Gender-specific association of SLC19A1 and MTHFR genetic polymorphism with oxidative stress biomarkers and plasma folate levels in older adults

• Published in: Experimental gerontology Vol. 178; p. 112208
• Main Authors: Wang, Xixiang, Wang, Ying, Ma, Xiaojun, Zhou, Shaobo, Xu, Jingjing, Guo, Yujie, Liu, Lu, Liu, Yu, Gao, Lifang, Yuan, Linhong
• Format: Journal Article
• Language: English
• Published: England Elsevier Inc 01-07-2023; Elsevier
• Subjects: Aged; Antioxidants - metabolism; Biomarkers - metabolism; Female; Folate; Folic Acid; Folic Acid Deficiency - genetics; Genetic polymorphism; Genotype; Homocysteine - metabolism; Humans; Male; Methylenetetrahydrofolate Reductase (NADPH2) - genetics; Methylenetetrahydrofolate Reductase (NADPH2) - metabolism; Older adults; Oxidative Stress; Polymorphism, Genetic; Reduced Folate Carrier Protein - genetics; Reduced Folate Carrier Protein - metabolism; Sex Characteristics; Superoxide Dismutase - genetics; Superoxide Dismutase - metabolism; Oxidative stress; Older adults; Folate; Genetic polymorphism
• ISSN: 0531-5565; 1873-6815
• DOI: 10.1016/j.exger.2023.112208

Plasma folate levels are closely related to antioxidant capacity and are regulated by folate pathway gene polymorphism. However, few studies have explored the gender-specific association of folate pathway gene polymorphism with oxidative stress biomarkers. The present study was designed to explore the gender-specific independent and combined impacts of solute carrier family 19 member 1 (SLC19A1) and methylenetetrahydrofolate reductase (MTHFR) genetic polymorphisms on oxidative stress biomarkers in older adults.
A total of 401 subjects were recruited, including 145 males and 256 females. Demographic characteristics of the participants were collected by using a self-administered questionnaire. Fasting venous blood samples were taken for folate pathway gene genotyping, circulating lipids parameters and erythrocyte oxidative stress biomarkers measurement. The difference of genotype distribution and the Hardy-Weinberg equilibrium was calculated by the Chi-square test. The general linear model was applied to compare the plasma folate levels and erythrocyte oxidative stress biomarkers. Multiple linear regression was used to explore the correlation between genetic risk scores and oxidative stress biomarkers. Logistic regression was used to explore the association of genetic risk scores of folate pathway gene with folate deficiency.
The male subjects have lower plasma folate and HDL-C levels than the female ones, and the male carrying MTHFR rs1801133 (CC) or MTHFR rs2274976 (GA) genotypes have higher erythrocyte SOD activity. The plasma folate levels, erythrocyte SOD and GSH-PX activities were negatively correlated with genetic risk scores in the male subjects. A positive correlation between the genetic risk scores and folate deficiency was observed in the male subjects.
There was association between folate pathway gene polymorphism of Solute Carrier Family 19 Member 1 (SLC19A1) and Methylenetetrahydrofolate Reductase (MTHFR) with erythrocyte SOD and GSH-PX activities, and folate levels in male but not in female aging subjects. Genetic variant of genes involved in folate metabolism has strong impact on plasma folate levels in the male aging subjects. Our data demonstrated that there was a potential interaction of gender and its genetic background in affecting the body's antioxidant capacity and the risk of folate deficiency in aging subjects.
•The erythrocyte SOD activities were SLC19A1 and MTHFR polymorphism and gender-dependent.•The combined effect of SLC19A1 and MTHFR polymorphisms was evaluated by constructing gene risk scores.•Genetic risk scores were negatively correlated with plasma folate level, erythrocyte SOD and GSH-PX activities.