Association of methylenetetrahydrofolate reductase () gene polymorphisms (C677T and A1298C) with thyroid dysfunction: A meta-analysis and trial sequential analysis.

Recent studies have shown that two common methylenetetrahydrofolate reductase () gene polymorphisms (C677T and A1298C) might correlate with thyroid dysfunction, but the results remain inconsistent. We carried out a meta-analysis aiming to assess the relationship of both polymorphisms with thyroid dysfunction. The PubMed, EMBASE, CNKI (China National Knowledge Infrastructure), CBMdisc (China Biology Medicine disc), WeiPu and Wanfang databases were searched up to September 2021. Case-control and cohort studies on polymorphism and thyroid dysfunction were identified. Eight studies from six publications were finally included in our meta-analysis, including 817 patients and 566 controls. After pooled analysis, we found that the C677T polymorphism was associated with an increased risk of hypothyroidism (TT CC+CT/recessive model: OR = 2.07, 95% CI: 1.02-4.20, P = 0.04; TT CC/homozygote model: OR = 2.35, 95% CI: 1.13-4.86, P = 0.02), while trial sequential analysis (TSA) revealed that it could be a false positive result. The A1298C polymorphism was related to a decreased risk of hypothyroidism (C A/allele model: OR = 0.63, 95% CI: 0.44-0.92, P = 0.02; CC AC+AA/recessive model: OR = 0.42, 95% CI: 0.22-0.79, P = 0.007; CC AA/homozygote model: OR = 0.43, 95% CI: 0.25-0.85, P = 0.02), which was conclusive according to TSA. The results of this meta-analysis suggest that A1298C seems to be a protective factor for hypothyroidism, while the C677T polymorphism may be a risk factor. However, more well-designed studies with larger sample sizes are needed to obtain more reliable results of the association between the C677T polymorphism and hypothyroidism.