Derivation of a Protein Risk Score for Cardiovascular Disease Among a Multiracial and Multiethnic HIV+ Cohort

Author:

Safo Sandra E.1ORCID,Haine Lillian1ORCID,Baker Jason2ORCID,Reilly Cavan1,Duprez Daniel1ORCID,Neaton James D.1ORCID,Jain Mamta K.3ORCID,Arenas‐Pinto Alejandro4ORCID,Polizzotto Mark5ORCID,Staub Therese6,

Affiliation:

1. University of Minnesota Minneapolis MN USA

2. Hennepin County Medical Center Minneapolis MN USA

3. University of Texas Southwestern Dallas TX USA

4. MRC Clinical Trials Unit at University College London Institute of Clinical Trials & Methodology London UK

5. Australian National University Canberra Australia

6. Luxembourg Hospital Center Luxembourg City Luxembourg

Abstract

Background Cardiovascular disease risk prediction models underestimate CVD risk in people living with HIV (PLWH). Our goal is to derive a risk score based on protein biomarkers that could be used to predict CVD in PLWH. Methods and Results In a matched case–control study, we analyzed normalized protein expression data for participants enrolled in 1 of 4 trials conducted by INSIGHT (International Network for Strategic Initiatives in Global HIV Trials). We used dimension reduction, variable selection and resampling methods, and multivariable conditional logistic regression models to determine candidate protein biomarkers and to generate a protein score for predicting CVD in PLWH. We internally validated our findings using bootstrap. A protein score that was derived from 8 proteins (including HGF [hepatocyte growth factor] and interleukin‐6) was found to be associated with an increased risk of CVD after adjustment for CVD and HIV factors (odds ratio: 2.17 [95% CI: 1.58–2.99]). The protein score improved CVD prediction when compared with predicting CVD risk using the individual proteins that comprised the protein score. Individuals with a protein score above the median score were 3.10 (95% CI, 1.83–5.41) times more likely to develop CVD than those with a protein score below the median score. Conclusions A panel of blood biomarkers may help identify PLWH at a high risk for developing CVD. If validated, such a score could be used in conjunction with established factors to identify CVD at‐risk individuals who might benefit from aggressive risk reduction, ultimately shedding light on CVD pathogenesis in PLWH.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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