Kim Young Ree, Hong Seung-Ho
Department of Laboratory Medicine, School of Medicine, Jeju National University, Jeju, 63243, Republic of Korea.
Department of Science Education, Teachers College, Jeju National University, Jeju, 63294, Republic of Korea.
Genes Genomics. 2019 Aug;41(8):983-991. doi: 10.1007/s13258-019-00840-8. Epub 2019 Jun 18.
Hyperhomocysteinemia is a potential risk factor for the development of metabolic syndrome (MetS). Among genes involved in homocysteine metabolism, polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene are known to be associated with MetS incidence. However, effects of polymorphisms of other folate metabolism-related genes on MetS susceptibility are not well known yet.
This study was to determine whether methionine synthase (MTR) 2756A > G, methionine synthase reductase (MTRR) 66A > G, and thymidylate synthase enhancer region (TSER) 2R/3R polymorphisms might be associated with risks of MetS development in the Korean population.
Genotype analysis of the three polymorphisms was performed for a total of 483 subjects including 236 MetS patients and 247 unrelated healthy controls using polymerase chain reaction-restriction fragment length polymorphism technique.
The present study revealed that MTRR and TSER polymorphisms were associated with susceptibility to MetS. Several genotypes and allele combinations from the three polymorphisms were also related to the MetS prevalence. When polymorphism data were stratified according to the risk components of MetS, MTR polymorphism was significantly associated with an increased risk of MetS in subjects with systolic blood pressure < 132.7 mmHg (AOR 1.842, 95% CI 1.039-3.266, P = 0.037) and fasting blood glucose level < 106.3 mg/dL (AOR 1.772, 95% CI 1.069-2.937, P = 0.027). MTRR polymorphism was significantly associated with a decreased risk of MetS in subjects with triglyceride level < 216.3 mg/dL (AOR 0.616, 95% CI 0.399-0.951, P = 0.029). To the best of our knowledge, this is the first to provide reliable evidence about the association of other folate metabolism-related gene polymorphisms besides MTHFR with MetS susceptibility and its risk factors.
Results of this study suggest that MTRR and TSER polymorphisms might be potential genetic markers for the risk of MetS development in Korean population.
高同型半胱氨酸血症是代谢综合征(MetS)发生的潜在危险因素。在参与同型半胱氨酸代谢的基因中,亚甲基四氢叶酸还原酶(MTHFR)基因多态性与MetS发病率相关。然而,其他叶酸代谢相关基因多态性对MetS易感性的影响尚不明确。
本研究旨在确定甲硫氨酸合成酶(MTR)2756A>G、甲硫氨酸合成酶还原酶(MTRR)66A>G和胸苷酸合成酶增强子区域(TSER)2R/3R多态性是否与韩国人群中MetS发生风险相关。
采用聚合酶链反应-限制性片段长度多态性技术,对包括236例MetS患者和247例无亲缘关系的健康对照在内的483名受试者进行了三种多态性的基因分型分析。
本研究表明,MTRR和TSER多态性与MetS易感性相关。三种多态性的几种基因型和等位基因组合也与MetS患病率有关。当根据MetS的风险成分对多态性数据进行分层时,MTR多态性与收缩压<132.7 mmHg的受试者中MetS风险增加显著相关(比值比1.842,95%置信区间1.039-3.266,P = 0.037),以及空腹血糖水平<106.3 mg/dL的受试者中MetS风险增加显著相关(比值比1.772,95%置信区间1.069-2.937,P = 0.027)。MTRR多态性与甘油三酯水平<216.3 mg/dL的受试者中MetS风险降低显著相关(比值比0.616,95%置信区间0.399-0.951,P = 0.029)。据我们所知,这是首次提供除MTHFR外其他叶酸代谢相关基因多态性与MetS易感性及其危险因素关联的可靠证据。
本研究结果表明,MTRR和TSER多态性可能是韩国人群中MetS发生风险的潜在遗传标志物。