Relationship between Inflammatory Markers, Endothelial Activation Markers, and Carotid Intima-Media Thickness in HIV-Infected Patients Receiving Antiretroviral Therapy

被引:196
作者
Ross, Allison C. [2 ,3 ]
Rizk, Nesrine [2 ,3 ]
O'Riordan, Mary Ann [3 ]
Dogra, Vikram [5 ]
El-Bejjani, Dalia [2 ]
Storer, Norma [2 ,3 ]
Harrill, Danielle [3 ]
Tungsiripat, Marisa [4 ]
Adell, Jerome [2 ]
McComsey, Grace A. [1 ,2 ,3 ]
机构
[1] Rainbow Babies & Childrens Hosp, Dept Infect Dis, Cleveland, OH 44106 USA
[2] Univ Hosp Case, Med Ctr, Cleveland, OH USA
[3] Case Western Reserve Univ, Cleveland, OH 44106 USA
[4] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[5] Univ Rochester, Rochester, NY USA
关键词
CORONARY-HEART-DISEASE; NECROSIS-FACTOR-ALPHA; C-REACTIVE-PROTEIN; MYOCARDIAL-INFARCTION; RISK-FACTORS; SUBCLINICAL ATHEROSCLEROSIS; CARDIOVASCULAR-DISEASE; ARTERY INTIMA; E-SELECTIN; EVENTS;
D O I
10.1086/605578
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Human immunodeficiency virus (HIV)-infected patients are at increased risk of cardiovascular disease, which may be related to chronic inflammation and endothelial dysfunction despite virological control with antiretroviral therapy. The relationship between carotid intima-media thickness (IMT), a surrogate marker for cardiovascular disease, proinflammatory cytokines, and endothelial activation markers has not been fully explored in HIV-infected patients who are receiving antiretroviral therapy. Methods. We conducted a prospective, cross-sectional, observational study of treated HIV-infected patients and healthy control subjects to evaluate the relationship between carotid IMT, proinflammatory cytokines, endothelial activation biomarkers, and metabolic parameters in treated HIV-infected patients, compared with healthy control subjects. Results. We enrolled 73 HIV-infected patients and 21 control subjects. Common carotid artery and internal carotid artery IMT measurements, as well as tumor necrosis factor-a, high-sensitivity C-reactive protein, interleukin-6, myeloperoxidase, and soluble vascular cell adhesion molecule-1 levels were higher in the HIV-infected group. High-sensitivity C-reactive protein was the only biomarker that was positively correlated with carotid IMT in both groups. In the HIV-infected group, soluble vascular cell adhesion molecule-1 was positively correlated with all inflammatory cytokine levels. In multiple regression analysis, soluble vascular cell adhesion molecule-1, myeloperoxidase, and tumor necrosis factor-a levels were all associated with internal carotid artery IMT in the HIV-infected group, whereas age was associated with both common carotid artery and internal carotid artery IMT. Conclusions. Enhanced endothelial activation, inflammation, and increased carotid IMT occur in HIV-infected patients despite antiretroviral therapy. Inflammatory markers are associated with endothelial activation, and both are associated with internal carotid artery IMT, supporting a potential role of inflammation in endothelial activation and cardiovascular disease in HIV infection.
引用
收藏
页码:1119 / 1127
页数:9
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