Retrospective, descriptive study of acute myelitis in French Guyana

IF 2.3 4区 医学 Q2 CLINICAL NEUROLOGY Revue neurologique Pub Date : 2025-03-01 Epub Date: 2025-01-31 DOI:10.1016/j.neurol.2025.01.002
P. Grimont , A. Montcuquet , F. Quet , B. De Toffol , N. Deschamps
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Abstract

Background

Acute myelitis is a neurological entity, often posing the problem of etiology. The two main causes are infectious or autoimmune. French Guyana is a region of the world where infectious etiologies are multiple, in particular human immunodeficiency virus infection, and autoimmune diseases appear to be emerging. The aim of our study was firstly to determine the proportion of each etiology of acute myelitis in French Guyana, and secondly to describe the clinical, paraclinical and epidemiological characteristics of autoimmune myelitis in French Guyana, with particular reference to neuromyelitis optica spectrum disorder (NMOSD).

Methods

This retrospective, observational study included all patients who presented with acute myelitis between January 2015 and August 2023 at Cayenne Hospital Center. Each patient's chart was reviewed and patients were classified according to etiology. Demographic and clinical data were collected, as well as blood, lumbar puncture, and cerebral and spinal cord magnetic resonance imaging results.

Results

Of the 40 patients included, immune etiology was found in 74%, including 49% with NMOSD (37% with positive anti-aquaporin-4 antibodies) compared with three patients with infectious etiology. There was no statistically significant difference in complementary examinations between immune and infectious etiologies. The prevalence of NMOSD in French Guyana was estimated at 8/100,000 (6/100,000 for patients with positive anti-aquaporin-4 antibodies). No significant difference in the geographic distribution of patients with NMOSD in French Guyana was demonstrated.

Conclusions

Our results show a high proportion of autoimmune etiology of acute myelitis in French Guyana, and more particularly of NMOSD. There is a high prevalence of NMOSD, the second highest in the world after the French West Indies. Given this high proportion of autoimmune myelitis, several hypotheses can be put forward, with genetic and environmental factors in the foreground. For patients with acute myelitis in French Guyana, an immune cause is the most likely. It is therefore important to think about this and look for NMOSD in particular, without ignoring an infectious etiology.
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法属圭亚那急性脊髓炎的回顾性描述性研究。
背景:急性脊髓炎是一种神经系统疾病,常引起病因问题。两种主要原因是感染或自身免疫。法属圭亚那是世界上传染病病因多种多样的一个区域,特别是人体免疫缺陷病毒感染,自身免疫性疾病似乎正在出现。我们研究的目的是首先确定法属圭亚那急性脊髓炎的各种病因的比例,其次描述法属圭亚那自身免疫性脊髓炎的临床、临床和流行病学特征,特别是参考视神经脊髓炎频谱障碍(NMOSD)。方法:这项回顾性观察性研究纳入了卡宴医院中心2015年1月至2023年8月期间出现急性脊髓炎的所有患者。对每位患者的病历进行回顾,并根据病因对患者进行分类。收集了人口统计学和临床资料,以及血液、腰椎穿刺、脑和脊髓磁共振成像结果。结果:在所纳入的40例患者中,免疫病因占74%,其中NMOSD占49%(抗水通道蛋白-4抗体阳性占37%),感染性病因占3例。在免疫和感染性病因的补充检查中,差异无统计学意义。法属圭亚那NMOSD的患病率估计为8/100,000(6/100,000为抗水通道蛋白-4抗体阳性的患者)。法属圭亚那NMOSD患者的地理分布无显著差异。结论:我们的结果显示法属圭亚那急性脊髓炎的自身免疫性病因比例很高,尤其是NMOSD。NMOSD的患病率很高,在世界上仅次于法属西印度群岛。鉴于自身免疫性脊髓炎的高比例,可以提出几种假设,遗传和环境因素是前景。对于法属圭亚那的急性脊髓炎患者,免疫原因是最有可能的。因此,重要的是要考虑这一点,特别是寻找NMOSD,而不要忽视感染性病因。
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来源期刊
Revue neurologique
Revue neurologique 医学-临床神经学
CiteScore
4.80
自引率
0.00%
发文量
598
审稿时长
55 days
期刊介绍: The first issue of the Revue Neurologique, featuring an original article by Jean-Martin Charcot, was published on February 28th, 1893. Six years later, the French Society of Neurology (SFN) adopted this journal as its official publication in the year of its foundation, 1899. The Revue Neurologique was published throughout the 20th century without interruption and is indexed in all international databases (including Current Contents, Pubmed, Scopus). Ten annual issues provide original peer-reviewed clinical and research articles, and review articles giving up-to-date insights in all areas of neurology. The Revue Neurologique also publishes guidelines and recommendations. The Revue Neurologique publishes original articles, brief reports, general reviews, editorials, and letters to the editor as well as correspondence concerning articles previously published in the journal in the correspondence column.
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