Li Yanrong, Yuan Huiping, Sun Liang, Zhou Qi, Yang Fan, Yang Ze, Liu Deping
1 Department of Cardiology, Beijing Hospital, National Center of Gerontology, Beijing, People's Republic of China.
2 The MOH Key Laboratory of Geriatrics, Beijing Hospital, National Center of Gerontology, Beijing, People's Republic of China.
Genet Test Mol Biomarkers. 2019 Feb;23(2):124-137. doi: 10.1089/gtmb.2018.0153. Epub 2019 Jan 22.
β-Adrenergic receptors (ADRBs) play a pivotal role in cardiovascular disease. Recently, genetic polymorphisms of ADRB1 and ADRB2 have been suggested to be associated with cardiovascular events and all-cause mortality in coronary artery disease (CAD) patients, but the results of relevant studies are inconsistent and controversial. Therefore, we performed a meta-analysis to investigate the association between ADRB1 and ADRB2 polymorphisms with cardiovascular events and all-cause mortality in CAD patients.
The PubMed, Ovid, EMBASE, Cochrane, and CINAHL databases were searched for eligible studies published before April 2018. A total of 5495 patients from eight studies were included in our meta-analysis.
We found that CAD patients harboring the ADRB2 rs1042714 Glu27 allele exhibited a positive association with cardiovascular events (risk ratio [RR] = 1.31, 95% confidence interval [CI]: 1.08-1.58, p = 0.006), but not with all-cause mortality (RR = 0.97, 95% CI: 0.70-1.35, p = 0.859), compared with patients who were Gln27 homozygotes. No other significant associations were observed between ADRB1 (rs1801252, rs1801253), ADRB2 (rs1042713, rs1800888) polymorphisms and cardiovascular events or all-cause mortality in CAD patients.
This study suggests that the identified ADRB2 polymorphism could influence the outcomes of CAD patients, showing important clinical value.
β-肾上腺素能受体(ADRBs)在心血管疾病中起关键作用。最近,有人提出ADRB1和ADRB2的基因多态性与冠心病(CAD)患者的心血管事件和全因死亡率相关,但相关研究结果并不一致且存在争议。因此,我们进行了一项荟萃分析,以研究ADRB1和ADRB2基因多态性与CAD患者心血管事件和全因死亡率之间的关联。
检索了PubMed、Ovid、EMBASE、Cochrane和CINAHL数据库,以查找2018年4月之前发表的符合条件的研究。我们的荟萃分析纳入了来自八项研究的共5495例患者。
我们发现,与携带Gln27纯合子的患者相比,携带ADRB2 rs1042714 Glu27等位基因的CAD患者与心血管事件呈正相关(风险比[RR]=1.31,95%置信区间[CI]:1.08-1.58,p=0.006),但与全因死亡率无关(RR=0.97,95%CI:0.70-1.35,p=0.859)。在CAD患者中,未观察到ADRB1(rs1801252、rs1801253)、ADRB2(rs1042713、rs1800888)基因多态性与心血管事件或全因死亡率之间的其他显著关联。
本研究表明,所鉴定的ADRB2基因多态性可能影响CAD患者的预后,具有重要的临床价值。