Plasma Interleukin-6 (IL-6), Angiopoietin-2, and C-Reactive Protein Levels Predict Subsequent Type 1 Myocardial Infarction in Persons With Treated HIV Infection

Author:

Graham Susan M.123ORCID,Nance Robin M.2,Chen Junmei4,Wurfel Mark M.2,Hunt Peter W.5,Heckbert Susan R.3,Budoff Matthew J.6,Moore Richard D.7,Jacobson Jeffrey M.8,Martin Jeffrey N.9,Crane Heidi M.210,López José A.4,Liles W. Conrad121112

Affiliation:

1. Global Health;

2. Medicine; and

3. Epidemiology, University of Washington, Seattle, WA;

4. Bloodworks Northwest Research Institute, Seattle, WA;

5. Department of Medicine, University of California at San Francisco, San Francisco, CA;

6. Department of Medicine, University of California at Los Angeles, Los Angeles, CA;

7. Department of Medicine, Johns Hopkins, Baltimore, MD;

8. Department of Medicine, Case Western Reserve University, Cleveland, OH;

9. Departments of Epidemiology and Biostatistics, University of California at San Francisco, San Francisco, CA;

10. Department of Health Services, University of Washington, Seattle, WA;

11. Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA; and

12. Department of Pharmacology, University of Washington, Seattle, WA.

Abstract

Background: HIV infection leads to endothelial activation, promoting platelet adhesion, and accelerating atherosclerosis. Our goal was to determine whether biomarkers of endothelial activation and hemostasis/thrombosis were elevated in people with treated HIV (PWH) before myocardial infarction (MI). Methods: In a case–control study nested within the CFAR Network of Integrated Clinical Systems (CNICS) cohort, we compared 69 adjudicated cases with type 1 MI with 138 controls matched for antiretroviral therapy regimen. We measured angiopoietin-1, angiopoietin-2 (ANG-2), intercellular adhesion molecule 1 (ICAM-1), vascular cell adhesion molecule 1 (VCAM-1), a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13), von Willebrand factor, C-reactive protein (CRP), interleukin-6 (IL-6), plasminogen activation inhibitor-1, P-selectin, serum amyloid-A, soluble CD14, and apolipoprotein A1 in stored plasma. Conditional logistic regression identified associations with subsequent MI, with and without adjustment for Atherosclerotic Cardiovascular Disease (ASCVD) and Veterans Aging Cohort Study (VACS) scores. Results: Higher IL-6 was associated with MI after adjustment for ASCVD score (adjusted odds ratio [AOR] 1.51, 95% confidence interval [95% CI]: 1.05 to 2.17 per standard-deviation-scaled log2 increment). In a separate model adjusting for VACS score, higher ANG-2 (AOR 1.49, 95% CI: 1.04 to 2.14), higher CRP (AOR 1.45, 95% CI: 1.06 to 2.00), and higher IL-6 (AOR 1.68, 95% CI: 1.17 to 2.41) were associated with MI. In a sensitivity analysis excluding PWH with viral load ≥400 copies/mL, higher IL-6 remained associated with MI after adjustment for ASCVD score and after adjustment for VACS score. Conclusions: Among PWH, higher levels of plasma IL-6, CRP, and ANG-2 predict subsequent type 1 MI, independent of conventional risk scores. IL-6 had the most consistent associations with type 1 MI, regardless of viral load suppression.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Infectious Diseases

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