Esclerosis múltiple

精索硬化症
  • 文章类型: Journal Article
    背景:近年来,多发性硬化症(MS)患者的认知康复研究有所增加;然而,其中很少分析对认知储备等变量的影响。该研究旨在探索认知康复计划的效果,该计划包括认知和体育锻炼的组合,以及提高认知能力的小组会议,情绪状态,和认知储备指数。
    方法:将50例MS患者分为2组:对照组,进行有氧运动(n=25),和实验组(n=25),参加了综合认知康复计划(ICRP)。所有参与者均接受3次评估(基线,治疗后,和长期)与简短的可重复的神经心理学测试电池,认知储备量表,贝克抑郁量表,以及评估特质和状态焦虑的量表。
    结果:与对照组相比,实验组患者的认知功能有所改善,随着信息处理速度的显著变化,注意,记忆,认知储备指数,和长期的情绪。
    结论:ICRP可有效改善MS的认知和情绪功能,提高了认知储备指数。
    BACKGROUND: In recent years, there has been an increase of studies dedicated to cognitive rehabilitation in patients with multiple sclerosis (MS); however, few of these analyze the impact on such variables as cognitive reserve. The study aims to explore the effects of a cognitive rehabilitation program comprising a combination of cognitive and physical exercises, as well as group sessions to improve cognitive performance, emotional state, and cognitive reserve index.
    METHODS: Fifty patients with MS were subdivided into 2 groups: the control group, which performed aerobic exercise (n=25), and the experimental group (n=25), which participated in the integrated cognitive rehabilitation program (ICRP). All participants were evaluated 3 times (baseline, post-treatment, and long-term) with the Brief Repeatable Battery of Neuropsychological Tests, Cognitive Reserve Scale, Beck Depression Inventory, and a scale evaluating trait and state anxiety.
    RESULTS: Compared with the control group, patients in the experimental group showed improvements in cognitive function, with significant changes in measures of information processing speed, attention, memory, cognitive reserve index, and long-term mood.
    CONCLUSIONS: The ICRP was effective in improving cognitive and emotional function in MS, and increased the cognitive reserve index.
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  • 文章类型: Journal Article
    背景:LEMVIDA是一项真实世界的前瞻性研究,对西班牙接受阿仑珠单抗治疗的多发性硬化症(MS)患者的生活质量进行3年随访。
    方法:这是一项中期分析,评估2016年10月至2018年9月期间开始使用阿仑珠单抗的患者的基线特征。对于另外3例亚分析患者,按基线EDSS评分进行分类;招募期间开始阿仑珠单抗的时间(队列1:2016年10月至2017年3月,队列2:2017年4月至9月,队列3:2017年10月至2018年3月,队列4:2018年4月至9月);以及是否存在高活性MS标准。
    结果:分析了161例患者:67.1%为女性,年龄38.7±9.4岁,MS持续时间8.5±6.0年,EDSS3.3±1.7,前2年复发次数1.8±1.3。48.3%的患者出现钆增强(Gd)病变(平均:5.2±6.9),63.1%的患者先前接受过芬戈莫德或那他珠单抗治疗。队列1的基线EDSS评分和Gd+病变数量高于队列4(4.1±1.8vs.3.2±1.7;p=0.040和10.9±11.9vs.4.5±5.7;p=0.020)。先前用芬戈莫德和那他珠单抗治疗的频率在队列4中(60.6%)低于队列1(70.6%)(未分析的组间比较)。
    结论:与阿仑珠单抗的3期研究不同,LEMVIDA的患者年龄较大,MS持续时间较长,更高的残疾和以前接受过免疫抑制剂。然而,在整个招聘期间,阿仑单抗治疗有早期开始的趋势,可能是由于MS早期阶段有效性较高的证据。
    BACKGROUND: LEMVIDA is a real-world prospective study of 3-year follow-up on quality of life of patients with multiple sclerosis (MS) receiving alemtuzumab in Spain.
    METHODS: This is an interim analysis evaluating the baseline characteristics of patients who started alemtuzumab between October 2016-September 2018. For 3 additional subanalysis patients were categorised by baseline EDSS score; time of alemtuzumab initiation during the recruitment period (cohort 1: October 2016-March 2017, cohort 2: April-September 2017, cohort 3: October 2017-March 2018 and cohort 4: April-September 2018); and the presence of highly active MS criteria.
    RESULTS: 161 patients were analysed: 67.1% female, age 38.7 ± 9.4 years, MS duration 8.5 ± 6.0 years, EDSS 3.3 ± 1.7 and number of relapses in the previous 2 years 1.8 ± 1.3. 48.3% of patients presented gadolinium-enhanced (Gd+) lesions (mean: 5.2 ± 6.9) and 63.1% had received prior treatment with fingolimod or natalizumab. Baseline EDSS scores and number of Gd+ lesions were higher in cohort 1 than in cohort 4 (4.1 ± 1.8 vs 3.2 ± 1.7; P = .040 and 10.9 ± 11.9 vs 4.5 ± 5.7; P = .020). The frequency of prior treatment with fingolimod and natalizumab was lower in cohort 4 (60.6%) than in cohort 1 (70.6%) (comparison between groups not analysed).
    CONCLUSIONS: Unlike phase 3 studies of alemtuzumab, the patients included in LEMVIDA are older, have a longer duration of MS, higher disability and have received previous immunosuppressants. However, throughout the recruitment period, there is a tendency towards an early beginning of treatment with alemtuzumab, probably due to the evidence of higher effectiveness in the early stages of MS.
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  • 文章类型: Journal Article
    背景:多发性硬化症(MS)是一种免疫介导的疾病,与几种危险因素有关,例如各种病毒感染。我们进行这项研究是为了确定COVID-19感染与MS严重程度之间的关系。
    方法:在一项病例对照研究中,我们招募了复发缓解型多发性硬化(RRMS)患者.在登记阶段结束时,根据COVID-19PCR阳性将患者分为两组。对每位患者进行前瞻性随访12个月。人口统计,临床,在常规临床实践期间收集既往病史.每6个月进行一次评估;在登记时和12个月后进行MRI检查。
    结果:三百六十二名患者参与了这项研究。合并COVID-19感染的MS患者的MRI病灶数量(p:0.019,OR(CI):6.37(1.54-26.34))和EDSS评分(p:0.017)明显增加,但总的年复发率或复发率没有差异。COVID-19感染与EDSS进展(p:0.02)和新的MRI病变数量(p:0.004)呈正相关,并预测新的MRI病变数量的可能性为5.92(p:0.018)。
    结论:COVID-19可能导致RRMS人群的残疾评分更高,并且与MRI成像中出现新的Gd增强病变有关。然而,两组间随访期间复发次数无差异.
    Multiple sclerosis (MS) is an immune-mediated disease that has been related to several risk factors such as various viral infections. We carried out this study in order to establish a relationship between COVID-19 infection and MS severity.
    In a case-control study, we recruited patients with relapsing-remitting multiple sclerosis (RRMS). Patients were divided into two groups based on positive COVID-19 PCR at the end of the enrollment phase. Each patient was prospectively followed for 12 months. Demographical, clinical, and past medical history were collected during routine clinical practice. Assessments were performed every six months; MRI was performed at enrollment and 12 months later.
    Three hundred and sixty-two patients participated in this study. MS patients with COVID-19 infection had significantly higher increases in the number of MRI lesions (p: 0.019, OR(CI): 6.37(1.54-26.34)) and EDSS scores (p: 0.017), but no difference was found in total annual relapses or relapse rates. COVID-19 infections were positively correlated with EDSS progression (p: 0.02) and the number of new MRI lesions (p: 0.004) and predicted the likelihood of the number of new MRI lesions by an odds of 5.92 (p: 0.018).
    COVID-19 may lead to higher disability scores in the RRMS population and is associated with developing new Gd-enhancing lesions in MRI imaging. However, no difference was observed between the groups regarding the number of relapses during follow-up.
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  • 文章类型: Journal Article
    背景:近年来,多发性硬化症(MS)患者的认知康复研究有所增加;然而,其中很少分析对认知储备等变量的影响。该研究旨在探索认知康复计划的效果,该计划包括认知和体育锻炼的组合,以及提高认知能力的小组会议,情绪状态,和认知储备指数。
    方法:将50例MS患者分为2组:对照组,进行有氧运动(n=25),和实验组(n=25),参加了综合认知康复计划(ICRP)。所有参与者均接受3次评估(基线,治疗后,和长期)与简短的可重复的神经心理学测试电池,认知储备量表,贝克抑郁量表,以及评估特质和状态焦虑的量表。
    结果:与对照组相比,实验组患者的认知功能有所改善,随着信息处理速度的显著变化,注意,记忆,认知储备指数,和长期的情绪。
    结论:ICRP可有效改善MS的认知和情绪功能,提高了认知储备指数。
    BACKGROUND: In recent years, there has been an increase of studies dedicated to cognitive rehabilitation in patients with multiple sclerosis (MS); however, few of these analyze the impact on such variables as cognitive reserve. The study aims to explore the effects of a cognitive rehabilitation program comprising a combination of cognitive and physical exercises, as well as group sessions to improve cognitive performance, emotional state, and cognitive reserve index.
    METHODS: Fifty patients with MS were subdivided into 2 groups: the control group, which performed aerobic exercise (n=25), and the experimental group (n=25), which participated in the integrated cognitive rehabilitation program (ICRP). All participants were evaluated 3 times (baseline, post-treatment, and long-term) with the Brief Repeatable Battery of Neuropsychological Tests, Cognitive Reserve Scale, Beck Depression Inventory, and a scale evaluating trait and state anxiety.
    RESULTS: Compared with the control group, patients in the experimental group showed improvements in cognitive function, with significant changes in measures of information processing speed, attention, memory, cognitive reserve index, and long-term mood.
    CONCLUSIONS: The ICRP was effective in improving cognitive and emotional function in MS, and increased the cognitive reserve index.
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  • 文章类型: Journal Article
    背景:疼痛在多发性硬化症(MS)患者中非常普遍;50%的病例是慢性的,被归类为伤害性,神经病,或混合型。疼痛影响生活质量,睡眠,和日常生活活动。电疗是治疗MS疼痛的一种有趣的替代或补充治疗方法,不断出现新的创新。
    方法:本研究评估脉冲电磁场(PEMF)单极介电传输治疗MS相关疼痛的有效性。我们做了一个随机的,安慰剂对照临床试验,包括24名患者,用简短的疼痛量表评估了他们,多发性硬化症国际生活质量问卷,贝克抑郁量表,和修正的疲劳冲击量表。
    结果:在最大和平均疼痛评分方面观察到统计学上显著的改善,以及疼痛对工作的影响,个人关系,睡觉和休息。在治疗组和安慰剂组之间没有发现显著差异。
    结论:用PEMF治疗可有效减轻MS患者的疼痛,尽管需要进一步的研究来确认其相对于安慰剂的有效性,并区分哪种类型的疼痛可能更容易受到这种治疗的影响。
    BACKGROUND: Pain is highly prevalent in patients with multiple sclerosis (MS); it is chronic in 50% of cases and is classified as nociceptive, neuropathic, or mixed-type. Pain affects quality of life, sleep, and the activities of daily living. Electrotherapy is an interesting alternative or complementary treatment in the management of pain in MS, with new innovations constantly appearing.
    METHODS: This study evaluates the effectiveness of treatment with monopolar dielectric transmission of pulsed electromagnetic fields (PEMF) for pain associated with MS. We performed a randomised, placebo-controlled clinical trial including 24 patients, who were assessed with the Brief Pain Inventory, the Multiple Sclerosis International Quality of Life questionnaire, the Beck Depression Inventory, and the Modified Fatigue Impact Scale.
    RESULTS: Statistically significant improvements were observed in maximum and mean pain scores, as well as in the impact of pain on work, personal relationships, and sleep and rest. Not significant differences were found between the treatment and placebo groups.
    CONCLUSIONS: Treatment with PEMF may be effective in reducing pain in patients with MS, although further research is necessary to confirm its effectiveness over placebo and to differentiate which type of pain may be more susceptible to this treatment.
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  • 文章类型: Case Reports
    In multiple sclerosis (MS), foetal exposure to disease-modifying drugs (DMDs) carries varying degrees of risk. We sought to analyse the clinical and obstetric outcomes of MS patients (MSp) exposed to DMDs during pregnancy.
    Observational study. We analysed the clinical-obstetric data of a cohort MSp, who became pregnant between 2007-2017. They were prospectively followed up during pregnancy and postpartum.
    healthy pregnant women (HPW) and MSp unexposed to DMDs.
    Sixty-eight pregnancies in MSp. Fifty-six HPW. Thirteen MSp were exposed to DMDs during pregnancy. Obstetric outcome: 2 (15%) infants had low birth weight, no preterm deliveries. Fifty-five MSp were not exposed to DMDs: 22 (40%) discontinued DMD before pregnancy, 33(60%) naïve. Five infants (9%) had low birth weight and 7 (12%) were preterm. HPW: 56. Low birth weight 6 (11%), preterm delivery 6 (11%). There were no differences in relapse incidence during pregnancy-puerperium between MSp groups. There were no differences in birth weight, gestation time, delivery-caesarean section. We found no special obstetric morbidity in women exposed to DMDs.
    There were no significant differences in the clinical and obstetric variables analysed between pregnant women exposed to DMDs, unexposed, and HPW.
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  • 文章类型: Journal Article
    BACKGROUND: Multiple sclerosis is an autoimmune, chronic and inflammatory disease of the central nervous system with axonal demyelination, gliosis and neurodegeneration. It is considered a frequent cause of neurological disability in young adults. In this work, an Experimental Autoimmune Encephalomyelitis (EAE) model was optimised by injecting a myelin oligodendrocyte glycoprotein (MOG35-55). The ophthalmological effects were studied, as well as its use as an experimental model in other studies of retinal ganglion cell degeneration (RGC) and optic nerve (ON).
    METHODS: The study included 16 mice of 10 weeks that were placed into 2 study groups: a control group of 10 animals and another group of 6 animals with EAE that were injected with MOG35-55. The animals of the EAE model were monitored using motor disability scales. The retinas and optic nerves were processed for morphological examination by optical microscopy and ultrastructure studies.
    RESULTS: The animal models presented with motor symptoms of spinal cord injury, with the first symptoms appearing between the 7th and 19th day post-injection, with a maximum disability mean of 3.5 points. In the retina, the mean RGC in the EAE group was 0.0891μm, compared with 0.1678μm of the control group (p=.0003). The ON was strongly affected with reactive gliosis, increased axonal damage and decreased density axonal (control group 0.38038 axons/μm2 versus EAE group 0.16 axons/μm2, p=.00032).
    CONCLUSIONS: In this work an animal model of EAE has been characterised and detailed for the study of demyelinating alterations in the retina and the ON. Its characteristics make it an excellent tool for the study of neurodegenerative ophthalmic diseases.
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  • 文章类型: Clinical Trial
    Hippotherapy is being used as a promising method in the physical treatment of multiple sclerosis (MS).
    Comparative open clinical pre-post study into hippotherapy intervention during a 6-month period in patients with MS (n=6). Not randomised and with control group (n=4). The study was performed by MHG Foundation.
    A statistically significant improvement was observed in the therapy group in: spasticity pre-post measured by the modified Ashworth scale (P=.01). Statistically significant improvement in fatigue impact (P<.0001) measured with FIS; in general, perception of heath outcome in urinary quality of life scale KHQ (P=.033), and in subscales 2, 3 and 4 of MSQOL-54 (P=.011). Control group showed no improvement in any scale.
    This study reinforces current literature that supports hippotherapy as an adequate intervention for MS patients. Further studies with more participants, control groups and blinded research would be logical steps for future research in this field.
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  • 文章类型: Journal Article
    背景:多发性硬化症(MS)是一种慢性,脱髓鞘,引起神经炎症的中枢神经系统自身免疫性疾病。实验性自身免疫性脑炎(EAE)是该疾病的模型。MS通常用干扰素β(IFN-β)和醋酸格拉替雷(GA)处理。已报道褪黑激素(MLT)调节免疫系统应答。本研究的目的是与MS(IFN-β和GA)的一线治疗相比,分析MLT给药的效果。
    方法:在雄性Sprague-Dawley大鼠中诱导EAE;动物随后接受IFN-β,GA,或MLT。通过多重测定分析脑脊液(CSF)样品以确定促炎细胞因子的水平。还记录了EAE的神经学评价。
    结果:所有免疫动物均发生EAE。我们评估了第一个复发-缓解周期,观察IFN-β和GA在临床评估中的效果优于MLT。EAE或任何治疗都不施用改良的CSFIL-1β和IL-12p70浓度。然而,IFN-β和MLT确实降低了CSFTNF-α浓度。
    结论:需要进一步的研究来评估EAE中MLT行为的分子机制,并量化不同生物介质中的其他细胞因子,以便将MLT视为能够调节MS的抗炎剂。
    BACKGROUND: Multiple sclerosis (MS) is a chronic, demyelinating, autoimmune disease of the central nervous system causing neuroinflammation. Experimental autoimmune encephalitis (EAE) is a model of the disease. MS is classically treated with interferon beta (IFN-β) and glatiramer acetate (GA). Melatonin (MLT) has been reported to modulate immune system responses. The aim of the present study is to analyse the effects of MLT administration in comparison with the first-line treatments for MS (IFN-β and GA).
    METHODS: EAE was induced in male Sprague-Dawley rats; the animals subsequently received either IFN-β, GA, or MLT. Cerebrospinal fluid (CSF) samples were analysed by multiplex assay to determine the levels of proinflammatory cytokines. The neurological evaluation of EAE was also recorded.
    RESULTS: All immunised animals developed EAE. We evaluated the first relapse-remission cycle, observing that IFN-β and GA had better results than MLT in the clinical evaluation. Neither EAE nor any of the treatments administered modified CSF IL-1β and IL-12p70 concentrations. However, IFN-β and MLT did decrease CSF TNF-α concentrations.
    CONCLUSIONS: Further studies are needed to evaluate the molecular mechanisms involved in the behaviour of MLT in EAE, and to quantify other cytokines in different biological media in order for MLT to be considered an anti-inflammatory agent capable of regulating MS.
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  • 文章类型: Journal Article
    BACKGROUND: The contrast sensitivity test determines the quality of visual function in patients with multiple sclerosis (MS). The purpose of this study is to analyse changes in visual function in patients with relapsing-remitting MS with and without a history of optic neuritis (ON).
    METHODS: We conducted a longitudinal study including 61 patients classified into 3 groups as follows: a) disease-free patients (control group); b) patients with MS and no history of ON; and c) patients with MS and a history of unilateral ON. All patients underwent baseline and 6-year follow-up ophthalmologic examinations, which included visual acuity and monocular and binocular Pelli-Robson contrast sensitivity tests.
    RESULTS: Monocular contrast sensitivity was significantly lower in MS patients with and without a history of ON than in controls both at baseline (P=.00 and P=.01, respectively) and at 6 years (P=.01 and P=.02). Patients with MS and no history of ON remained stable throughout follow-up whereas those with a history of ON displayed a significant loss of contrast sensitivity (P=.01). Visual acuity and binocular contrast sensitivity at baseline and at 6 years was significantly lower in the group of patients with a history of ON than in the control group (P=.003 and P=.002 vs P=.006 and P=.005) and the group with no history of ON (P=.04 and P=.038 vs P=.008 and P=.01). However, no significant differences were found in follow-up results (P=.1 and P=.5).
    CONCLUSIONS: Monocular Pelli-Robson contrast sensitivity test may be used to detect changes in visual function in patients with ON.
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