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Updated: May 16, 2026

Measuring Frailty in HIV-infected Individuals. Identification of Frail Patients is the First Step to Amelioration and Reversal of Frailty
Published on: July 24, 2013
Renal impairment is associated with coronary heart disease in HIV-positive men
Lucy J Campbell1, Mitesh Desai, Aseel Hegazi
1School of Medicine, King's College, London, UK.
Insights
Impaired kidney function, indicated by an estimated glomerular filtration rate (eGFR) below 75 mL/min, increases the risk of coronary heart disease (CHD) events in HIV-positive individuals. Prioritizing traditional CHD risk factor management is crucial for these patients.
Area of Science:
- Cardiology
- Nephrology
- Infectious Diseases (HIV/AIDS)
Background:
- Chronic kidney disease (CKD) is a known risk factor for coronary heart disease (CHD).
- The relationship between renal impairment and CHD in HIV-positive individuals is not well understood.
Purpose of the Study:
- To determine the incidence of CHD in a cohort of HIV-positive patients.
- To investigate the association between reduced estimated glomerular filtration rate (eGFR) and new-onset CHD.
Main Methods:
- A cohort of 7,828 HIV-positive patients was followed from 2004 to 2009.
- CHD events were identified via electronic records and elevated troponin levels.
- Multivariate Poisson regression was used to analyze factors associated with CHD in HIV-positive men.
Main Results:
- CHD incidence was 1.2 per 1,000 person-years; 32 events occurred in 28 patients.
- Older age and hepatitis C virus (HCV) status were significantly associated with CHD.
- An eGFR <75 mL/min was linked to incident CHD, independent of age.
Conclusions:
- The incidence of CHD in this HIV-positive cohort was low.
- Impaired renal function identifies HIV-positive patients at higher risk for CHD.
- Management of traditional CHD risk factors should be prioritized in these patients.
Background:
Chronic kidney disease is a risk factor for coronary heart disease (CHD). The association between renal impairment and CHD in HIV-positive patients remains poorly described.
Objective:
To describe the CHD incidence in a cohort of HIV-positive patients and to examine the relationship between reduced estimated glomerular filtration rate (eGFR) and incident CHD.
Methods:
We studied 7,828 HIV-positive patients who were followed up at 3 South London clinics between January 2004 and December 2009. CHD events were identified from electronic records and through elevated troponin levels. Multivariate Poisson regression analysis was used to identify factors associated with CHD among HIV-positive men.
Results:
The incidence of CHD among men was 1.2 (95% CI, 0.8-1.8) per 1,000 person-years of follow-up, with 28 patients (0.4%) having experienced 32 CHD events. In adjusted analyses, older age (incidence rate ratios [IRR], 2.81; 95% CI, 1.51-5.25) and hepatitis C virus (HCV) status (IRR, 3.94; 95% CI, 1.00-15.5) were significantly associated with CHD. Although eGFR as a continuous variable was not associated with CHD, an eGFR <75 mL/min remained associated with incident CHD (IRR, 4.30; 95% CI, 1.33-14.5) after adjustment for age. No association between CHD and abacavir exposure was observed (IRR, 0.94; 95% CI, 0.30-2.99).
Conclusions:
The incidence of CHD in this ethnically diverse cohort was low. Our data suggest that impaired renal function identifies patients at increased risk of CHD events in whom management of traditional CHD risk factors should be prioritized.
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