Ogura Masatsune, Hori Mika, Harada-Shiba Mariko
From the Department of Molecular Innovation in Lipidology, National Cerebral and Cardiovascular Center Research Institute, Osaka, Japan.
Arterioscler Thromb Vasc Biol. 2016 Jan;36(1):181-8. doi: 10.1161/ATVBAHA.115.306665. Epub 2015 Nov 5.
Patients with familial hypercholesterolemia (FH) are at high risk for premature atherosclerotic cardiovascular disease (ASCVD), especially because of long-term exposure to high low-density lipoprotein cholesterol levels. It has been reported that low-density lipoprotein-lowering therapy delays the onset of ASCVD. However, it still remains difficult to prevent it. Therefore, novel biomarkers and therapeutic targets are necessary to evaluate and prevent atherosclerosis in FH. The aim of this study was to investigate associations of cholesterol efflux capacity with the presence of ASCVD and clinical features in patients with heterozygous FH.
We measured cholesterol efflux capacity in 227 patients with heterozygous FH under pharmaceutical treatment. Seventy-six (33.5%) of them were known to have ASCVD. In a logistic-regression analysis adjusted for risk factors, increased efflux capacity was associated with decreased risk of ASCVD even after the addition of high-density lipoprotein cholesterol level as a covariate (odds ratio per 1-SD increase, 0.95; 95% confidence interval, 0.90-0.99; P<0.05). Decreased cholesterol efflux capacity was associated with the presence of corneal arcus after adjusting for age and sex. In addition, inverse relationships between cholesterol efflux capacity and Achilles tendon thickness, as well as carotid intima-media thickness, were observed after adjustment for age, sex, and traditional cardiovascular risk factors.
Cholesterol efflux capacity was independently and inversely associated with the presence of ASCVD in heterozygous FH. In view of residual risks after treatment with statins, cholesterol efflux capacity might be a novel biomarker and a therapeutic target for preventing atherosclerosis in patients with FH.
家族性高胆固醇血症(FH)患者过早发生动脉粥样硬化性心血管疾病(ASCVD)的风险很高,尤其是由于长期暴露于高低密度脂蛋白胆固醇水平。据报道,降低低密度脂蛋白的治疗可延迟ASCVD的发病。然而,预防它仍然很困难。因此,需要新的生物标志物和治疗靶点来评估和预防FH患者的动脉粥样硬化。本研究的目的是调查胆固醇流出能力与杂合子FH患者ASCVD的存在及临床特征之间的关联。
我们测量了227例接受药物治疗的杂合子FH患者的胆固醇流出能力。其中76例(33.5%)已知患有ASCVD。在针对风险因素进行调整的逻辑回归分析中,即使将高密度脂蛋白胆固醇水平作为协变量加入后,流出能力增加仍与ASCVD风险降低相关(每增加1个标准差的优势比为0.95;95%置信区间为0.90-0.99;P<0.05)。在调整年龄和性别后,胆固醇流出能力降低与角膜弓的存在相关。此外,在调整年龄、性别和传统心血管风险因素后,观察到胆固醇流出能力与跟腱厚度以及颈动脉内膜中层厚度之间呈负相关。
在杂合子FH中,胆固醇流出能力与ASCVD的存在独立且呈负相关。鉴于他汀类药物治疗后的残余风险,胆固醇流出能力可能是预防FH患者动脉粥样硬化的一种新的生物标志物和治疗靶点。