Kurian Mathew, Khera Nikhil
General Internal Medicine, University of Leicester Hospitals, Leicester, GBR.
General Practice, University of Leicester Hospitals, Leicester, GBR.
Cureus. 2024 Sep 20;16(9):e69791. doi: 10.7759/cureus.69791. eCollection 2024 Sep.
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, DRB104:04 and DRB103, 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-DRB104:04 and DRB103 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.
重症肌无力(MG)是一种自身免疫性疾病,其特征是由于针对突触后受体产生的抗体导致肌肉无力。随着人口老龄化,MG的影响可能会很大。人类白细胞抗原(HLA)是与自身免疫性疾病相关的多态性基因。确定与MG相关的HLA等位基因可能有助于对有MG风险的个体进行诊断、筛查和早期管理。本研究旨在确定与世界各地MG患病率相关的II类HLA等位基因,并识别可能易患该病的等位基因。使用系统评价和Meta分析的首选报告项目(PRISMA)流程图以及包括Scopus和PubMed在内的各种数据库以及其他来源,以查找有关与MG相关的HLA II类等位基因以及各国MG患病率的合适论文。从网站allelefrequencies.net获取选定区域中选定HLA等位基因的频率。据此计算相关系数和p值,以研究MG的频率与HLA等位基因的患病率是否存在显著关联。结果突出显示两个HLA等位基因DRB104:04和DRB103与MG的患病率呈显著正相关。这些等位基因的频率存在区域差异,欧洲国家,尤其是北欧,频率最高。HLA-DRB104:04和DRB103与MG的患病率呈显著正相关,突出表明这些等位基因可能是该病的病因。对这些等位基因进行筛查,特别是在北欧,可能有助于识别易患MG的个体。