Magvanjav Oyunbileg, McDonough Caitrin W, Gong Yan, McClure Leslie A, Talbert Robert L, Horenstein Richard B, Shuldiner Alan R, Benavente Oscar R, Mitchell Braxton D, Johnson Julie A
From the Department of Pharmacotherapy and Translational Research, Center for Pharmacogenomics, College of Pharmacy, University of Florida, Gainesville (O.M., C.W.M., Y.G., J.A.J.); Department of Epidemiology and Biostatistics, Dornsife School of Public Health, Drexel University, Philadelphia, PA (L.A.M.); College of Pharmacy, University of Texas, Austin (R.L.T.); Division of Endocrinology, Diabetes and Nutrition and Program for Personalized and Genomic Medicine, University of Maryland School of Medicine, Baltimore (R.B.H., A.R.S., B.D.M.); Department of Neurology, University of British Columbia, Vancouver, Canada (O.R.B.); and Geriatrics Research and Education Clinical Center, Baltimore Veterans Administration Medical Center, MD (B.D.M.).
Stroke. 2017 May;48(5):1337-1343. doi: 10.1161/STROKEAHA.116.015936. Epub 2017 Mar 28.
Functional polymorphisms (Ser49Gly and Arg389Gly) in have been associated with cardiovascular and β-blocker response outcomes. Herein we examined associations of these polymorphisms with major adverse cardiovascular events (MACE), with and without stratification by β-blocker treatment in patients with a history of stroke.
Nine hundred and twenty-six participants of the SPS3 trial's (Secondary Prevention of Small Subcortical Strokes) genetic substudy with hypertension were included. MACE included stroke, myocardial infarction, and all-cause death. Kaplan-Meier and multivariable Cox regression analyses were used. Because the primary component of MACE was ischemic stroke, we tested the association of Ser49Gly with ischemic stroke among 41 475 individuals of European and African ancestry in the NINDS (National Institute of Neurological Disorders and Stroke) SiGN (Stroke Genetics Network).
MACE was higher in carriers of the Gly49 allele than in those with the Ser49Ser genotype (10.5% versus 5.4%, log-rank =0.005). Gly49 carrier status was associated with MACE (hazard ratio, 1.62; 95% confidence interval, 1.00-2.68) and ischemic stroke (hazard ratio, 1.81; 95% confidence interval, 1.01-3.23) in SPS3 and with small artery ischemic stroke (odds ratio, 1.14; 95% confidence interval, 1.03-1.26) in SiGN. In SPS3, β-blocker-treated Gly49 carriers had increased MACE versus non-β-blocker-treated individuals and noncarriers (hazard ratio, 2.03; 95% confidence interval, 1.20-3.45). No associations were observed with the Arg389Gly polymorphism.
Among individuals with previous small artery ischemic stroke, the Gly49 polymorphism was associated with MACE, particularly small artery ischemic stroke, a risk that may be increased among β-blocker-treated individuals. Further research is needed to define β-blocker benefit among ischemic stroke patients by genotype.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00059306.
[具体基因]中的功能多态性(Ser49Gly和Arg389Gly)与心血管及β受体阻滞剂反应结局相关。在此,我们研究了这些多态性与主要不良心血管事件(MACE)的关联,以及在有卒中病史的患者中按β受体阻滞剂治疗与否进行分层后的情况。
纳入了SPS3试验(皮质下小卒中二级预防)基因亚研究中926例患有高血压的参与者。MACE包括卒中、心肌梗死和全因死亡。采用Kaplan-Meier和多变量Cox回归分析。由于MACE的主要组成部分是缺血性卒中,我们在国立神经疾病与卒中研究所(NINDS)的卒中遗传学网络(SiGN)中41475例欧洲和非洲血统个体中测试了Ser49Gly与缺血性卒中的关联。
Gly49等位基因携带者的MACE高于Ser49Ser基因型者(10.5%对5.4%,对数秩检验P = 0.005)。在SPS3中,Gly49携带者状态与MACE(风险比,1.62;95%置信区间,1.00 - 2.68)和缺血性卒中(风险比,1.81;95%置信区间,1.01 - 3.23)相关,在SiGN中与小动脉缺血性卒中(优势比,1.14;95%置信区间,1.03 - 1.26)相关。在SPS3中,接受β受体阻滞剂治疗的Gly49携带者与未接受β受体阻滞剂治疗的个体及非携带者相比,MACE增加(风险比,2.03;95%置信区间,1.20 - 3.45)。未观察到与Arg389Gly多态性的关联。
在既往有小动脉缺血性卒中的个体中,[具体基因]的Gly49多态性与MACE相关,尤其是小动脉缺血性卒中,这种风险在接受β受体阻滞剂治疗的个体中可能增加。需要进一步研究以根据[具体基因]基因型确定缺血性卒中患者使用β受体阻滞剂的获益情况。