuit for external load test analysis, and (<b>b</b>) current-voltage measurements of graphene-encapsulated and amorphous-carbon-coated SiMPs [<a href="#B32-molecules-29-04411" class="html-bibr">32</a>]. (<b>B</b>) Experimental set-up of (<b>a</b>) in situ bias arrangements of tungsten tip and Cu wire inside TEM, (<b>b</b>) low-magnification TEM showing the contact, (<b>c</b>) high-magnification TEM showing the contact between tip, wire, and SEI layer, and (<b>d</b>) TEM showing the surface SEI layer assembly of the integrated set-up, and (<b>e</b>) current-voltage plot indicating critical voltage [<a href="#B33-molecules-29-04411" class="html-bibr">33</a>]. (<b>C</b>) Lithiation of electrochemically biased and (<b>a</b>) arc-discharged MWCNT which is glued to an Al rod (working electrode), Li<sub>2</sub>O grown on Li surface acts as a solid electrolyte, bulk Li metal scratched from tungsten rod acts as counter electrode, (<b>b</b>) pristine MWCNT before coming in contact with Li<sub>2</sub>O/Li electrode, (<b>c</b>) lithiated MWCNT showing uniform Li<sub>2</sub>O layer formation on the surface, and (<b>d</b>–<b>f</b>) corresponding EELS mapping of C, Li, and O, respectively, indicating the nanotube lithiation [<a href="#B34-molecules-29-04411" class="html-bibr">34</a>]. (<b>D</b>) Crack formation in the lithiated Si NWs, (<b>a</b>–<b>i</b>) morphological evolution showing anisotropic elongation and crack during the lithiation of solid cells after contacting the Li<sub>2</sub>O/Li electrode. Red arrows in the panel indicate the propagation of reaction front [<a href="#B38-molecules-29-04411" class="html-bibr">38</a>]. (<b>E</b>) In situ electrochemical functional cell for operando TEM characterization of battery materials [<a href="#B41-molecules-29-04411" class="html-bibr">41</a>]. Figures reproduced with permission from [<a href="#B32-molecules-29-04411" class="html-bibr">32</a>,<a href="#B33-molecules-29-04411" class="html-bibr">33</a>,<a href="#B34-molecules-29-04411" class="html-bibr">34</a>,<a href="#B38-molecules-29-04411" class="html-bibr">38</a>,<a href="#B41-molecules-29-04411" class="html-bibr">41</a>].</p>
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<p>In situ thermal-induced TEM characterization of energy materials. (<b>A</b>) Thermal welding type experiment of nano solder Sn sheet and Cu structure, showing (<b>a</b>) TEM images of their interface at room temperature (Red, and green parts represent Sn, and Cu, respectively) and (<b>d</b>) after heating (enlarged version (<b>b</b>,<b>e</b>) and HRTEM images (<b>c</b>,<b>f</b>) before and after heating, respectively) [<a href="#B50-molecules-29-04411" class="html-bibr">50</a>]. (<b>B</b>) STEM-HAADF images of samples at all four conditions of the perovskite layer (varying the temperature from 50 to 250 °C) showed no visible changes until 150 °C [<a href="#B1-molecules-29-04411" class="html-bibr">1</a>]. (<b>C</b>) Direct transitions of perovskite structures from tetragonal to trigonal crystalline structure, (<b>a</b>–<b>c</b>) degradation process focusing on single MAPbI<sub>3</sub> grains (scale bar = 2 nm), and (<b>d</b>) MAPbI<sub>3</sub> transition from tetragonal phase to PbI<sub>2</sub> with a trigonal configuration [<a href="#B51-molecules-29-04411" class="html-bibr">51</a>]. (<b>D</b>) Cross-sectional view of in situ analysis showing HAADF images of a perovskite solar cell with a device structure of glass/ITO/TiO<sub>2</sub>/CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub>/spiro-OMeTAD/Ag, and stability check: day 1 shows bright images due to FIB beam focus damage, day 2 shows beam-sensitiveness slowly disappeared, days 7–15 show growth of electron-beam damaged area, and days 20–30 show no further changes (later day-30 samples underwent heating-induced degradation at different time intervals as shown by arrows) [<a href="#B52-molecules-29-04411" class="html-bibr">52</a>]. Figures reproduced with permission from [<a href="#B1-molecules-29-04411" class="html-bibr">1</a>,<a href="#B50-molecules-29-04411" class="html-bibr">50</a>,<a href="#B51-molecules-29-04411" class="html-bibr">51</a>,<a href="#B52-molecules-29-04411" class="html-bibr">52</a>].</p>
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<p>In situ gas-cell type TEM characterization for energy materials. (<b>A</b>) Schematic demonstration of operando ETEM equipped with windowed gas cell. (<b>B</b>) HAADF-STEM characterization depicting the atomic orientation of Ni/TiO<sub>2</sub> (<b>a</b>) catalyst (exposed to H<sub>2</sub>) prepared under in situ conditions at 400 °C (white arrow: Ni NPs of TiO<sub>2</sub> support, solid lines: TiO<sub>x</sub>-covered Ni atomic planes, and dashed lines: unoccupied facets), (<b>b</b>) strain maps showing atomic displacements, (<b>c</b>) catalyst (exposed to CO<sub>2</sub>:H<sub>2</sub> (0.25 bar:0.75 bar) mixture) at 400 °C showing complete re-exposure of Ni and NPs restructuring, and (<b>d</b>) estimated atomic displacements/reorientations [<a href="#B59-molecules-29-04411" class="html-bibr">59</a>]. (<b>C</b>) Concept of loading ZnO nanowires onto SiN<sub>x</sub> observing windows in a gas-cell setup with built-in MEMS chip (SO<sub>2</sub> atm conditions). (<b>D</b>) In situ TEM imaging taken after exposure to SO<sub>2</sub> gaseous conditions shows (<b>a</b>–<b>h</b>) the nanostructure’s morphological evolution, and (<b>i</b>) its corresponding EDS mapping [<a href="#B61-molecules-29-04411" class="html-bibr">61</a>]. (<b>E</b>) The concept of particle formation and growth observed during the reduction of nickel-phyllosilicate-based catalyst precursor was investigated in an in situ gaseous state. (<b>F</b>) In situ TEM images were observed at different time intervals during the reduction of nickel-phyllosilicates under 1 bar pressure (0.1 sccm gas flow rate at 425 °C) with an electron imaging dose of 30 e<sup>−</sup>·A<sup>−2</sup>·s<sup>−1</sup> showing the nucleation and growth of nanoparticles only in the presence of the electron beam [<a href="#B63-molecules-29-04411" class="html-bibr">63</a>]. Figures reproduced with permission from [<a href="#B59-molecules-29-04411" class="html-bibr">59</a>,<a href="#B61-molecules-29-04411" class="html-bibr">61</a>,<a href="#B63-molecules-29-04411" class="html-bibr">63</a>].</p>
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<p>In situ liquid-cell/electrochemistry integrated TEM characterization for energy materials. (<b>A</b>) Schematic diagram showing a cross-sectional view of TEM holder, (<b>a</b>) conduit-like silicon nitride membranes encapsulating fluid layer and in situ electrochemical workstation, (<b>b</b>) system of three patterned electrodes with top chip, (<b>c</b>,<b>d</b>) electrochemical activity of Pt cyclic voltammetry (CV) with thick and thin liquid (~150 nm) layers, and (<b>e</b>) Temporal evolution (<b>a</b>–<b>h</b>) occurring in LiFePO<sub>4</sub>/FePO<sub>4</sub> cluster during cycling (charge/discharge). Red, and yellow arrows indicate the propagation of delithiation in core–shell, and left to right pathways [<a href="#B75-molecules-29-04411" class="html-bibr">75</a>]. (<b>B</b>) Schematic representation of (<b>a</b>) in situ liquid-cell nanobattery setup analyzing the lithiation process, (<b>b</b>) SEM images of the electrochemically biased chip with (<b>b</b>) inner side, (<b>c</b>) its magnified view, and (<b>d</b>) Si NW electrode welded onto the Pt contact [<a href="#B76-molecules-29-04411" class="html-bibr">76</a>]. (<b>C</b>) Graphene liquid-cell (GLC) TEM illustration: (<b>a</b>) Si NPs were immersed in liquid electrolyte and placed between graphene layers in a sandwich structure, (<b>b</b>) the whole assembly was mounted on a holey amorphous carbon TEM grid (SEM image, scale bar: 1 μm), and (<b>c</b>) STEM mapping images of O, C, Si, P, and F in the GLC (scale bar: 100 nm) [<a href="#B77-molecules-29-04411" class="html-bibr">77</a>]. (<b>D</b>) Schematic diagram of in situ liquid-cell visualization of (<b>a</b>) MOS<sub>2</sub> reaction on Ti electrodes, (<b>b</b>) assembled cell window area for capturing the dynamic lithiation/de-lithiation process, (<b>c</b>) schematic diagram for nanobeam diffraction characterization on the SEI layer or residual MoS<sub>2</sub> reaction after the process, and (<b>d</b>) typical example showing bright-field or dark-field image reconstruction of the diffraction pattern [<a href="#B78-molecules-29-04411" class="html-bibr">78</a>]. Figures reproduced with permission from [<a href="#B75-molecules-29-04411" class="html-bibr">75</a>,<a href="#B76-molecules-29-04411" class="html-bibr">76</a>,<a href="#B77-molecules-29-04411" class="html-bibr">77</a>,<a href="#B78-molecules-29-04411" class="html-bibr">78</a>].</p>
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<p>In situ light-induced TEM characterization of energy materials. (<b>A</b>) Schematic representation of integrated optical fiber setup with TEM holder [<a href="#B91-molecules-29-04411" class="html-bibr">91</a>]. (<b>B</b>) Customized fiber connection with cut fiber end projecting inside the microscope vacuum with a 15° angle to avoid optical loss, and the opposite angle cut by 30° to produce a beam that can illuminate the TEM sample [<a href="#B92-molecules-29-04411" class="html-bibr">92</a>]. (<b>C</b>) Schematic representation of in situ light-induced TEM with an integrated gas flow and heating controller inside the compact sample chamber. (<b>D</b>) In situ HRTEM imaging of anatase nanocrystals at 150 °C with/without 1 Torr water pressure: (<b>a</b>–<b>f</b>) diverse experimental conditions starting from no water to fresh water presence even after 40 h in a water/gas environment before exposure to the electron beam [<a href="#B93-molecules-29-04411" class="html-bibr">93</a>]. (<b>E</b>) TEM holder modification with liquid-cell chip arrangement. (<b>a</b>,<b>c</b>,<b>d</b>) schematic representations, (<b>b</b>) liquid cell, and (<b>e</b>) real photograph. (<b>F</b>) HRTEM analysis depicting transition in the morphology of Cu<sub>2</sub>O samples observed at different (<b>a</b>–<b>c</b>) irradiation time intervals such as 1 h, 2 h, 3 h, and (<b>d</b>) schematic showing its evolution over time [<a href="#B95-molecules-29-04411" class="html-bibr">95</a>]. (<b>G</b>) Schematic diagram displaying in situ fabrication of TiO<sub>2</sub>/CdSe nanowire QD solar cell integrated with LED and electrical measurement system in the STM-TEM [<a href="#B8-molecules-29-04411" class="html-bibr">8</a>]. (<b>H</b>) Light-induced rapid phase transformation (through <span class="html-italic">α</span> phase and hydrogen-rich <span class="html-italic">β</span> phase) reaction in the antenna–reactor configuration with illumination at 690 nm (scale bars: 50 nm) visualized over different short time intervals: (<b>a</b>,<b>b</b>) phase transformation at difffernt locations., in both cases (I–V) represents snapshots taken at different time (s) interval. Figures reproduced with permission from [<a href="#B8-molecules-29-04411" class="html-bibr">8</a>,<a href="#B91-molecules-29-04411" class="html-bibr">91</a>,<a href="#B92-molecules-29-04411" class="html-bibr">92</a>,<a href="#B93-molecules-29-04411" class="html-bibr">93</a>,<a href="#B95-molecules-29-04411" class="html-bibr">95</a>,<a href="#B97-molecules-29-04411" class="html-bibr">97</a>].</p>
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<p>In situ Cryo-TEM characterization of MOF nanostructures. (<b>A</b>) Schematic representation of Cryo-TEM technique for MOF nanostructures for monitoring its dynamics under cryogenic conditions [<a href="#B100-molecules-29-04411" class="html-bibr">100</a>]. (<b>B</b>) HRTEM images of (<b>a</b>) MOF-525(Pt) and (<b>b</b>) PCN-224(Pt) (insets: FFT depicting the predominant lattice fringes) [<a href="#B102-molecules-29-04411" class="html-bibr">102</a>]. (<b>C</b>) HRTEM images of (<b>a</b>) intact MOF-5 crystals with inset FFT corresponding to [<a href="#B100-molecules-29-04411" class="html-bibr">100</a>] zone axis orientation as illustrated in (<b>b</b>); the selected inset from the filtered version (<b>c</b>) was simulated noise-free with (<b>d</b>) HRTEM image (thickness 15.5 nm, Δf = +12 nm, Cs +20 μm), and (<b>e</b>) illustrated structure of MOF-5 crystals (white stripes: terephthalate linker, grey color: pores) [<a href="#B103-molecules-29-04411" class="html-bibr">103</a>]. Figures reproduced with permission from [<a href="#B100-molecules-29-04411" class="html-bibr">100</a>,<a href="#B102-molecules-29-04411" class="html-bibr">102</a>,<a href="#B103-molecules-29-04411" class="html-bibr">103</a>].</p>
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<p>In situ Cryo-TEM characterization for SEI layer and Li metal interfaces in rechargeable batteries. (<b>A</b>) The method for preserving and stabilizing Li metal by Cryo-TEM whereby the specimen was placed onto the Cryo-TEM holder while maintaining cryogenic conditions, and during insertion of TEM column the temperature is maintained not above −170 °C. (<b>B</b>) Cryo-TEM observations (<b>a</b>) depicting kinked Li metal dendrite and SEI that changes from &lt;211&gt; to &lt;110&gt; and finally comes back to &lt;211&gt; growth lattice projection, (<b>b</b>) Li deposition on Cu TEM grid and storage under cryogenic conditions, (<b>c</b>) atomic-resolution images showing the transition from (i) &lt;211&gt; to &lt;110&gt; and (ii) &lt;110&gt; changes back to &lt;211&gt; lattice orientation, (<b>d</b>) mosaic model, and (<b>e</b>) multi-layer model of dendritic Li deposition on SEI under different carbonate electrolyte conditions [<a href="#B101-molecules-29-04411" class="html-bibr">101</a>]. (<b>C</b>) Detailed representation of Li dissolution under (<b>a</b>,<b>c</b>,<b>e</b>) mosaic SEI, and (<b>b</b>,<b>d</b>,<b>f</b>) multi-layer SEIs [<a href="#B3-molecules-29-04411" class="html-bibr">3</a>]. (<b>D</b>) Structural composition and elemental mapping of Li dendrites formed at the interface; the morphology was differentiated and analyzed under (<b>a</b>,<b>b</b>) Cryo-FIB, (<b>c</b>,<b>d</b>) Cryo-STEM, and (<b>e</b>,<b>f</b>) Cryo-EELS for type I dendrites and type II dendrites, respectively. Scale bar in (<b>a</b>,<b>b</b>), and (<b>c</b>–<b>f</b>) are equal to 1 µM, and 300 nm, respectively [<a href="#B4-molecules-29-04411" class="html-bibr">4</a>]. Figures reproduced with permission from [<a href="#B3-molecules-29-04411" class="html-bibr">3</a>,<a href="#B4-molecules-29-04411" class="html-bibr">4</a>,<a href="#B101-molecules-29-04411" class="html-bibr">101</a>].</p>
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<p>In situ Cryo-TEM characterization of electron-beam sensitive perovskites. (<b>A</b>) Schematic representation displaying (<b>a</b>) integrated galvanostatic and current-voltage measurements under Cryo-TEM conditions, and (<b>b</b>) five galvanostatic curves between mixed and only electronic states measured at the temperature range from 100 to 295 K. (<b>B</b>) Dynamic changes in optical images of perovskite films from (<b>a</b>–<b>c</b>) dark conditions to 20 mW cm<sup>−2</sup> illumination, (<b>d</b>) schematic illustration depicting the migration of cations MA<sup>+</sup> and anions I<sup>−</sup> through the film [<a href="#B105-molecules-29-04411" class="html-bibr">105</a>]. (<b>C</b>) Drop casting of (<b>a</b>) pristine or UV/moisture-exposed perovskite nanowires onto the TEM grid in nitrogen glove box conditions, in comparison with using (<b>b</b>) Cryo-TEM showing preserved structures, (<b>c</b>) conventional TEM techniques showing electron beam-damaged structures with atomic-level resolution in lattice fringes, (<b>d</b>) TEM image of MAPI<sub>3</sub> NWs after exposing to electron beam, and (<b>e</b>) decomposition of MAPI<sub>3</sub> in to PBI<sub>2</sub> [<a href="#B106-molecules-29-04411" class="html-bibr">106</a>]. Figures reproduced with permission from [<a href="#B105-molecules-29-04411" class="html-bibr">105</a>,<a href="#B106-molecules-29-04411" class="html-bibr">106</a>].</p>
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<p>Overview of diverse methodologies adapted for in situ TEM characterization of energy materials.</p>
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19 pages, 735 KiB  
Article
The Role of Secreted Frizzled-Related Protein 5 (Sfrp5) in Overweight and Obesity in Childhood and Adolescence
by Diamanto Koutaki, George Paltoglou, Maria Manou, Aikaterini Vourdoumpa, Eleni Ramouzi, Anastasia-Maria Tzounakou, Athanasios Michos, Flora Bacopoulou, Emilia Mantzou, Emmanouil Zoumakis, Marina Papadopoulou, Penio Kassari and Evangelia Charmandari
Nutrients 2024, 16(18), 3133; https://doi.org/10.3390/nu16183133 (registering DOI) - 17 Sep 2024
Abstract
Background/Objective: Secreted frizzled-related protein 5 (Sfrp5) is an anti-inflammatory adipokine that has been implicated in the pathophysiology of obesity and its metabolic complications. Despite the fact that numerous studies have been carried out in adults, limited data on Sfrp5 exist for youth, especially [...] Read more.
Background/Objective: Secreted frizzled-related protein 5 (Sfrp5) is an anti-inflammatory adipokine that has been implicated in the pathophysiology of obesity and its metabolic complications. Despite the fact that numerous studies have been carried out in adults, limited data on Sfrp5 exist for youth, especially in relation to overweight and obesity. Methods: In our study, we assessed the concentrations of Sfrp5, total oxidative (TOS) and antioxidative (TAS) status, high-sensitivity C-reactive protein (hs-CRP), and several cytokines (IL-1α, IL-1β, IL-2, IL-6, IL-8, IL-12, TNF-α) in 120 children and adolescents (mean age ± SE: 11.48 ± 0.25 years; 48 prepubertal, 72 pubertal; 74 males and 46 females) before and 1 year after the implementation of a personalized, structured, lifestyle intervention program of healthy diet, sleep, and physical exercise. Results: Based on the body mass index (BMI), participants were categorized as having morbid obesity (n = 63, 52.5%), obesity (n = 21, 17.5%), overweight (n = 22, 18.33%), or normal BMIs (n = 14, 11.67%), based on the International Obesity Task Force (IOTF) cut-off points. Following the 1-year lifestyle intervention program, a significant improvement in anthropometric measurements (BMI, BMI-z score, diastolic blood pressure, WHR, and WHtR), body-composition parameters, hepatic enzymes, lipid profile, inflammation markers, and the insulin-sensitivity profile (HbA1C, HOMA index) was observed in all subjects. Sfrp5 decreased in subjects with obesity (p < 0.01); however, it increased significantly (p < 0.05) in patients with morbid obesity. Linear regression analysis indicates that TNF-α and systolic blood pressure were the best positive predictors and hs-CRP was the best negative predictor for Sfpr5 concentration at initial assessment and glucose concentration for ΔSfrp5, while TNF-α and TAS were the best positive predictors for Sfpr5 concentration at annual assessment. Conclusions: These results indicate that Sfrp5 is associated with severe obesity and is increased following weight loss in children and adolescents with morbid obesity. It is also related to metabolic homeostasis, as well as inflammation and oxidative status. Full article
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<p>Concentrations of Sfrp5 at initial and annual assessment. The asterisk (*) indicates statistically significant difference.</p>
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<p>BMI <span class="html-italic">z</span>-score at initial and annual assessment based on BMI category. *: indicates significant difference from initial assessment. †: indicates significant difference from subjects with morbid obesity. ‡: indicates significant difference from subjects with obesity. #: Indicates significant difference from subjects with overweight.</p>
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10 pages, 434 KiB  
Article
Asthma and Obstructive Sleep Apnea Overlap in a Sample of Older American Indian Adults: The Strong Heart Study
by Huimin Wu, Dorothy A. Rhoades, Jessica A. Reese and Kellie R. Jones
J. Clin. Med. 2024, 13(18), 5492; https://doi.org/10.3390/jcm13185492 (registering DOI) - 17 Sep 2024
Abstract
Study Objectives: Our study aimed to investigate the association between asthma and obstructive sleep apnea (OSA) in American Indian communities, a historically underrepresented population in clinical research with a high prevalence of asthma and OSA risk factors like smoking and obesity. Methods: This [...] Read more.
Study Objectives: Our study aimed to investigate the association between asthma and obstructive sleep apnea (OSA) in American Indian communities, a historically underrepresented population in clinical research with a high prevalence of asthma and OSA risk factors like smoking and obesity. Methods: This cross-sectional study used data retrieved from the Strong Heart Study cohort. Participants who attended both the Asthma Sub-study and the Sleep Heart Health Study around the same time were compared for active asthma diagnosis, OSA diagnosis, and potential risk factors for asthma and OSA. The association between asthma and OSA was then evaluated. Results: Among the 2480 participants who attended the Strong Heart Study Phase III exam, 123 participated in both the Asthma Sub-study and the Sleep Heart Health Study. Of these, 13 were diagnosed with OSA, with 4 having moderate to severe OSA. There was no statistically significant difference in OSA prevalence between the active asthma group and the non-active asthma group (former asthma or no asthma) (9.6% vs. 12.5%, p = 0.63). Additionally, body mass index did not differ significantly between participants with both active asthma and OSA and those without active asthma, OSA, or both. OSA diagnosis was significantly associated with male sex (Odds Ratio [OR] 9.2 [1.85–45.87], p = 0.007) and body mass index (OR 1.1 [1.02–1.26], p = 0.016) but not with age or a diagnosis of active asthma. Conclusions: In this American Indian cohort, no significant difference in OSA prevalence was observed between participants with and without active asthma, contradicting previous studies. Further research is needed to explore the underlying reasons for this discrepancy. Full article
(This article belongs to the Section Pulmonology)
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<p>Participant enrollment.</p>
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13 pages, 348 KiB  
Article
The Role of Social Determinants of Health in Self-Reported Psychological Distress among United States Adults Post-COVID-19 Pandemic
by Kingsley Kalu, Gulzar H. Shah, Elizabeth Ayangunna, Bushra Shah and Nandi Marshall
Int. J. Environ. Res. Public Health 2024, 21(9), 1219; https://doi.org/10.3390/ijerph21091219 (registering DOI) - 17 Sep 2024
Abstract
Psychological distress, an emotional condition with symptoms of anxiety and depression, leads to impaired function, behavior, and personal traits. The current study examined the association between social determinants of health and the severity of psychological distress among adults in the United States after [...] Read more.
Psychological distress, an emotional condition with symptoms of anxiety and depression, leads to impaired function, behavior, and personal traits. The current study examined the association between social determinants of health and the severity of psychological distress among adults in the United States after the COVID-19 pandemic. Using multinomial multivariable logistic regression, we analyzed data from 5106 (n = 5106) participants in the Health Information National Trends Survey (HINTS) 6. Compared to non-Hispanic Whites, African Americans (AOR = 0.62, CI = 0.42–0.93) had lower odds of reporting mild psychological distress rather than no stress. Other variables associated with a higher likelihood of reporting moderate to severe psychological distress, rather than no distress, are being in the 50–64 years age group (AOR = 2.77, CI = 1.45–5.28), divorced (AOR = 2.50, CI = 1.70–3.69), and widowed (AOR = 3.78, CI = 2.15–6.64). Respondents living in an urban area had lower odds of reporting moderate to severe psychological distress (AOR = 0.56, CI = 0.39–0.80) compared to those living in rural areas. Our findings identify several risk factors for psychological distress by sociodemographic characteristics such as age, race, marital status, and urban living, providing empirical evidence for interventions in behavioral health. These findings suggest there is an utmost need for a multi-sectoral approach to address the social determinants of health associated with psychological distress post-COVID-19 pandemic. Full article
14 pages, 2039 KiB  
Article
Metabolomic Effects of Liraglutide Therapy on the Plasma Metabolomic Profile of Patients with Obesity
by Assim A. Alfadda, Anas M. Abdel Rahman, Hicham Benabdelkamel, Reem AlMalki, Bashayr Alsuwayni, Abdulaziz Alhossan, Madhawi M. Aldhwayan, Ghalia N. Abdeen, Alexander Dimitri Miras and Afshan Masood
Metabolites 2024, 14(9), 500; https://doi.org/10.3390/metabo14090500 (registering DOI) - 17 Sep 2024
Abstract
Background: Liraglutide, a long-acting glucagon-like peptide-1 receptor agonist (GLP1RA), is a well-established anti-diabetic drug, has also been approved for the treatment of obesity at a dose of 3 mg. There are a limited number of studies in the literature that have looked at [...] Read more.
Background: Liraglutide, a long-acting glucagon-like peptide-1 receptor agonist (GLP1RA), is a well-established anti-diabetic drug, has also been approved for the treatment of obesity at a dose of 3 mg. There are a limited number of studies in the literature that have looked at changes in metabolite levels before and after liraglutide treatment in patients with obesity. To this end, in the present study we aimed to explore the changes in the plasma metabolomic profile, using liquid chromatography-high resolution mass spectrometry (LC-HRMS) in patients with obesity. Methods: A single-center prospective study was undertaken to evaluate the effectiveness of 3 mg liraglutide therapy in twenty-three patients (M/F: 8/15) with obesity, mean BMI 40.81 ± 5.04 kg/m2, and mean age of 36 ± 10.9 years, in two groups: at baseline (pre-treatment) and after 12 weeks of treatment (post-treatment). An untargeted metabolomic profiling was conducted in plasma from the pre-treatment and post-treatment groups using LC-HRMS, along with bioinformatics analysis using ingenuity pathway analysis (IPA). Results: The metabolomics analysis revealed a significant (FDR p-value ≤ 0.05, FC 1.5) dysregulation of 161 endogenous metabolites (97 upregulated and 64 downregulated) with distinct separation between the two groups. Among the significantly dysregulated metabolites, the majority of them were identified as belonging to the class of oxidized lipids (oxylipins) that includes arachidonic acid and its derivatives, phosphorglycerophosphates, N-acylated amino acids, steroid hormones, and bile acids. The biomarker analysis conducted using MetaboAnalyst showed PGP (a21:0/PG/F1alpha), an oxidized lipid, as the first metabolite among the list of the top 15 biomarkers, followed by cysteine and estrone. The IPA analysis showed that the dysregulated metabolites impacted the pathway related to cell signaling, free radical scavenging, and molecular transport, and were focused around the dysregulation of NF-κB, ERK, MAPK, PKc, VEGF, insulin, and pro-inflammatory cytokine signaling pathways. Conclusions: The findings suggest that liraglutide treatment reduces inflammation and modulates lipid metabolism and oxidative stress. Our study contributes to a better understanding of the drug’s multifaceted impact on overall metabolism in patients with obesity. Full article
(This article belongs to the Special Issue Metabolomics in Human Diseases and Health)
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<p>(<b>A</b>) Receiver operating characteristic (ROC) curve utilizing PLS-DA as the classification and feature ranking method. The top 15 variants had an area under the curve (AUC) of 0.852. (<b>B</b>) Frequency plot showing the top 15 significantly dysregulated metabolites in the pre- and post-liraglutide treatment groups. ROC curves are shown of individual metabolite biomarkers: (<b>C</b>) N-linoleoyl tryptophan, with an AUC of 0.881, and box plot (<span class="html-italic">p</span> ≤ 0.05 and fold change ≥ 1.5), where red represents the post-liraglutide treatment group and green represents the pre-liraglutide treatment group; and (<b>D</b>) epinephrine glucuronide, with an AUC of 0.849, and box plot (<span class="html-italic">p</span> ≤ 0.05 and fold change ≥ 1.5), where red represents the post-liraglutide treatment group and green represents the pre-liraglutide treatment group.</p>
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<p>Schematic representation of the (<b>A</b>) highest scoring network pathways depicting the involvement of the differentially regulated metabolites between the pre- and post-liraglutide treatment groups. The dotted lines indicate indirect relationships, and the straight lines indicate direct relationships. The network pathways identified between the two groups were related to cell signalling, free radical scavenging, and molecular transport, with a score of 36 and 14 focus molecules (represented in bold <a href="#app1-metabolites-14-00500" class="html-app">Supplementary Table S4</a>). The interaction networks were generated through IPA (QIAGEN, Aarhus, Denmark). (<b>B</b>) The top canonical pathways dysregulated after 12 weeks of treatment with liraglutide.</p>
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<p>Schematic representation of the (<b>A</b>) highest scoring network pathways depicting the involvement of the differentially regulated metabolites between the pre- and post-liraglutide treatment groups. The dotted lines indicate indirect relationships, and the straight lines indicate direct relationships. The network pathways identified between the two groups were related to cell signalling, free radical scavenging, and molecular transport, with a score of 36 and 14 focus molecules (represented in bold <a href="#app1-metabolites-14-00500" class="html-app">Supplementary Table S4</a>). The interaction networks were generated through IPA (QIAGEN, Aarhus, Denmark). (<b>B</b>) The top canonical pathways dysregulated after 12 weeks of treatment with liraglutide.</p>
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12 pages, 1204 KiB  
Article
Sperm Migration and Hyaluronic Acid Binding: Implications for Male Fertility Evaluation
by Katarzyna Marchlewska, Marta Erkiert-Kusiak, Renata Walczak-Jędrzejowska and Jolanta Słowikowska-Hilczer
Int. J. Mol. Sci. 2024, 25(18), 9995; https://doi.org/10.3390/ijms25189995 (registering DOI) - 17 Sep 2024
Abstract
Mature, vital, and motile spermatozoa are essential for reaching the oocyte and binding to hyaluronic acid (HA) in the cumulus oophorus matrix. This study aims to determine the relationship between sperm-migration ability and HA-binding potential, as well as the relationship between sperm concentration [...] Read more.
Mature, vital, and motile spermatozoa are essential for reaching the oocyte and binding to hyaluronic acid (HA) in the cumulus oophorus matrix. This study aims to determine the relationship between sperm-migration ability and HA-binding potential, as well as the relationship between sperm concentration and motility. Semen samples were collected from 702 men aged 20–56 years (median 34.8). We evaluated the sperm concentration and motility from basic semen analysis, the swim-up test (expressed as millions per mL and the migration efficiency percentage), and the hyaluronan-binding assay (HBA). A moderate positive correlation was found between the migration test results and HBA (R = 0.48). The highest correlation was observed between the concentration of motile spermatozoa and the migration test results (R = 0.85) and HBA (R = 0.4). The sperm migration efficiency strongly correlated with progressive motility (R = 0.6). Although significantly higher sperm migration was observed in patients with normal HBA results, the results of the functional tests were found to differ in some cases. For infertility treatment, the current diagnostic algorithm should be enhanced with more comprehensive seminological methods that assess the sperm-migration ability and HA-binding potential. We also recommend incorporating the swim-up method into the diagnostic protocol before planning assisted reproductive technology (ART) treatment. Full article
(This article belongs to the Special Issue Male Infertility: From Molecular Mechanisms to Therapeutic Strategies)
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<p>Correlation between the results of the HBA and (<b>A</b>) of the migration test, expressed as post-wash sperm count and (<b>B</b>) efficiency of sperm migration in the swim-up test (S). Blue line—reference value for HBA (Spearman’s R); green line—cut-off value for post-wash sperm count and S in the migration test, established specifically for this study; red line—trend estimation based on linear regression (trend line).</p>
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<p>Results of (<b>A</b>) swim-up test (post-wash sperm count) and (<b>B</b>) efficiency of sperm migration in the swim-up test (S) in groups with normal and &lt;80% HBA results. Mann–Whitney test (<span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>The changes occurring in the hyaluronic acid-binding receptor during the capacitation process.</p>
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12 pages, 1354 KiB  
Article
Neonatal Markers of Prematurity as Predictors of Permanent Childhood Hearing Loss and Neurodevelopmental Impairment in Children Admitted to the Neonatal Intensive Care Unit
by Hayma Moosan, Derek J. Hoare, Dulip Jayasinghe, Karen R. Willis, Katherine Martin and Sally K. Thornton
Brain Sci. 2024, 14(9), 926; https://doi.org/10.3390/brainsci14090926 (registering DOI) - 17 Sep 2024
Abstract
Need for admission to the neonatal intensive care unit (NICU) confers an increased risk of hearing loss in the newborn and of later neurodevelopmental impairment. In this retrospective longitudinal case-controlled study, we assess how the degree of prematurity, measured via gestational age, birth [...] Read more.
Need for admission to the neonatal intensive care unit (NICU) confers an increased risk of hearing loss in the newborn and of later neurodevelopmental impairment. In this retrospective longitudinal case-controlled study, we assess how the degree of prematurity, measured via gestational age, birth weight, and z-scores, in 138 infants admitted to the NICU are associated with permanent childhood hearing loss (PCHI) and 2-year developmental outcomes. Logistic regression analyses, Kruskal–Wallis analysis of variance, and Chi-squared tests were used. Independent of prematurity, PCHI and NICU admission were predictive of poor developmental outcomes. Twenty-one (47%) children with PCHI had a moderate-to-severe developmental delay, compared to three (7%) matched controls. Days in the NICU but not z-scores predicted PCHI. Z-score was not prognostic of moderate or severe developmental impairment in children with PCHI. The odds ratio of moderate-to-severe neurodevelopmental impairment with PCHI was high, at 12.48 [95% CI = 3.37–46.40]. Children with PCHI were significantly more likely to have cerebral palsy than their matched counterparts (30% vs. 2%). These findings challenge the conventional focus on gestational age and birth weight on neurodevelopmental outcomes for children with PCHI and NICU admission. A more nuanced approach to monitoring and intervention is needed. Full article
(This article belongs to the Special Issue Recent Advances in Hearing Impairment)
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<p>Full range of gestational ages and birth weights recorded for PCHI cases and peer-matched controls. Data from the cases with permanent childhood hearing impairment (PCHI) are shown as red symbols, peer-matched controls are shown as blue symbols. The peer-matched controls have also been admitted to the NICU and are matched on birth date, sex, and city location.</p>
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<p>Children with PCHI were more likely to have moderate or severe developmental delay compared to matched controls and were not restricted to the most premature gestational ages. Blue shaded box indicates children who would be suitable for increased surveillance according to local guidelines. Dotted line indicates those children who would be followed up according to national NICE guidance. PCHI = permanent childhood hearing impairment. There was a strong positive correlation (assessed using Spearmen’s correlation) between birth weight and gestational age for cases with PCHI who have normal developmental delay (r<sup>2</sup> = 0.77, <span class="html-italic">p</span> &lt; 0.0001); mild developmental delay (r<sup>2</sup> = 0.77; <span class="html-italic">p</span> = 0.0009); moderate developmental delay (r<sup>2</sup> = 0.95, <span class="html-italic">p</span> &lt; 0.001); and severe developmental delay (r<sup>2</sup> = 0.82; <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Birth weight z-scores were not significantly different between the groups. There were no statistically significant differences in the z-scores between groups (Kruskal–Wallis; <span class="html-italic">p</span> &gt; 0.05). The horizontal bars represent the means, and the error bars the standard deviations. The blue dotted line indicates the z-scores of infants born small for gestational age (z-score &lt; −1.28, 10th percentile) as defined by birth weight, gestational age, and sex.</p>
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<p>Z-scores and centiles for children with PCHI and different degrees of neurodevelopmental impairment. The two plots show the means (horizontal line) ±standard deviations (error bars) for the group with PCHI. Z-scores are shown on the left and centiles for birth weight, gestational age, and sex are shown on the right. The blue dotted line indicates the z-scores of infants born small for gestational age (z-score &lt; −1.28, 10th percentile and centiles &lt; 10%) as defined by birth weight, gestational age, and sex. * Indicates a level of significance of <span class="html-italic">p</span> &lt; 0.05 when comparing the groups with normal/mild developmental delay to those with moderate/severe developmental delay for z-scores and centiles.</p>
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14 pages, 2707 KiB  
Article
Effect of Purified Resveratrol Butyrate Ester Monomers against Hypertension after Maternal High-Fructose Intake in Adult Offspring
by You-Lin Tain, Chih-Yao Hou, Hong-Tai Tzeng, Shu-Fen Lin, Guo-Ping Chang-Chien, Wei-Chia Lee, Kay L. H. Wu, Hong-Ren Yu, Julie Y. H. Chan and Chien-Ning Hsu
Nutrients 2024, 16(18), 3132; https://doi.org/10.3390/nu16183132 (registering DOI) - 17 Sep 2024
Viewed by 46
Abstract
Background: Offspring hypertension arising from adverse maternal conditions can be mitigated through dietary nutritional supplementation, including resveratrol. Previously, we identified derivatives of resveratrol butyrate ester (RBE), specifically 3,4′-di-O-butanoylresveratrol (ED2) and 3-O-butanoylresveratrol (ED4), demonstrating their superior antioxidant capabilities compared to RBE itself. This study [...] Read more.
Background: Offspring hypertension arising from adverse maternal conditions can be mitigated through dietary nutritional supplementation, including resveratrol. Previously, we identified derivatives of resveratrol butyrate ester (RBE), specifically 3,4′-di-O-butanoylresveratrol (ED2) and 3-O-butanoylresveratrol (ED4), demonstrating their superior antioxidant capabilities compared to RBE itself. This study sought to assess the protective impact of maternal supplementation with ED2 or ED4 on offspring hypertension in a rat model subjected to a high-fructose (HF) diet during pregnancy and lactation. Methods: Female Sprague–Dawley rats were distributed into distinct dietary groups throughout pregnancy and lactation: (1) standard chow; (2) HF diet (60%); (3) HF diet supplemented with ED2 (25 mg/L); and (4) HF diet supplemented with ED4 (25 mg/L). Male offspring were euthanized at the age of 12 weeks. Results: The maternal HF diet induced hypertension in the offspring, which was mitigated by perinatal supplementation with either ED2 or ED4. These protective effects were attributed to the antioxidant properties of ED2 and ED4, resulting in an increased availability of nitric oxide (NO). Additionally, supplementation with ED2 was connected to an increased abundance of Bifidobacterium and Clostridium genera, which was accompanied by a decrease in Angelakisella and Christensenella. On the other hand, ED4 supplementation shielded rat offspring from hypertension by elevating concentrations of short-chain fatty acids (SCFAs) and their receptors while reducing trimethylamine-N-oxide (TMAO) levels. Conclusions: These findings highlight the potential of purified RBE monomers, ED2 and ED4, as preventive measures against hypertension resulting from a maternal high-fructose diet. Further research is warranted to explore their clinical applications based on these promising results. Full article
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<p>Effects of ED2 and ED4 on systolic blood pressures in offspring from week 3 to 12. Statistical analysis by a one-way ANOVA with Tukey’s post hoc test. * <span class="html-italic">p</span> &lt; 0.05 vs. ND; # <span class="html-italic">p</span> &lt; 0.05 vs. HF.</p>
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<p>Concentrations of (<b>A</b>) arginine, (<b>B</b>) asymmetric dimethylarginine (ADMA), (<b>C</b>) symmetric dimethylarginine (SDMA), and (<b>D</b>) the ratio of arginine to ADMA (AAR) in the plasma. Statistical analysis by a one-way ANOVA with Tukey’s post hoc test. * <span class="html-italic">p</span> &lt; 0.05 vs. ND; # <span class="html-italic">p</span> &lt; 0.05 vs. HF.</p>
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<p>The assessment of gut microbial community α-diversity is demonstrated in (<b>A</b>) Faith’s phylogenetic diversity (PD) index and (<b>B</b>) the Shannon index. (<b>C</b>) Principal coordinate analysis (PCoA) plots were used to visualize beta diversity, with each data point representing one sample and each color corresponding to a different group. # <span class="html-italic">p</span> &lt; 0.05 vs. HF.</p>
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<p>Linear discriminant analysis effect size (LEfSe) was employed to identify taxa that were significantly differentially abundant between groups. Taxa with a linear discriminant analysis (LDA) score greater than 3 were primarily highlighted. Statistical analysis by the Wilcoxon test.</p>
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<p>Genus-based comparison between the HF and HFED2 group showing relative abundance of (<b>A</b>) <span class="html-italic">Bifidobacterium</span>, (<b>B</b>) <span class="html-italic">Clostridium</span>, (<b>C</b>) <span class="html-italic">Angelakisella</span>, and (<b>D</b>) <span class="html-italic">Christensenella</span>. Genus-based comparison between the HF and HFED4 group showing relative abundance of (<b>E</b>) <span class="html-italic">Angelakisella</span> and (<b>F</b>) <span class="html-italic">Christensenella</span>. The dots represent the outliers. Statistical analysis by using <span class="html-italic">p</span>-values adjusted for multiple comparisons with the false discovery rate (FDR) method. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.005.</p>
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<p>Plasma concentrations of (<b>A</b>) acetate, (<b>B</b>) propionate, (<b>C</b>) butyrate, and (<b>D</b>) mRNA expression of their receptors in rat kidneys, including G protein-coupled receptor 41 (GPR41), GPR43, GPR109A, and olfactory receptor 78 (Oflr78). Statistical analysis by a one-way ANOVA with Tukey’s post hoc test. * <span class="html-italic">p</span> &lt; 0.05 vs. ND; # <span class="html-italic">p</span> &lt; 0.05 vs. HF.</p>
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11 pages, 266 KiB  
Article
Intact FGF23 and Markers of Iron Homeostasis, Inflammation, and Bone Mineral Metabolism in Acute Pediatric Infections
by Eleni Papastergiou, Dimitrios Rallis, Afroditi Papagianni, Vasileios Cholevas, Nikolaos Katzilakis, Ekaterini Siomou, Eftichia Stiakaki and Alexandros Makis
Biology 2024, 13(9), 728; https://doi.org/10.3390/biology13090728 (registering DOI) - 17 Sep 2024
Viewed by 80
Abstract
We intend to evaluate the association of intact Fibroblast Growth Factor 23 (i-FGF23), a phosphaturic hormone that contributes to anemia of inflammation, with markers of iron homeostasis, inflammation, and bone mineral metabolism in acute pediatric infections. Seventy-nine children, aged 1 month–13 years, out [...] Read more.
We intend to evaluate the association of intact Fibroblast Growth Factor 23 (i-FGF23), a phosphaturic hormone that contributes to anemia of inflammation, with markers of iron homeostasis, inflammation, and bone mineral metabolism in acute pediatric infections. Seventy-nine children, aged 1 month–13 years, out of which forty-two were males and thirty-seven females, participated in this study. Children with diseases and nutrient deficiencies causing anemia were excluded. Twenty-six patients had bacterial infections, twenty-six had viral infections, and twenty-seven children served as healthy controls. Complete blood count, markers of inflammation, iron and mineral metabolism, serum hepcidin, and i-FGF23 were compared between the groups. Thirty-nine percent of patients with bacterial infection and twelve percent of patients with viral infection presented characteristics of anemia of inflammation (p < 0.001). Ninety-two percent of patients with bacterial infection and eighty-one percent of patients with viral infection had functional iron deficiency (p < 0.001). Hepcidin was significantly positively correlated with the duration of fever, markers of inflammation, and negatively with iron, mineral metabolism parameters, and i-FGF23. i-FGF23 was positively correlated with iron metabolism parameters and negatively with the duration of fever, markers of inflammation, and hepcidin. Hepcidin levels increase, whereas i-FGF23 levels decrease in acute pediatric infections. Further research is required to understand the role of FGF23 in the hepcidin–ferroportin axis and for hepcidin in the diagnosis of bacterial infections and mineral metabolism. Full article
(This article belongs to the Section Infection Biology)
35 pages, 5486 KiB  
Review
Complex Pathophysiology of Acute Kidney Injury (AKI) in Aging: Epigenetic Regulation, Matrix Remodeling, and the Healing Effects of H2S
by Shreyasi Gupta, Subhadeep Mandal, Kalyan Banerjee, Hebah Almarshood, Sathnur B. Pushpakumar and Utpal Sen
Biomolecules 2024, 14(9), 1165; https://doi.org/10.3390/biom14091165 (registering DOI) - 17 Sep 2024
Viewed by 87
Abstract
The kidney is an essential excretory organ that works as a filter of toxins and metabolic by-products of the human body and maintains osmotic pressure throughout life. The kidney undergoes several physiological, morphological, and structural changes with age. As life expectancy in humans [...] Read more.
The kidney is an essential excretory organ that works as a filter of toxins and metabolic by-products of the human body and maintains osmotic pressure throughout life. The kidney undergoes several physiological, morphological, and structural changes with age. As life expectancy in humans increases, cell senescence in renal aging is a growing challenge. Identifying age-related kidney disorders and their cause is one of the contemporary public health challenges. While the structural abnormalities to the extracellular matrix (ECM) occur, in part, due to changes in MMPs, EMMPRIN, and Meprin-A, a variety of epigenetic modifiers, such as DNA methylation, histone alterations, changes in small non-coding RNA, and microRNA (miRNA) expressions are proven to play pivotal roles in renal pathology. An aged kidney is vulnerable to acute injury due to ischemia-reperfusion, toxic medications, altered matrix proteins, systemic hemodynamics, etc., non-coding RNA and miRNAs play an important role in renal homeostasis, and alterations of their expressions can be considered as a good marker for AKI. Other epigenetic changes, such as histone modifications and DNA methylation, are also evident in AKI pathophysiology. The endogenous production of gaseous molecule hydrogen sulfide (H2S) was documented in the early 1980s, but its ameliorative effects, especially on kidney injury, still need further research to understand its molecular mode of action in detail. H2S donors heal fibrotic kidney tissues, attenuate oxidative stress, apoptosis, inflammation, and GFR, and also modulate the renin–angiotensin–aldosterone system (RAAS). In this review, we discuss the complex pathophysiological interplay in AKI and its available treatments along with future perspectives. The basic role of H2S in the kidney has been summarized, and recent references and knowledge gaps are also addressed. Finally, the healing effects of H2S in AKI are described with special emphasis on epigenetic regulation and matrix remodeling. Full article
(This article belongs to the Special Issue Homocysteine and H2S in Health and Disease)
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<p>Effect of H<sub>2</sub>S in pathophysiological AKI: In the absence or at the low physiological level of H<sub>2</sub>S blood pressure [<a href="#B22-biomolecules-14-01165" class="html-bibr">22</a>,<a href="#B23-biomolecules-14-01165" class="html-bibr">23</a>], oxidative damage [<a href="#B24-biomolecules-14-01165" class="html-bibr">24</a>,<a href="#B25-biomolecules-14-01165" class="html-bibr">25</a>,<a href="#B26-biomolecules-14-01165" class="html-bibr">26</a>], inducible NO synthase [<a href="#B27-biomolecules-14-01165" class="html-bibr">27</a>,<a href="#B28-biomolecules-14-01165" class="html-bibr">28</a>], NF-kB activation [<a href="#B28-biomolecules-14-01165" class="html-bibr">28</a>,<a href="#B42-biomolecules-14-01165" class="html-bibr">42</a>], and apoptosis increase [<a href="#B29-biomolecules-14-01165" class="html-bibr">29</a>,<a href="#B30-biomolecules-14-01165" class="html-bibr">30</a>] and Heme oxygenase 1 decreases [<a href="#B28-biomolecules-14-01165" class="html-bibr">28</a>,<a href="#B31-biomolecules-14-01165" class="html-bibr">31</a>,<a href="#B32-biomolecules-14-01165" class="html-bibr">32</a>] in aging AKI. When H<sub>2</sub>S is supplemented, these changes are reversed (shown on the right side of the schematic images).</p>
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<p>H<sub>2</sub>S production pathway in a cell. In cytosol, L-Methionine is converted into L-homocysteine by S-Adenosylmethionine synthase (SAM) and S-Adenosyl homocysteine hydrolase (SAH). L-homocysteine is condensed with serine by cystathionine β-synthase (CBS) to generate L-cystathionine, which is converted to L-cysteine by cystathionine γ-lyase (CSE). L-cysteine can be used as a substrate by both CBS and CSE to produce hydrogen sulfide (H<sub>2</sub>S). CSE catalyzes H<sub>2</sub>S production by two pathways; one is the conversion of L-homocysteine to L-homolanthionine. Additionally, CSE also catalyzes H<sub>2</sub>S production by the conversion of L-homocysteine to α-ketoglutarate. L-cysteine is transported into mitochondria, and it is converted by aspartate aminotransferase (AAT) in the presence of α-ketoglutarate to form 3-mercaptopyruvate (3-MP) and L-glutamate. Another enzyme, 3-mercaptopyruvate sulfurtransferase (3-MST), contributes to the endogenous H<sub>2</sub>S production in the mitochondria by using 3-mercaptopyruvate (3-MP) as a substrate. Peroxisome resident D-amino acid oxidase (DAO) catalyzes D-cysteine into 3-mercaptopyruvate (3-MP), which is then transported into mitochondria and utilized by 3-MST for the production of H<sub>2</sub>S.</p>
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<p>Effects of H<sub>2</sub>S on renal function. (<b>A</b>) H<sub>2</sub>S inhibits the activity of tubular Na<sup>+</sup>-K<sup>+</sup>-2C<sup>−</sup> channels and Na<sup>+</sup>/K<sup>+</sup>-ATPase channels, thereby enhancing renal excretory function, such as RBF and GFR, and the restoration of the oxygen level. (<b>B</b>) H<sub>2</sub>S as an O<sub>2</sub> sensor in the kidney. In normoxic conditions, H<sub>2</sub>S is metabolized into sulfates in the presence of O<sub>2</sub>; in hypoxic conditions, the shortage of O<sub>2</sub> leads to the accumulation of H<sub>2</sub>S, which helps to restore the O<sub>2</sub> level by enhancing blood flow and suppressing tubular transport activity in the kidney. H<sub>2</sub>S, hydrogen sulfide; RBF, renal blood flow; GFR, glomerular filtration rate; Una.V, urinary sodium; Uk.V, urinary potassium.</p>
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<p>Schematic representation of non-coding RNAs (ncRNAs) that play a role in acute kidney injury (AKI) and subsequent kidney repair. Non-coding RNAs (ncRNAs) are the genome transcripts that function at the RNA level instead of the protein level. AKI, mainly induced by sepsis, renal ischemia-reperfusion, and nephrotoxicity, is pathologically characterized by the injury and death of renal tubular epithelial cells. Complete repair restores the structural integrity and full normal function of the kidney, while maladaptive or incomplete repair leads to chronic pathologies and likely progression to chronic kidney disease (CKD). ncRNAs play regulatory roles in both kidney injury and repair processes, with some being protective and others being pathogenic.</p>
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<p>Schematic overview of canonical and non-canonical biogenesis pathways of miRNA: The canonical miRNA pathway produces Pri-miRNA transcripts from miRNA genes by RNA polymerase II, which is processed into pre-miRNAs by the DROSHA/DGCR8 complex. In the non-canonical pathway, pre-miRNAs are directly produced by the splicing of short introns without DROSHA/DGCR8 processing. After transportation to the cytoplasm via Exportin 5, these pre-miRNAs are converted into a double-stranded miRNA/miRNA duplex by DICER. After that, the mature miRNA integrates into RISC. One strand of this duplex is loaded onto AGO and incorporated into the RNA-induced silencing complex (RISC), leading to gene silencing by mRNA degradation and/or translational repression.</p>
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<p>Two subtypes of macrophages (mφ)-M1 and M2 and their role in AKI. Distinct macrophage phenotypes are involved in renal injury and repair, especially in ischemia-reperfusion injury. Mφ are broadly classified into two subpopulations according to their phenotype and function. So-called “classically activated” pro-inflammatory macrophages (M1) infiltrate the kidney 24 h after reperfusion and contribute to kidney injury. M1 contributes to inflammation by the secretion of cytokines and reactive oxygen species (ROS). M1 also promotes kidney fibrosis through the release of MMP-9. In contrast, “Alternatively” activated anti-inflammatory macrophages (M2) are detected in the kidney 3 days after reperfusion, dampening renal inflammation and promoting tissue repair. M2 macrophages mediate kidney repair by the secretion of Wnt7b, BRP-39, and heme oxygenase-1 (HO-1). Additionally, galectin-3 and TGF-β, released by M2 macrophages, may induce renal fibrosis.</p>
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<p>Schematic diagram showing some of the current therapeutic options of AKI.</p>
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8 pages, 382 KiB  
Article
Standardized Usage of Electronic Patient-Reported Outcome Measurements is Time-Efficient and Feasible
by Thilo Khakzad, Michael Putzier, Alexander Bartschke, Rasim Atakan Poyraz and Nima Taheri
J. Pers. Med. 2024, 14(9), 986; https://doi.org/10.3390/jpm14090986 (registering DOI) - 17 Sep 2024
Viewed by 91
Abstract
(1) Background: Digitization is of the utmost importance in improving the transfer of medical data. In order to emphasize the need for the greater implementation of digital solutions, we compared analog PROMs (aPROMs) to electronic PROMs (ePROMs) to emphasize the time benefits for [...] Read more.
(1) Background: Digitization is of the utmost importance in improving the transfer of medical data. In order to emphasize the need for the greater implementation of digital solutions, we compared analog PROMs (aPROMs) to electronic PROMs (ePROMs) to emphasize the time benefits for clinical everyday life. (2) Methods: This prospective, observational study compared the evaluation of SF-36 in patients between 18 and 80 years old with musculoskeletal pathologies. We performed an age-independent and age-dependent analysis. (3) Results: After the import of aPROMs data, ePROMs took significantly less time (11.97 ± 3.00 min vs. 9.41 ± 3.12 min, p = 0.002, d = 0.797). There were no significant differences associated with age for aPROMs (7.23 ± 2.57 min vs. 8.38 ± 2.71 min, p = 0.061, d = −0.607) or ePROMs (8.72 ± 2.19 min vs. 10.09 ± 3.80 min, p = 0.130, d = −0.436), respectively. (4) Conclusions: This study indicates that ePROMs are a time-feasible method for collecting data to guide patient-personalized treatment approaches. Full article
(This article belongs to the Special Issue Personalized Medicine in Orthopaedics, 2nd Edition)
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<p>Comparison of time needed for completion of aPROMs and ePROMs before and after hospital information system (HIS) import; aPROMs = analog PROMs, ePROMs = digital PROMs; * = <span class="html-italic">p</span> &lt; 0.05.</p>
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Case Report
Unambiguous Interpretation of the Pathogenicity of the GLA c.547+3A>G Variant Causing Fabry Disease
by Mario Urtis, Claudia Cavaliere, Viviana Vilardo, Chiara Paganini, Alexandra Smirnova, Carmelina Giorgianni, Alessandro Di Toro, Luisa Chiapparini, Carlo Pellegrini, Maurizia Grasso and Eloisa Arbustini
Genes 2024, 15(9), 1212; https://doi.org/10.3390/genes15091212 (registering DOI) - 17 Sep 2024
Viewed by 159
Abstract
Objectives: This study aims to demonstrate the role of case-level American College of Medical Genetics (ACMG) criteria, such as familial segregation and pathology data, in providing conclusive evidence for the pathogenicity of ultrarare GLA variants causing Anderson–Fabry disease when gene-level and variant-level criteria [...] Read more.
Objectives: This study aims to demonstrate the role of case-level American College of Medical Genetics (ACMG) criteria, such as familial segregation and pathology data, in providing conclusive evidence for the pathogenicity of ultrarare GLA variants causing Anderson–Fabry disease when gene-level and variant-level criteria provide ambiguous or discrepant results. Case/family description: A 52-year-old woman presented with new-onset shortness of breath, chest pain, and palpitations. Echocardiography revealed mild left ventricular wall thickening (14 mm) and mild diastolic dysfunction. She was the second of three siblings born to unrelated parents, both of whom died from malignancies. Family screening identified brothers, one affected 55-year-old with hypertension and asthma and one unaffected 47-year-old. The 15-year-old son of the proband complained of exercise-induced burning feet acral pain his electrocardiogram showed a short PR interval and signs of early hypertrophy. Results: Endomyocardial biopsies of the proband and the affected sibling demonstrated substrate accumulation (globotriaosylceramide). The anti-α-galactosidase-A immunostain showed a total loss of the enzyme in the hemizygous male and a mosaic pattern in the heterozygous female. The next-generation sequencing short-read multigene panel identified the c.547+3A>G variant in the GLA gene and excluded variants in other genes; Oxford-Nanopore long-read sequencing excluded known pathogenic deep intronic variants. A Multiplex-Ligation-dependent-Probe-Amplification assay excluded copy number variations. Based on the variant-level and gene-level ACMG criteria, the variant was classified as a Variant of Uncertain Significance or Likely Benign using different bioinformatic tools. By adding case-level functional data (endomyocardial biopsy, PS3_VeryStrong) and familial data (segregation of genotype with phenotype, PP2_Moderate), the variant was classified as Likely Pathogenic/Pathogenic. Conclusion: ACMG case-level data can unambiguously resolve uncertain interpretations of GLA variants. Full article
(This article belongs to the Section Human Genomics and Genetic Diseases)
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<p>The figure shows the pedigree (Panel (<b>A</b>)) of the family at the end of the clinical and genetic family screening and specifies the family members’ phenotypes (Panel (<b>B</b>)).</p>
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<p>The figure shows EMB findings from the heterozygous proband (II:2). Panel (<b>A</b>) shows the typical view of the EMB with optically empty myocytes (H&amp;E stain); Panel (<b>B</b>) shows common accompanying, non-substitutive interstitial fibrosis (Movat stain); Panel (<b>C</b>) shows intra-myocyte storage material specifically immuno-stained with anti-GB3 antibodies; Panel (<b>D</b>) shows a toluidine-blue stained semi-thin resin section with the intra-sarcoplasmic substrate accumulation (dark blue); Panel (<b>E</b>) shows the typical osmiophilic lamellar bodies substrate accumulation that are specifically immunogold-labeled with anti-GB3 antibodies in Panel (<b>F</b>).</p>
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<p>The figure shows EMB findings from the hemizygous proband brother (II:1). The findings replicate those observed in the EMB of the sister. Panel (<b>A</b>) shows the typical view of the EMB with optically empty myocytes (H&amp;E stain); Panel (<b>B</b>) shows interstitial fibrosis commonly observed in the affected myocardium (green) (Movat stain); Panel (<b>C</b>) shows intra-myocyte storage material specifically immune-stained with anti-GB3 antibodies; Panel (<b>D</b>) shows toluidine-blue stained semi-thin resin section with the intra-sarcoplasmic substrate accumulation (dark blue); Panel (<b>E</b>) shows the typical osmiophilic lamellar substrate accumulation that is specifically immunolabeled with anti-GB3 antibodies in Panel (<b>F</b>).</p>
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<p>Panel (<b>A</b>) shows the lack of expression of α-Gal A enzyme immunostain in optically empty myocytes of the hemizygous affected male (II:1). Panel (<b>B</b>) shows the mosaic pattern of expression of α-Gal A enzyme in the heterozygous affected female proband (II:2). The enzyme expression is nearly absent in optically empty myocytes indicated by red arrows. Panel (<b>C</b>) shows the ubiquitous expression of the a-Gal enzyme in a control myocardial sample from a donor heart.</p>
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<p>The figure illustrates the application of the scale point system of the ACMG classification to the c.547+3A&gt;G <span class="html-italic">GLA</span> variant. The green dashed line indicates the threshold between the Likely Benign and VUS classes, the orange dashed line indicates the threshold between the VUS and Likely Pathogenic classes, and the red dashed line indicates the threshold between the Likely Pathogenic and Pathogenic classes. The blue boxes indicate the pathogenicity class obtained using only variant-level and gene-level data (blue arrows). Starting from 0 points, Franklin and OSM activate PP3 (+1 point) and PM2 (+2 points) and classify the variant as VUS (3 points), while Varsome activates BP3_Moderate (−2 points) and PM2_Supporting (+1 point) and classifies the variant as Likely Benign (−1 point). The red boxes indicate the final classification obtained after the addition of criteria based on case-level data (red arrows). Family co-segregation meets the PP1_Moderate criterion (+2 point), and EMB functional data, confirmed by splicing assay from PMID: 37254000, meet the PS3_VeryStrong criterion (+8 points). Adding case-level criteria, the final classification changes from VUS to Pathogenic using Franklin and OSM (3 + 10 = 13 points capped to 12 points) and from Likely Benign to Likely Pathogenic using Varsome (−1+ 10 = 9 points).</p>
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