Department of Cardiology, Peking University People's Hospital, Xizhimen South Rd. No.11, Xicheng district, Beijing, 100044, China.
Beijing Key Laboratory of Early Prediction and Intervention of Acute Myocardial Infarction, Peking University People's Hospital, Beijing, China.
Lipids Health Dis. 2019 Apr 11;18(1):95. doi: 10.1186/s12944-019-1042-3.
The incidence of premature myocardial infarction (PMI) has gradually increased in recent years. Genetics plays a central role in the development of PMI. Familial hypercholesterolemia (FH) is one of the most common genetic disorders of cholesterol metabolism leading to PMI.
This study investigated the relationship between FH-associated genes and the phenotype of PMI to clarify the genetic spectrum of PMI diseases.
This study enrolled PMI patients (n = 225) and detected the mutations in their FH-associated genes (LDLR, APOB, PCSK9, LDLRAP1) by Sanger sequencing. At the same time, patients free of PMI (non-FH patients, n = 56) were enrolled as control, and a logistic regression analysis was used to identify risk factors associated with PMI. The diagnosis of FH was confirmed using "2018 Chinese expert consensus of FH screening and diagnosis" before the prevalence and clinical features of FH were analyzed.
Pathogenic mutations in LDLR, APOB, PCSK9 and LDLRAP1 genes were found in 17 of 225 subjects (7.6%), and all mutations were loss of function (LOF) and heterozygous. The genotype-phenotype relationship of patients carrying FH-associated mutations showed high heterogeneity. The logistic regression analysis showed that the smoking history, obesity and the family history of premature CHD were independent risk factors of PMI. In this study, a total of 19 patients (8.4%) were diagnosed as FH, and the proportion of smoking subjects in FH patients was higher than that in non-FH patients.
FH-associated gene mutations were present in about 7.6% of Chinese patients with PMI. In addition to genetic factors, smoking history, lifestyle and other environmental factors may play a synergistic role in determining the phenotype of PMI.
Essential gene mutation of cholesterol metabolism in patients with premature myocardial infarction. ChiCTR-OCH-12002349.Registered 26 December 2014, http://www.chictr.org.cn/showproj.aspx?proj=7201 .
近年来,过早心肌梗死(PMI)的发病率逐渐升高。遗传在 PMI 的发展中起着核心作用。家族性高胆固醇血症(FH)是导致 PMI 的最常见胆固醇代谢遗传紊乱之一。
本研究旨在探讨 FH 相关基因与 PMI 表型的关系,阐明 PMI 疾病的遗传谱。
本研究纳入了 225 名 PMI 患者(FH 患者),并通过 Sanger 测序检测了他们 FH 相关基因(LDLR、APOB、PCSK9、LDLRAP1)的突变。同时,纳入了 56 名无 PMI 的患者(非 FH 患者)作为对照,并采用 logistic 回归分析识别与 PMI 相关的危险因素。在分析 FH 的患病率和临床特征之前,使用“2018 年中国 FH 筛查与诊断专家共识”对 FH 进行了诊断。
在 225 名患者中发现了 LDLR、APOB、PCSK9 和 LDLRAP1 基因的致病性突变,共 17 例(7.6%),所有突变均为功能丧失(LOF)和杂合子。携带 FH 相关突变的患者的基因型-表型关系显示出高度异质性。logistic 回归分析显示,吸烟史、肥胖和早发冠心病家族史是 PMI 的独立危险因素。本研究共诊断出 19 例(8.4%)FH 患者,FH 患者的吸烟人数比例高于非 FH 患者。
在中国 PMI 患者中,约 7.6%存在 FH 相关基因突变。除遗传因素外,吸烟史、生活方式和其他环境因素可能在决定 PMI 的表型方面发挥协同作用。
胆固醇代谢关键基因在早发心肌梗死患者中的突变。ChiCTR-OCH-12002349. 注册于 2014 年 12 月 26 日,http://www.chictr.org.cn/showproj.aspx?proj=7201 。