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Family Planning for People with Multiple Sclerosis in Saudi Arabia: an Expert Consensus. 沙特阿拉伯多发性硬化症患者计划生育:专家共识。
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2021-02-15 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6667006
Mohammed Al Jumah, Yaser Al Malik, Nuha M AlKhawajah, Jameelah Saeedi, Ibtisam AlThubaiti, Saeed Bohlega, Reem F Bunyan, Edward J Cupler, Ahmed ElBoghdady, Ahmed Hassan, Eman Nassim Ali, Marinella Clerico

More than half of all patients with multiple sclerosis (MS) in the Kingdom of Saudi Arabia (KSA) are women of childbearing age. Raising a family is an important life goal for women in our region of the world. However, fears and misconceptions about the clinical course of relapsing-remitting MS (RRMS) and the effects of disease-modifying drugs (DMDs) on the foetus have led many women to reduce their expectations of raising a family, sometimes even to the point of avoiding pregnancy altogether. The increase in the number of DMDs available to manage RRMS and recent studies on their effects in pregnancy have broadened management options for these women. Interferon beta now has an indication in Europe for use during pregnancy (according to clinical need) and can be used during breastfeeding. Glatiramer acetate is a further possible option for women with lower levels of RRMS disease activity who are, or about to become, pregnant; natalizumab may be used up to 30 weeks in patients with higher levels of disease activity. Where possible, physicians need to support and encourage women to pursue their dream of a fulfilling family life, supported where necessary by active interventions for RRMS that are increasingly evidence based.

在沙特阿拉伯王国(KSA),超过一半的多发性硬化症(MS)患者是育龄妇女。在我们这个地区,养家是妇女重要的人生目标。然而,对复发缓解型多发性硬化症(RRMS)的临床病程以及疾病缓解药物(dmd)对胎儿的影响的恐惧和误解,导致许多妇女降低了抚养家庭的期望,有时甚至达到完全避免怀孕的程度。可用于管理RRMS的dmd数量的增加,以及最近关于其在怀孕期间影响的研究,扩大了这些妇女的管理选择。干扰素β现在在欧洲有妊娠期间使用的指征(根据临床需要),并可在母乳喂养期间使用。对于已经或即将怀孕的RRMS疾病活动度较低的女性,醋酸格拉替默是另一种可能的选择;Natalizumab可用于疾病活动度较高的患者长达30周。在可能的情况下,医生需要支持和鼓励妇女追求充实的家庭生活的梦想,必要时通过对RRMS的积极干预来支持,这些干预越来越多地基于证据。
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引用次数: 5
The Effect of Cannabis on the Clinical and Cytokine Profiles in Patients with Multiple Sclerosis. 大麻对多发性硬化症患者临床和细胞因子谱的影响
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2021-02-05 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6611897
Wessam Mustafa, Nadia Elgendy, Samer Salama, Mohamed Jawad, Khaled Eltoukhy

Background: Multiple studies have reported that cannabis administration in multiple sclerosis patients is associated with decreased symptom severity. This study was conducted to evaluate the prevalence of cannabis abuse in multiple sclerosis cases and to evaluate the effect of cannabis on serum cytokines in such cases. Patients and Methods. A total of 150 multiple sclerosis cases along with 150 healthy controls were included during the study period. All cases were subjected to history taking, neurological examination, and routine investigations. Cases were asked about cannabis intake which was confirmed by a urine test. Serum cytokines including IL-1, IL-2, IL-4, IL-10, IL-12, IL-17, IL-22, IFN-γ, IFN-β1, and TNF-α were ordered for all cases and controls.

Results: Twenty-eight cases were cannabis abusers (MS/cannabis group, 18.67%). The remaining 122 cases represented the MS group. There was no significant difference between the three groups regarding age, disease duration, or MS type. Male gender was more predominant in the MS/cannabis group, and the number of relapses was significantly lower in the same group. Fifteen cases (53.6%) reported that their symptoms were improved by cannabis. Proinflammatory cytokines were significantly elevated in the MS group compared to the MS/cannabis and control groups. Additionally, anti-inflammatory cytokines had significantly lower values in the MS group compared to the MS/cannabis and control groups. Most clinical symptoms were significantly improved in the MS/cannabis group compared to the MS group apart from sexual dysfunction, bladder symptoms, and visual disturbances. Mild side effects of cannabis were also reported.

Conclusion: Cannabis may have a positive impact on the cytokine and clinical profiles in cases with multiple sclerosis.

背景:多项研究报道,多发性硬化症患者服用大麻与症状严重程度降低有关。本研究旨在评估多发性硬化症病例中大麻滥用的流行程度,并评估大麻对此类病例中血清细胞因子的影响。患者和方法。在研究期间,共有150例多发性硬化症患者和150名健康对照者被纳入研究。所有病例均接受病史记录、神经学检查和常规检查。向病例询问大麻摄入量,并通过尿检予以证实。所有病例和对照组的血清细胞因子包括IL-1、IL-2、IL-4、IL-10、IL-12、IL-17、IL-22、IFN-γ、IFN-β1和TNF-α。结果:大麻滥用者28例(MS/大麻组,18.67%)。其余122例为多发性硬化症组。三组之间在年龄、病程或MS类型方面无显著差异。男性在MS/大麻组中更占优势,且同一组的复发次数明显较低。15例(53.6%)报告说,大麻改善了他们的症状。与MS/大麻组和对照组相比,MS组的促炎细胞因子显著升高。此外,与MS/大麻组和对照组相比,MS组的抗炎细胞因子值显着降低。除了性功能障碍、膀胱症状和视觉障碍外,MS/大麻组的大多数临床症状与MS组相比都得到了显著改善。大麻的轻微副作用也有报道。结论:大麻可能对多发性硬化症患者的细胞因子和临床表现有积极影响。
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引用次数: 4
miRNA-Dependent CD4+ T Cell Differentiation in the Pathogenesis of Multiple Sclerosis. mirna依赖性CD4+ T细胞分化在多发性硬化发病机制中的作用。
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2021-01-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8825588
Justyna Basak, Ireneusz Majsterek

Multiple sclerosis (MS) is characterized by multifocal lesions, chronic inflammatory condition, and degenerative processes within the central nervous system (CNS) leading to demyelination. The most important cells involved in its pathogenesis are those which are CD4+, particularly proinflammatory Th1/Th17 and regulatory Treg. Signal cascades associated with CD4+ differentiation are regulated by microRNAs (miRNAs): short, single-stranded RNAs, responsible for negative regulation of gene expression at the posttranscriptional level. Several miRNAs have been consistently reported as showing dysregulated expression in MS, and their expression patterns may be elevated or decreased, depending on the function of specific miRNA in the immune system. Studies in MS patients indicate that, among others, miR-141, miR-200a, miR-155, miR-223, and miR-326 are upregulated, while miR-15b, miR-20b, miR-26a, and miR-30a are downregulated. Dysregulation of these miRNAs may contribute to the imbalance between pro- and anti-inflammatory processes, since their targets are associated with the regulation of Th1/Th17 and Treg cell differentiation. Highly expressed miRNAs can in turn suppress translation of key Th1/Th17 differentiation inhibitors. miRNA dysregulation may result from the impact of various factors at each stage of their biogenesis. Immature miRNA undergoes multistage transcriptional and posttranscriptional modifications; therefore, any protein involved in the processing of miRNAs can potentially lead to disturbances in their expression. Epigenetic modifications that have a direct impact on miRNA gene transcription may also play an important role.

多发性硬化症(MS)的特点是多灶性病变、慢性炎症和中枢神经系统(CNS)退行性过程导致脱髓鞘。在其发病机制中最重要的细胞是CD4+,特别是促炎Th1/Th17和调节性Treg。与CD4+分化相关的信号级联是由microRNAs (miRNAs)调控的。microRNAs是一种短的单链rna,在转录后水平上负责基因表达的负调控。一些miRNA一直被报道在MS中表达失调,它们的表达模式可能升高或降低,这取决于特定miRNA在免疫系统中的功能。在MS患者中的研究表明,miR-141、miR-200a、miR-155、miR-223和miR-326上调,miR-15b、miR-20b、miR-26a和miR-30a下调。这些mirna的失调可能导致促炎和抗炎过程之间的不平衡,因为它们的靶标与Th1/Th17和Treg细胞分化的调节有关。高表达的mirna可以反过来抑制关键的Th1/Th17分化抑制剂的翻译。miRNA的失调可能是在其生物发生的各个阶段受到各种因素的影响。未成熟miRNA经历多阶段转录和转录后修饰;因此,任何参与mirna加工的蛋白质都可能导致其表达受到干扰。对miRNA基因转录有直接影响的表观遗传修饰也可能发挥重要作用。
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引用次数: 15
Teriflunomide Safety and Efficacy in Advanced Progressive Multiple Sclerosis. 特立氟米特治疗晚期进行性多发性硬化的安全性和有效性。
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2020-12-17 eCollection Date: 2020-01-01 DOI: 10.1155/2020/5471987
Vanessa F Moreira Ferreira, Danielle Caefer, Natalie Erlich-Malona, Brian C Healy, Tanuja Chitnis, James M Stankiewicz

Objectives: To explore the safety and efficacy profile of teriflunomide in progressive multiple sclerosis.

Methods: We conducted a single-center retrospective observational analysis of a progressive multiple sclerosis population, assessing safety and efficacy in patients treated at least one year with teriflunomide or glatiramer acetate. Sustained progression of expanded disability status scale and sustained worsening of timed 25-foot walk were compared using a Cox proportional hazards model.

Results: Teriflunomide group (n = 29) mean characteristics: age = 58 years (SD ± 7.6), disease duration = 16.7 years (SD ± 9.5), expanded disability status score = 5.9 (SD ± 1.3), and follow - up = 32.4 months (SD ± 13.6). Glatiramer acetate group (n = 30) mean characteristics: age = 52.4 years (SD ± 11.3), disease duration = 15.1 years (SD ± 10.4), expanded disability status score = 5.7 (SD ± 1.6), and follow - up = 46.9 months (SD ± 43.9). Both treatments were well tolerated without serious side effects. After adjustment for age, sex, and baseline expanded disability status score, sustained expanded disability status score progression did not differ between groups (hazard ratio = 1.17; 95% confidence interval: 0.45, 3.08; p = 0.75). Sustained timed 25-foot walk worsening after adjustment also did not differ (hazard ratio = 0.56; 95% confidence interval: 0.2, 1.53; p = 0.26).

Conclusion: In an advanced progressive multiple sclerosis population, no substantial differences in tolerability, safety, sustained EDSS progression, or sustained T25FW worsening over time were observed between glatiramer acetate and teriflunomide-treated groups. The small sample precluded definitive determination.

目的:探讨特立氟米特治疗进展性多发性硬化症的安全性和有效性。方法:我们对进行性多发性硬化症人群进行了一项单中心回顾性观察分析,评估了使用特立氟米特或醋酸格拉替雷默治疗至少一年的患者的安全性和有效性。使用Cox比例风险模型比较扩展残疾状态量表的持续进展和定时25英尺步行的持续恶化。结果:特利氟米特组(n = 29)平均特征:年龄= 58岁(SD±7.6),病程= 16.7年(SD±9.5),扩展残疾状态评分= 5.9 (SD±1.3),随访= 32.4个月(SD±13.6)。醋酸格拉替默组(n = 30)平均特征:年龄= 52.4岁(SD±11.3),病程= 15.1年(SD±10.4),扩展残疾状态评分= 5.7 (SD±1.6),随访= 46.9个月(SD±43.9)。两种治疗方法耐受性良好,无严重副作用。调整年龄、性别和基线扩展残疾状态评分后,两组间持续扩展残疾状态评分进展无差异(风险比= 1.17;95%置信区间:0.45,3.08;P = 0.75)。调整后持续计时25英尺步行恶化也没有差异(风险比= 0.56;95%置信区间:0.2,1.53;P = 0.26)。结论:在晚期进行性多发性硬化症人群中,醋酸格拉替雷默和特立氟米特治疗组在耐受性、安全性、持续EDSS进展或持续T25FW恶化方面没有观察到实质性差异。样本量小,无法作出确切的测定。
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引用次数: 0
Backward Walking and Dual-Task Assessment Improve Identification of Gait Impairments and Fall Risk in Individuals with MS. 后退行走和双任务评估提高了MS患者步态障碍和跌倒风险的识别。
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2020-09-08 eCollection Date: 2020-01-01 DOI: 10.1155/2020/6707414
Erin M Edwards, Deborah A Kegelmeyer, Anne D Kloos, Manon Nitta, Danya Raza, Deborah S Nichols-Larsen, Nora E Fritz

Background: Individuals with multiple sclerosis (MS) experience deficits in motor and cognitive domains, resulting in impairment in dual-task walking ability. The goal of this study was to compare performance of forward walking and backward walking in single- and dual-task conditions in persons with MS to age- and sex-matched healthy controls. We also examined relationships between forward and backward walking to cognitive function, balance, and retrospective fall reports.

Methods: All measures were collected in a single session. A 2 × 2 × 2 mixed model ANOVA was used to compare differences in forward and backward walking in single- and dual-task conditions between MS and healthy controls. Spearman correlations were used to examine relationships between gait and cognitive function, falls, and balance.

Results: Eighteen individuals with relapsing-remitting MS and 14 age- and sex-matched healthy controls participated. Backward walking velocity revealed significant differences between groups for both single-task (p = 0.015) and dual-task (p = 0.014) conditions. Persons with MS demonstrated significant differences between single- and dual-task forward and backward walking velocities (p = 0.023; p = 0.004), whereas this difference was only apparent in the backward walking condition for healthy controls (p = 0.004). In persons with MS, there were significant differences in double support time between single- and dual-task conditions in both backward (p < 0.001) and forward (p = 0.001) directions. More falls at six months were significantly associated with shorter backward dual-task stride length (r = -0.490; p = 0.046) and slower velocity (r = -0.483; p = 0.050).

Conclusion: Differences in MS and age- and sex-matched healthy controls are more pronounced during backward compared to forward walking under single- and dual-task conditions. Future work with a larger sample size is needed to validate the clinical utility of backward walking and dual-task assessments and mitigate the limited sensitivity of the current dual-task assessments that primarily rely upon forward walking.

背景:多发性硬化症(MS)患者在运动和认知领域存在缺陷,导致双任务行走能力受损。本研究的目的是比较MS患者在单任务和双任务条件下向前行走和向后行走的表现与年龄和性别匹配的健康对照。我们还研究了向前和向后行走与认知功能、平衡和回顾性跌倒报告之间的关系。方法:单次采集所有测量数据。采用2 × 2 × 2混合模型方差分析比较MS与健康对照在单任务和双任务条件下向前和向后行走的差异。Spearman相关性用于检查步态与认知功能、跌倒和平衡之间的关系。结果:18名复发缓解型MS患者和14名年龄和性别匹配的健康对照者参与了研究。在单任务(p = 0.015)和双任务(p = 0.014)条件下,组间后退行走速度均有显著差异。多发性硬化症患者在单任务和双任务的向前和向后行走速度上存在显著差异(p = 0.023;P = 0.004),而这种差异仅在健康对照组的后退行走条件下明显(P = 0.004)。在MS患者中,单任务和双任务条件下的双重支持时间在向后(p < 0.001)和向前(p = 0.001)两个方向上都有显著差异。6个月时跌倒次数越多,向后双任务步幅越短(r = -0.490;P = 0.046)和较慢的速度(r = -0.483;P = 0.050)。结论:在单任务和双任务条件下,MS与年龄和性别匹配的健康对照在后退行走时比向前行走时差异更明显。未来需要更大样本量的工作来验证向后行走和双任务评估的临床效用,并减轻当前主要依赖于向前行走的双任务评估的有限敏感性。
{"title":"Backward Walking and Dual-Task Assessment Improve Identification of Gait Impairments and Fall Risk in Individuals with MS.","authors":"Erin M Edwards,&nbsp;Deborah A Kegelmeyer,&nbsp;Anne D Kloos,&nbsp;Manon Nitta,&nbsp;Danya Raza,&nbsp;Deborah S Nichols-Larsen,&nbsp;Nora E Fritz","doi":"10.1155/2020/6707414","DOIUrl":"https://doi.org/10.1155/2020/6707414","url":null,"abstract":"<p><strong>Background: </strong>Individuals with multiple sclerosis (MS) experience deficits in motor and cognitive domains, resulting in impairment in dual-task walking ability. The goal of this study was to compare performance of forward walking and backward walking in single- and dual-task conditions in persons with MS to age- and sex-matched healthy controls. We also examined relationships between forward and backward walking to cognitive function, balance, and retrospective fall reports.</p><p><strong>Methods: </strong>All measures were collected in a single session. A 2 × 2 × 2 mixed model ANOVA was used to compare differences in forward and backward walking in single- and dual-task conditions between MS and healthy controls. Spearman correlations were used to examine relationships between gait and cognitive function, falls, and balance.</p><p><strong>Results: </strong>Eighteen individuals with relapsing-remitting MS and 14 age- and sex-matched healthy controls participated. Backward walking velocity revealed significant differences between groups for both single-task (<i>p</i> = 0.015) and dual-task (<i>p</i> = 0.014) conditions. Persons with MS demonstrated significant differences between single- and dual-task forward and backward walking velocities (<i>p</i> = 0.023; <i>p</i> = 0.004), whereas this difference was only apparent in the backward walking condition for healthy controls (<i>p</i> = 0.004). In persons with MS, there were significant differences in double support time between single- and dual-task conditions in both backward (<i>p</i> < 0.001) and forward (<i>p</i> = 0.001) directions. More falls at six months were significantly associated with shorter backward dual-task stride length (<i>r</i> = -0.490; <i>p</i> = 0.046) and slower velocity (<i>r</i> = -0.483; <i>p</i> = 0.050).</p><p><strong>Conclusion: </strong>Differences in MS and age- and sex-matched healthy controls are more pronounced during backward compared to forward walking under single- and dual-task conditions. Future work with a larger sample size is needed to validate the clinical utility of backward walking and dual-task assessments and mitigate the limited sensitivity of the current dual-task assessments that primarily rely upon forward walking.</p>","PeriodicalId":46096,"journal":{"name":"Multiple Sclerosis International","volume":"2020 ","pages":"6707414"},"PeriodicalIF":2.5,"publicationDate":"2020-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/6707414","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38409454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Evaluation of Lower Urinary Tract Dysfunction Impact on Quality of Life in Multiple Sclerosis Patients: Russian Translation and Validation of SF-Qualiveen. 评估多发性硬化症患者下尿路功能障碍对生活质量的影响:俄语翻译和SF-Qualiveen的验证。
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2020-07-25 eCollection Date: 2020-01-01 DOI: 10.1155/2020/4652439
Ekaterina S Philippova, Igor V Bazhenov, Alexander V Ziryanov, Ekaterina Y Moskvina

The Short Form Qualiveen (SF-Qualiveen) is an 8-item version of the Qualiveen questionnaire used to evaluate the impact of urinary symptoms on the quality of life in patients with urological dysfunction due to neurological disorders. The questionnaire was never available in the Russian language before. The study is aimed at providing the translation, cultural adaptation, and validation of a Russian version of the SF-Qualiveen for the use in patients with multiple sclerosis (MS). Materials and Methods. The original English language version of the SF-Qualiveen was translated into Russian according to the cultural and linguistic adaptation algorithm. The participants (50 MS patients with neurogenic bladder and 10 relatively healthy volunteers) filled out the finalized Russian version of the SF-Qualiveen and the Neurogenic Bladder Symptom Score (NBSS) twice, 2 weeks apart. The data obtained was used to determine the internal consistency (Cronbach's alpha), external validity (the Spearman correlation), and test-retest reliability (intraclass correlation coefficient (ICC)) of the questionnaire. Results. The mean SF-Qualiveen total score was 2.51 ± 0.79 in patients with a neurogenic bladder and 0.1 ± 0.02 in the control group (p < 0.001). Cronbach's alpha exceeded 0.9 indicating an excellent internal consistency of the questionnaire. The retest did not reveal any significant differences between the findings. The test-retest reliability was good for all items and domains (ICC 0.81-0.89). The total score demonstrated the highest ICC (0.89). The external validity was verified by a strong correlation demonstrated between the SF-Qualiveen and NBSS scores. Conclusions. The Russian SF-Qualiveen questionnaire is a reliable, valid, and consistent tool for the assessment of a urinary disorder impact on the quality of life in patients with MS.

简式Qualiveen (SF-Qualiveen)是一份由8个条目组成的Qualiveen问卷,用于评估由神经系统疾病引起的泌尿功能障碍患者的泌尿症状对生活质量的影响。以前从未有过俄文的调查表。该研究旨在为多发性硬化症(MS)患者提供俄语版SF-Qualiveen的翻译、文化适应和验证。材料与方法。原英文版本的SF-Qualiveen根据文化和语言适应算法被翻译成俄语。参与者(50名MS神经源性膀胱患者和10名相对健康的志愿者)填写了最终的俄语版SF-Qualiveen和神经源性膀胱症状评分(NBSS)两次,间隔2周。获得的数据用于确定问卷的内部一致性(Cronbach’s alpha)、外部效度(Spearman相关)和重测信度(类内相关系数(ICC))。结果。神经源性膀胱组SF-Qualiveen总分均值为2.51±0.79,对照组为0.1±0.02 (p < 0.001)。Cronbach’s alpha大于0.9,表明问卷内部一致性极佳。重新测试没有发现任何显著的差异。所有项目和领域的重测信度均良好(ICC 0.81-0.89)。总得分为0.89,是ICC最高的分数。外部效度通过SF-Qualiveen与NBSS分数之间的强相关性得到验证。结论。俄罗斯SF-Qualiveen问卷是评估泌尿系统疾病对MS患者生活质量影响的可靠、有效和一致的工具。
{"title":"Evaluation of Lower Urinary Tract Dysfunction Impact on Quality of Life in Multiple Sclerosis Patients: Russian Translation and Validation of SF-Qualiveen.","authors":"Ekaterina S Philippova,&nbsp;Igor V Bazhenov,&nbsp;Alexander V Ziryanov,&nbsp;Ekaterina Y Moskvina","doi":"10.1155/2020/4652439","DOIUrl":"https://doi.org/10.1155/2020/4652439","url":null,"abstract":"<p><p>The Short Form Qualiveen (SF-Qualiveen) is an 8-item version of the Qualiveen questionnaire used to evaluate the impact of urinary symptoms on the quality of life in patients with urological dysfunction due to neurological disorders. The questionnaire was never available in the Russian language before. <i>The study is aimed</i> at providing the translation, cultural adaptation, and validation of a Russian version of the SF-Qualiveen for the use in patients with multiple sclerosis (MS). <i>Materials and Methods</i>. The original English language version of the SF-Qualiveen was translated into Russian according to the cultural and linguistic adaptation algorithm. The participants (50 MS patients with neurogenic bladder and 10 relatively healthy volunteers) filled out the finalized Russian version of the SF-Qualiveen and the Neurogenic Bladder Symptom Score (NBSS) twice, 2 weeks apart. The data obtained was used to determine the internal consistency (Cronbach's alpha), external validity (the Spearman correlation), and test-retest reliability (intraclass correlation coefficient (ICC)) of the questionnaire. <i>Results</i>. The mean SF-Qualiveen total score was 2.51 ± 0.79 in patients with a neurogenic bladder and 0.1 ± 0.02 in the control group (<i>p</i> < 0.001). Cronbach's alpha exceeded 0.9 indicating an excellent internal consistency of the questionnaire. The retest did not reveal any significant differences between the findings. The test-retest reliability was good for all items and domains (ICC 0.81-0.89). The total score demonstrated the highest ICC (0.89). The external validity was verified by a strong correlation demonstrated between the SF-Qualiveen and NBSS scores. <i>Conclusions</i>. The Russian SF-Qualiveen questionnaire is a reliable, valid, and consistent tool for the assessment of a urinary disorder impact on the quality of life in patients with MS.</p>","PeriodicalId":46096,"journal":{"name":"Multiple Sclerosis International","volume":"2020 ","pages":"4652439"},"PeriodicalIF":2.5,"publicationDate":"2020-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/4652439","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38256298","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls. 氨基酸和酰基肉碱血浆谱的变化对多发性硬化症患者与健康对照的区别
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2020-07-15 eCollection Date: 2020-01-01 DOI: 10.1155/2020/9010937
Marat F Kasakin, Artem D Rogachev, Elena V Predtechenskaya, Vladimir J Zaigraev, Vladimir V Koval, Andrey G Pokrovsky

McDonald criteria and magnetic resonance imaging (MRI) are used for the diagnosis of multiple sclerosis (MS); nevertheless, it takes a considerable amount of time to make a clinical decision. Amino acid and fatty acid metabolic pathways are disturbed in MS, and this information could be useful for diagnosis. The aim of our study was to find changes in amino acid and acylcarnitine plasma profiles for distinguishing patients with multiple sclerosis from healthy controls. We have applied a targeted metabolomics approach based on tandem mass-spectrometric analysis of amino acids and acylcarnitines in dried plasma spots followed by multivariate statistical analysis for discovery of differences between MS (n = 16) and control (n = 12) groups. It was found that partial least square discriminant analysis yielded better group classification as compared to principal component linear discriminant analysis and the random forest algorithm. All the three models detected noticeable changes in the amino acid and acylcarnitine profiles in the MS group relative to the control group. Our results hold promise for further development of the clinical decision support system.

麦克唐纳标准和磁共振成像(MRI)用于多发性硬化症(MS)的诊断;然而,做出临床决定需要相当长的时间。氨基酸和脂肪酸代谢途径在MS中受到干扰,这一信息可能对诊断有用。我们研究的目的是发现氨基酸和酰基肉碱血浆谱的变化,以区分多发性硬化症患者和健康对照。我们应用了一种靶向代谢组学方法,该方法基于串联质谱分析干燥血浆斑点中的氨基酸和酰基肉碱,然后进行多元统计分析,以发现MS组(n = 16)和对照组(n = 12)之间的差异。结果表明,相对于主成分线性判别分析和随机森林算法,偏最小二乘判别分析具有更好的分类效果。三种模型均检测到MS组相对于对照组的氨基酸和酰基肉碱谱的明显变化。我们的研究结果为临床决策支持系统的进一步发展提供了希望。
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引用次数: 6
The Correlation between Using Social Networks and the General Health of Multiple Sclerosis Patients. 多发性硬化症患者使用社交网络与整体健康的关系
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2020-07-09 eCollection Date: 2020-01-01 DOI: 10.1155/2020/2791317
Atefeh Basirat, Hadi Raeisi Shahraki, Hamid Reza Farpour, Leila Habibi

Background: Multiple sclerosis (MS) threatens the patients' independency and ability to effectively participate in the society. The aim of this study was to determine the correlation between using social networks on the general health of multiple sclerosis patients.

Methods: This study was performed on 80 MS patients referring to Shiraz University of Medical Sciences, Chamran, and Imam Reza Hospital in 2017, whose condition had improved and were treated by a specialist physician. Tools for data collection were general health questionnaire (GHQ-28) and social networks use questionnaires.

Results: Amongst the 80 individuals with MS, 65 (81.3%) were female and 15 (18.8%) were male. Our results suggest that patients with higher levels of education had higher levels of health (P = 0.01). Telegram and WhatsApp, respectively, had a positive correlation with general health (P = 0.007, P = 0.007), anxiety (P = 0.003, P = 0.028), and social dysfunction (P = 0.007, P = 0.007). WhatsApp with 33.64% was the most popular application among MS patients. The correlation between general health and duration of using social networks was not statistically significant (r = 0.22, P = 0.06). Also, no significant correlation was found between the duration of using social networks and the general health (P = 0.62).

Conclusion: Our findings suggest that social networks, especially Telegram and WhatsApp, had a positive correlation with general health, anxiety, and social dysfunction of patients. Therefore, the use of social networks can be considered as a suitable option in reducing the aforementioned concerns among patients with MS. On the other hand, general health and mood status might as well influence the use of social network in MS patients.

背景:多发性硬化症(MS)威胁着患者的独立性和有效参与社会的能力。本研究的目的是确定使用社交网络与多发性硬化症患者总体健康状况之间的相关性。方法:选取设拉子医科大学、Chamran和Imam Reza医院2017年收治的病情好转并经专科医生治疗的80例MS患者为研究对象。数据收集工具为一般健康问卷(GHQ-28)和社交网络使用问卷。结果:80例MS患者中,女性65例(81.3%),男性15例(18.8%)。结果表明,受教育程度越高的患者健康水平越高(P = 0.01)。Telegram和WhatsApp分别与一般健康(P = 0.007, P = 0.007)、焦虑(P = 0.003, P = 0.028)和社交功能障碍(P = 0.007, P = 0.007)呈正相关。最受MS患者欢迎的应用是WhatsApp,占33.64%。一般健康状况与使用社交网络时间之间的相关性无统计学意义(r = 0.22, P = 0.06)。此外,使用社交网络的持续时间与总体健康状况之间没有显著相关性(P = 0.62)。结论:我们的研究结果表明,社交网络,特别是Telegram和WhatsApp,与患者的总体健康、焦虑和社交功能障碍呈正相关。因此,社交网络的使用可以被认为是减少MS患者上述担忧的一个合适的选择。另一方面,一般的健康状况和情绪状况也可能影响MS患者对社交网络的使用。
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引用次数: 2
Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis. Ocrelizumab治疗原发性进行性多发性硬化症的真实世界结果
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2020-06-15 eCollection Date: 2020-01-01 DOI: 10.1155/2020/5463451
K Daniels, P B van der Nat, S T F M Frequin, P J van der Wees, D H Biesma, E L J Hoogervorst, E M W van de Garde

Background: Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered.

Objective: The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting.

Methods: We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (n = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration).

Results: Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (Z = -2.81, p ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start.

Conclusion: Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab.

背景:最近,基于ORATORIO临床试验的数据,ocrelizumab (Ocrevus®)被批准用于治疗原发性进行性多发性硬化症(PPMS)。关于ocrelizumab临床有效性的实际数据尚未收集。目的:本研究的目的是提供关于ocrelizumab在现实世界中诊断为PPMS患者的临床有效性的数据。方法:我们对2018年4月至2018年12月31日期间在St. Antonius医院(Utrecht/Nieuwegein,荷兰)开始ocrelizumab治疗的所有PPMS患者(n = 21)进行了回顾性队列研究。主要结局是奥克雷珠单抗治疗前和治疗后的残疾恶化率(从首次给药前96周到首次给药后24周)。结果:治疗期间残疾加重率与治疗前残疾加重率差异有统计学意义(p < 0.01)。17例患者中有3例在治疗开始后出现临床相关的残疾状况改善。结论:Ocrelizumab可以稳定PPMS患者的残疾进展。一些患者甚至表现出与临床相关的残疾状况改善。进一步的研究应该有助于确定哪些患者从ocrelizumab中获益最多。
{"title":"Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis.","authors":"K Daniels,&nbsp;P B van der Nat,&nbsp;S T F M Frequin,&nbsp;P J van der Wees,&nbsp;D H Biesma,&nbsp;E L J Hoogervorst,&nbsp;E M W van de Garde","doi":"10.1155/2020/5463451","DOIUrl":"https://doi.org/10.1155/2020/5463451","url":null,"abstract":"<p><strong>Background: </strong>Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered.</p><p><strong>Objective: </strong>The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting.</p><p><strong>Methods: </strong>We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (<i>n</i> = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration).</p><p><strong>Results: </strong>Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (<i>Z</i> = -2.81, <i>p</i> ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start.</p><p><strong>Conclusion: </strong>Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab.</p>","PeriodicalId":46096,"journal":{"name":"Multiple Sclerosis International","volume":"2020 ","pages":"5463451"},"PeriodicalIF":2.5,"publicationDate":"2020-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/5463451","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38109787","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
Neuromyelitis Optica Spectrum Disorder Attack Triggered by Herpes Zoster Infection. 带状疱疹感染引发的视神经脊髓炎频谱障碍发作。
IF 2.5 Q3 CLINICAL NEUROLOGY Pub Date : 2020-04-25 eCollection Date: 2020-01-01 DOI: 10.1155/2020/6151258
Emanuela Claudia Turco, Erica Curti, Valentina Maffini, Francesco Pisani, Franco Granella

Neuromyelitis optica spectrum disorder is a severe autoimmune disease of the central nervous system characterized by recurrent inflammatory events primarily involving the optic nerves and spinal cord. Recently, a triggering role of infectious events in the development of NMOSD has been suggested. Varicella zoster virus is the most common viral infection involved, though the linkage with anti-aquaporin-4 antibodies is so far unknown. We report, to the best of our knowledge, the first pediatric case report about NMOSD relapse triggered by herpes zoster infection. The strict temporal relationship between VZV infection and NMO attacks seems to be more than simply due to chance; however, further reports are needed to be confirmed.

视神经脊髓炎是一种严重的中枢神经系统自身免疫性疾病,以复发性炎症事件为特征,主要累及视神经和脊髓。最近,有研究认为感染事件在NMOSD的发展中起着触发作用。水痘带状疱疹病毒是最常见的病毒感染,尽管与抗水通道蛋白-4抗体的联系迄今尚不清楚。据我们所知,我们报告了第一例由带状疱疹感染引发的NMOSD复发的儿科病例。VZV感染与NMO攻击之间的严格时间关系似乎不仅仅是偶然的;但是,还需要进一步的报告加以证实。
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引用次数: 7
期刊
Multiple Sclerosis International
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