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Search Results (785)

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Keywords = botulinum toxin A

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19 pages, 528 KiB  
Systematic Review
Use of Botulinum Toxin in Upper-Limb Tremor: Systematic Review and Perspectives
by Damien Motavasseli, Cécile Delorme, Nicolas Bayle, Jean-Michel Gracies, Emmanuel Roze and Marjolaine Baude
Toxins 2024, 16(9), 392; https://doi.org/10.3390/toxins16090392 - 13 Sep 2024
Viewed by 393
Abstract
Background: Tremor is the most common movement disorder, with significant functional and psychosocial consequences. Oral medications have been disappointing or limited by side effects. Surgical techniques are effective but associated with risks and adverse events. Botulinum toxin (BT) represents a promising avenue but [...] Read more.
Background: Tremor is the most common movement disorder, with significant functional and psychosocial consequences. Oral medications have been disappointing or limited by side effects. Surgical techniques are effective but associated with risks and adverse events. Botulinum toxin (BT) represents a promising avenue but there is still no double-blind evidence of efficacy on upper limb function. A systematic review on the effects of BT in upper-limb tremor was conducted. Methods: A systematic search of the literature was conducted up to July 2023, including the keywords “botulinum toxin” and “tremor”. All randomized controlled trials (RCTs) and open-label studies were analyzed. Independent reviewers assessed their methodological quality. Results: There were only eight published RCTs and seven published open-label studies, with relatively small sample sizes. This review suggests that BT is more effective when injections are patient-tailored, with analyses based on clinical judgement or kinematics. Subjective and objective measures frequently improve but transient weakness may occur after injections, especially if wrist or fingers extensors are targeted. A number of studies had methodological limitations. Conclusions: The authors discuss how to optimize tremor assessments and effects of BT injection. Controlled evidence is still lacking but it is suggested that distal “asymmetric” BT injections (targeting flexors/pronators while sparing extensors/supinators) and proximal injections, involving shoulder rotators when indicated, may avoid excessive weakness while optimizing functional benefit. Full article
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<p>Flowchart of study selection.</p>
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13 pages, 1367 KiB  
Article
An Ultrasonographic Analysis of the Deep Inferior Tendon in the Masseter Muscle: Implications for Botulinum Toxin Injections
by Jia Shi, Chenyang Li, Jinbo Zhou, Xinyu Guo, Guo Li and Meng You
Toxins 2024, 16(9), 391; https://doi.org/10.3390/toxins16090391 - 11 Sep 2024
Viewed by 263
Abstract
(1) Background: With the increasing aesthetic pursuit of facial features, the clinical use of Botulinum Toxin Type A (BoNT-A) injections for masseter hypertrophy has been on the rise. However, due to variations in masseter muscle structure and differences in clinicians’ injection techniques, blind [...] Read more.
(1) Background: With the increasing aesthetic pursuit of facial features, the clinical use of Botulinum Toxin Type A (BoNT-A) injections for masseter hypertrophy has been on the rise. However, due to variations in masseter muscle structure and differences in clinicians’ injection techniques, blind injections may lack precision, potentially compromising treatment accuracy and increasing the risk of complications. (2) Objectives: The study aims to use ultrasonography to detail the deep inferior tendon (DIT) within the masseter muscle in a young Chinese cohort, refine its classification, analyze muscle belly thickness and variations across groups, and propose a customized ultrasound-guided BoNT-A injection protocol. (3) Methods: Ultrasound imaging was used to observe the bilateral masseter muscles at rest and during clenching. The features of the DIT were classified from these images, and the thickness of the masseter’s distinct bellies associated with the DIT types was measured in both states. (4) Results: The study cohort included 103 participants (27 male, 76 female), with 30 muscles in the normal masseter group and 176 muscles in the hypertrophy group. The DIT was categorized as Type A, B (subtypes B1, B2), and C. The distribution of these types was consistent across normal, hypertrophic, and gender groups, all following the same trend (B > A > C). In hypertrophy, Type B1 showed uniform thickness across masseter bellies, B2 presented with a thinner intermediate belly, and Type C had mainly superficial muscle enlargement. Changes in muscle thickness during clenching were noted but not statistically significant among different bellies. (5) Conclusions: The study evidences individual variation in the DIT, highlighting the importance of precise DIT classification for effective BoNT-A injections. A tailored ultrasound-guided BoNT-A injection strategy based on this classification may enhance safety and efficacy of the therapy. Full article
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<p>Transverse ultrasonography images and their corresponding schematics. Ultrasonography images of Type A (<b>A</b>), B1 (<b>B</b>), B2 (<b>C</b>), and C (<b>D</b>) along with their corresponding schematics: (<b>E</b>) Type A, (<b>F</b>) Type B1, (<b>G</b>) Type B2, and (<b>H</b>) Type C. P, posterior; M, mandible; PD, parotid gland; DIT, deep inferior tendon.</p>
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<p>Measurement diagrams for muscle belly thickness. (<b>A</b>,<b>D</b>) Type B1; (<b>B</b>,<b>E</b>) Type B2; and (<b>C</b>,<b>F</b>) Type C. Relaxed state images are shown on the left (<b>A</b>–<b>C</b>); clenched state images are shown on the right (<b>D</b>–<b>F</b>). SB, superficial belly; IB, intermediate belly; DB, deep belly; DIT, deep inferior tendon.</p>
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<p>The recommended procedural flowchart for injecting BoNT-A. * Ultrasound Evaluation: Evaluate the injection effect by ultrasound at 1, 2, 3, and 4 weeks post-injection. Throughout the 4 subsequent assessments, observe the condition of the muscle fibers and dynamically monitor whether the masseter muscle contracts evenly. At the 4-week mark, compare the thickness of the masseter muscle before and after the injection. Good Injection Effect: By the 4th week, the masseter muscle thickness is reduced to achieve the desired injection outcome, with no complications. Poor Injection Effect: Ineffective injections or complications may arise within 4 weeks. DIT, deep inferior tendon.</p>
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17 pages, 1260 KiB  
Review
Opportunistic Features of Non-Clostridium botulinum Strains Containing bont Gene Cluster
by Tomasz Grenda, Anna Grenda, Anna Jakubczyk and Kamila Rybczyńska-Tkaczyk
Pathogens 2024, 13(9), 780; https://doi.org/10.3390/pathogens13090780 - 10 Sep 2024
Viewed by 409
Abstract
The cluster of genes determining the production of botulinum toxins is an attribute of not only the Clostridium botulinum species. This cluster is also found in other members of the Clostridium genus, such as C. baratii, C. butyricum, and C. sporogenes [...] Read more.
The cluster of genes determining the production of botulinum toxins is an attribute of not only the Clostridium botulinum species. This cluster is also found in other members of the Clostridium genus, such as C. baratii, C. butyricum, and C. sporogenes. The occurrence of a botulinum-like cluster has also been recorded in strains of other genera, i.e., Enterococcus faecium, as well as in a Gram-negative species isolated from freshwater sediments; however, the biological activity of bont-related genes has not been noted. It can be said that the mentioned species have a dual nature. Another species with a dual nature is C. butyricum. This bacterium is a common human and animal gut commensal bacterium and is also frequently found in the environment. Although non-toxigenic strains are currently used as probiotics in Asia, other strains have been implicated in pathological conditions, such as botulism in infants or necrotizing enterocolitis in preterm neonates. Additionally, C. baratii strains are rare opportunistic pathogens associated with botulism intoxication. They have been isolated from food and soil and can be carried asymptomatically or cause botulism outbreaks in animals and humans. In addition to the mentioned clostridia, the other microorganisms considered as non-toxigenic have also been suspected of carrying botulinum cluster Gram-negative bacteria, such as Chryseobacterium piperi isolated from freshwater sediments; however, the biological activity of bont-related genes has not been noted. Additionally, Enterococcus faecium strains have been discovered carrying BoNT-related clusters (BoNT/En). Literature data regarding the heterogeneity of BoNT-producing strains indicate the requirement to reclassify C. botulinum species and other microorganisms able to produce BoNTs or possess botulinum-like gene clusters. This article aims to show the dual nature of Clostridium strains not belonging to the C. botulinum species that are sporadically able to carry bont clusters, which are usually considered saprophytic and even probiotic, and bont-like clusters in microorganisms from other genera. The aim was also to consider the genetic mechanisms of botulinum cluster expression in strains that are considered opportunistic and the microbiological safety aspects associated with their occurrence in the environment. Full article
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<p>Horizontal <span class="html-italic">bont</span> gene transfer among <span class="html-italic">Clostridium</span> strains.</p>
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<p>Dual nature of <span class="html-italic">C. butyricum</span> species.</p>
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15 pages, 1235 KiB  
Review
The Pathomechanism and Current Treatments for Chronic Interstitial Cystitis and Bladder Pain Syndrome
by Wan-Ru Yu, Jia-Fong Jhang, Yuan-Hong Jiang and Hann-Chorng Kuo
Biomedicines 2024, 12(9), 2051; https://doi.org/10.3390/biomedicines12092051 - 10 Sep 2024
Viewed by 433
Abstract
Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic and debilitating condition characterized by symptoms such as bladder pain, frequent urination, and nocturia. Pain is typically perceived in the lower abdomen, pelvic floor, or urethra, causing significant discomfort and impacting quality of life. Due [...] Read more.
Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic and debilitating condition characterized by symptoms such as bladder pain, frequent urination, and nocturia. Pain is typically perceived in the lower abdomen, pelvic floor, or urethra, causing significant discomfort and impacting quality of life. Due to the similarity of its symptoms with those of overactive bladder and acute bacterial cystitis, patients often face misdiagnosis and delayed appropriate treatment. Hunner’s (HIC) and non-Hunner’s IC (NHIC), each with distinct clinical presentations, urothelial dysfunction, chronic inflammation, and central sensitization and thus multimodal symptomatic treatment approaches, may be the most common pathogeneses of IC/BPS. Treatment of IC/BPS should involve identifying the different clinical phenotypes and underlying pathophysiology causing clinical symptoms and developing strategies tailored to the patient’s needs. This review discusses the roles of urine biomarkers, bladder inflammation, and glycosaminoglycans in the pathogenesis of IC/BPS. Various bladder treatment modalities are explored, including glycosaminoglycan replenishment, botulinum toxin A injection, platelet-rich plasma injection, low-energy shock waves, immunosuppression, and low-dose oral prednisolone. Pelvic floor muscle physiotherapy and bladder therapy combined with psychiatric consultation can help alleviate psychological stress and enhance the quality of life of patients with IC/BPS. Elucidating the pathological mechanisms and exploring diverse treatment options would help advance the care of individuals suffering from this challenging bladder condition. Full article
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<p>Electron microscopic (EM) examination of the ultrastructure of bladder urothelium in patients with (<b>A</b>) a normal urothelium (scanning EM), (<b>B</b>) non-Hunner’s interstitial cystitis (IC; scanning EM), and (<b>C</b>) Hunner’s IC (transmission EM).</p>
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<p>Cystoscopic findings of interstitial cystitis/bladder pain syndrome under hydrodistension: (<b>A</b>) normal urothelium, no glomerulation; (<b>B</b>) grade 1 glomerulation; (<b>C</b>) grade 2 glomerulation; (<b>D</b>) grade 3 glomerulation; (<b>E</b>) Hunner’s lesion with urothelial crack; and (<b>F</b>) Hunner’s lesion with hemorrhagic patch. Magnification ×10.</p>
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<p>Multimodal therapy and strategy for the treatment of interstitial cystitis/bladder pain syndrome (IC/BPS). Abbreviations: U/A: urinalysis, U/C: urine culture, Qmax: maximum flow rate, PVR: post-void residual, NSAID: non-steroidal anti-inflammatory agent, PFM: pelvic floor muscle, UDS: urodynamic study, VUDS: videourodynamic study, KCl: potassium chloride, BND: bladder neck dysfunction, DV: dysfunctional voiding, DO: detrusor overactivity, TUR: transurethral resection, CT: computed tomography, HIC: Hunner’s interstitial cystitis, MBC: maximum bladder capacity, Gr: grade, EBV: Epstein–Barr virus, LUTS: lower urinary tract symptoms, PFMT: pelvic floor muscle training, PTNS: percutaneous tibial nerve stimulation, TTNS: transcutaneous tibial nerve stimulation, SNS: sacral nerve stimulation, PRP: platelet-rich plasma, LESW: low-energy shock wave.</p>
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9 pages, 1345 KiB  
Article
Prospective Analysis of the Effectiveness of Targeted Botulinum Toxin Type A Injection Using an Ultrasound-Guided Single-Point Injection Technique for Lower Face Contouring
by Hyun-Jung Ryoo, Ho Kwon, Jae-Seon Choi, Bo-Seong Sohn, Ja-Young Yoo and Hyung-Sup Shim
J. Clin. Med. 2024, 13(17), 5337; https://doi.org/10.3390/jcm13175337 - 9 Sep 2024
Viewed by 403
Abstract
Background: Botulinum toxin type A (BoNT-A) injection is widely used for masseter hypertrophy. Traditional BoNT-A injection methods often incorporate landmark-guided blind injections, which approximate the shape of the masseter muscle inject across various points. Conversely, ultrasound (US)-guided injection techniques offer real-time visualization [...] Read more.
Background: Botulinum toxin type A (BoNT-A) injection is widely used for masseter hypertrophy. Traditional BoNT-A injection methods often incorporate landmark-guided blind injections, which approximate the shape of the masseter muscle inject across various points. Conversely, ultrasound (US)-guided injection techniques offer real-time visualization and dynamic monitoring, enhancing accuracy. Patients and Methods: 50 patients who underwent BoNT-A injections were included in this trial. One on the face side received a landmark-guided injection, and the other side was treated with a US-guided injection. Initial and post-procedure measurements of muscle thickness at the upper, middle, and lower regions were collected using ultrasound. Results: Both methods led to a significant reduction in muscle thickness one month after injection. In the upper area, the absolute difference in muscle thickness between the two methods was observed as a mean ± standard deviation (SD) value of 0.37 ± 0.0314 (p < 0.0001), indicating a superior effect with US-guided injection. Similarly, in the middle area, the mean ± SD difference was 0.41 ± 0.0608 (p < 0.0001) and in the lower area, the mean ± SD difference was 0.24 ± 0.0134 (p = 0.0004). Conclusions: This study demonstrated that the US-guided single-point injection technique is a more effective and accurate method for BoNT-A injection compared to the conventional method. Full article
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<p>A landmark-guided BoNT-A injection procedure. The borders of the masseter muscle were identified by palpation, and BoNT-A first was injected at the thickest region, followed by two subsequent injections about 1–1.5 cm away.</p>
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<p>Ultrasound image before BoNT-A injection. Prior to the procedure, the thickest location of the masseter muscle was pre-identified using ultrasound. (* represents the thickest part of the masseter muscle).</p>
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<p>Ultrasound (US)-guided BoNT-A injection. With the US system set to B-mode, the thickest region was identified, and injections were administered in that specific area. Real-time monitoring using US confirmed the accurate delivery of injections.</p>
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<p>Ultrasound image showing injection dynamics after BoNT-A injection. (<b>A</b>) The yellow arrow notes the BoNT-A injection needle. Puncture was performed using a 1-cc syringe, with injection into the thickest region of the masseter muscle. (<b>B</b>) Immediate post-injection view.</p>
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<p>Changes in masseter muscle thickness before and after Botox injections. (<b>A</b>) In the upper area, masseter muscle thickness in the landmark-guided group measured 9.92 mm and 8.99 mm before and after the procedure, respectively, while that in the ultrasound-guided group measured 9.93 mm and 8.63 mm. (<b>B</b>) In the middle area, masseter muscle thickness values in the landmark-guided group were 10.22 mm and 8.72 mm before and after the procedure, respectively, while corresponding values in the ultrasound-guided group were 10.83 mm and 8.92 mm. (<b>C</b>) In the lower area, the masseter muscle measured 8.16 mm and 7.49 mm before and after the procedure in the landmark-guided group and 8.43 mm and 7.52 mm in the ultrasound-guided group, respectively.</p>
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18 pages, 18199 KiB  
Article
Comparison of Neural Recovery Effects of Botulinum Toxin Based on Administration Timing in Sciatic Nerve-Injured Rats
by Minsu Seo, Seokjoon Hwang, Tae Heon Lee and Kiyeun Nam
Toxins 2024, 16(9), 387; https://doi.org/10.3390/toxins16090387 - 5 Sep 2024
Viewed by 404
Abstract
This study aimed to assess the effects of the timing of administering botulinum neurotoxin A (BoNT/A) on nerve regeneration in rats. Sixty 6-week-old rats with a sciatic nerve injury were randomly divided into four groups: the immediately treated (IT) group (BoNT/A injection administered [...] Read more.
This study aimed to assess the effects of the timing of administering botulinum neurotoxin A (BoNT/A) on nerve regeneration in rats. Sixty 6-week-old rats with a sciatic nerve injury were randomly divided into four groups: the immediately treated (IT) group (BoNT/A injection administered immediately post-injury), the delay-treated (DT) group (BoNT/A injection administered one week post-injury), the control group (saline administered one week post-injury), and the sham group (only skin and muscle incisions made). Nerve regeneration was assessed 3, 6, and 9 weeks post-injury using various techniques. The levels of glial fibrillary acid protein (GFAP), astroglial calcium-binding protein S100β (S100β), growth-associated protein 43 (GAP43), neurofilament 200 (NF200), and brain-derived neurotrophic factor (BDNF) in the IT and DT groups were higher. ELISA revealed the highest levels of these proteins in the IT group, followed by the DT and control groups. Toluidine blue staining revealed that the average area and myelin thickness were higher in the IT group. Electrophysiological studies revealed that the CMAP in the IT group was significantly higher than that in the control group, with the DT group exhibiting significant differences starting from week 8. The findings of the sciatic functional index analysis mirrored these results. Thus, administering BoNT/A injections immediately after a nerve injury is most effective for neural recovery. However, injections administered one week post-injury also significantly enhanced recovery. BoNT/A should be administered promptly after nerve damage; however, its administration during the non-acute phase is also beneficial. Full article
(This article belongs to the Special Issue Botulinum Toxins: New Uses in the Treatment of Diseases (Volume II))
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<p>Effect of botulinum neurotoxin A (BoNT/A) on glial fibrillary acid protein (GFAP) expression. (<b>A</b>) Image depicting immunofluorescence staining (scale bar = 150 µm; 200× magnification). (<b>B</b>) The ELISA results indicate that GFAP expression in the IT and DT groups was significantly higher than that in the control at all time points. However, no differences were observed between the IT and DT groups. * indicates IT group vs. control group, # indicates DT group vs. control group (<span class="html-italic">p</span> &lt; 0.05). n = 5 in each group. The error bars indicate the standard error of the mean.</p>
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<p>Effect of BoNT/A on astroglial calcium-binding protein S100β (S100β) expression: (<b>A</b>) Image depicting immunofluorescence staining (scale bar = 150 µm; 200× magnification). (<b>B</b>) ELISA results revealed significantly higher S100β levels in the IT and DT groups compared with that in the control, with a significant difference being observed between the IT and DT groups at week 6. * indicates IT group vs. control group, ∆ indicates IT group vs. DT group, and # indicates DT group vs. control group (<span class="html-italic">p</span> &lt; 0.05). n = 5 in each group. The error bars indicate the standard error of the mean.</p>
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<p>Effect of BoNT/A on growth associated protein 43 (GAP43) expression. (<b>A</b>) Image depicting immunofluorescence staining (scale bar = 150 µm; 200× magnification). (<b>B</b>) The ELISA results indicate significantly higher expression of GAP43 in the IT and DT groups compared with that in the control group at all time points, with a significant difference being observed between the IT and DT groups at week 3. * indicates IT group vs. control group, ∆ indicates IT group vs. DT group, and # indicates DT group vs. control group (<span class="html-italic">p</span> &lt; 0.05). n = 5 in each group. The error bars indicate the standard error of the mean.</p>
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<p>Effect of BoNT/A on neurofilament 200 (NF200) expression. (<b>A</b>) Image depicting immunofluorescence staining (scale bar = 150 µm; 200× magnification). (<b>B</b>) The ELISA results revealed that the expression of NF200 in the IT and DT groups at weeks 6 and 9 was significantly higher than that in the control group. No statistically significant difference was observed between the IT and DT groups at any time point. * indicates IT group vs. control group, # indicates DT group vs. control group (<span class="html-italic">p</span> &lt; 0.05). n = 5 in each group. The error bars indicate the standard error of the mean.</p>
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<p>Effect of BoNT/A on brain-derived neurotrophic factor (BDNF) expression. (<b>A</b>) Image of immunofluorescence staining (scale bar = 150 µm; 200× magnification). (<b>B</b>) ELISA results indicate significantly higher BDNF levels in the IT group compared to the DT and control groups at weeks 3 and 9, with no significant differences observed between the DT group and the control group. * indicates IT group vs. control group, ∆ indicates IT group vs. DT group. n = 5 in each group. The error bars indicate the standard error of the mean.</p>
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<p>Effect of BoNT/A on axonal regeneration and remyelination. (<b>A</b>) Images depicting embedded sciatic nerve sections stained with toluidine blue (scale bar = 20 µm; 1000× magnification). (<b>B</b>) Average area, (<b>C</b>) mean diameter of the myelin sheath, and (<b>D</b>) remyelination degree of axons (G-ratio). The quantitative analysis revealed that the average axon area and myelin thickness in the IT group were significantly greater at week 9 compared with those in the DT and control groups. The G-ratio analysis revealed a significantly lower value in the IT group at week 9, indicating better remyelination. * indicates IT group vs. control group, ∆ indicates IT group vs. DT group. n = 5 in each group. The error bars indicate the standard error of the mean.</p>
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<p>Effect of BoNT/A on functional recovery. (<b>A</b>) CMAP amplitude (mV) and (<b>B</b>) SFI (score) were measured weekly for up to 9 weeks following neural damage (n = 5 per group). (<b>A</b>) The CMAP amplitude in the IT group was significantly greater than that in the control group starting from week 2 after injury (<span class="html-italic">p</span> &lt; 0.05). No statistically significant differences were observed between the DT and control groups until week 7; however, significantly greater CMAP values were observed from week 8 onwards (<span class="html-italic">p</span> &lt; 0.05). (<b>B</b>) The SFI scores exhibited similar trends, with the IT group exhibiting significantly improved functional recovery compared with the control group starting from week 2 and the DT group exhibited significant improvements starting from week 7. The IT group exhibited results comparable with those of the sham group by week 9. * indicates IT group vs. control group, ◦ indicates IT group vs. sham group, ∆ indicates IT group vs. DT group, and # indicates DT group vs. control group (<span class="html-italic">p</span> &lt; 0.05). n = 5 in each group. The error bars indicate the standard error of the mean.</p>
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<p>(<b>A</b>) Schematic diagram. (<b>B</b>) Experimental protocols.</p>
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11 pages, 777 KiB  
Article
Predictive Factors for the Successful Outcome of Urethral Sphincter Injections of Botulinum Toxin A for Non-Neurogenic Dysfunctional Voiding in Women
by Chia-Cheng Yang, Yuan-Hong Jiang and Hann-Chorng Kuo
Toxins 2024, 16(9), 386; https://doi.org/10.3390/toxins16090386 - 5 Sep 2024
Viewed by 360
Abstract
Purpose: Dysfunctional voiding (DV) is not uncommon in women with non-neurogenic voiding dysfunction. Because of its unknown pathophysiology, effective and durable treatment is lacking. This study aimed to analyze the results of treatment and predictive factors for a successful outcome of botulinum toxin [...] Read more.
Purpose: Dysfunctional voiding (DV) is not uncommon in women with non-neurogenic voiding dysfunction. Because of its unknown pathophysiology, effective and durable treatment is lacking. This study aimed to analyze the results of treatment and predictive factors for a successful outcome of botulinum toxin A (BoNT-A) treatment in female patients with DV. Methods: In total, 66 women with DV confirmed by a videourodynamic study (VUDS) were treated with a BoNT-A injection into the urethral sphincter once (n = 33) or several times (n = 33). VUDS was performed before (baseline) and after the BoNT-A treatment. Patients with a global response assessment of the voiding condition of 2 or 3 and a voiding efficiency (VE) of >20% than baseline were considered to have a successful outcome. The baseline demographics, VUDS parameters, and VUDS DV subtypes were compared between the successful and failed groups. Predictive factors for a successful outcome were investigated by logistic regression analyses. Results: Successful and failed outcomes were achieved in 27 (40.9%) and 39 (59.1%) women, respectively. After BoNT-A injections, the maximum flow rate (Qmax), voided volume, and VE all significantly increased, and the postvoid residual (PVR) was slightly improved. No significant difference in the number of injections and medical comorbidity was found between the groups. However, the successful group had a higher incidence of previous pelvic surgery. No significant difference in the treatment outcome was found among patients with different urethral obstruction sites. Significant improvements in Qmax, voided volume, PVR, VE, and the bladder outlet obstruction (BOO) index were noted in the successful group. A lower VE at baseline and a history of surgery were identified as predictive factors for a successful outcome of BoNT-A injections for treating DV. Conclusion: BoNT-A injections into the urethral sphincter can effectively improve VE in 40.9% of women with DV. Women with higher BOO grades and previous pelvic surgery are predicted to have a successful treatment outcome. Full article
(This article belongs to the Section Bacterial Toxins)
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<p>VUDS characteristics of bladder outlet obstruction in women with dysfunctional voiding (DV), with urethral narrowing (arrow) at the (<b>A</b>) mid-urethra, (<b>B</b>) distal urethra, (<b>C</b>) bladder neck before transurethral incision of the bladder neck (TUI-BN), and (<b>D</b>) DV at the mid-urethra after TUI-BN of the woman shown in <a href="#toxins-16-00386-f001" class="html-fig">Figure 1</a>C.</p>
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14 pages, 2647 KiB  
Article
Long-Term Management of Post-Stroke Spasticity with Botulinum Toxin: A Retrospective Study
by Nicoletta Falcone, Fabrizio Leo, Carmelo Chisari and Stefania Dalise
Toxins 2024, 16(9), 383; https://doi.org/10.3390/toxins16090383 - 3 Sep 2024
Viewed by 576
Abstract
Stroke-induced spasticity is a prevalent condition affecting stroke survivors, significantly impacting their quality of life. Botulinum Toxin A injections are widely used for its management, yet the long-term effects and optimal management strategies remain uncertain. This retrospective study analyzed medical records of 95 [...] Read more.
Stroke-induced spasticity is a prevalent condition affecting stroke survivors, significantly impacting their quality of life. Botulinum Toxin A injections are widely used for its management, yet the long-term effects and optimal management strategies remain uncertain. This retrospective study analyzed medical records of 95 chronic stroke patients undergoing long-term BoNT-A treatment for spasticity. Demographic data, treatment duration, dosage variability, and dropout rates were assessed over a period ranging from 2 to 14 years. The study revealed a notable extension of the interval between BoNT-A injections throughout the treatment duration. Dropout rates peaked during the initial 5 years of treatment, perhaps due to perceived treatment ineffectiveness. Additionally, a trend of escalating dosage was observed across all groups, indicating a potential rise in the severity of spasticity or changes in treatment response over time. BoNT-A injections emerged as the predominant treatment choice for managing post-stroke spasticity. The delayed initiation of BoNT-A treatment underscores the need for heightened awareness among healthcare providers to recognize and manage spasticity promptly post-stroke. Patients’ expectations and treatment goals should be clearly defined to optimize treatment adherence, while the observed escalation in dosage and treatment intervals emphasizes the dynamic nature of spasticity and underscores the importance of monitoring long-term treatment outcomes. Full article
(This article belongs to the Section Bacterial Toxins)
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<p>Number of dropouts by year of treatment. Numbers above the bars indicate the cumulative percentage of dropouts.</p>
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<p>(<b>A</b>) Distribution of the mean intervals between injections in the first and last year of treatment in all patients. Horizontal lines indicate medians and black dots indicate means. Whiskers extend to points that lie within 1.5 interquartile ranges of the lower and upper quartiles. (<b>B</b>) Distribution of the mean intervals between injections in the first (red) and last year (cyan) of treatment separately for the SIT and LIT groups. The same graphical conventions are used as in panel (<b>A</b>). Asterisks indicate larger intervals in the last year of treatment than in the first. ***, <span class="html-italic">p</span> &lt; 0.001, *, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>(<b>A</b>) Distribution of the dosage in the first and in the last injection in all patients. Horizontal lines indicate medians and black dots indicate means. Whiskers extend to points that lie within 1.5 interquartile ranges of the lower and upper quartiles. (<b>B</b>) Distribution of the dosage in the first (red) and last injection (cyan) of treatment separately for the SIT and LIT groups. The same graphical conventions were are as in panel (<b>A</b>). Asterisks indicate a greater dosage in the last injection than in the first. **, <span class="html-italic">p</span> &lt; 0.01, *, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Flow chart of the retrospective patients’ selection for data acquisition and statistical analysis.</p>
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<p>Distribution of the mean intervals between injections for each year of treatment. Horizontal lines indicate medians and black dots indicate means. Whiskers extend to points that lie within 1.5 interquartile ranges of the lower and upper quartiles.</p>
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<p>Distribution of the mean dosage for each year of treatment. Horizontal lines indicate medians and black dots indicate means. Whiskers extend to points that lie within 1.5 interquartile ranges of the lower and upper quartiles.</p>
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<p>Mean intervals between injections of individual patients who took anti-spasticity drugs (open red circles) and those who did not take anti-spasticity drugs (open cyan circles) represented as a scatterplot, with intervals in the first year of treatment shown on the abscissa and intervals in the last year of treatment shown on the ordinate. A jitter was added to the data points to limit the superposition of circles. Larger filled color-coded circles represent the mean values of each group.</p>
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<p>Dosages of individual patients who took anti-spasticity drugs (open red circles) and those who did not take anti-spasticity drugs (open cyan circles) represented as a scatterplot, with the first dosage of treatment shown on the abscissa and the last dosage of treatment shown on the ordinate. A jitter was added to the data points to limit the superposition of circles. Larger filled color-coded circles represent the mean values of each group.</p>
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29 pages, 2887 KiB  
Article
Constraint-Induced Movement Therapy (CIMT) and Neural Precursor Cell (NPC) Transplantation Synergistically Promote Anatomical and Functional Recovery in a Hypoxic-Ischemic Mouse Model
by Prakasham Rumajogee, Svetlana Altamentova, Junyi Li, Nirushan Puvanenthirarajah, Jian Wang, Azam Asgarihafshejani, Derek Van Der Kooy and Michael G. Fehlings
Int. J. Mol. Sci. 2024, 25(17), 9403; https://doi.org/10.3390/ijms25179403 - 29 Aug 2024
Viewed by 400
Abstract
Cerebral palsy (CP) is a common neurodevelopmental disorder characterized by pronounced motor dysfunction and resulting in physical disability. Neural precursor cells (NPCs) have shown therapeutic promise in mouse models of hypoxic-ischemic (HI) perinatal brain injury, which mirror hemiplegic CP. Constraint-induced movement therapy (CIMT) [...] Read more.
Cerebral palsy (CP) is a common neurodevelopmental disorder characterized by pronounced motor dysfunction and resulting in physical disability. Neural precursor cells (NPCs) have shown therapeutic promise in mouse models of hypoxic-ischemic (HI) perinatal brain injury, which mirror hemiplegic CP. Constraint-induced movement therapy (CIMT) enhances the functional use of the impaired limb and has emerged as a beneficial intervention for hemiplegic CP. However, the precise mechanisms and optimal application of CIMT remain poorly understood. The potential synergy between a regenerative approach using NPCs and a rehabilitation strategy using CIMT has not been explored. We employed the Rice–Vannucci HI model on C57Bl/6 mice at postnatal day (PND) 7, effectively replicating the clinical and neuroanatomical characteristics of hemiplegic CP. NPCs were transplanted in the corpus callosum (CC) at PND21, which is the age corresponding to a 2-year-old child from a developmental perspective and until which CP is often not formally diagnosed, followed or not by Botulinum toxin injections in the unaffected forelimb muscles at PND23, 26, 29 and 32 to apply CIMT. Both interventions led to enhanced CC myelination and significant functional recovery (as shown by rearing and gait analysis testing), through the recruitment of endogenous oligodendrocytes. The combinatorial treatment indicated a synergistic effect, as shown by newly recruited oligodendrocytes and functional recovery. This work demonstrates the mechanistic effects of CIMT and NPC transplantation and advocates for their combined therapeutic potential in addressing hemiplegic CP. Full article
(This article belongs to the Section Molecular Neurobiology)
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<p>Experimental design and timeline. HI injury at PND7 included ischemia (i.e., right common carotid artery cauterization) and hypoxia (8% O<sub>2</sub> for 45 min) (<b>A</b>). The regeneration strategy was based on NPC transplantation in the right/injured corpus callosum at PND21 (developmentally comparable to a 2-year old child, the age until which CP is not formally diagnosed) and the rehabilitation strategy was based on Botox injections into the biceps, triceps, and supraspinous muscles of the right/unaffected forelimb at PND23, 25, 29, and 32 to reproduce CIMT (<b>B</b>). Timeline of the experimental procedures in neurobehavioural testing, the PND77 time-point was skipped as the analysis of the partial data obtained at PND70 showed a “plateau” of the values, and consequently, a time-point after two weeks (PND84 following PND70) was sought (<b>C</b>). Time-points of the experimental procedures (<b>D</b>). The body weights of animals under CIMT or CIMT + NPC were comparable to the control body weights (see <a href="#app1-ijms-25-09403" class="html-app">Supplemental Figure S1</a>). Green arrow represents the NPC transplantation. Blue arrows represent the Botox injections.</p>
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<p>Transplanted NPCs survive, migrate, differentiate morphologically, and integrate in the corpus callosum (CC). MRI picture showing the location of transplantation of YFP-NPCs, i.e., the right/injured CC, ipsilateral to the common carotid occlusion (<b>A</b>). Survival rate of transplanted NPCs in the sham, HI, and HI + CIMT mice (<b>B</b>). Transplanted NPCs migrate, differentiate morphologically, and integrate in the brain tissue of the sham (<b>C</b>), HI (<b>D</b>), and HI + CIMT mice (<b>E</b>). The vast majority of transplanted NPCs remain Nestin-positive (<b>F</b>).</p>
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<p>The treatments significantly improved various brain structures following HI injury. Representative pictures of LFB/H&amp;E staining of the whole brain coronal sections at 3 Bregma levels (i.e., Bregma −1.2, 0 and +1 mm) for the sham (<b>A</b>–<b>C</b>), HI (<b>D</b>–<b>F</b>), HI + NPC (<b>G</b>–<b>I</b>), HI + CIMT (<b>J</b>–<b>L</b>), and HI + NPC + CIMT (<b>M</b>–<b>O</b>) mice. Yellow arrows indicate brain structures such as the CC, lateral ventricle (LV), caudate putamen (CPu), hippocampus (Hpc), and cortex. L and R indicate the left- and right-hand sides of the brain, respectively.</p>
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<p>Assessment of structural integrity and neuronal populations in various brain structures following NPC, CIMT, and NPC + CIMT treatments. Following HI, various brain structures were reduced in size and displayed a decreased number of neurons. The brain hemisphere area decrease was not restored following any of the treatments (<b>A</b>). Even though the reduced hippocampus area was not fully restored, it was significantly improved when compared to the sham group. CIMT and NPC + CIMT treatments led to better recovery than NPCs used alone (<b>B</b>). The CA1 neuronal population significantly improved after treatments but was fully restored only following NPC + CIMT treatment (<b>C</b>). The CA3 neuronal population significantly improved after CIMT and NPC + CIMT, but not NPC treatment, and was fully restored after NPC + CIMT treatment (<b>D</b>). The somatosensory cortex thickness was partially restored after all treatments (<b>E</b>), while the neuronal population increased only slightly (<b>F</b>). The primary motor cortex thickness was partially restored after all treatments (<b>G</b>) while the neuronal population slightly increased (<b>H</b>). The CC area (<b>I</b>) and volume (<b>J</b>) were fully restored after all treatments. The lateral ventricle area significantly improved, but was not fully restored, after any treatments. However, NPC + CIMT led to better recovery than both treatments alone (<b>K</b>). The % sign indicates that the left side was normalized to 100% and compared with the right side. The dashed versus plain bars represent the right versus left side. * <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; 0.001, n.s.—no significance.</p>
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<p>Pictures of fluorescent NeuN-positive cells in the hippocampus and the cortex following NPC, CIMT, and NPC + CIMT treatments. Following HI, the neuronal population was reduced in various brain structures such as the CA1 (<b>A</b>) and CA3 (<b>B</b>) of the hippocampus, as well as the somatosensory (<b>C</b>) and primary motor cortex (<b>D</b>).</p>
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<p>Effect of the treatments on the oligodendrocyte population in the corpus callosum. Following HI, the oligodendrocyte population (Olig2+ cells) was dramatically reduced in the ipsilateral brain (red dashed bar) when compared to the contralateral brain (control side, red plain bar). After all treatments, the OL population increased above normal levels. Following the NPC + CIMT treatment, this increase was significantly higher than after both treatments alone (<b>A</b>). The mature oligodendrocyte population (Olig2+/CC1+ cells) returned to normal levels after all treatments (<b>B</b>). Representative pictures of immunostaining for oligodendrocytes (Olig2+/CC1−; black arrows), astrocytes (Olig2−/CC1+; white arrows), and mature oligodendrocytes (CC1+/Olig2+; yellow arrowheads) in the CC of the sham and HI animals after treatments (NPC, CIMT, and NPC + CIMT). The white squares indicate an example of mature oligodendrocyte enlarged five times (<b>C</b>). The left side was normalized to 100% and compared with the right side. The dashed versus plain bars represent the right versus left side. * <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; 0.001, n.s.—no significance.</p>
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<p>All treatments led to functional myelination, with an enhanced synergistic effect observed with the combinatorial treatment. Representative pictures of coronal brain sections prepared for electrophysiology (<b>A</b>). Diagram of the suction electrode recording method for the CC with a conduction distance of 2.8 mm (<b>B</b>). Averaged compound action potential (CAP) recordings from the right/injured side of the CC of the sham animals (black line); HI injured animals (red line); and HI injured animals treated with NPCs (green line), CIMT (blue line), and NPC + CIMT (dark-blue line) ((<b>C</b>) inset: the measurement of CAP amplitudes). Statistical assessment of Peak 1 and Peak 2 amplitude (mV), conduction velocity CV1 and CV2 (m/s), and Peak 2/Peak 1 ratio amplitude in the right/injured side of the CC compared to the left/control side of the CC for all studied animal groups: sham animals (black bar, <span class="html-italic">n</span> = 21); HI injured animals (red bar, <span class="html-italic">n</span> = 9); HI injured animals treated with NPC (green bar, <span class="html-italic">n</span> = 8), CIMT (blue bar, <span class="html-italic">n</span> = 8), and NPC + CIMT (dark-blue bar, <span class="html-italic">n</span> = 8) (<b>D</b>). See the statistical table in <a href="#app1-ijms-25-09403" class="html-app">Supplemental Table S1</a>. One-way ANOVA followed by Tukey’s multiple comparisons test, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, n.s.—no significance.</p>
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<p>All treatments led to functional recovery. The cylinder test showed a clear preference for using the unaffected right forelimb in HI mice ((<b>A</b>), baseline time-point—BL). A progressive recovery was observed following all treatments when compared to the sham group (black line). The combinatorial treatment (NPC + CIMT; dark blue line) led to earlier and greater recovery than NPC transplantation (green line) or CIMT (blue line) alone (<b>A</b>). Similarly, the test also showed a strong preference for the HI mice to use the unaffected right forelimb to initiate a rearing sequence. Progressive recovery was observed following all treatments when compared to the sham group. NPC + CIMT led to earlier and enhanced recovery as compared to using NPC transplantation or CIMT alone (<b>B</b>). The CatWalk test demonstrated an impairment of HI animals for several parameters, including Swing Speed (<b>C</b>), Stride Length (<b>D</b>), and Paw Intensity (<b>E</b>) when compared to the sham mice (black bars) at baseline. A progressive improvement was observed after NPC (green bars), CIMT (blue bars), and NPC + CIMT (dark blue bars) treatments. NB: Following the onset of the treatments, recordings were not reliable for CIMT and NPC + CIMT animals for the first 3 time-points (i.e., PND28, 35, and 42) and were not reported. Furthermore, the PND77 time-point was skipped as the analysis of the partial data obtained at PND70 showed a “plateau” of the values, and consequently, a time-point after two weeks (PND84 following PND70) was sought. Green and blue arrows show the timing of, respectively, the NPC and the CIMT treatments. * <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; 0.001, n.s.—no significance.</p>
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11 pages, 672 KiB  
Article
Impact of Urethral Sphincter Electrophysiology on Botulinum Toxin A Treatment in Women with Non-Neurogenic Dysfunctional Voiding
by Tien-Lin Chang, Yuan-Hong Jiang and Hann-Chorng Kuo
Biomedicines 2024, 12(8), 1902; https://doi.org/10.3390/biomedicines12081902 - 20 Aug 2024
Viewed by 388
Abstract
Dysfunctional voiding (DV) is an abnormal urethral sphincter activity during voiding in neurologically normal individuals. Urethral sphincter botulinum toxin A (BoNT-A) injection has been used to treat DV, but the results have not been completely satisfactory. This study investigated the neurological characteristics of [...] Read more.
Dysfunctional voiding (DV) is an abnormal urethral sphincter activity during voiding in neurologically normal individuals. Urethral sphincter botulinum toxin A (BoNT-A) injection has been used to treat DV, but the results have not been completely satisfactory. This study investigated the neurological characteristics of women with DV using the lower urinary tract electrophysiology (EP) study and the therapeutic efficacy of BoNT-A injection. In total, 48 women with DV and 16 women with normal voiding were included. Videourodynamic studies were conducted to diagnose DV before BoNT-A injection. EP studies, including urethral sphincter electromyography, bulbocavernosus reflex, and pudendal nerve conduction velocity, were conducted. Polyphasic motor unit action potentials suggestive of reinnervation were detected in 58.3% of patients with DV and 18.8% of controls (p = 0.001). Significant improvement in the corrected maximum flow rate (cQmax) was observed in patients with reinnervation at 1 and 3 months after BoNT-A injections into the urethral sphincter. Urethral sphincter denervation or reinnervation activity was commonly noted in 62.5% of women with DV. Repeated BoNT-A injections into the urethral sphincter provided effective treatment in 47.9% of patients, with mild improvement in cQmax observed in patients with urethral sphincter reinnervation. However, the improvement was not superior to those without reinnervation. Full article
(This article belongs to the Section Molecular and Translational Medicine)
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<p>Different electromyographic findings in patients with dysfunctional voiding. (<b>A</b>) Positive sharp waves and the presence of fibrillation indicating denervation changes. (<b>B</b>) Polyphasic motor-unit action potential indicating reinnervation changes. (<b>C</b>) Normal motor unit action potentials. X-labeling: time (millisecond), Y-labeling: Voltage, Div: Digital input group voltage.</p>
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15 pages, 1647 KiB  
Article
Phase-Based Gait Prediction after Botulinum Toxin Treatment Using Deep Learning
by Adil Khan, Omar Galarraga, Sonia Garcia-Salicetti and Vincent Vigneron
Sensors 2024, 24(16), 5343; https://doi.org/10.3390/s24165343 - 18 Aug 2024
Viewed by 566
Abstract
Gait disorders in neurological diseases are frequently associated with spasticity. Intramuscular injection of Botulinum Toxin Type A (BTX-A) can be used to treat spasticity. Providing optimal treatment with the highest possible benefit–risk ratio is a crucial consideration. This paper presents a novel approach [...] Read more.
Gait disorders in neurological diseases are frequently associated with spasticity. Intramuscular injection of Botulinum Toxin Type A (BTX-A) can be used to treat spasticity. Providing optimal treatment with the highest possible benefit–risk ratio is a crucial consideration. This paper presents a novel approach for predicting knee and ankle kinematics after BTX-A treatment based on pre-treatment kinematics and treatment information. The proposed method is based on a Bidirectional Long Short-Term Memory (Bi-LSTM) deep learning architecture. Our study’s objective is to investigate this approach’s effectiveness in accurately predicting the kinematics of each phase of the gait cycle separately after BTX-A treatment. Two deep learning models are designed to incorporate categorical medical treatment data corresponding to the injected muscles: (1) within the hidden layers of the Bi-LSTM network, (2) through a gating mechanism. Since several muscles can be injected during the same session, the proposed architectures aim to model the interactions between the different treatment combinations. In this study, we conduct a comparative analysis of our prediction results with the current state of the art. The best results are obtained with the incorporation of the gating mechanism. The average prediction root mean squared error is 2.99° (R2 = 0.85) and 2.21° (R2 = 0.84) for the knee and the ankle kinematics, respectively. Our findings indicate that our approach outperforms the existing methods, yielding a significantly improved prediction accuracy. Full article
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<p>Process of converting each patient’s trial into normalized gait phases (stance and swing). (<b>a</b>,<b>b</b>) knee and ankle trials of a random Patient i, respectively; (<b>c</b>,<b>d</b>) knee and ankle cycles of Patient i extracted from their trials; (<b>e</b>,<b>f</b>) One cycle of the knee and ankle joints, respectively; (<b>g</b>,<b>i</b>) normalized stance phase of knee and ankle joints from given cycles, respectively; (<b>h</b>,<b>j</b>) normalized swing phase of knee and ankle joints, respectively.</p>
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<p>Flowchart of data preprocessing. We acquired the trajectories of patient trials from the database and extracted all cycles from the trials for the knee and ankle joints. After that, we selected each cycle and segmented them into stance and swing phases. Finally, we normalized the phases.</p>
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<p>(<b>a</b>) Multi-task learning architecture with Bi-LSTM sub-models: processing of MTD in each sub-model. (<b>b</b>) Multi-task learning architecture with Bi-LSTM sub-models: incorporating MTD through a gating mechanism.</p>
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<p>Comparison of MTD-GM prediction and post-treatment kinematics for a patient with a given disease.</p>
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<p>Outliers.</p>
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<p>Detailed results of all patients using the MTD-GM model.</p>
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15 pages, 2218 KiB  
Article
Real-World Observational Analysis of Clinical Characteristics and Treatment Patterns of Patients with Chronic Sialorrhea
by Michael A. Hast, Amanda M. Kong, Jenna Abdelhadi, Rohan Shah, Andrew Szendrey and Jordan Holmes
Toxins 2024, 16(8), 366; https://doi.org/10.3390/toxins16080366 - 17 Aug 2024
Viewed by 627
Abstract
Chronic sialorrhea is a condition characterized by excessive drooling, often associated with neurological and neuromuscular disorders such as Parkinson’s disease, cerebral palsy, and stroke. Despite its prevalence, it remains underdiagnosed and poorly understood, leading to a lack of comprehensive data on patient demographics, [...] Read more.
Chronic sialorrhea is a condition characterized by excessive drooling, often associated with neurological and neuromuscular disorders such as Parkinson’s disease, cerebral palsy, and stroke. Despite its prevalence, it remains underdiagnosed and poorly understood, leading to a lack of comprehensive data on patient demographics, clinical characteristics, and treatment patterns. This study aimed to help fill these existing gaps by analyzing real-world data using Optum’s de-identified Clinformatics® Data Mart Database. Patients were required to have a diagnosis indicative of sialorrhea plus evidence of sialorrhea treatment between 1/1/2007 and 5/31/2022. Two cohorts were analyzed: patients with evidence of newly diagnosed sialorrhea and associated treatment, and sialorrhea patients initiating incobotulinumtoxinA. Clinical characteristics, comorbidities, symptoms, and treatment utilization were described before and after diagnosis and incobotulinumtoxinA initiation. No formal statistical comparisons were performed. Patients were predominantly aged 65 or older, male, and non-Hispanic white. Parkinson’s disease and cerebral palsy were the most common comorbidities among adults and children, respectively. Treatment patterns suggest that anticholinergics are more commonly used than botulinum toxin therapy. The findings offer valuable information for improving diagnosis and treatment approaches and suggest a need for further research into treatment effectiveness, safety, and disease burden. Full article
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<p>(<b>A</b>,<b>B</b>) Patient attrition of overall chronic sialorrhea cohort and incobotulinumtoxinA cohort.</p>
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<p>(<b>A</b>,<b>B</b>) Patient attrition of overall chronic sialorrhea cohort and incobotulinumtoxinA cohort.</p>
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14 pages, 928 KiB  
Article
Treatment of Acquired Deforming Hypertonia with Botulinum Toxin in Older Population: A Retrospective Study
by Pablo Maldonado, Hugo Bessaguet, Cédric Chol, Pascal Giraux, Ludovic Lafaie, Ahmed Adham, Romain David, Thomas Celarier and Etienne Ojardias
Toxins 2024, 16(8), 365; https://doi.org/10.3390/toxins16080365 - 16 Aug 2024
Viewed by 634
Abstract
Acquired deforming hypertonia (ADH) affects the daily care of numerous nursing home residents. The aim of this study was to analyze the practice, aims, and effectiveness of botulinum toxin injections (BTxis) in the treatment of older patients with contractures, an indication for which [...] Read more.
Acquired deforming hypertonia (ADH) affects the daily care of numerous nursing home residents. The aim of this study was to analyze the practice, aims, and effectiveness of botulinum toxin injections (BTxis) in the treatment of older patients with contractures, an indication for which BTxis are still underused. Data were extracted retrospectively from medical records regarding population, contractures, and injections. A prospective analysis was conducted to evaluate treatment goals set by goal attainment scaling (GAS) at T0 and at T1, to evaluate the therapeutic effects. We also recorded the occurrence of side effects, using a telephone questionnaire. This study included 41 patients older than 70 years who had received one or more BTxis for the first time between January 2018 and December 2021. Most of the older people we included lived in an institution (66%), manifested severe dependence, and presented significant morbi-mortality (37% of the patients died in the year after the last injection). The main objectives of these injections were purely comfort, without any functional goals. The GAS scores suggested effectiveness for comfort GAS scores. No complications were recorded. This study highlights the BTxis potential to address the needs of a larger number of older patients with ADH. Full article
(This article belongs to the Special Issue Uses of Botulinum Toxin Injection in Medicine)
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<p>Survival curve of patients receiving botulinum toxin injections (BTxis) to treat acquired deforming hypertonia (ADH); (time in months elapsed between the first injection and death). Legend F1: This survival curve represents the survival of the population during the treatment follow-up period. Time 0 on the <span class="html-italic">x</span>-axis corresponds to the first BTxi for each patient (100% of the population alive, <span class="html-italic">y</span>-axis). At the end of the study period (24 months), 50% of the population is alive.</p>
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<p>Mean GAS score for each goal (with minimum and maximum values) at the time of individual re-evaluation (T1) (aggregate data for all individuals; symbols) and percentage frequency of each goal among all the goals chosen (histograms). Legend F2: This graph shows the frequency of goals set at the start of treatment with BTxi (right <span class="html-italic">y</span>-axis) and the mean of GAS T1 scores by goal category after treatment (left <span class="html-italic">y</span>-axis) with minimum and maximum values.</p>
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13 pages, 3988 KiB  
Article
Intramuscular Botulinum Toxin as an Adjunct to Arthrocentesis with Viscosupplementation in Temporomandibular Disorders: A Proof-of-Concept Case–Control Investigation
by Luca Guarda Nardini, Daniele Manfredini, Anna Colonna, Edoardo Ferrari Cagidiaco, Marco Ferrari and Matteo Val
Toxins 2024, 16(8), 364; https://doi.org/10.3390/toxins16080364 - 16 Aug 2024
Viewed by 561
Abstract
Background: The reduction in joint load is a potential beneficial factor in managing osteoarthritis of the temporomandibular joint (TMJ). This paper aims to compare the effectiveness of the intramuscular injection of botulinum toxin (BTX-A) as an adjunct to TMJ arthrocentesis plus viscosupplementation with [...] Read more.
Background: The reduction in joint load is a potential beneficial factor in managing osteoarthritis of the temporomandibular joint (TMJ). This paper aims to compare the effectiveness of the intramuscular injection of botulinum toxin (BTX-A) as an adjunct to TMJ arthrocentesis plus viscosupplementation with arthrocentesis plus viscosupplementation alone in the management of TMJ osteoarthritis. Methods: A pilot clinical retrospective study examined TMJ osteoarthritis treatments. Patients were divided into two groups: Group A received BTX-A injections and arthrocentesis with viscosupplementation, while Group B received only arthrocentesis with viscosupplementation. The study assessed outcomes based on mouth opening (MO), pain at rest (PR), pain at mastication (PF), and masticatory efficiency (ME) at various time points (baseline (T0), 1 week (T1), 2 weeks (T2), 3 weeks (T3), and 4 weeks (T4)) up to 2 months after treatment. Results: The study included two groups, each with five patients. Group A received five weekly sessions of arthrocentesis plus viscosupplementation and a single BTX-A injection during the first arthrocentesis appointment. Group B underwent the five-session protocol of arthrocentesis plus viscosupplementation alone. MO, PF, PR, and ME improved quickly in T2 in both groups, but the improvement was of greater importance over the following weeks and lasted longer in Group A. Conclusions: Arthrocentesis with viscosupplementation associated with BTX-A was found to be more effective than arthrocentesis alone in improving clinical outcomes. This suggests that patients with TMJ osteoarthritis and myofascial pain may benefit from reduced muscle tone and joint load. Full article
(This article belongs to the Section Bacterial Toxins)
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<p>Variations in pain at rest (score according to VAS scale) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group A.</p>
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<p>Variations in pain at rest (score according to VAS scale) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group B.</p>
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<p>Variations in pain during chewing (score according to VAS scale) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group A.</p>
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<p>Variations in pain during chewing (score according to VAS scale) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group B.</p>
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<p>Mastication efficiency variations (score according to VAS scale) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group A.</p>
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<p>Mastication efficiency variations (score according to VAS scale) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group B.</p>
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<p>Functional limitation variations (0, absent; 1, slight; 2, moderate; 3, intense; 4, severe) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group A.</p>
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<p>Functional limitation variations (0, absent; 1, slight; 2, moderate; 3, intense; 4, severe) in T0 (before treatment), T1, T2, T3, T4, and T5 (2 months after last arthrocentesis in T4) in Group B.</p>
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<p>Site of injection of BTX in masseter and temporalis muscle. The dots indicate the injection sites for BTX, while the lines outline the recommended areas for injecting the masseter muscle inferiorly and the anterior portion of the temporalis muscle superiorly.</p>
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13 pages, 1759 KiB  
Article
Patient Characteristics and Real-World Use of Botulinum Toxins for the Treatment of Cervical Dystonia, Blepharospasm, and Hemifacial Spasm
by Michael A. Hast, Amanda M. Kong, Shaina Desai, Soo Back, Sahar Syed and Jordan Holmes
Toxins 2024, 16(8), 362; https://doi.org/10.3390/toxins16080362 - 16 Aug 2024
Viewed by 612
Abstract
Movement disorders such as cervical dystonia, blepharospasm, and hemifacial spasm negatively impact the quality of life of people living with these conditions. Botulinum toxin (BoNT) injections are commonly used to treat these disorders. We sought to describe patient characteristics, BoNT utilization, and potential [...] Read more.
Movement disorders such as cervical dystonia, blepharospasm, and hemifacial spasm negatively impact the quality of life of people living with these conditions. Botulinum toxin (BoNT) injections are commonly used to treat these disorders. We sought to describe patient characteristics, BoNT utilization, and potential adverse events (AEs) among patients with cervical dystonia, blepharospasm, and hemifacial spasm using Optum’s de-identified Clinformatics® Data Mart Database. Patients were required to have a diagnosis of the specific condition plus evidence of treatment with BoNT between 8/1/2010 and 5/31/2022. Cervical dystonia patients were commonly females (76%) and aged 45 and older (78%); both blepharospasm and hemifacial spasm patients were commonly females (both 69%) and aged 65 and older (61% and 56%, respectively). Anticholinergics were commonly used (65–82% across cohorts), as were peripheral muscle relaxants for cervical dystonia patients specifically (31%). The median number of injections per year was 2 with the median weeks between injections being between 13 and 15. Of the AEs evaluated, dyspnea was identified frequently across all the cohorts (14–20%). The findings were similar for different BoNT formulations. More research is needed to thoroughly describe BoNT utilization, such as the doses injected, and to optimize treatment for patients with these conditions. Full article
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<p>Patient attrition for cervical dystonia, blepharospasm, and hemifacial spasm patient populations.</p>
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<p>(<b>A</b>,<b>B</b>) Proportions of Patients Experiencing a Potential AE within 5 Months of Botulinum Toxin Administration.</p>
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