Correlation Between the Prevalence of Myasthenia Gravis and the Frequency of Class II Human Leucocyte Antigen Alleles in Various Geographical Locations Around the World.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2024-09-20 eCollection Date: 2024-09-01 DOI:10.7759/cureus.69791
Mathew Kurian, Nikhil Khera
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Abstract

Myasthenia gravis (MG) is an autoimmune condition characterised by muscle weakness due to antibodies produced against post-synaptic receptors. The impact of MG can be significant, especially with an ageing population. Human leukocyte antigens (HLA) are polymorphic genes associated with autoimmune conditions. Establishing the HLA alleles associated with MG may aid in the diagnosis, screening and early management of individuals at risk of MG. This research aims to establish the class II HLA alleles associated with the prevalence of MG in various regions of the world and identify the alleles that could predispose to the condition. A Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow chart and various databases including, Scopus and PubMed as well as other sources were used to find appropriate papers on HLA class II alleles associated with MG and the prevalence of MG in various countries. The frequency of selected HLA alleles in selected regions were obtained from the website, allelefrequencies.net. From this, a correlation coefficient and p-value were calculated to investigate whether the frequency of MG and the prevalence of HLA alleles had a significant association.  The results highlighted two HLA alleles, DRB1*04:04 and DRB1*03, to have a significant positive association with the prevalence of MG. The frequency of the alleles showed regional variation, with European countries, particularly Northern Europe, exhibiting the highest frequencies. A significant positive correlation between HLA-DRB1*04:04 and DRB1*03 showed with the prevalence of MG, highlighting these alleles as a possible cause of the disease. Screening for these alleles, particularly in Northern Europe, may help identify individuals susceptible to MG.

全球不同地理位置的肌无力患病率与 II 类人类白细胞抗原等位基因频率之间的相关性。
重症肌无力(MG)是一种自身免疫性疾病,其特点是由于针对突触后受体产生抗体而导致肌肉无力。肌无力症的影响很大,尤其是在人口老龄化的情况下。人类白细胞抗原(HLA)是与自身免疫性疾病相关的多态基因。确定与 MG 相关的 HLA 等位基因有助于对 MG 高危人群进行诊断、筛查和早期管理。本研究旨在确定与世界各地区 MG 患病率相关的 II 类 HLA 等位基因,并找出可能导致该病的等位基因。研究采用了系统综述和元分析首选报告项目(PRISMA)流程图和各种数据库,包括 Scopus 和 PubMed 以及其他来源,以查找与 MG 相关的 HLA II 类等位基因和各国 MG 患病率的相关论文。从网站 allelefrequencies.net 上获得了选定地区 HLA 等位基因的频率。由此计算出相关系数和 P 值,以研究 MG 的发病率与 HLA 等位基因的流行率是否有显著关联。 结果表明,DRB1*04:04 和 DRB1*03 这两个 HLA 等位基因与 MG 患病率呈显著正相关。等位基因的频率显示出地区差异,欧洲国家,尤其是北欧国家的频率最高。HLA-DRB1*04:04和DRB1*03与MG发病率呈明显的正相关,这表明这些等位基因可能是导致该病的原因之一。对这些等位基因进行筛查,尤其是在北欧地区,可能有助于识别对 MG 易感的个体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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