Polymorphic variants of genes encoding MTHFR, MTR, and MTHFD1 and the risk of depression in postmenopausal women in Poland

ObjectiveDisturbances in the folate-dependent one-carbon metabolism have been reported in depression. Polymorphic variants of genes encoding key enzymes of folate and methionine metabolism may have an impact on catecholamine catabolism conducted by catechol-O-methyltransferase.MethodsThe distribution of polymorphisms of genes encoding methylenetetrahydrofolate reductase (MTHFR); methionine synthase (MTR); 5,10-methylenetetrahydrofolate dehydrogenase, 5,10-methenyltetrahydrofolate cyclohydrolase and 10-formyltetrahydrofolate synthetase (MTHFD1) was examined in postmenopausal women with (n = 83) and without depression (n = 89).ResultsWe found a significant contribution of the MTHFR 677C > T polymorphic variants to depression in postmenopausal women. Odds ratio (OR) for women with depression and MTHFR TT genotype was 3.478 (95% CI = 1.377–8.783), P = 0.0096 and OR of the TT and CT genotypes was 2.345 (95% CI = 1.258–4.373), P = 0.0086. Moreover, after stratification based on depression severity in postmenopausal women, we found that the MTHFR TT genotype displayed a 4.831-fold increased risk of moderate and severe depression (95% CI = 1.975–11.820, P = 0.0008). We did not observe statistical differences in the distribution of MTR 2756A > G and MTHFD1 1958G > A polymorphic variants in groups of postmenopausal women with and without depression. However, the MTR GG genotype exhibited a 5.750-fold increased risk of moderate and severe depression in postmenopausal women (95% CI = 1.547–21.379, P = 0.013).ConclusionsOur findings indicate a significant role of folate and possible methionine metabolism involvement in the development of depression in postmenopausal women.