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Inflammatory Biomarkers Predicting Major Adverse Cardiovascular Events in People Living With HIV: A Systematic Review and Meta‐Analysis

Abstract:
Introduction: Chronic inflammation is a unique contributor to cardiovascular disease (CVD) risk among people living with HIV, yet there is a lack of consensus on the predictive utility of inflammatory biomarkers in this population. We conducted a systematic review assessing the predictive value of inflammatory biomarkers for major adverse cardiovascular events in people living with HIV to inform their potential integration into CVD risk assessment. Methods: MEDLINE, Embase and Google Scholar were searched for articles published up to 01 May 2024. We included prospective cohort and nested case‐control studies of adults living with HIV with inflammatory biomarker measurements in blood and at least one year of follow‐up to major adverse cardiovascular events. Risk of bias was assessed using the Quality in Prognostic Studies (QUIPS) tool. Where at least two studies reported the same type of effect measure for a biomarker, results were pooled using an inverse variance heterogeneity model. Results: Among 5156 screened citations, 21 studies reporting 31 inflammatory biomarkers met inclusion criteria. Meta‐analysis showed high‐sensitivity C‐reactive protein (hsCRP) positively associated with future cardiovascular events (hazard ratio = 1.86 per log10 unit; 95% CI 1.39–2.50, n = 5,254). Three biomarkers, interleukin 6 (IL‐6), D‐dimer, and N‐terminal pro‐brain natriuretic peptide (NT‐proBNP), demonstrated positive, statistically significant associations with adverse cardiovascular outcomes in at least two non‐overlapping studies, though heterogeneous effect measures precluded meta‐analysis. Most research (14/21 studies) was conducted exclusively in high‐income settings, and female representation was low (median proportion = 15.5%; IQR 8.4–20.9%). All but three studies had a moderate or high risk of bias in at least one domain. Discussion: We identified several inflammatory biomarkers with potential prognostic value, but most associations were derived from single or heterogeneous studies. The certainty of evidence is reduced by methodological heterogeneity, few high‐quality studies and the underrepresentation of low‐ and middle‐income countries (LMICs). Conclusions: Consistent positive associations between inflammatory biomarkers and future CVD in people living with HIV support a central role of inflammation in HIV‐related CVD. Representative, large‐scale studies that include women and LMICs are needed to guide the integration of candidate biomarkers into CVD risk prediction models. PROSPERO Number: CRD42024542944
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/jia2.70101

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Institution:
University of Oxford
Role:
Author
ORCID:
0009-0000-9780-7617
More by this author
Institution:
University of Oxford
Role:
Author
More by this author
Institution:
University of Oxford
Role:
Author
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-8952-4262


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Funder identifier:
10.13039/501100009978
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Funder identifier:
https://ror.org/05hq0zw41


Publisher:
Wiley
Journal:
Journal of the International AIDS Society More from this journal
Volume:
29
Issue:
4
Article number:
e70101
Publication date:
2026-04-27
Acceptance date:
2026-03-19
DOI:
EISSN:
1758-2652
ISSN:
1758-2652


Language:
English
Keywords:
Subtype:
Review
Pubs id:
2412506
Local pid:
pubs:2412506
Source identifiers:
3990008
Deposit date:
2026-04-27
ARK identifier:
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