Jones Gregory T, van Rij Andre M, Cole Jennifer, Williams Michael J A, Bateman Emma H, Marcovina Santica M, Deng Meiying, McCormick Sally P A
Department of Medical and Surgical Sciences, University of Otago, Dunedin, New Zealand.
Clin Chem. 2007 Apr;53(4):679-85. doi: 10.1373/clinchem.2006.079947. Epub 2007 Feb 15.
Increased lipoprotein(a) [Lp(a)] concentrations are predictive for coronary artery disease (CAD). The risk conferred by Lp(a) for other types of vascular disease compared with CAD has not been investigated within a single population. This study aimed to investigate Lp(a) risk association for 4 different types of vascular disease (including CAD) within a predominantly white population.
We used an Lp(a) ELISA that measures Lp(a) independently of apolipoprotein(a) size to measure plasma Lp(a) in patients [384 CAD, 262 peripheral vascular disease, 184 ischemic stroke (stroke), 425 abdominal aortic aneurysm] and 230 disease-free controls. We then conducted association studies with logistic regression, integrating the potential confounding effects of age, sex, diabetes, plasma lipids, and a history of previous hypertension, hypercholesterolemia, and smoking.
Multivariate analyses with Lp(a) concentrations of >45 nmol/L (the 75th percentile value for controls) as the clinical cutoff showed increased Lp(a) concentrations to be a risk factor for all disease groups, with adjusted odds ratios ranging from 1.96 [95% confidence interval (CI) 1.24-3.08] for CAD to 2.33 (95% CI 1.39-3.89) for PVD. The risk conferred by Lp(a) appeared to be independent of other confounders, including exposure to statin/fibrate therapies. Similar odds ratios and CIs between disease groups indicated that increased Lp(a) conferred a similar risk for all groups studied.
Lp(a) constitutes a stable risk factor of similar magnitude for 4 major forms of vascular disease. This association was not altered by exposure to standard lipid-lowering therapy.
脂蛋白(a)[Lp(a)]浓度升高是冠状动脉疾病(CAD)的预测指标。与CAD相比,Lp(a)对其他类型血管疾病的风险尚未在单一人群中进行研究。本研究旨在调查在以白人为主的人群中,Lp(a)与4种不同类型血管疾病(包括CAD)的风险关联。
我们使用一种独立于载脂蛋白(a)大小来测量Lp(a)的Lp(a)酶联免疫吸附测定法,对患者[384例CAD、262例周围血管疾病、184例缺血性卒中(中风)、425例腹主动脉瘤]和230例无疾病对照者的血浆Lp(a)进行测量。然后我们进行了逻辑回归关联研究,综合考虑年龄、性别、糖尿病、血脂以及既往高血压、高胆固醇血症和吸烟史的潜在混杂效应。
以Lp(a)浓度>45 nmol/L(对照组的第75百分位数)作为临床临界值的多变量分析显示,Lp(a)浓度升高是所有疾病组的危险因素,调整后的比值比范围从CAD的1.96[95%置信区间(CI)1.24 - 3.08]到周围血管疾病的2.33(95%CI 1.39 - 3.89)。Lp(a)所带来的风险似乎独立于其他混杂因素,包括他汀类/贝特类药物治疗。疾病组之间相似的比值比和置信区间表明,Lp(a)升高给所有研究组带来相似的风险。
Lp(a)是4种主要血管疾病形式的相似程度的稳定危险因素。这种关联不受标准降脂治疗的影响。