Provident Clinical Research, 489 Taft Avenue, Glen Ellyn, IL 60137, USA.
Radiant Research, Chicago, IL, USA; The University of Chicago Pritzker School of Medicine, Chicago, IL, USA.
J Clin Lipidol. 2011 May-Jun;5(3):141-151. doi: 10.1016/j.jacl.2011.02.003. Epub 2011 Feb 12.
The rate of carotid intima media thickness (CIMT) progression has been widely used in clinical trials as a surrogate marker for subclinical atherosclerosis.
The aim of this study was to investigate relationships between coronary heart disease (CHD) risk markers and progression of CIMT in patients at moderate CHD risk.
Participants included men (45-75 years) and women (55-74 years) in the control arm of a clinical trial. All had at least one major CHD risk factor and baseline posterior wall CIMT 0.7-2.0 mm, without significant stenosis. Posterior (n = 134) and anterior wall (in a subset, n = 72) CIMT were assessed with B-mode ultrasound at baseline and 12 and ∼18 months. Fasting lipoprotein lipid, apolipoprotein (Apo), inflammatory, and oxidative stress markers were evaluated.
Baseline CIMT was inversely associated (P < .001) with CIMT progression. After adjustment for baseline CIMT, significant predictors of anterior wall CIMT progression in linear regression analyses included glucose (P = .044), high-density lipoprotein cholesterol (HDL-C, inverse, P = .006), triglycerides (TG, P = .006), and ratios of total cholesterol (TC)/HDL-C (P = .013), TG/HDL-C (P = .005), and Apo B/HDL-C (P = .021). Posterior wall CIMT progressed on average, whereas anterior wall CIMT regressed (0.0078 vs -0.0164 mm/year, P = .014). Significant baseline CIMT-adjusted predictors of posterior wall CIMT progression included TC (P = .028), low-density lipoprotein-C (P = .035), non-HDL-C (P = .004), TG (P = .016), Apo B (P = .005), and ratios of TC/HDL-C (P < .001), TG/HDL-C (P = .015), Apo B/Apo AI (P = .012) and Apo B/HDL-C (P = .004).
The strongest predictors for CIMT progression in anterior and posterior walls were lower baseline CIMT, increased TG, and elevated ratios, including TC/HDL-C, TG/HDL-C and Apo B/HDL-C.
颈动脉内膜中层厚度(CIMT)进展率已被广泛用于临床试验中,作为亚临床动脉粥样硬化的替代标志物。
本研究旨在探讨在中等冠心病风险患者中,冠心病(CHD)风险标志物与 CIMT 进展之间的关系。
该研究的参与者包括临床试验对照组的男性(45-75 岁)和女性(55-74 岁)。所有参与者均至少有一个主要的 CHD 风险因素,且基线时后侧壁 CIMT 在 0.7-2.0mm 之间,无明显狭窄。基线时用 B 型超声评估后壁(n=134)和前壁(亚组 n=72)CIMT,12 个月和 18 个月时再次评估。检测空腹脂蛋白脂质、载脂蛋白(Apo)、炎症和氧化应激标志物。
基线 CIMT 与 CIMT 进展呈负相关(P<0.001)。在校正基线 CIMT 后,线性回归分析中前壁 CIMT 进展的显著预测因子包括血糖(P=0.044)、高密度脂蛋白胆固醇(HDL-C,负相关,P=0.006)、甘油三酯(TG,P=0.006)和总胆固醇(TC)/HDL-C(P=0.013)、TG/HDL-C(P=0.005)和 ApoB/HDL-C(P=0.021)比值。后壁 CIMT 平均进展,而前壁 CIMT 出现逆转(0.0078 与-0.0164mm/年,P=0.014)。校正基线 CIMT 后,后壁 CIMT 进展的显著预测因子包括 TC(P=0.028)、低密度脂蛋白-C(LDL-C,P=0.035)、非高密度脂蛋白-C(non-HDL-C,P=0.004)、TG(P=0.016)、ApoB(P=0.005)和 TC/HDL-C(P<0.001)、TG/HDL-C(P=0.015)、ApoB/Apo AI(P=0.012)和 ApoB/HDL-C(P=0.004)比值。
在前壁和后壁 CIMT 中,最强的 CIMT 进展预测因子是较低的基线 CIMT、升高的 TG 以及升高的比值,包括 TC/HDL-C、TG/HDL-C 和 ApoB/HDL-C。