The association of C-reactive protein with subclinical cardiovascular disease in HIV-infected and HIV-uninfected women

被引:0
|
作者
Moran, Caitlin A. [1 ,2 ]
Sheth, Anandi N. [1 ,2 ]
Mehta, C. Christina [3 ]
Hanna, David B. [4 ]
Gustafson, Deborah R. [5 ]
Plankey, Michael W. [6 ]
Mack, Wendy J. [7 ]
Tien, Phyllis C. [8 ,9 ]
French, Audrey L. [10 ,11 ]
Golub, Elizabeth T. [12 ]
Quyyumi, Arshed [1 ]
Kaplan, Robert C. [4 ]
Ofotokun, Ighovwerha [1 ,2 ]
机构
[1] Emory Univ, Dept Med, Atlanta, GA 30303 USA
[2] Grady Healthcare Syst, Dept Med, Atlanta, GA USA
[3] Emory Univ, Dept Biostat & Bioinformat, Atlanta, GA 30303 USA
[4] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[5] State Univ New York Downstate, Dept Neurol, New York, NY USA
[6] Georgetown Univ, Med Ctr, Dept Med, Washington, DC 20007 USA
[7] Univ Southern Calif, Dept Prevent Med, Los Angeles, CA USA
[8] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[9] Dept Vet Affairs, San Francisco, CA USA
[10] John H Stroger Jr Hosp Cook Cty, Dept Med, Chicago, IL USA
[11] Rush Univ, Dept Med, Med Ctr, Chicago, IL 60612 USA
[12] Johns Hopkins Univ, Dept Epidemiol, Baltimore, MD USA
关键词
atherosclerosis; C-reactive protein; HIV; subclinical cardiovascular disease; women; HUMAN-IMMUNODEFICIENCY-VIRUS; INTIMA-MEDIA THICKNESS; MYOCARDIAL-INFARCTION; INTERAGENCY HIV; RISK; ATHEROSCLEROSIS; INFLAMMATION; PROGRESSION; BIOMARKERS; EVENTS;
D O I
10.1097/QAD.0000000000001785
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: HIV is a cardiovascular disease (CVD) risk factor. However, CVD risk is often underestimated in HIV-infected women. C-reactive protein (CRP) may improve CVD prediction in this population. We examined the association of baseline plasma CRP with subclinical CVD in women with and without HIV. Design: Retrospective cohort study. Methods: A total of 572 HIV-infected and 211 HIV-uninfected women enrolled in the Women's Interagency HIV Study underwent serial high-resolution B-mode carotid artery ultrasonography between 2004 and 2013 to assess carotid intima-media thickness (CIMT) and focal carotid artery plaques. We used multivariable linear and logistic regression models to assess the association of baseline high (>= 3 mg/l) high-sensitivity (hs) CRP with baseline CIMT and focal plaques, and used multivariable linear and Poisson regression models for the associations of high hsCRP with CIMT change and focal plaque progression. We stratified our analyses by HIV status. Results: Median (interquartile range) hsCRP was 2.2 mg/l (0.8-5.3) in HIV-infected, and 3.2 mg/l (0.9-7.7) in HIV-uninfected, women (P = 0.005). There was no statistically significant association of hsCRP with baseline CIMT [adjusted mean difference -3.5 mu m (95% confidence interval: -19.0 to 12.1)] or focal plaques [adjusted odds ratio: 1.31 (0.67-2.67)], and no statistically significant association of hsCRP with CIMT change [adjusted mean difference 11.4 mu m (-2.3 to 25.1)]. However, hsCRP at least 3 mg/l was positively associated with focal plaque progression in HIV-uninfected [adjusted rate ratio: 5.97 (1.46-24.43)], but not in HIV-infected [adjusted rate ratio: 0.81 (0.47-1.42)] women (P = 0.042 for interaction). Conclusion: In our cohort of women with similar CVD risk factors, higher baseline hsCRP is positively associated with carotid plaque progression in HIV-uninfected, but not HIV-infected, women, suggesting that subclinical CVD pathogenesis may be different HIV-infected women. Copyright (C) 2018 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:999 / 1006
页数:8
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