Petersen Gabriela, Inzunza Andrés, Levy Michael
Neurology Department, Massachusetts General Hospital, Boston, MA, United States.
Ophthalmology Department, Massachusetts Eye and Ear, Boston, MA, United States; Harvard Medical School, Boston, MA, United States.
Mult Scler Relat Disord. 2025 Oct;102:106604. doi: 10.1016/j.msard.2025.106604. Epub 2025 Jun 30.
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune neurological disease. NMOSD is more common in non-Caucasian populations, with some Latin American and Caribbean (LAC) populations having some of the highest reported prevalences globally. Previous research suggests that populations in the LAC region may present with distinctive clinical and paraclinical features. However, despite these potential population-specific differences, such characteristics remain poorly defined and understudied.
Following the PRISMA guidelines and the PROSPERO registration (CRD42024598746), a systematic review was conducted in October 2024 to evaluate the epidemiological, clinical, and paraclinical characteristics of NMOSD in Latin America. The outcomes of interest included age at onset, female-to-male ratio, mean disease duration, mean Expanded Disability Status Scale (EDSS) score, seropositivity for aquaporin-4 antibodies, and the prevalence proportion of NMOSD. Studies were included based on predefined inclusion and exclusion criteria. Risk of bias was assessed for all studies using the JBI critical appraisal tools. Pooled single-group summary estimates were calculated using a random effects model. Forest plots were generated to visualize the pooled results. Data analysis was performed using STATA version 18.
A systematic search of PubMed and Embase was conducted. A total of 303 studies were screened, 74 articles underwent full-text evaluation, and 33 studies were included for data extraction and analysis. An overall population of 5,105 patients was analyzed. The mean age at onset was 36.08 years (95% CI: 34.77-37.39). The female-to-male ratio was approximately 4:1, with a pooled proportion of females of 0.81 (95% CI: 0.79-0.83). The mean disease duration was 6.57 years (95% CI: 5.13-8.01), with a mean Expanded Disability Status Scale score of 4.27 (95% CI: 3.87-4.67). The proportion of patients seropositive for aquaporin-4 antibodies was 0.64 (I² = 85.81%, 95% CI: 0.59-0.69). The pooled prevalence proportion of NMOSD in Latin America was 3.03 per 100,000 inhabitants (95% CI: 0.87-5.20), with high heterogeneity in prevalence estimates among the included studies.
The prevalence of NMOSD in Latin America is highly heterogeneous. The clinical and paraclinical characteristics of patients with NMOSD included in this study are consistent with those reported in other regions globally.
视神经脊髓炎谱系障碍(NMOSD)是一种自身免疫性神经疾病。NMOSD在非白种人群中更为常见,一些拉丁美洲和加勒比地区(LAC)人群的报告患病率在全球范围内处于较高水平。先前的研究表明,LAC地区的人群可能具有独特的临床和副临床特征。然而,尽管存在这些潜在的人群特异性差异,但这些特征仍定义不明确且研究不足。
遵循PRISMA指南和PROSPERO注册(CRD42024598746),于2024年10月进行了一项系统评价,以评估拉丁美洲NMOSD的流行病学、临床和副临床特征。感兴趣的结果包括发病年龄、女性与男性比例、平均病程、平均扩展残疾状态量表(EDSS)评分、水通道蛋白-4抗体血清阳性率以及NMOSD的患病率。根据预先定义的纳入和排除标准纳入研究。使用JBI批判性评价工具对所有研究进行偏倚风险评估。使用随机效应模型计算合并的单组汇总估计值。生成森林图以直观显示合并结果。使用STATA 18版进行数据分析。
对PubMed和Embase进行了系统检索。共筛选了303项研究,74篇文章进行了全文评估,33项研究纳入数据提取和分析。共分析了5105例患者。平均发病年龄为36.08岁(95%CI:34.77 - 37.39)。女性与男性比例约为4:1,女性合并比例为0.81(95%CI:0.79 - 0.83)。平均病程为6.57年(95%CI:5.13 - 8.01),平均扩展残疾状态量表评分为4.27(95%CI:3.87 - 4.67)。水通道蛋白-4抗体血清阳性患者的比例为0.64(I² = 85.81%,95%CI:0.59 - 0.69)。拉丁美洲NMOSD的合并患病率为每10万居民3.03例(95%CI:0.87 - 5.20),纳入研究中的患病率估计值存在高度异质性。
拉丁美洲NMOSD的患病率高度异质性。本研究纳入的NMOSD患者的临床和副临床特征与全球其他地区报告的特征一致。