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Search Results (20,749)

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19 pages, 716 KiB  
Review
Genetic Variants of Obesity in Malaysia: A Scoping Review
by Siti Sarah Hamzah, Liyana Ahmad Zamri, Norhashimah Abu Seman and Nur Azlin Zainal Abidin
Genes 2024, 15(10), 1334; https://doi.org/10.3390/genes15101334 (registering DOI) - 17 Oct 2024
Abstract
Background: Obesity is a pressing public health issue in Malaysia, involving not only excess weight but also complex metabolic and physiological changes. Addressing these complexities requires comprehensive strategies, including understanding the population-level differences in obesity susceptibility. This review aims to compile the genetic [...] Read more.
Background: Obesity is a pressing public health issue in Malaysia, involving not only excess weight but also complex metabolic and physiological changes. Addressing these complexities requires comprehensive strategies, including understanding the population-level differences in obesity susceptibility. This review aims to compile the genetic variants studied among Malaysians and emphasize their implications for obesity risk. Methods: Relevant articles published up to March 2024 were extracted from the Scopus, PubMed, and ScienceDirect databases. The review process was conducted in accordance with the PRISMA-ScR guidelines. From an initial pool of 579 articles, 35 of these were selected for the final review. Results: The identified gene variants, including LEPR (K656N), LEP (G2548A—Indian only), ADIPOQ (rs17366568), UCP2 (45bp-I/D), ADRB3 (rs4994), MC3R (rs3827103), PPARγ (pro12Ala—Malay only), IL1RA (intron 2 VNTR), NFKB1 (rs28362491), and FADS1 (rs174547—Indian only), showed significant associations with obesity as measured by the respective studies. Conclusions: Overall, more intensive genetic research is needed, starting with population-based profiling of genetic data on obesity, including among children. Sociocultural contexts and environmental factors influence variations in genetic elements, highlighting the need for targeted interventions to mitigate the impacts of obesity in the population. Full article
(This article belongs to the Special Issue Genetics and Epigenetics of Metabolic Diseases)
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<p>PRISMA flowchart outlining selection process for including studies in the review.</p>
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<p>STRING protein networks of genes associated with monogenic obesity.</p>
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2 pages, 182 KiB  
Correction
Correction: Patias et al. Effect of Liposomal Protium heptaphyllum (Alb.) March Extract in the Treatment of Obesity Induced by High-Calorie Diet. Biology 2024, 13, 535
by Naiéle Sartori Patias, Eveline Aparecida Isquierdo Fonseca de Queiroz, Stela Regina Ferrarini, Gisele Facholi Bomfim, Danilo Henrique Aguiar, Adilson Paulo Sinhorin, Alexandre Aymberé Bello, Geovana Vicentini Fazolo da Silva, Larissa Cavalheiro and Valéria Dornelles Gindri Sinhorin
Biology 2024, 13(10), 833; https://doi.org/10.3390/biology13100833 (registering DOI) - 17 Oct 2024
Abstract
In the original publication [...] Full article
(This article belongs to the Special Issue Physiology and Pathophysiology of Obesity)
11 pages, 488 KiB  
Article
Macronutrients in Human Milk and Early Childhood Growth—Is Protein the Main Driver?
by Jie Ma, Debra J. Palmer, Ching Tat Lai, Susan L. Prescott, Nina D’Vaz, Philip Vlaskovsky, Lisa F. Stinson, Zoya Gridneva and Donna T. Geddes
Nutrients 2024, 16(20), 3514; https://doi.org/10.3390/nu16203514 (registering DOI) - 16 Oct 2024
Abstract
Background: Infant growth trajectories reflect current health status and may predict future obesity and metabolic diseases. Human milk is tailored to support optimal infant growth. However, nutrient intake rather than milk composition more accurately predicts growth outcomes. Although the role of protein leverage [...] Read more.
Background: Infant growth trajectories reflect current health status and may predict future obesity and metabolic diseases. Human milk is tailored to support optimal infant growth. However, nutrient intake rather than milk composition more accurately predicts growth outcomes. Although the role of protein leverage in infant growth is unclear, protein intake is important for early infancy growth. Materials and methods: This study of exclusively breastfeeding mothers with allergies (n = 161) from the Infant Fish Oil Supplementation Study assessed relationships between intake of human milk macronutrients and infant growth. Human milk fat, protein and lactose concentrations were measured at 3 months postpartum, and infant daily intakes were estimated using an average milk intake of 800 mL/day. Results: Higher human milk protein:energy ratio was associated with higher weight-for-age z-score at 2.5 years compared to 3 months and higher body mass index-for-age z-score change (6 months to 1 year compared to 3–6 months). Maternal atopy and birth season (summer) were negatively associated with human milk lactose concentration. Passive smoke exposure was associated with reduced energy and fat concentrations and increased lactose:energy ratio. Conclusions: Our results indicate that intake of human milk macronutrients may impact early childhood growth. Full article
(This article belongs to the Special Issue Prenatal and Early Postnatal Nutrition to Promote Offspring's Health)
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<p>Relationships of macronutrient and energy ratios with total daily energy intake. (<b>a</b>) protein: fat + lactose; (<b>b</b>) protein:fat; (<b>c</b>) protein:lactose. Red colour indicates females and blue indicates males.</p>
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9 pages, 248 KiB  
Brief Report
Severity Profile of COVID-19 in Hospitalized Pediatric Patients
by Vânia Chagas da Costa, Ulisses Ramos Montarroyos, Katiuscia Araújo de Miranda Lopes and Ana Célia Oliveira dos Santos
Children 2024, 11(10), 1249; https://doi.org/10.3390/children11101249 - 16 Oct 2024
Abstract
Objective: We aimed to describe the clinical characteristics associated with severity in children hospitalized with COVID-19. Method: This was an epidemiological cohort study conducted in two hospitals, one of which was a reference center for the treatment of COVID-19 cases. Data were collected [...] Read more.
Objective: We aimed to describe the clinical characteristics associated with severity in children hospitalized with COVID-19. Method: This was an epidemiological cohort study conducted in two hospitals, one of which was a reference center for the treatment of COVID-19 cases. Data were collected from the reports generated by the hospital epidemiology centers and the medical records of patients aged between 0 and 14 years with a diagnosis of COVID-19, hospitalized between March 2020 and June 2021. To analyze the association between the clinical profile and severity, the cases were classified as severe (severe and critical) and non-severe (asymptomatic, mild, and moderate). Results: Of the 191 children followed up in the cohort, 73.3% developed the severe form. The percentage of children with oxygen saturation below 95% was 46.6%. In the multivariate analysis, a higher risk of severity was estimated among children with uncontrolled asthma (RR = 13.2), who were overweight or obese (RR = 3.21), who had cough symptoms (RR = 2.72), and those aged under one year (RR = 3.23). Conclusions: This result underscores the need to improve healthcare at every level for children and for the management of asthma and nutrition when considering children with this clinical profile who are diagnosed with COVID-19. Full article
(This article belongs to the Special Issue COVID-19 and Pediatric Emergency Medicine)
12 pages, 2076 KiB  
Article
Liraglutide Therapy in Obese Patients Alters Macrophage Phenotype and Decreases Their Tumor Necrosis Factor Alpha Release and Oxidative Stress Markers—A Pilot Study
by Łukasz Bułdak, Aleksandra Bołdys, Estera Skudrzyk, Grzegorz Machnik and Bogusław Okopień
Metabolites 2024, 14(10), 554; https://doi.org/10.3390/metabo14100554 - 16 Oct 2024
Abstract
Introduction: Obesity is one of the major healthcare challenges. It affects one in eight people around the world and leads to several comorbidities, including type 2 diabetes, hyperlipidemia, and arterial hypertension. GLP-1 analogs have become major players in the therapy of obesity, [...] Read more.
Introduction: Obesity is one of the major healthcare challenges. It affects one in eight people around the world and leads to several comorbidities, including type 2 diabetes, hyperlipidemia, and arterial hypertension. GLP-1 analogs have become major players in the therapy of obesity, leading to significant weight loss in patients. However, benefits resulting from their usage seem to be greater than simple appetite reduction and glucose-lowering potential. Recent data show better cardiovascular outcomes, which are connected with the improvements in the course of atherosclerosis. Macrophages are crucial cells in the forming and progression of atherosclerotic lesions. Previously, it was shown that in vitro treatment with GLP-1 analogs can affect macrophage phenotype, but there is a paucity of in vivo data. Objective: To evaluate the influence of in vivo treatment with liraglutide on basic phenotypic and functional markers of macrophages. Methods: Basic phenotypic features were assessed (including inducible nitric oxide synthase, arginase 1 and mannose receptors), proinflammatory cytokine (IL-1β, TNFα) release, and oxidative stress markers (reactive oxygen species, malondialdehyde) in macrophages obtained prior and after 3-month therapy with liraglutide in patients with obesity. Results: Three-month treatment with subcutaneous liraglutide resulted in the alteration of macrophage phenotype toward alternative activation (M2) with accompanying reduction in the TNFα release and diminished oxidative stress markers. Conclusions: Our results show that macrophages in patients treated with GLP-1 can alter their phenotype and function. Those findings may at least partly explain the pleiotropic beneficial cardiovascular effects seen in subjects treated with GLP-1 analogs. Full article
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<p>Flowchart of the study.</p>
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<p>Basic phenotypical features of macrophages during the course of in vivo treatment with liraglutide and ex vivo challenge with LPS. The expression of mRNA for <span class="html-italic">NOS2</span> (<b>a</b>), <span class="html-italic">ARG1</span> (<b>b</b>), and <span class="html-italic">MRC1</span> (<b>c</b>). Protein expression of iNOS (<b>d</b>), arg1 (<b>e</b>), and MR (<b>f</b>). Representative Western blots for assessment of protein expression (<b>g</b>). Immunofluorescent staining of macrophages for iNOS and MR (<b>h</b>). Bar represents 50 µm (<span class="html-italic">n</span> = 3–7). *—<span class="html-italic">p</span> &lt; 0.05; **—<span class="html-italic">p</span> &lt; 0.01. Abbreviations: <span class="html-italic">ARG1</span>/arg1—arginase 1; <span class="html-italic">NOS2</span>/iNOS—inducible nitric oxide; LPS—lipopolysaccharide; <span class="html-italic">MRC1</span>/MR—mannose receptor; ROS—relative optical density; RU—relative units.</p>
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<p>Markers of proinflammatory response: TNFα (<b>a</b>) and IL-1β (<b>b</b>) (<span class="html-italic">n</span> = 7). *—<span class="html-italic">p</span> &lt; 0.05; **—<span class="html-italic">p</span> &lt; 0.01. Abbreviation: LPS—lipopolysaccharide.</p>
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<p>Markers of oxidative stress: reactive oxygen species (<b>a</b>) and malondialdehyde (<b>b</b>) (<span class="html-italic">n</span> = 8). *—<span class="html-italic">p</span> &lt; 0.05; **—<span class="html-italic">p</span> &lt; 0.01. Abbreviation: LPS—lipopolysaccharide.</p>
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14 pages, 775 KiB  
Article
Nutritional Status, Diet, and Intestinal Permeability of Mexican Children with Autism Spectrum Disorders
by Karina Alejandra Pedroza-García, Miriam Aracely Anaya-Loyola, Dolores Ronquillo, María del Carmen Caamaño, David Masuoka, Jorge Palacios-Delgado and Jorge L. Rosado
Gastroenterol. Insights 2024, 15(4), 912-925; https://doi.org/10.3390/gastroent15040064 (registering DOI) - 16 Oct 2024
Abstract
Introduction: Autism spectrum disorder (ASD) comprises a group of developmental disorders characterized by deficits in social interaction and behavioral patterns. Children with ASD may face nutritional challenges, primarily due to their restrictive behaviors and frequent gastrointestinal issues. Objective: The objective of the present [...] Read more.
Introduction: Autism spectrum disorder (ASD) comprises a group of developmental disorders characterized by deficits in social interaction and behavioral patterns. Children with ASD may face nutritional challenges, primarily due to their restrictive behaviors and frequent gastrointestinal issues. Objective: The objective of the present study was to assess nutritional status, dietary habits, and intestinal permeability in a sample of individuals with ASD. Methods: A cross-sectional study was conducted with 24 children and adolescents (both sexes), aged 4 to 18 years, living in two cities of Mexico (Aguascalientes and Querétaro). Weight and height were measured, and body mass index for age was calculated and compared using WHO Z-scores. Diet was assessed through three 24 h dietary recalls and a food frequency questionnaire. Intestinal permeability was evaluated using a lactulose/mannitol test by HPLC. Results: A high prevalence of malnutrition was observed; 12.5% of the participants were underweight, and 45.8% were overweight or obese. Children had a low intake of fiber, vitamin E, folate, potassium, zinc, and phosphorus and a high intake of sodium. On average, the intestinal permeability ratio was 0.09 ± 0.05, with 54.2% of the children exhibiting high intestinal permeability. Conclusions: It is advisable to develop food counseling strategies for children with ASD to prevent micronutrient deficiencies, promote healthy weight, and improve gastrointestinal integrity. Full article
(This article belongs to the Section Gastrointestinal Disease)
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<p>Evaluation of body mass index-for-age (BMI/A) indicator in children and adolescents with ASD (Z-scores interpretation). (<b>A</b>) BMI/A in 4-to-8-year-old children (n = 9); (<b>B</b>) BMI/A in 9-to-13-year-old children (n = 9); (<b>C</b>) BMI/A in 14-to-18-year-old children (n = 6).</p>
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<p>Comparison of energy and macronutrient intake stratified by age group in children and adolescents with ASD. (<b>A</b>) Comparison of total energy intake (TEI) by age group. (<b>B</b>) Comparison of carbohydrate intake by age groups. (<b>C</b>) Comparison of protein intake by age groups. (<b>D</b>) Comparison of lipid intake by age groups. Data are presented as mean and SEM. Statistical test used: ANOVA, significance at <span class="html-italic">p</span> &lt; 0.05. ns: not significant.</p>
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15 pages, 1910 KiB  
Article
Effects of Chitosan and N-Succinyl Chitosan on Metabolic Disorders Caused by Oral Administration of Olanzapine in Mice
by Balzhima Shagdarova, Viktoria Melnikova, Valentina Kostenko, Mariya Konovalova, Vsevolod Zhuikov, Valery Varlamov and Elena Svirshchevskaya
Biomedicines 2024, 12(10), 2358; https://doi.org/10.3390/biomedicines12102358 - 16 Oct 2024
Abstract
Background: The issue of human mental health is gaining more and more attention nowadays. However, most mental disorders are treated with antipsychotic drugs that cause weight gain and metabolic disorders, which include olanzapine (OLZ). The search for and development of natural compounds for [...] Read more.
Background: The issue of human mental health is gaining more and more attention nowadays. However, most mental disorders are treated with antipsychotic drugs that cause weight gain and metabolic disorders, which include olanzapine (OLZ). The search for and development of natural compounds for the prevention of obesity when taking antipsychotic drugs is an urgent task. The biopolymer chitosan (Chi) and its derivatives have lipid-lowering and anti-diabetic properties, which makes them potential therapeutic substances for use in the treatment of metabolic disorders. The purpose of this work was to analyze the effect of the natural biopolymer Chi, its derivative N-succinyl chitosan (SuChi), and Orlistat (ORL) as a control on the effects caused by the intake of OLZ in a mouse model. Methods: Mice were fed with pearl barley porridge mixed with OLZ or combinations OLZ + Chi, OLZ + SuChi, or OLZ + ORL for 2 months. The weight, lipid profile, blood chemokines, expression of genes associated with appetite regulation, and behavior of the mice were analyzed in dynamics. Results: For the first time, data were obtained on the effects of Chi and SuChi on metabolic changes during the co-administration of antipsychotics. Oral OLZ increased body weight, food and water intake, and glucose, triglyceride, and cholesterol levels in blood. ORL and SuChi better normalized lipid metabolism than Chi, decreasing triglyceride and cholesterol levels. OLZ decreased the production of all chemokines tested at the 4th week of treatment and increased CXCL1, CXCL13, and CCL22 chemokine levels at the 7th week. All of the supplements corrected the level of CXCL1, CXCL13, and CCL22 chemokines but did not recover suppressed chemokines. SuChi and ORL stimulated the expression of satiety associated proopiomelanocortin (POMC) and suppressed the appetite-stimulating Agouti-related protein (AgRP) genes. All supplements improved the locomotion of mice. Conclusions: Taken collectively, we found that SuChi more than Chi possessed an activity close to that of ORL, preventing metabolic disorders in mice fed with OLZ. As OLZ carries positive charge and SuChi is negatively charged, we hypothesized that SuChi’s protective effect can be explained by electrostatic interaction between OLZ byproducts and SuChi in the gastrointestinal tract. Full article
(This article belongs to the Special Issue Advanced Research in Metabolic Syndrome)
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<p>Stack of <sup>1</sup>H NMR spectra of (<b>a</b>) chitosan and (<b>b</b>) <span class="html-italic">N</span>-succinyl chitosan.</p>
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<p>Effects of olanzapine (OLZ) and food supplements on body weight, glucose level, and water and food intake. Mice were fed with pearl barley porridge mixed with dry OLZ only or supplemented with chitosan (Chi), <span class="html-italic">N</span>-succinyl chitosan (SuChi), or orlistat (ORL). (<b>a</b>) Body weight was calculated as a ratio to the weight at the start of the experiment for each mouse and averaged. (<b>b</b>) Glucose level was estimated in the blood at the 4th and 7th weeks of the experiment. (<b>c</b>,<b>d</b>) Water (<b>c</b>) and food (<b>d</b>) intake were measured once a week from the 1st to 4th (4 weeks) and 5th to 8th weeks (7 weeks) per group of five mice and averaged. Data are shown as the mean ± SEM. Significant differences (<span class="html-italic">p</span> &lt; 0.05, Mann–Whitney) are shown by brackets.</p>
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<p>Effects of olanzapine (OLZ) and food supplements on lipid metabolism. Triglyceride (<b>a</b>), total cholesterol (<b>b</b>), high density lipoproteins (HDL) (<b>c</b>), low density lipoproteins (LDL) (<b>d</b>), and LDL to HDL ratios at the 4th (<b>e</b>) and 7th (<b>f</b>) weeks of the treatment in the blood of mice fed with dry OLZ only or supplemented with chitosan (Chi), <span class="html-italic">N</span>-succinyl chitosan (SuChi), or orlistat (ORL). Data are shown as mean ± SEM. Significant differences (<span class="html-italic">p</span> &lt; 0.05, Mann–Whitney) are shown by brackets.</p>
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<p>Effects of olanzapine (OLZ) and food supplements on blood chemokines. (<b>a</b>–<b>c</b>) Intact blood homeostatic chemokine concentrations (<b>a</b>) and the effect of OLZ and the combination of OLZ with chitosan (Chi), <span class="html-italic">N</span>-succinyl chitosan (SuChi), or orlistat (ORL) at week 4 (<b>b</b>) or 7 (<b>c</b>). (<b>d</b>–<b>f</b>) Intact blood inducible chemokine concentrations (<b>d</b>) and OLZ and OLZ plus the supplements at weeks 4 (<b>e</b>) and 7 (<b>f</b>) of the treatment. Data are shown and mean ± SEM (<b>a</b>) or as the ratios of experimental sample concentrations to the control intact blood ones. Significant differences (<span class="html-italic">p</span> &lt; 0.05, Mann–Whitney) are shown by brackets only for the increased by OLZ chemokines.</p>
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<p>Expression of appetite-associated genes in the hypothalamus of olanzapine-treated mice. (<b>a</b>) Scheme of hypothalamic isolation. Incisions were made rostrally (r) at the level of the optic chiasma and caudally (c) along the pituitary pedicle, dorsally along the border of the third ventricle (3v). The drawing was created using the BioRender program (<a href="https://app.biorender.com" target="_blank">https://app.biorender.com</a>). (<b>b</b>–<b>f</b>) An analysis of gene expression associated with metabolic changes in the hypothalamus of mice treated orally with olanzapine (OLZ) alone and in combination with orlistat (OLZ-ORL), chitosan (OLZ-Chi), or <span class="html-italic">N</span>-succinyl chitosan (OLZ-SuChi). Data are shown as the relative expression calculated as DeltaCt<sub>experiment</sub>/DeltaCt<sub>control</sub>, where experiment corresponds to OLZ-treated samples and control corresponds to intact mice. Significant differences (<span class="html-italic">p</span> &lt; 0.05, Mann–Whitney) are shown by brackets.</p>
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<p>Effect of olanzapine (OLZ) and food supplementation on the locomotion and rearings of mice in an open field test (OFT). Mice fed with OLZ alone or supplemented with chitosan (Chi), <span class="html-italic">N</span>-succinyl chitosan (SuChi), or orlistat (ORL) were run for 4 min in an OFT (3 min in the light and the last min in the dark, shown by the gray bar). (<b>a</b>,<b>b</b>) Number of sectors crossed at the 4th (<b>a</b>) and 7th (<b>b</b>) weeks. (<b>c</b>,<b>d</b>) Total number of rearing at the 4th (<b>c</b>) and 7th (<b>d</b>) weeks. Significant differences (<span class="html-italic">p</span> &lt; 0.05, Mann–Whitney) are shown by brackets (* in (<b>a</b>)).</p>
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16 pages, 1324 KiB  
Article
Association between Serum Fatty Acids Profile and MetScore in Women with Severe Obesity
by Emilly Santos Oliveira, Fabiana Martins Kattah, Glaucia Carielo Lima, Maria Aderuza Horst, Nayra Figueiredo, Gislene Batista Lima, Renata Guimarães Moreira Whitton, Gabriel Inacio de Morais Honorato de Souza, Lila Missae Oyama, Erika Aparecida Silveira and Flávia Campos Corgosinho
Nutrients 2024, 16(20), 3508; https://doi.org/10.3390/nu16203508 - 16 Oct 2024
Abstract
Background: Metabolic syndrome (MetS) is a set of conditions associated with an increased cardiovascular risk. Several serum fatty acids (FAs) seem to play an essential role in the development of cardiometabolic diseases and mortality. Thus, it is imperative to explore the impact of [...] Read more.
Background: Metabolic syndrome (MetS) is a set of conditions associated with an increased cardiovascular risk. Several serum fatty acids (FAs) seem to play an essential role in the development of cardiometabolic diseases and mortality. Thus, it is imperative to explore the impact of FAs on MetS parameters, using an early MetS screening tool such as MetScore, which is readily available in clinical practice. Aim: The aim of this study was to assess the potential correlation between serum FAs and cardiovascular risk using a MetScore. Methods: This cross-sectional study involved 41 women with severe obesity. The MetScore was calculated, and participants were categorized into high- and low-cardiovascular-risk groups based on the median MetScore value. Gas chromatography was used to quantify serum FAs. Generalized Linear Models were used to compare group means. The association was assessed through simple logistic regression, and an adjusted logistic regression was conducted to validate the association between Metscore and serum FAs. Results: The high-cardiovascular-risk group exhibited elevated values of HOMA-IR, palmitic, oleic, cis-vaccenic, and monounsaturated fatty acids, as well as the SCD-18C, indicating a heightened cardiovascular risk. Conversely, HDL-c, QUICK, gamma-linolenic, and eicosatetraenoic fatty acids showed lower values compared to the low-risk group. Conclusions: Women with severe obesity and high cardiovascular risk have lower values of some omega-3 and omega-6 FAs, considered cardioprotective and anti-inflammatory, and have higher lipogenic activity and FAs, correlated with high cardiovascular risk. These findings emphasize the need to address lipid metabolism in this population as a therapeutic target to reduce cardiovascular risk. Future research should explore clinical interventions that modulate fatty acid metabolism to mitigate cardiometabolic complications. Full article
(This article belongs to the Section Nutrition in Women)
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<p>Graphical illustration of the study design: stages of participant recruitment and data collection.</p>
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<p>Illustration of linoleic acid bioconversion pathway, eicosanoid synthesis, and cardiovascular risk. Green arrows: anti-inflammatory pathways; Red arrow: inflammatory pathways.</p>
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<p>The mechanism by which PUFA [n3] decreases triacylglycerol biosynthesis.</p>
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21 pages, 1748 KiB  
Review
The Role of Dietary Ingredients and Herbs in the Prevention of Non-Communicable Chronic Liver Disease
by Monika Maćków, Tomasz Dziubyna, Tatiana Jamer, Dmytro Slivinskyi, Tomasz Pytrus, Katarzyna Neubauer, Małgorzata Zwolińska-Wcisło, Andrzej Stawarski, Ewa Piotrowska and Dorian Nowacki
Nutrients 2024, 16(20), 3505; https://doi.org/10.3390/nu16203505 - 16 Oct 2024
Abstract
Background: Liver diseases are among the most commonly diagnosed conditions, with the main risk factors being inappropriate lifestyles, including poor diet, excessive alcohol consumption, low physical activity and smoking, including electronic cigarettes. Non-communicable chronic liver diseases also often develop as a result of [...] Read more.
Background: Liver diseases are among the most commonly diagnosed conditions, with the main risk factors being inappropriate lifestyles, including poor diet, excessive alcohol consumption, low physical activity and smoking, including electronic cigarettes. Non-communicable chronic liver diseases also often develop as a result of accompanying overweight and obesity, as well as type 2 diabetes. Methods: The literature on risk factors for non-communicable chronic liver diseases, which show a high strong influence on their occurrence, was analysed. Results: Measures to prevent non-communicable chronic liver disease include the selection of suitable food ingredients that have proven protective effects on the liver. Such ingredients include dietary fibre, probiotics, herbs, various types of polyphenols and fatty acids (omega-3). Conclusions: Because of their liver-protective effects, nutritionists recommend consuming vegetables, fruits, herbs and spices that provide valuable ingredients with anti-inflammatory and anti-cancer effects. These components should be provided with food and, in the case of probiotics, supplementation appears to be important. As a preventive measure, a diet rich in these nutrients is therefore recommended, as well as one that prevents overweight and other diseases that can result in liver disease. Full article
(This article belongs to the Special Issue Nutrition in the Liver Damage)
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<p>Negative and positive factors influencing the development of non-communicable chronic liver diseases.</p>
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<p>Schematic representation of key herbal components in liver disease prevention. Signs: ↑ increasees, ↓ decreases.</p>
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10 pages, 746 KiB  
Article
Growth Parameters and Prevalence of Obesity in PKU Patients and Peers: Is This the Right Comparison?
by Giulia Paterno, Vito Di Tullio, Rosa Carella, Giada De Ruvo, Fabrizio Furioso, Aleksandra Skublewska-D’Elia, Donatella De Giovanni and Albina Tummolo
Pediatr. Rep. 2024, 16(4), 892-901; https://doi.org/10.3390/pediatric16040076 (registering DOI) - 16 Oct 2024
Abstract
Background: One of the main objectives of Phenylketonuria (PKU) management is represented by optimising the growth trend under restricted protein diet regimen. The data on long-term growth in PKU children are limited and mostly based on earlier studies. Methods: The data for this [...] Read more.
Background: One of the main objectives of Phenylketonuria (PKU) management is represented by optimising the growth trend under restricted protein diet regimen. The data on long-term growth in PKU children are limited and mostly based on earlier studies. Methods: The data for this twelve-year longitudinal study were collected from 34 PKU children and 37 healthy peers, whose auxological parameters were taken at 7 time-points over the follow-up. The weight-for-length ratio (WLR) z-score and body mass index (BMI) z-score were considered according to age. Prevalence of overweight/obesity was evaluated at last assessment. Results: The median BMI z-score of PKU children was normal and not statistically different from that of controls on all the seven time-point assessments. Their distributions tended to be wider than those of peers, with the upper limit exceeding the normal range since 12 months old, with a peak specifically at 3 years of age. In controls, there was a tendency to approach the BMI z-score values of overweight in later childhood. The prevalence of overweight was comparable (29% vs. 25%, p: 0.78) between the two groups at last assessment, and obese subjects (3/37) were only detected in the control group. Conclusions: In this study, we report data from a long-term follow-up on growth, highlighting that the median BMI z-score of PKU children was normal and not statistically different from that of controls. Also, the prevalence of obesity at 12 years of age was overlapping. However, the high prevalence of overweight children in the general population may explain the lack of difference and does not reassure about patients’ nutritional risk. Full article
(This article belongs to the Section Inborn Errors and Neonatal Screening)
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<p>BMI z-score trends at the 7 time-points for patients and controls.</p>
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<p>Pie charts on BMI z-score category percentage at last assessment.</p>
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33 pages, 12115 KiB  
Article
Effects of Nitric Oxide on Bladder Detrusor Overactivity through the NRF2 and HIF-1α Pathways: A Rat Model Induced by Metabolic Syndrome and Ovarian Hormone Deficiency
by Hung-Yu Lin, Jian-He Lu, Rong-Jyh Lin, Kuang-Shun Chueh, Tai-Jui Juan, Jing-Wen Mao, Yi-Chen Lee, Shu-Mien Chuang, Mei-Chen Shen, Ting-Wei Sun and Yung-Shun Juan
Int. J. Mol. Sci. 2024, 25(20), 11103; https://doi.org/10.3390/ijms252011103 - 16 Oct 2024
Abstract
Metabolic syndrome (MetS) includes cardiovascular risk factors like obesity, dyslipidemia, hypertension, and glucose intolerance, which increase the risk of overactive bladder (OAB), characterized by urgency, frequency, urge incontinence, and nocturia. Both MetS and ovarian hormone deficiency (OHD) are linked to bladder overactivity. Nitric [...] Read more.
Metabolic syndrome (MetS) includes cardiovascular risk factors like obesity, dyslipidemia, hypertension, and glucose intolerance, which increase the risk of overactive bladder (OAB), characterized by urgency, frequency, urge incontinence, and nocturia. Both MetS and ovarian hormone deficiency (OHD) are linked to bladder overactivity. Nitric oxide (NO) is known to reduce inflammation and promote healing but its effect on bladder overactivity in MetS and OHD is unclear. This study aimed to investigate NO’s impact on detrusor muscle hyperactivity in rats with MetS and OHD. Female Sprague-Dawley rats were divided into seven groups based on diet and treatments involving L-arginine (NO precursor) and L-NAME (NOS inhibitor). After 12 months on a high-fat, high-sugar diet with or without OVX, a cystometrogram and tracing analysis of voiding behavior were used to identify the symptoms of detrusor hyperactivity. The MetS with or without OHD group had a worse bladder contractile response while L-arginine ameliorated bladder contractile function. In summary, MetS with or without OHD decreased NO production, reduced angiogenesis, and enhanced oxidative stress to cause bladder overactivity, mediated through the NF-kB signaling pathway, whereas L-arginine ameliorated the symptoms of detrusor overactivity and lessened oxidative damage via the NRF2/HIF-1α signaling pathway in MetS with or without OHD-induced OAB. Full article
(This article belongs to the Section Molecular Biology)
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<p>L-arginine treatment ameliorated fatty liver and improved serum parameters in rats. The changes in liver morphology (<b>A</b>–<b>G</b>) and physical indicators (<b>H</b>) after 12 months of standard diet feeding (control group, <b>A</b>) and HFHS diet feeding without OVX in the MetS group (<b>B</b>), the MetS + L-arginine group (<b>C</b>), and the MetS + L-NAME group (<b>D</b>) were shown, as were HFHS diet feeding with OVX in the MetS + OVX group (<b>E</b>), the MetS + OVX + L-arginine group (<b>F</b>), and the MetS + OVX + L-NAME group (<b>G</b>). (<b>A</b>–<b>G</b>): The control group (<b>A</b>) exhibited a dark red liver appearance. However, the liver photographs after MetS with or without OVX displayed a fatty and swollen liver appearance. Particularly, liver appearance in the MetS + OVX group (<b>E</b>) and the MetS + OVX + L-NAME group (<b>G</b>) was obviously fatty and edematous. However, the appearance of the MetS + L-arginine group showed signs of improvement compared to other groups, suggesting a beneficial effect of L-arginine treatment. (<b>H</b>): Serum parameters were significantly elevated in the MetS with or without HFHS diet feeding groups as compared to the control group, including GOT, GPT, triglycerides, cholesterol, LDL, glucose, and LDH (except insulin level). Treatment with L-arginine decreased the levels in the MetS + L-arginine group and the MetS + OVX + L-arginine group. Note: GOT, glutamate oxaloacetate transaminase; GPT, glutamate pyruvate transaminase; HDL, high-density lipoprotein; LDL, low-density lipoprotein; OHD, ovarian hormone deficiency. Data were expressed as mean ± SD for <span class="html-italic">n</span> = 6. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 versus the control group. <sup>†</sup> <span class="html-italic">p</span> &lt; 0.05; <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05; <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS + OVX group.</p>
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<p>L-arginine improved voiding behavior and alleviated detrusor hyperactivity in a rat model. Urodynamic analysis of cystometric parameters (<b>A</b>), including micturition pressure (<b>A</b>,<b>C</b>), voiding frequency, contraction (arrows), and non-voiding contraction (asterisks), in the different groups. Tracing analysis of 24-h voiding behavior by metabolic cage, including voiding frequency (<b>B</b>,<b>D</b>) and volume (<b>B</b>,<b>E</b>) in the different groups. The MetS + OVX group exhibited increased bladder micturition pressure, voiding contractions, non-voiding contractions, and micturition frequency, whereas the L-arginine groups showed an improved bladder voiding pattern and volume. Note: MetS, metabolic syndrome; OHD, ovarian hormone deficiency. Data were expressed as mean ± SD for <span class="html-italic">n</span> = 6. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 versus the control group. <sup>†</sup> <span class="html-italic">p</span> &lt; 0.05; <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 versus the MetS + OVX group.</p>
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<p>L-arginine treatment improved the bladder detrusor contractile response. After 12-month HFHS feeding with or without OVX, bladder strips induced by EFS (<b>A</b>,<b>E</b>), carbachol (<b>B</b>,<b>E</b>), KCl (<b>C</b>,<b>E</b>), and ATP (<b>D</b>,<b>E</b>) in the MetS group, the MetS + L-NAME group, the MetS + OVX group, and the MetS + OVX + L-NAME group, they had higher contractile responses compared with the control group, whereas the MetS + L-arginine and MetS + OVX + L-arginine groups demonstrated significantly lower contractile responses compared to the MetS and MetS + OVX groups. L-arginine treatment significantly ameliorated the detrusor contractile response to various forms of stimulation in the MetS + L-arginine group and the MetS + OVX + L-arginine group. Note: EFS, electrical field stimulation; OVX, bilateral ovariectomy. Data were expressed as mean ± SD for <span class="html-italic">n</span> = 6. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 versus the control group. <sup>†</sup> <span class="html-italic">p</span> &lt; 0.05; <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05; <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS + OVX group.</p>
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<p>The bladder pathological features induced by the HFHS diet and OHD were shown by Masson’s trichrome staining and fibrosis marker expressions. (<b>A</b>–<b>G</b>): Bladder pathological features of the control group (<b>A</b>,<b>A’</b>), the MetS group (<b>B</b>,<b>B’</b>), the MetS + L-arginine group (<b>C</b>,<b>C’</b>) the MetS + L-NAME group (<b>D</b>,<b>D’</b>), the MetS + OVX group (<b>E</b>,<b>E’</b>), the MetS + OVX + L-arginine group (<b>F</b>,<b>F’</b>), and the MetS + OVX + L-NAME group (<b>G</b>,<b>G’</b>). Masson’s trichrome staining revealed red-stained smooth muscle and green-stained collagen. In the control group (<b>A</b>), there were three to five layers of the urothelium (UL, black arrows) with sparse collagen (green arrows) distributed in the submucosal layer (SL, lamina propria). In the MetS + OVX group (<b>B</b>), the morphology was characterized by a thinner UL (black arrows) and increased interstitial fibrosis (green arrows). In contrast, the MetS + L-arginine group (<b>C</b>) and the MetS + OVX + L-arginine group (<b>F</b>) exhibited an improved bladder condition with a thicker UL (black arrows) and reduced interstitial fibrosis (green arrows), compared to the MetS group (<b>B</b>) and the MetS + OVX group (<b>E</b>). The MetS + OVX group also showed increased bladder fibrosis (arrows), denuded urothelial mucosa (arrowheads), and a thinning UL. Therapeutic effects of NO improved pathological alteration induced by MetS with or without OHD. (<b>A</b>–<b>G</b>), magnification × 200; Scale bar (grey) = 200 μm.; (<b>A’</b>–<b>G’</b>), magnification × 400; Scale bar (grey) = 100 μm. (<b>H</b>,<b>I</b>): Western Blots for fibrosis marker expression were measured by TGF-β1, fibronectin, and type I collagen in each group. Compared to the control group, the expression of TGF-β1, fibronectin, and type I collagen proteins was significantly elevated in the MetS group compared to the MetS + L-arginine group, as well as in the MetS + OVX group compared to the MetS + OVX + L-arginine group. Therefore, L-arginine administration greatly decreased fibrosis marker expression. Quantifications of the percentage of TGF-β1, fibronectin, and type I collagen expressions to β-actin were shown. Results were normalized as the control = 100%. Note: MetS, metabolic syndrome; ML, muscular layer; OVX, bilateral ovariectomy; OHD, ovarian hormone deficiency; SL, suburothelial layer; UL, urothelial layer. Data were expressed as mean ± SD for <span class="html-italic">n</span> = 6. ** <span class="html-italic">p</span> &lt; 0.01 versus the control group. <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS group. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS + OVX group.</p>
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<p>L-arginine improved bladder urothelial regeneration and interstitial cell generation. In a rat model of MetS with or without OHD-induced detrusor hyperactivity, urothelial marker (E-Cadherin), cell proliferating proteins (CK14), and IC markers (C-Kit, vimentin, and PDGFR) were quantified by immunostaining (<b>A</b>–<b>G</b>) and Western Blots (<b>H</b>,<b>I</b>). (<b>A</b>–<b>G</b>): In the control group (<b>A</b>), E-Cadherin staining showed the urothelial layer (UL; yellow arrows) consisting of three to five layers. However, following a HFHS diet with or without OVX, the bladders displayed a thinner and defective urothelial mucosa in the UL. Morphological evaluation in the MetS + L-arginine group (<b>C</b>) and the MetS + OVX + L-arginine group (<b>F</b>) showed an increased thicker layer of UL to improve bladder damage induced by MetS with or without OHD. (<b>A</b>–<b>G</b>) magnification × 400; Scale bar (grey) = 100 μm. (<b>H</b>,<b>I</b>): Western Blot analysis of E-Cadherin, CK14, C-Kit, vimentin, and PDGFR expressions was investigated. All expressions in the MetS group and the MetS + OVX group were significantly declined as compared with the control group, whereas all expressions in the MetS + L-arginine group and the MetS + OVX + L-arginine group were significantly enhanced compared to the MetS group and the MetS + OVX group. Results were normalized as the control = 100%. Note: IC, interstitial cell; MetS, metabolic syndrome; ML, muscular layer; UL, urothelial layer; SL, suburothelial layer; OVX, bilateral ovariectomy; OHD, ovarian hormone deficiency. Data were expressed as mean ± SD for <span class="html-italic">n</span> = 6. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 versus the control group. <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS group. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS + OVX group.</p>
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<p>The effect of L-arginine enhanced bladder angiogenesis. (<b>A</b>–<b>G</b>): The distribution of α-SMA (yellow arrows) for angiogenesis was shown by immunostaining. In the control group (<b>A</b>), α-SMA staining (yellow arrows) was abundantly expressed on the microvasculature at SL and ML while the staining was decreased in the SL and ML of the MetS group (<b>B</b>) and the MetS + OVX group (<b>E</b>). The immunostaining of the MetS + L-arginine group (<b>C</b>) and the MetS + OVX + L-arginine group (<b>F</b>) showed an enhancement of the expression. (<b>A</b>–<b>G</b>) magnification × 400; Scale bar (grey) = 100 μm. (<b>H</b>,<b>I</b>): the protein levels of angiogenesis (α-SMA, Laminin, and VEGF) were evaluated by Western Blot analysis. The levels of α-SMA, Laminin, and VEGF markers were significantly decreased in the MetS group and the MetS + OVX group compared to the control group, whereas all expressions in the MetS + L-arginine group and the MetS + OVX + L-arginine group were significantly enhanced compared to the MetS group and the MetS + OVX group. Note: α-SMA, α-smooth muscle actin; UL, urothelial layer; SL, suburothelial layer; ML, muscular layer; OHD, ovarian hormone deficiency; PDGFR, platelet-derived growth factor receptor; VEGF, vascular endothelial growth factor. Nuclear DNA was labeled with DAPI (blue). Results were normalized as the control = 100%. Data were expressed as mean ± SD for <span class="html-italic">n</span> = 8, * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 versus the sham group. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the OVX group. <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the OVX + SW4 group.</p>
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<p>The effect of L-arginine increased neuronal regeneration, synaptic transmission, and receptor response. The expressions of neuronal endogenous markers (neurofilament, NeuN, GFAP), muscarinic receptor (M2 and M3) markers, and purinergic receptor (P2X3 and P2X7) markers were assessed by immunostaining (<b>A</b>–<b>H</b>) and Western Blots (<b>I</b>). (<b>A</b>–<b>G</b>): The distribution of neurofilament for neurogenesis was shown by immunostaining. Neurofilament immunostaining (yellow arrows) and ganglion (green arrows) were prominently expressed in the SL and ML of the control group (<b>A</b>). In contrast, the MetS group (<b>B</b>) and the MetS + OVX group (<b>E</b>) showed reduced neurofilament staining (yellow arrows) and ganglion (green arrows) in the thinner and defective urothelial mucosa of the SL and ML. However, neurofilament expression (yellow arrows) was significantly increased in the MetS + L-arginine group (<b>C</b>) and the MetS + OVX + L-arginine group (<b>F</b>) compared to the MetS group (<b>B</b>) and the MetS + OVX group (<b>E</b>). This indicates that L-arginine enhances bladder synaptic transmission, receptor response, and neurogenesis, thereby improving detrusor contractile. (<b>A</b>–<b>G</b>) magnification × 400; Scale bar (grey) = 100 μm. (<b>H</b>,<b>I</b>): Quantifications of the percentage of neurogenesis-related markers, muscarinic receptors, and purinergic receptors were evaluated by Western Blotting. Nuclear DNA was labeled with DAPI (blue). Note: NF, neurofilament; NeuN, neuronal nuclear antigen and neuron; GFAP, glial fibrillary acidic protein; ML, muscular layer. Results were normalized as the control = 100%. Data were expressed as mean ± SD for <span class="html-italic">n</span> = 8, ** <span class="html-italic">p</span> &lt; 0.01 versus the sham group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05; <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the OVX group; <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the OVX + SW4 group.</p>
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<p>The effects of L-arginine on the expressions of oxidative stress markers in the status of MetS and OHD. (<b>A</b>) The expression levels of NOS (iNOS, eNOS, and nNOS), transcription factors (HIF-1α, NRF2, and NFkB), and oxidative stress markers (DNP and nitrotyrosine) by Western Blots. (<b>B</b>) Quantifications of the percentage of the proteins to β-actin in different experimental groups. The expression levels were significantly enhanced in the MetS group and the MetS + OVX group. Results were normalized as the control = 100%. Data were represented as mean ± SD for <span class="html-italic">n</span> = 6. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 versus the control group. <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS group. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS + OVX group.</p>
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<p>Up-regulation of the subunits of mitochondrial respiratory enzymes with MetS and OHD. (<b>A</b>) The expression levels of mitochondrial respiratory enzyme subunits (NDUFS3, SDHA, UQCRC1, COX-2, and ATPB) were analyzed by Western Blotting. (<b>B</b>) Quantification of these mitochondrial respiratory enzymes as a percentage relative to β-actin. Results were normalized to the control group, set at 100%. The expression levels of these subunits were elevated in the MetS group and significantly enhanced in both the MetS and MetS + OVX groups. Results were normalized as the control = 100%. Data were represented as mean ± SD for <span class="html-italic">n</span> = 6. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 versus the control group. <sup>††</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS group. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 versus the MetS + OVX group.</p>
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<p>Proposed mechanistic model illustrating how MetS and OHD induce oxidative stress through mitochondria-mediated pathways and the potential mitigating effect of L-arginine on bladder overactivity. MetS and OHD induced mitochondria to release ROS to induce the generation of oxidative stress. However, L-arginine treatment reduced oxidative stress induced by MetS, with or without OHD; enhanced neurogenesis and angiogenesis; and alleviated the symptoms of OAB. Note: α-SMA, alpha smooth muscle actin; GFAP, glial fibrillary acidic protein; HIF-1α, hypoxia-inducible factor-1α; L-NAME, NG-nitro-L-arginine methyl ester; MetS, metabolic syndrome; NeuN, neuronal nuclei; NO, nitric oxide; NFκB, nuclear factor kappa-light-chain-enhancer of activated B cells; NRF2, nuclear factor erythroid 2-related factor 2; OAB, overactive bladder; OHD, ovarian hormone deficiency; OVX, bilateral ovariectomy; ROS, reactive oxygen species; TGF-β, transforming growth factor-β; TRPV, transient receptor potential vanilloid 1; VEGF, vascular endothelial growth factor.</p>
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<p>Schematic diagram of the experimental procedure.</p>
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16 pages, 3021 KiB  
Article
From Mother to Child: Epigenetic Signatures of Hyperglycemia and Obesity during Pregnancy
by Marica Franzago, Paola Borrelli, Marta Di Nicola, Pierluigi Cavallo, Ebe D’Adamo, Luciano Di Tizio, Diego Gazzolo, Liborio Stuppia and Ester Vitacolonna
Nutrients 2024, 16(20), 3502; https://doi.org/10.3390/nu16203502 (registering DOI) - 16 Oct 2024
Abstract
Background: In utero exposure to maternal hyperglycemia and obesity can trigger detrimental effects in the newborn through epigenetic programming. We aimed to assess the DNA methylation levels in the promoters of MC4R and LPL genes from maternal blood, placenta, and buccal swab samples [...] Read more.
Background: In utero exposure to maternal hyperglycemia and obesity can trigger detrimental effects in the newborn through epigenetic programming. We aimed to assess the DNA methylation levels in the promoters of MC4R and LPL genes from maternal blood, placenta, and buccal swab samples collected in children born to mothers with and without obesity and Gestational Diabetes Mellitus (GDM). Methods: A total of 101 Caucasian mother–infant pairs were included in this study. Sociodemographic characteristics, clinical parameters, physical activity, and adherence to the Mediterranean diet were evaluated in the third trimester of pregnancy. Clinical parameters of the newborns were recorded at birth. Results: A negative relationship between MC4R DNA methylation on the fetal side of the GDM placenta and birth weight (r = −0.630, p = 0.011) of newborns was found. MC4R DNA methylation level was lower in newborns of GDM women (CpG1: 2.8% ± 3.0%, CpG2: 3.8% ± 3.3%) as compared to those of mothers without GDM (CpG1: 6.9% ± 6.2%, CpG2: 6.8% ± 5.6%; p < 0.001 and p = 0.0033, respectively), and it was negatively correlated with weight (r = −0.229; p = 0.035), head circumference (r = −0.236; p = 0.030), and length (r = −0.240; p = 0.027) at birth. LPL DNA methylation was higher on the fetal side of the placenta in obese patients as compared to normal-weight patients (66.0% ± 14.4% vs. 55.7% ± 15.2%, p = 0.037), and it was associated with maternal total cholesterol (r = 0.770, p = 0.015) and LDL-c (r = 0.783, p = 0.012). Conclusions: These results support the role of maternal MC4R and LPL methylation in fetal programming and in the future metabolic health of children. Full article
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<p>Schematic representation of the genes analyzed and localization of the CpGs ((<b>a</b>): <span class="html-italic">LPL</span> gene; (<b>b</b>): <span class="html-italic">MC4R</span> gene).</p>
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<p>The genotypes distribution of the <span class="html-italic">LPL</span> rs326 based on additive (<b>a</b>), dominant (<b>b</b>), and recessive (<b>c</b>) inheritance genetic models in women and newborns by NGT/GDM and NW/OB groups.</p>
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<p>The genotypes distribution of the <span class="html-italic">LPL</span> rs326 based on additive (<b>a</b>), dominant (<b>b</b>), and recessive (<b>c</b>) inheritance genetic models in women and newborns by NGT/GDM and NW/OB groups.</p>
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15 pages, 453 KiB  
Article
Exploring Food Preferences as a Pre-Step for Developing Diabetes-Friendly Options in Adults with Diabetes and Prediabetes
by Sungeun Choi and Jihee Choi
Foods 2024, 13(20), 3276; https://doi.org/10.3390/foods13203276 (registering DOI) - 16 Oct 2024
Abstract
Given the low compliance with healthy eating among patients with diabetes, personalized dietary plans incorporating their food preferences are urgently needed. However, few studies have explored the food preferences of adults with diabetes or prediabetes (AdDMP). We aimed to examine taste and food [...] Read more.
Given the low compliance with healthy eating among patients with diabetes, personalized dietary plans incorporating their food preferences are urgently needed. However, few studies have explored the food preferences of adults with diabetes or prediabetes (AdDMP). We aimed to examine taste and food preferences among AdDMP, comparing them by sex, age, and weight status. A total of 415 AdDMP completed the survey via Amazon Mechanical Turk in 2023 (53% women, 47% men; 20–70 years old). Food/taste preferences were measured using Likert-type scales for six taste-cluster food groups, as well as basic tastes/spicy flavor. Open-ended questions assessed comfort, favorite, and least favorite foods, which were then categorized into five groups. Independent t-tests, analysis of variance, and Tukey–HSD were performed to compare outcomes across the groups. Men, the 41–70-year-old group, and the obese group regarded warm food as a comfort food more than in other comparable groups, while women and the 20–30-year-old group tend to prefer fruits and vegetables. Additionally, men expressed a significantly higher preference for salty-/umami-/fat-tasting foods compared to women. These findings underscore the need to align dietary expectations with reality for AdDMP. Future research should focus on strategies to accommodate their preferences within a healthy eating framework. Full article
(This article belongs to the Special Issue Consumer Behavior and Food Choice—Volume III)
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<p>Regional distribution of survey participants’ (<span class="html-italic">n</span> = 415) residences in the United States.</p>
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17 pages, 2192 KiB  
Article
Metabolite, Biochemical, and Dietary Intake Alterations Associated with Lifestyle Interventions in Obese and Overweight Malaysian Women
by Fatin Saparuddin, Mohd Naeem Mohd Nawi, Liyana Ahmad Zamri, Fazliana Mansor, Mohd Fairulnizal Md Noh, Mohd Azahadi Omar, Nur Shahida Abdul Aziz, Norasyikin A. Wahab, Ahmed Mediani, Nor Fadilah Rajab and Razinah Sharif
Nutrients 2024, 16(20), 3501; https://doi.org/10.3390/nu16203501 (registering DOI) - 16 Oct 2024
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Abstract
Differences in metabolic regulation among obesity phenotypes, specifically metabolically healthy obese (MHO) and metabolically unhealthy obese (MUO) women, may lead to varied responses to interventions, which could be elucidated through metabolomics. Therefore, this study aims to investigate the differences in metabolite profiles between [...] Read more.
Differences in metabolic regulation among obesity phenotypes, specifically metabolically healthy obese (MHO) and metabolically unhealthy obese (MUO) women, may lead to varied responses to interventions, which could be elucidated through metabolomics. Therefore, this study aims to investigate the differences in metabolite profiles between MHO and MUO women and the changes following a lifestyle intervention. Serum samples from 36 MHO and 34 MUO women who participated in a lifestyle intervention for weight loss were analysed using untargeted proton nuclear magnetic resonance spectroscopy (1H NMR) at baseline and 6 months post-intervention. Anthropometric, clinical, and dietary intake parameters were assessed at both time points. Both groups showed differential metabolite profiles at baseline and after six months. Seven metabolites, including trimethylamine-N-oxide (TMAO), arginine, ribose, aspartate, carnitine, choline, and tyrosine, significantly changed between groups post-intervention, which all showed a decreasing pattern in MHO. Significant reductions in body weight and body mass index (BMI) in the MUO correlated with changes in the carnitine and tyrosine levels. In conclusion, metabolite profiles differed significantly between MHO and MUO women before and after a lifestyle intervention. The changes in carnitine and tyrosine levels in MUO were correlated with weight loss, suggesting potential targets for therapeutic intervention. Full article
(This article belongs to the Section Nutrition in Women)
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<p>Summary of the lifestyle intervention programme.</p>
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<p>Metabolites that significantly changed between MHO and MUO following intervention.</p>
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<p>Metabolic pathways affected at sixth month.</p>
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<p>Heatmap of correlation between the significantly changed metabolites with body weight, BMI, WC, and systolic blood pressure in MUO. Correlation determined using Pearson correlation. Green indicates a positive correlation, while red indicates a negative correlation.</p>
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<p>Heatmap of correlation between the significantly changed metabolites with changes in anthropometry, clinical, and biochemical variables. Correlation determined using Pearson correlation analysis in both groups combined. Blue indicates a positive correlation, while red indicates a negative correlation.</p>
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18 pages, 1953 KiB  
Article
The Abdominal Adiposity Index (A Body Shape Index) Predicts 10-Year All-Cause Mortality in Elderly Active Non-Obese Subjects
by Alessio Nunnari, Filippo Giorgio Di Girolamo, Kaja Teraž, Nicola Fiotti, Boštjan Šimunič, Filippo Mearelli, Rado Pišot and Gianni Biolo
J. Clin. Med. 2024, 13(20), 6155; https://doi.org/10.3390/jcm13206155 - 16 Oct 2024
Viewed by 102
Abstract
Background/Objectives: A Body Shape Index (ABSI), which accounts for waist circumference relative to mass and height, shows a robust association with mortality risk. The present study evaluates the effectiveness of ABSI as a predictor of 10-year all-cause mortality in physically active, non-obese [...] Read more.
Background/Objectives: A Body Shape Index (ABSI), which accounts for waist circumference relative to mass and height, shows a robust association with mortality risk. The present study evaluates the effectiveness of ABSI as a predictor of 10-year all-cause mortality in physically active, non-obese elderly individuals. Methods: This prospective cohort study included 159 volunteers (94 women, aged 60–80 years), recruited in the frame of the “Physical Activity and Nutrition for Great Ageing” (PANGeA) Cross-border Cooperation Program Slovenia–Italy 2007–2013, and followed for 10 years. Baseline characteristics included anthropometric measurements, bioelectrical impedance analysis, and cardiovascular fitness tests (VO2max). Statistical analyses (Cox regression, Kaplan–Meier survival) were conducted to examine the relationship between ABSI and mortality. Results: During the 10-year follow-up, 10 deaths (6.7%) were recorded. ABSI (adjusted for age, smoking, comorbidities, and therapy) was an independent predictor of mortality (hazard ratio = 4.65, p < 0.001). Higher ABSI scores were linked to reduced VO2max (r = −0.190, p = 0.017) and increased systolic blood pressure (r = 0.262, p = 0.001). An ABSI-based predictive model showed strong discriminatory power (AUROC = 0.91). Conclusions: ABSI is a reliable predictor of 10-year mortality in active, non-obese elderly individuals and may improve risk stratification in clinical practice. Full article
(This article belongs to the Section Endocrinology & Metabolism)
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<p>Flow diagram of the inclusion and exclusion criteria.</p>
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<p>Comparison of the standardized ABSI alone and the logistic regression model with ABSI, cancer, cigarette use, and pharmacological therapy for heart rhythm: Receiver Operating Characteristic for predicting 10-year mortality.</p>
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<p>Kaplan–Meier curves for mortality risk at 10 years stratified for the ABSI cutoff of 0.77.</p>
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<p>Correlation matrix of ABSI with age, systolic pressure, maximum oxygen consumption, and muscle strength. Warm colors indicate a negative correlation, while cold colors indicate a positive correlation; the strengths of the correlations can be deduced from the pie charts.</p>
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