Inclusion of ALKBH5 as a candidate gene for the susceptibility of autoimmune thyroid disease

• Published in: Advances in medical sciences 2021-09, Vol.66 (2), p.351-358
• Main Authors: Song, Rong-hua, Zhao, Jing, Gao, Chao-qun, Qin, Qiu, Zhang, Jin-an
• Format: Article
• Language: English
• Subjects: AlkB Homolog 5, RNA Demethylase; ALKBH5; Autoimmune thyroid disease (AITD); Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Graves' disease; Hashimoto Disease; Hashimoto's thyroiditis; Humans; Polymorphism; Polymorphism, Single Nucleotide - genetics
• ISSN: 1896-1126; 1898-4002
• DOI: 10.1016/j.advms.2021.07.006

RNA demethylase AlkB homolog 5 (ALKBH5) gene is pivotal in N6-methyladenosine (m6A) modification. Therefore, this study aimed to explore the potential relationship between polymorphisms of ALKBH5 gene and the development of autoimmune thyroid disease (AITD). A case-control study of 979 AITD patients, including 620 Graves' disease (GD) and 359 Hashimoto's thyroiditis (HT), and 732 normal controls of the Chinese Han population was performed using high-throughput sequencing (HiSeq) genotyping method for detecting 5 variants in ALKBH5 gene (rs12936694, rs2124370, rs4925144, rs8068517, and rs9913266). In addition, the associations between ALKBH5 single nucleotide polymorphisms (SNPs) and clinical phenotypes of AITD were investigated. Compared to normal controls, rs9913266 displayed significant differences in allele and genotype distributions in AITD and GD. rs12936694 also showed significantly different frequencies of alleles in AITD and GD. The link of these 2 loci polymorprhisms to AITD and GD also existed after adjusting for age and gender. When stratified by sex, the minor allele of rs9913266 was associated with the risk of female AITD and HT development before and after adjusting for age and gender. There was a significant association between rs8068517 locus and GD in females after adjusting for the confounders. Finally, we observed significant correlations of haplotypes CGACA and CAGCG to the susceptibility of AITD and GD. Our results provided evidence of association of polymorphisms in ALKBH5 gene with AITD, GD, and HT patients, and hence ALKBH5 might be the candidate gene for susceptibility to AITD.