Wang Shuxia, Fu Chunyan, Wang Hu, Shi Yi, Xu Xiqi, Chen Jingzhou, Song Xiaodong, Sun Kai, Wang Jianwei, Fan Xiaohan, Wang Hongjian, Yang Xiaomin, Huan Tujun, Hui Rutai
Sino-German Laboratory for Molecular Medicine, Key Laboratory for Clinical Cardiovascular Genetics of the Ministry of Education, Beijing, PR China.
Clin Chem Lab Med. 2007;45(8):962-7. doi: 10.1515/CCLM.2007.189.
The clinical phenotype of both hypertrophic cardiomyopathy (HCM) and left ventricular hypertrophy (LVH) induced by hypertension is heterogeneous. Genetic factors may contribute to this heterogeneity. Evidence is accumulating that the peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1alpha) gene plays a role in cardiac hypertrophy. The aim of our study was to identify the association between PGC-1alpha gene polymorphisms and cardiac hypertrophy.
A total of 270 consecutive HCM patients and 2486 hypertensive patients, comprising 1180 with LVH and 1306 without LVH, as well as 894 healthy controls, were successfully investigated. Polymorphisms of the PGC-1alpha gene were genotyped by PCR-restriction fragment length polymorphism and confirmed by sequencing.
The Ser482 allele (rs8192678 G>A and A>A) and CC genotype of Thr394Thr (rs2970847) conferred increased risk for HCM [odds ratio (OR) 1.52, 95% confidence interval (CI) 1.11-2.11; OR 1.49, 95% CI 1.15-1.98, respectively]. The maximum ventricular thickness was greater in HCM patients carrying the Ser482 risk allele than in carriers of the non-risk allele (20.7+/-4.1 vs. 19.1+/-4.3 mm, p<0.05) and for the CC Thr394Thr genotype (20.9+/-4.6 vs. 19.0+/-4.2 mm, p<0.05). No association was found between PGC-1alpha polymorphism and hypertension with or without LVH.
Our data indicate that variants of the PGC-1alpha gene are correlated with increased risk for HCM.
肥厚型心肌病(HCM)和高血压所致左心室肥厚(LVH)的临床表型均具有异质性。遗传因素可能导致这种异质性。越来越多的证据表明,过氧化物酶体增殖物激活受体γ共激活因子1α(PGC-1α)基因在心脏肥大中起作用。我们研究的目的是确定PGC-1α基因多态性与心脏肥大之间的关联。
共成功调查了270例连续性HCM患者、2486例高血压患者(其中1180例有LVH,1306例无LVH)以及894例健康对照者。通过聚合酶链反应-限制性片段长度多态性对PGC-1α基因多态性进行基因分型,并通过测序进行确认。
Ser482等位基因(rs8192678 G>A和A>A)以及Thr394Thr的CC基因型(rs2970847)使HCM风险增加[比值比(OR)分别为1.52,95%置信区间(CI)1.11-2.11;OR 1.49,95%CI 1.15-1.98]。携带Ser482风险等位基因的HCM患者的最大心室厚度大于非风险等位基因携带者(20.7±4.1对19.1±4.3 mm,p<0.05),CC Thr394Thr基因型患者也是如此(20.9±4.6对19.0±4.2 mm,p<0.05)。未发现PGC-1α多态性与有或无LVH的高血压之间存在关联。
我们的数据表明,PGC-1α基因变异与HCM风险增加相关。