CTH G1208T and MTHFR A1298C polymorphisms are associated with a higher risk of a first myocardial infarction with fatal outcome among women.

Q2 Pharmacology, Toxicology and Pharmaceutics Drug metabolism and personalized therapy Pub Date : 2023-03-01 DOI:10.1515/dmpt-2022-0119
Elisabet Söderström, Jonas Andersson, Stefan Söderberg, Bethany van Guelpen, Torbjörn K Nilsson, Johan Hultdin
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引用次数: 1

Abstract

Objectives: Cystathionine-gamma-lyase (CSE) in the transsulfuration pathway generates hydrogen sulfide (H2S), suggested regulating cardiovascular function. The G1208T polymorphism in the CTH gene, rs1021737, has, in addition to MTHFR, been found to increase homocysteine, related to myocardial infarction (MI) risk. This study aimed, for the first time, to investigate the associations of the polymorphisms CTH G1208T, MTHFR C677T, and A1298C with the prospective risk of developing a fatal or non-fatal first MI.

Methods: This case-referent study included 545 cases later developing a first-ever MI and 1,054 referents from the Northern Sweden Health and Disease Study. Fatal MI was defined as death within 28 days after MI symptoms.

Results: Women, but not men, had a positive association between fatal MI and the CTH G1208T, odds ratio [95% confidence interval] 3.14 [1.16-8.54] for heterozygotes, and the dominant model 3.22 [1.22-8.51], and for the MTHFR A1298C heterozygotes 3.24 [1.26-8.34] and the dominant model 2.63 [1.06-6.50]. The MTHFR C677T polymorphism was not related to MI.

Conclusions: This study indicates that the minor alleles of CTH G1208T and MTHFR A1298C polymorphisms are associated with a higher risk for a fatal MI among women but not for non-fatal MI. No association was found in men.

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在女性中,CTH G1208T和MTHFR A1298C多态性与首次心肌梗死的高风险相关。
目的:半胱硫氨酸- γ -裂解酶(CSE)在转硫途径中产生硫化氢(H2S),可能调节心血管功能。CTH基因rs1021737的G1208T多态性,除MTHFR外,已被发现增加同型半胱氨酸,与心肌梗死(MI)风险相关。本研究旨在首次探讨CTH G1208T、MTHFR C677T和A1298C多态性与致死性或非致死性首次心肌梗死的前瞻性风险之间的关系。方法:本研究纳入了来自瑞典北部健康与疾病研究的545例首次心肌梗死病例和1054例参照物。致死性心肌梗死定义为心肌梗死症状出现后28天内死亡。结果:致死性心肌梗死与CTH G1208T呈正相关,女性,而非男性,杂合子的比值比为3.14[1.16-8.54],优势模型为3.22 [1.22-8.51],MTHFR A1298C杂合子的比值比为3.24[1.26-8.34],优势模型为2.63[1.06-6.50]。结论:本研究表明,CTH G1208T和MTHFR A1298C多态性的次要等位基因与女性致死性心肌梗死的高风险相关,而与非致死性心肌梗死无关。在男性中未发现相关。
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来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
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