Knudsen Andreas, Katzenstein Terese L, Benfield Thomas, Jørgensen Niklas R, Kronborg Gitte, Gerstoft Jan, Obel Niels, Kjær Andreas, Lebech Anne-Mette
aDepartment of Infectious Diseases, Copenhagen University Hospital, Hvidovre bDepartment of Clinical Physiology, Nuclear Medicine & PET, Copenhagen University Hospital, Rigshospitalet and Cluster for Molecular Imaging, Faculty of Health and Medical Sciences, University of Copenhagen cDepartment of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet dResearch Center for Ageing and Osteoporosis, Departments of Diagnostics and Medicine, Copenhagen University Hospital, Glostrup, Denmark.
AIDS. 2014 May 15;28(8):1171-9. doi: 10.1097/QAD.0000000000000247.
Biomarkers of endothelial dysfunction, inflammation and coagulation are associated with atherosclerosis and cardiovascular disease, but their association and possible predictive value remain controversial among HIV-1-infected individuals. We sought to investigate the association of seven biomarkers with first-time myocardial infarction (MI) in an HIV-1-infected population.
A matched case-control study of 54 cases and 54 controls.
We compared 54 HIV-1-infected patients with verified first-time MI and 54 HIV-1-infected controls matched for age, duration of antiretroviral therapy, sex, smoking and no known cardiovascular disease. Levels of high-sensitivity C-reactive protein, soluble endothelial selectin, soluble vascular cell adhesion molecule, soluble intercellular adhesion molecule, matrix metalloprotease 9, myeloperoxidase, and plasminogen activator inhibitor 1 (PAI-1) were measured using a Luminex assay in plasma samples from routine visits both 12 and 2 months prior to the case patient's MI.
The two groups had similar HIV characteristics and traditional cardiovascular risk factors. In univariate analysis, PAI-1 levels were associated with MI, whereas none of the other markers showed any association.In multivariate analyses adjusting for the D:A:D risk score, HIV viral load and high-sensitivity C-reactive protein, PAI-1 levels in the highest quartile were associated with a six to seven-fold increased risk of MI in both samples.
High levels of PAI-1 were associated with risk of first-time MI in HIV-1-infected individuals independently of cardiovascular risk factors, HIV parameters and antiretroviral therapy. Therefore PAI-1 may be used for risk stratification and prediction of CHD, but further studies are needed.
内皮功能障碍、炎症和凝血的生物标志物与动脉粥样硬化和心血管疾病相关,但其在HIV-1感染个体中的关联及可能的预测价值仍存在争议。我们旨在研究HIV-1感染人群中7种生物标志物与首次心肌梗死(MI)的关联。
一项54例病例与54例对照的匹配病例对照研究。
我们比较了54例经证实为首次MI的HIV-1感染患者与54例年龄、抗逆转录病毒治疗持续时间、性别、吸烟情况及无已知心血管疾病的HIV-1感染对照。在病例患者发生MI前12个月和2个月的常规就诊血浆样本中,使用Luminex检测法测量高敏C反应蛋白、可溶性内皮选择素、可溶性血管细胞黏附分子、可溶性细胞间黏附分子、基质金属蛋白酶9、髓过氧化物酶和纤溶酶原激活物抑制剂1(PAI-1)的水平。
两组具有相似的HIV特征和传统心血管危险因素。单因素分析中,PAI-1水平与MI相关,而其他标志物均未显示出任何关联。在对D:A:D风险评分、HIV病毒载量和高敏C反应蛋白进行校正的多因素分析中,两个样本中最高四分位数的PAI-1水平与MI风险增加6至7倍相关。
高水平的PAI-1与HIV-1感染个体首次MI的风险相关,独立于心血管危险因素、HIV参数和抗逆转录病毒治疗。因此,PAI-1可用于冠心病的风险分层和预测,但还需要进一步研究。