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Traditional risk factors and D-dimer predict incident cardiovascular disease events in chronic HIV infection
被引:157
|作者:
Ford, Emily S.
[1
]
Greenwald, Jamieson H.
[1
]
Richterman, Aaron G.
[1
]
Rupert, Adam
[2
]
Dutcher, Lauren
[1
]
Badralmaa, Yunden
[2
]
Natarajan, Ven
[2
]
Rehm, Catherine
[1
]
Hadigan, Colleen
[1
]
Sereti, Irini
[1
]
机构:
[1] NIAID, NIH, Bethesda, MD 20892 USA
[2] NCI, AIDS Monitoring Lab, SAIC Frederick Inc, Frederick, MD 21701 USA
来源:
基金:
美国国家卫生研究院;
关键词:
cardiovascular disease;
D-dimer;
HIV;
myocardial infarction;
smoking;
tissue factor;
vascular cell adhesion molecule-1;
CORONARY-ARTERY-DISEASE;
ACUTE MYOCARDIAL-INFARCTION;
C-REACTIVE PROTEIN;
ANTIRETROVIRAL THERAPY;
INSULIN-RESISTANCE;
IMMUNE ACTIVATION;
STABLE ANGINA;
ATHEROSCLEROSIS;
INFLAMMATION;
MONOCYTES;
D O I:
10.1097/QAD.0b013e32833ad914
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Objective: Cardiovascular disease (CVD) contributes significantly to HIV-related morbidity and mortality. Chronic immune activation and inflammation are thought to augment the progression of atherosclerotic disease. In this retrospective, case-control study of HIV-infected individuals, we investigated the association of traditional cardiac risk factors, HIV-related disease, and inflammation with CVD events. Methods: HIV-infected individuals who experienced an incident CVD event while enrolled in National Institutes of Health clinical protocols from 1995 to 2009 were matched 2 : 1 to HIV-infected individuals without known CVD. Markers of inflammation and cell activation were measured in serum or plasma using ELISA-based assays and peripheral mononuclear cells by four-color flow cytometry. Results: Fifty-two patients experienced an incident CVD event. Events were related to smoking, dyslipidemia, hyperglycemia, and family history as well as elevated D-dimer, soluble vascular cell adhesion molecule-1, tissue inhibitor of metalloproteinase-1, and soluble tissue factor, but not high-sensitivity C-reactive protein. No significant differences in antiviral therapy, CD4(+) T-cell count, or CD38 and human leukocyte antigen-DR expression were identified between patients and controls. In multivariable analysis, smoking, family history, D-dimer, and glucose were independently related to CVD risk. Conclusion: In this cohort, CVD risk was related to traditional CVD risk factors and markers of thrombosis and endothelial damage, but not to high-sensitivity C-reactive protein or markers of T-cell activation such as CD38/human leukocyte antigen-DR coexpression. D-dimer may help identify HIV-infected patients at elevated CVD risk. (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
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页码:1509 / 1517
页数:9
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