Alvarenga M P, Schimidt Sergio, Alvarenga Rm Papais
Department of Neurology, Hospital Federal da Lagoa, Brazil.
Universidade Federal do Estado do Rio de Janeiro, Brazil.
Mult Scler J Exp Transl Clin. 2017 Sep 25;3(3):2055217317730098. doi: 10.1177/2055217317730098. eCollection 2017 Jul-Sep.
A major development over the past two decades was the recognition of recurrent neuromyelitis optica (NMO) as a particular central nervous system disorder different from multiple sclerosis (MS). Here we reviewed the epidemiology of NMO in Latin America (LATAM). A predominance of a mixed population is found in this region. Recurrent NMO in black women was described in the Caribbean Islands and in Rio de Janeiro. The prevalence of NMO in LATAM varied from 0.37/100,000 (Volta Redonda city) to 4.2/100,000 inhabitants (Caribbean Islands). NMO differs significantly from MS with respect to gender, ethnicity, morbidity and genetic susceptibility. An association of the HLA DRB1*03 alleles with NMO was described in the French Antilles, Ribeirão Preto, Rio de Janeiro and Mexico. It is not common to find familial forms of NMO. NMO represents 11.8% of all inflammatory idiopathic diseases in South America (SA). In SA, the highest frequency of NMO occurs in African Brazilian young women. The overall relative frequency of NMO among MS cases in this region was 14%, decreasing following a north-south gradient, which parallels the percentage of nonwhite people.
过去二十年中的一项重大进展是,复发性视神经脊髓炎(NMO)被确认为一种不同于多发性硬化症(MS)的特殊中枢神经系统疾病。在此,我们回顾了拉丁美洲(LATAM)NMO的流行病学情况。该地区以混合人群为主。在加勒比群岛和里约热内卢曾有关于黑人女性复发性NMO的描述。拉丁美洲NMO的患病率从0.37/10万(沃尔塔雷东达市)到4.2/10万居民(加勒比群岛)不等。NMO在性别、种族、发病率和遗传易感性方面与MS有显著差异。在法属安的列斯群岛、里贝朗普雷图、里约热内卢和墨西哥曾有HLA DRB1*03等位基因与NMO相关的描述。NMO的家族形式并不常见。在南美洲(SA),NMO占所有炎症性特发性疾病的11.8%。在南美洲,NMO的最高发病频率出现在非洲裔巴西年轻女性中。该地区MS病例中NMO的总体相对频率为14%,呈南北梯度下降,这与非白人的比例情况相似。