Department of Neurology, High Specialty Medical Unit, Western National Medical Center of the Mexican Institute of Social Security, Guadalajara, Jalisco, Mexico.
Department of Neurology, Hospital General Regional No 45 of the Mexican Institute of Social Security, Guadalajara, Jalisco, Mexico.
Mult Scler Relat Disord. 2022 May;61:103733. doi: 10.1016/j.msard.2022.103733. Epub 2022 Mar 11.
Neuromyelitis Optica Spectrum Disorders (NMOSD) are a group of inflammatory diseases of the Central Nervous System (CNS) that primarily affect the optic nerve and spinal cord, usually with a severe and relapsing course. Due to the scarce information in non-Caucasian populations, we aimed to describe incidence, prevalence, and main clinical characteristics of NMOSD in a defined region in Mexico.
Descriptive, retrospective analysis of all reported cases of NMOSD attended in the neurology department of the UMAE-HE, CMNO, IMSS, the biggest third level hospital in Western Mexico. We searched the electronic medical records of the hospital for patients with a diagnosis of NMO, and reviewed all cases to confirm if they fulfilled NMOSD 2015 diagnostic criteria. Data were collected through a structured form. We described adjusted incidence and prevalence according to the WHO method, for the IMSS affiliated total population in Jalisco state in 2019.
67 NMOSD patients were included in the analysis of clinical data, with a mean age at onset of symptoms of 36 years ((Rivera et al., 2008-65). Most patients were female (74.6%). 53 patients living in Jalisco by the end of 2019 were included in the analysis of prevalence and incidence. Adjusted prevalence was 0.71/100,000 (95% CI 0.55-0.92), while adjusted incidence was 1.87/1,000,000 person-years (95% CI 1.11-3.16). In the full cohort, the first symptom of NMOSD was optic neuritis in 49.3% of the patients, followed by transverse myelitis (23.9%) and area postrema syndrome (10.4%). 62 patients relapsed in a mean follow-up of 2 years (0-7). 5 patients with less than 6 months of follow up had not relapsed. 55.2% of the patients were AQP4-IgG +, 14.9% AQP4-IgG -, and 29.9% unknown status.
Although NMOSD prevalence is similar to other reports around the world, incidence is higher than in Caucasian populations. We believe that this high incidence is related to an increased awareness of the disease in the era of new NMOSD treatments. Recurrent disease is very frequent in our cohort.
视神经脊髓炎谱系疾病(NMOSD)是一组中枢神经系统(CNS)的炎症性疾病,主要影响视神经和脊髓,通常具有严重和复发性病程。由于非白种人群的信息匮乏,我们旨在描述在墨西哥一个特定地区 NMOSD 的发病率、患病率和主要临床特征。
对 UMAE-HE、CMNO、IMSS 神经病学系收治的所有 NMOSD 报告病例进行描述性、回顾性分析,该医院是墨西哥西部最大的三级医院。我们在医院的电子病历中搜索 NMO 诊断患者,并对所有病例进行复查以确认是否符合 NMOSD 2015 年诊断标准。通过结构化表格收集数据。我们根据世界卫生组织(WHO)的方法,对 2019 年伊达尔戈州 IMSS 附属总人口进行了调整后的发病率和患病率的描述性分析。
67 例 NMOSD 患者纳入临床数据分析,症状发病平均年龄为 36 岁((Rivera 等人,2008-65 岁)。大多数患者为女性(74.6%)。2019 年底,53 名居住在哈利斯科州的患者纳入患病率和发病率分析。调整后的患病率为 0.71/100,000(95%CI 0.55-0.92),而调整后的发病率为 1.87/1,000,000 人年(95%CI 1.11-3.16)。在全队列中,NMOSD 的首发症状为视神经炎占 49.3%,其次为横贯性脊髓炎(23.9%)和后区综合征(10.4%)。62 例患者在平均 2 年(0-7 年)的随访中复发。5 例随访不足 6 个月的患者未复发。55.2%的患者 AQP4-IgG+,14.9%的患者 AQP4-IgG-,29.9%的患者状态未知。
尽管 NMOSD 的患病率与世界各地的其他报告相似,但发病率高于白种人群。我们认为,这种高发病率与新的 NMOSD 治疗时代对该病的认识提高有关。在我们的队列中,复发性疾病非常常见。