4.5 Article

Earlier onset and shorter survival of amyotrophic lateral sclerosis in Jewish patients of North African origin - A clue to modifying genetic factors?

期刊

JOURNAL OF THE NEUROLOGICAL SCIENCES
卷 258, 期 1-2, 页码 39-43

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jns.2007.02.021

关键词

amyotrophic lateral sclerosis; motor neuron disease; epidemiology; ethnicity

向作者/读者索取更多资源

Arnyotrophic lateral sclerosis (ALS) is a multifactorial disease, with many genetic and environmental factors contributing to its outcome. The population of Israel is comprised of immigrants from all over the world as well as by Arabs. People with different ethnic backgrounds who live in the same environment provide a unique opportunity to analyze genetic and environmental influences on ALS. We performed a retrospective analysis of 374 sporadic ALS patients whose origin was European in 211, North African in 53, Oriental in 43, Balkan in 19, Arab in 9, and Yemenite in 7, comparing their age at disease onset, gender, disease form at onset, survival, smoking habits, cognitive dysfunction and apolipoprotein E genotype. Patients of North African origin were significantly younger and had a shorter duration of disease relative to their age compared to other ethnic groups, adjusted for age. The difference between the patient groups might be related to a genetic burden in North African patients and war-rants further investigation. (c) 2007 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据