Kulshreshtha Ambar, Zheng Yan, Quyyumi Arshed A, Veledar Emir, Votaw John, Uphoff Irina, Bremner Douglas J, Goldberg Jack, Vaccarino Viola
Department of Epidemiology, Emory University School of Public Health, Atlanta, GA ; Division of Cardiology, Emory University School of Medicine, Atlanta, GA.
Department of Epidemiology, Emory University School of Public Health, Atlanta, GA.
IJC Metab Endocr. 2014 Sep 1;4:28-32. doi: 10.1016/j.ijcme.2014.07.004.
Silent myocardial ischemia is common in asymptomatic subjects without a prior history of coronary artery disease (CAD) and is associated with increased morbidity and mortality. Our objective was to determine whether endothelial dysfunction is associated with silent myocardial ischemia and whether the association is independent of genetic and familial factors.
We examined 416 male monozygotic and dizygotic twins aged 47 to 63 years, free of symptomatic CAD. Subclinical ischemia was diagnosed by [13N] ammonia positron emission tomography at rest and after adenosine stress. Endothelial function was measured by flow-mediated dilation (FMD) of the brachial artery. Generalized estimating equations were used for analysis.
Fixed perfusion defects were found in 24 (6%) twins and reversible perfusion defects in 90 (22%) twins, indicating subclinical ischemia. There was an inverse correlation between FMD and the reversible perfusion defect score (r = - 0.14, p=0.01) but not the fixed defect score (r= -0.017, p=0.73). From the lowest to the highest quartile of FMD, the prevalence of reversible defects decreased 28% to 14%, p=0.008. In multivariable analysis, reversible defects were significantly associated with each quartile of decreasing FMD (OR =1.3; 95% 1.1, 2.5). In 54 twin pairs discordant for endothelial dysfunction (FMD ≤ 7% dilation from baseline), twins with endothelial dysfunction had 9% higher likelihood of having perfusion defects than their co-twins without endothelial dysfunction (p=0.041).
Endothelial dysfunction is independently associated with silent ischemia and this association is not confounded by genetic or other shared familial factors.
无症状性心肌缺血在无冠心病(CAD)既往史的无症状受试者中很常见,且与发病率和死亡率增加相关。我们的目的是确定内皮功能障碍是否与无症状性心肌缺血相关,以及这种关联是否独立于遗传和家族因素。
我们检查了416名年龄在47至63岁之间、无有症状CAD的男性同卵和异卵双胞胎。通过静息和腺苷负荷后的[13N]氨正电子发射断层扫描诊断亚临床缺血。通过肱动脉的血流介导的扩张(FMD)测量内皮功能。使用广义估计方程进行分析。
在24名(6%)双胞胎中发现了固定灌注缺损,在90名(22%)双胞胎中发现了可逆灌注缺损,表明存在亚临床缺血。FMD与可逆灌注缺损评分之间存在负相关(r = -0.14,p = 0.01),但与固定缺损评分无相关性(r = -0.017,p = 0.73)。从FMD的最低四分位数到最高四分位数,可逆缺损的患病率从28%降至14%,p = 0.008。在多变量分析中,可逆缺损与FMD降低的每个四分位数显著相关(OR = 1.3;95% 1.1,2.5)。在54对内皮功能障碍不一致(FMD自基线扩张≤7%)的双胞胎中,有内皮功能障碍的双胞胎出现灌注缺损的可能性比其无内皮功能障碍的双胞胎高9%(p = 0.041)。
内皮功能障碍与无症状性缺血独立相关,且这种关联不受遗传或其他共同家族因素的混淆。