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Multiple sclerosis and human leukocyte antigen genotypes: Focus on the Middle East and North Africa region

机译:多发性硬化症和人类白细胞抗原基因型:集中在中东和北非地区

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摘要

Recent reports have demonstrated that the prevalence of multiple sclerosis (MS) is increasing in the Middle East and North Africa region. There is also emerging evidence regarding the genetic components of MS risk. This review provides an overview of the role of genetic factors in MS susceptibility by examining human leukocyte antigen loci in patients within the Middle East and North Africa region. Most of the genetic studies conducted in the Middle East and North Africa region have been based on case–control designs, which cannot confirm direct causality of genetic variants on MS susceptibility. Moreover, there are very limited and inconsistent studies on human leukocyte antigen class I and II (DQA and DQB) in MS patients of the Middle East and North Africa region. To identify common risk haplotypes in the Middle East and North Africa region or its sub-populations, further longitudinal studies will be required.
机译:最近的报告表明,中东和北非地区的多发性硬化症(MS)患病率正在上升。也有关于MS风险的遗传成分的新兴证据。这篇综述通过检查中东和北非地区患者的人类白细胞抗原基因座,概述了遗传因素在MS易感性中的作用。在中东和北非地区进行的大多数遗传研究均基于病例对照设计,这些研究无法证实遗传变异对MS易感性的直接因果关系。此外,在中东和北非地区的MS患者中,关于人类白细胞抗原I和II类(DQA和DQB)的研究非常有限且不一致。为了确定中东和北非地区或其子种群的常见风险单倍型,将需要进一步的纵向研究。

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