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

• Published in: Maturitas 2008-11, Vol.61 (3), p.252-255
• Main Authors: Słopien, R, Jasniewicz, K, Meczekalski, B, Warenik-Szymankiewicz, A, Lianeri, M, Jagodziński, P.P
• Format: Article
• Language: English
• Subjects: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase - genetics; Adult; Adult and adolescent clinical studies; Aged; Biological and medical sciences; Depression; Depression - enzymology; Depression - genetics; Depression - psychology; DNA - chemistry; DNA - genetics; Female; Formate-Tetrahydrofolate Ligase - genetics; Genotype; Gynecology. Andrology. Obstetrics; Humans; Internal Medicine; Medical sciences; Methylenetetrahydrofolate Dehydrogenase (NADP) - genetics; Methylenetetrahydrofolate Reductase (NADPH2) - genetics; Middle Aged; Mood disorders; MTHFD1; MTHFR; MTR; Obstetrics and Gynecology; Poland; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Polymorphisms; Postmenopause - genetics; Postmenopause - psychology; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Puberal and climacteric disorders (male and female)
• ISSN: 0378-5122; 1873-4111
• DOI: 10.1016/j.maturitas.2008.08.002

Abstract Objective Disturbances 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. Methods The 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). Results We 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). Conclusions Our findings indicate a significant role of folate and possible methionine metabolism involvement in the development of depression in postmenopausal women.