• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

同型半胱氨酸水平和 MTHFR 多态性与年轻急性心肌梗死患者:病例对照研究。

Homocysteine levels and MTHFR polymorphisms in young patients with acute myocardial infarction: a case control study.

机构信息

Cardiology Department, Nicosia General Hospital, 215 Old Road Nicosia-Limassol, Strovolos, Nicosia, Cyprus.

出版信息

Hellenic J Cardiol. 2012 May-Jun;53(3):189-94.

PMID:22653243
Abstract

INTRODUCTION

Increased levels of homocysteine are known to be associated with coronary artery disease (CAD). The most common form of genetic hyperhomocysteinemia results from MTHFR polymorphisms. To examine the role of homocysteine levels and MTHFR polymorphisms in premature CAD and acute myocardial infarction (MI) in the Cypriot population, a case control study was performed in Nicosia General Hospital.

METHODS

Sixty-three male patients less than 50 years old who presented with MI in Nicosia General Hospital were compared with 54 controls without CAD. Fasting homocysteine and lipids were tested within 24 hrs from admission, while MTHFR C677T and A1298C polymorphisms were also tested.

RESULTS

Mean homocysteine levels were 14.5 mol/L in patients and 12.3 mol/L in controls (p=0.017). Mutant homozygous MTHFR C677T was present in 17.7% of the patients and 19.2% of the controls (p=0.838), while mutant homozygous MTHFR A1298C was found in 16.1% of patients and 13.5% of controls (p=0.690). Mean homocysteine levels were 12.6 mol/L in patients with single-vessel CAD and 15.5 mol/L in patients with multi-vessel CAD (p=0.025). Lower HDL appeared to be associated with higher levels of homocysteine with an odds ratio of 0.901, indicating that for each unit increase in HDL, the expected odds of having high homocysteine levels decreased by approximately 10%.

CONCLUSIONS

Higher levels of homocysteine are associated with acute MI and multi-vessel disease in Cypriot patients under the age of 50. The existence and extent of disease are not associated with MTHFR polymorphisms. Lower HDL is associated with higher levels of homocysteine.

摘要

简介

已知同型半胱氨酸水平升高与冠状动脉疾病(CAD)有关。最常见的遗传性高同型半胱氨酸血症是由于 MTHFR 多态性引起的。为了研究同型半胱氨酸水平和 MTHFR 多态性在塞浦路斯人早发 CAD 和急性心肌梗死(MI)中的作用,在尼科西亚综合医院进行了一项病例对照研究。

方法

尼科西亚综合医院 63 名年龄小于 50 岁的 MI 患者与 54 名无 CAD 的对照组进行比较。在入院后 24 小时内检测空腹同型半胱氨酸和血脂,同时检测 MTHFR C677T 和 A1298C 多态性。

结果

患者的平均同型半胱氨酸水平为 14.5 μmol/L,对照组为 12.3 μmol/L(p=0.017)。患者中突变纯合 MTHFR C677T 为 17.7%,对照组为 19.2%(p=0.838),而患者中突变纯合 MTHFR A1298C 为 16.1%,对照组为 13.5%(p=0.690)。单支血管 CAD 患者的平均同型半胱氨酸水平为 12.6 μmol/L,多支血管 CAD 患者为 15.5 μmol/L(p=0.025)。较低的高密度脂蛋白(HDL)似乎与较高的同型半胱氨酸水平相关,优势比为 0.901,这表明每增加一个单位的 HDL,同型半胱氨酸水平升高的预期几率就会降低约 10%。

结论

塞浦路斯 50 岁以下患者的同型半胱氨酸水平升高与急性 MI 和多支血管疾病相关。MTHFR 多态性与疾病的存在和严重程度无关。较低的 HDL 与较高的同型半胱氨酸水平相关。

相似文献

1
Homocysteine levels and MTHFR polymorphisms in young patients with acute myocardial infarction: a case control study.同型半胱氨酸水平和 MTHFR 多态性与年轻急性心肌梗死患者:病例对照研究。
Hellenic J Cardiol. 2012 May-Jun;53(3):189-94.
2
Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery disease.亚甲基四氢叶酸还原酶基因C677T和A1298C多态性、血浆同型半胱氨酸、叶酸和维生素B12水平与冠状动脉疾病的程度
Am J Cardiol. 2004 May 15;93(10):1201-6. doi: 10.1016/j.amjcard.2004.02.009.
3
The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.亚甲基四氢叶酸还原酶基因C677T突变、血浆同型半胱氨酸浓度与冠状动脉疾病风险
Kardiol Pol. 2003 Jul;59(7):17-26; discussion 26.
4
Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).亚甲基四氢叶酸还原酶基因、同型半胱氨酸与冠状动脉疾病:A1298C多态性至关重要。一项病例研究(葡萄牙马德拉岛)的推论
Thromb Res. 2008;122(5):648-56. doi: 10.1016/j.thromres.2008.02.005. Epub 2008 Apr 1.
5
Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients.亚甲基四氢叶酸还原酶(C677T 和 A1298C)多态性、高同型半胱氨酸血症与突尼斯患者的缺血性脑卒中。
J Stroke Cerebrovasc Dis. 2013 May;22(4):465-9. doi: 10.1016/j.jstrokecerebrovasdis.2013.03.011.
6
Polymorphisms in MTHFR, MS and CBS genes and premature acute myocardial infarction in a Pakistani population.MTHFR、MS和CBS基因多态性与巴基斯坦人群过早急性心肌梗死
Pak J Pharm Sci. 2016 Nov;29(6):1901-1906.
7
Folate, homocysteine levels, methylenetetrahydrofolate reductase (MTHFR) 677C --> T variant, and the risk of myocardial infarction in young women: effect of female hormones on homocysteine levels.叶酸、同型半胱氨酸水平、亚甲基四氢叶酸还原酶(MTHFR)677C→T变异与年轻女性心肌梗死风险:女性激素对同型半胱氨酸水平的影响
J Thromb Haemost. 2004 Jan;2(1):35-41. doi: 10.1111/j.1538-7836.2004.00508.x.
8
Correlation between C677T MTHFR gene polymorphism, plasma homocysteine levels and the incidence of CAD.C677T亚甲基四氢叶酸还原酶(MTHFR)基因多态性、血浆同型半胱氨酸水平与冠心病发病率之间的相关性
Am J Cardiovasc Drugs. 2001;1(5):353-61. doi: 10.2165/00129784-200101050-00005.
9
Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and variations of homocysteine concentrations in patients with Behcet's disease.亚甲基四氢叶酸还原酶 C677T 和 A1298C 多态性与白塞病患者同型半胱氨酸浓度的变化。
Gene. 2013 Sep 15;527(1):306-10. doi: 10.1016/j.gene.2013.06.041. Epub 2013 Jul 1.
10
Hyperhomocysteinaemia, methylenetetrahydrofolate reductase polymorphism and risk of coronary artery disease.高同型半胱氨酸血症、亚甲基四氢叶酸还原酶多态性与冠状动脉疾病风险
Ann Clin Biochem. 2006 May;43(Pt 3):200-6. doi: 10.1258/000456306776865232.

引用本文的文献

1
Methylenetetrahydrofolate Reductase Gene Polymorphism as a Risk Factor for Coronary Artery Disease.亚甲基四氢叶酸还原酶基因多态性作为冠状动脉疾病的一个危险因素
Indian J Clin Biochem. 2025 Jan;40(1):25-31. doi: 10.1007/s12291-023-01162-z. Epub 2023 Nov 23.
2
Effect of MTHFR A1298C Gene Polymorphism on Acute Coronary Syndrome.亚甲基四氢叶酸还原酶A1298C基因多态性对急性冠状动脉综合征的影响
ARYA Atheroscler. 2023 Feb;19(2):8-13. doi: 10.48305/ARYA.2022.39221.2830.
3
Association between homocysteine and coronary artery disease-trend over time and across the regions: a systematic review and meta-analysis.
同型半胱氨酸与冠状动脉疾病之间的关联——随时间推移及不同地区的趋势:一项系统评价与荟萃分析
Egypt Heart J. 2024 Feb 27;76(1):29. doi: 10.1186/s43044-024-00460-y.
4
ATR1 A1166C (rs5186), FII G20210A (rs1799963), FV G1691A (rs6025), FXIII 97G > T (rs11466016) and MTHFR A1298C (rs1801131) polymorphisms and the risk of ST-elevation myocardial infarction in young Mexican individuals.ATR1 A1166C(rs5186)、FII G20210A(rs1799963)、FV G1691A(rs6025)、FXIII 97G > T(rs11466016) 和 MTHFR A1298C(rs1801131) 多态性与年轻墨西哥个体 ST 段抬高型心肌梗死的风险。
Mol Biol Rep. 2024 Jan 25;51(1):208. doi: 10.1007/s11033-023-09027-7.
5
gene polymorphisms and susceptibility to myocardial infarction: Evidence from meta-analysis and trial sequential analysis.基因多态性与心肌梗死易感性:来自荟萃分析和试验序贯分析的证据。
Int J Cardiol Heart Vasc. 2023 Nov 22;49:101293. doi: 10.1016/j.ijcha.2023.101293. eCollection 2023 Dec.
6
Biochemical Association of MTHFR C677T Polymorphism with Myocardial Infarction in the Presence of Diabetes Mellitus as a Risk Factor.在糖尿病作为危险因素存在的情况下,亚甲基四氢叶酸还原酶(MTHFR)C677T多态性与心肌梗死的生化关联
Metabolites. 2023 Feb 9;13(2):251. doi: 10.3390/metabo13020251.
7
Biomarkers for Premature Coronary Artery Disease (PCAD): A Case Control Study.早发性冠状动脉疾病(PCAD)的生物标志物:一项病例对照研究。
Diagnostics (Basel). 2023 Jan 4;13(2):188. doi: 10.3390/diagnostics13020188.
8
Role of plasma homocysteine levels and other associated factors with coronary artery disease among Palestinian patients in North Palestine: a case control study.血浆同型半胱氨酸水平及其他相关因素在巴勒斯坦北部地区冠心病患者中的作用:一项病例对照研究。
Pan Afr Med J. 2022 Jul 6;42:180. doi: 10.11604/pamj.2022.42.180.34264. eCollection 2022.
9
Genetic polymorphisms in early-onset myocardial infarction in a sample of Iraqi patients: a pilot study.伊拉克患者样本中早发性心肌梗死的基因多态性:一项初步研究。
BMC Res Notes. 2020 Nov 24;13(1):541. doi: 10.1186/s13104-020-05367-w.
10
Interplay between 3'-UTR polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene and the risk of ischemic stroke.亚甲基四氢叶酸还原酶(MTHFR)基因 3'-UTR 多态性与缺血性脑卒中风险之间的相互作用。
Sci Rep. 2017 Sep 29;7(1):12464. doi: 10.1038/s41598-017-12668-x.