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Inflammatory Biomarkers Predicting Major Adverse Cardiovascular Events in People Living With HIV: A Systematic Review
Ashley Murray1, Niamh Louwman2, Augustine Luk3,4
1Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
Inflammation significantly increases cardiovascular disease (CVD) risk in people with HIV. High-sensitivity C-reactive protein (hsCRP) and other biomarkers show potential for predicting CVD events in this population.
Area of Science:
- Cardiology
- Infectious Diseases
- Immunology
Background:
- Chronic inflammation is a key factor in cardiovascular disease (CVD) risk for people living with HIV.
- Current consensus on the predictive value of inflammatory biomarkers for CVD in this population is lacking.
Purpose of the Study:
- To systematically review the predictive value of inflammatory biomarkers for major adverse cardiovascular events (MACE) in people living with HIV.
- To inform the potential integration of these biomarkers into CVD risk assessment strategies.
Main Methods:
- A systematic search of MEDLINE, Embase, and Google Scholar was conducted up to May 1, 2024.
- Included studies were prospective cohorts or nested case-control studies of adults living with HIV with biomarker measurements and at least one year of follow-up for MACE.
- Risk of bias was assessed using the Quality in Prognostic Studies (QUIPS) tool, and meta-analysis was performed where appropriate.
Main Results:
- Twenty-one studies identified 31 inflammatory biomarkers. High-sensitivity C-reactive protein (hsCRP) was positively associated with future CVD events (HR=1.86 per log10 unit).
- Interleukin-6 (IL-6), D-dimer, and N-terminal pro-brain natriuretic peptide (NT-proBNP) showed significant associations in at least two studies, but meta-analysis was precluded by heterogeneity.
- Most studies were from high-income settings with low female representation, and a moderate to high risk of bias was common.
Conclusions:
- Several inflammatory biomarkers show potential for predicting CVD in people with HIV, supporting inflammation's role in HIV-related CVD.
- However, evidence is limited by study heterogeneity, methodological quality, and underrepresentation of women and low- and middle-income countries (LMICs).
- Larger, representative studies are needed to validate these biomarkers for clinical risk prediction models.
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