# Pericoronary adipose tissue density a novel CT-derived marker of local inflammation and coronary artery disease in people living with HIV

> **NIH NIH R01** · MASSACHUSETTS GENERAL HOSPITAL · 2024 · $419,880

## Abstract

PROJECT SUMMARY/ABSTRACT
People with HIV (PWH) have a heightened coronary artery disease (CAD) and adverse event risk even after
controlling for traditional cardiovascular (CV) risk factors. Hence, there is an unmet need for improved CV risk
stratification among PWH. HIV infection is associated with increased systemic immune activation and
inflammation that is not part of the traditional CV risk assessment. Importantly, work to date in PWH has been
limited to evaluating systemic inflammatory biomarkers or utilizing functional imaging assessments of vascular
inflammation at vessels larger than the coronary arteries. Assessing large vessels prevents direct assessment
of the local coronary inflammatory milieu that drives the development of coronary plaques. Nevertheless,
recent advances in cardiac computed tomography (CT), specifically assessing the density of peri-coronary
adipose tissue (PCAT) that directly surrounds the coronary arteries, suggest that PCAT density may be an
accurate non-invasive index of coronary artery inflammation. In the proposed study, we will leverage data
obtained from the Randomized Trial to Prevent Vascular Events in HIV (REPRIEVE), in which we have shown
high rates of vulnerable plaque, in association with key systemic inflammatory markers, among asymptomatic
PWH on ART, with only low to moderate traditional atherosclerotic cardiovascular disease (ASCVD) risk. We
will first assess the relationship of coronary inflammation to critical cardiac CT and deep immune phenotyping
parameters, including noncalcified plaque volume, obtained in the mechanistic substudy of REPRIEVE. We will
further leverage the trial design, encompassing a randomized treatment trial of statin therapy and serial
assessments of CTA parameters to assess the natural history of coronary inflammation and plaque and the
key effects of statin therapy in PWH. Specifically, we will analyze the unique relation of coronary inflammation,
measured as PCAT density, to coronary plaque development and changes in plaque composition in
relationship to other CV risk factors, the effects of statins on coronary inflammation in relation to changes in
plaque volume, and the relationship to MACE in exploratory analyses. Successful completion of this study will
inform the field of the critical, independent role of coronary inflammation in the development of coronary plaque
in PWH and determine for the first time whether a reduction in coronary inflammation contributes to statin-
related effects on plaque parameters in this population. Data from this grant, leveraging a key ASCVD
prevention trial, will thus inform the development of more targeted CV risk reduction strategies among PWH.

## Key facts

- **NIH application ID:** 10914266
- **Project number:** 5R01HL170877-02
- **Recipient organization:** MASSACHUSETTS GENERAL HOSPITAL
- **Principal Investigator:** Borek Foldyna
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $419,880
- **Award type:** 5
- **Project period:** 2023-09-01 → 2027-05-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10914266

## Citation

> US National Institutes of Health, RePORTER application 10914266, Pericoronary adipose tissue density a novel CT-derived marker of local inflammation and coronary artery disease in people living with HIV (5R01HL170877-02). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10914266. Licensed CC0.

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