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Updated: Jun 17, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Kidney function and the risk of cardiovascular events in HIV-1-infected patients
Elizabeth George1, Gregory M Lucas, Girish N Nadkarni
1All India Institute of Medical Sciences, New Delhi, India.
Insights
Reduced kidney function and proteinuria significantly increase cardiovascular event risk in HIV patients. This highlights the importance of monitoring kidney health to prevent cardiovascular complications in this population.
Area of Science:
- Nephrology
- Cardiology
- Infectious Diseases
Background:
- Cardiovascular events (CVEs) are a major cause of mortality in individuals with HIV/AIDS.
- Kidney function impairment is increasingly recognized as a risk factor for CVEs.
Purpose of the Study:
- To investigate the association between kidney function and the risk of CVEs in HIV-infected patients.
- To determine if proteinuria is an independent predictor of CVEs in this cohort.
Main Methods:
- A nested, matched, case-control study was conducted with 315 HIV-infected patients (63 cases with CVEs, 252 controls).
- Estimated glomerular filtration rate (eGFR) and proteinuria were assessed as primary exposures.
- eGFR was calculated using the CKD-EPI and MDRD equations.
Main Results:
- Patients with CVEs had significantly lower mean eGFR compared to controls (P < 0.001).
- An eGFR < 60 ml/min/1.73 m² was associated with a 15.9-fold increased odds of CVEs (P < 0.001).
- Proteinuria was present in approximately double the proportion of cases vs. controls (51% vs. 25%, P < 0.001) and was independently associated with CVEs.
Conclusions:
- Decreased kidney function, indicated by lower eGFR and proteinuria, is significantly and independently associated with an increased risk of CVEs in HIV-1-infected patients.
- These findings underscore the critical role of renal health in cardiovascular risk stratification for HIV-infected individuals.
Objective:
Cardiovascular events (CVEs) are a significant cause of mortality in HIV/AIDS patients. The objective is to determine the correlation between kidney function and the risk of CVEs in the HIV-infected population.
Design:
Nested, matched, case-control study design was employed.
Methods:
: We performed a single-center study of 315 HIV-infected patients (63 patients who had CVEs and 252 controls). Estimated glomerular filtration rate (eGFR), calculated by the Chronic Kidney Disease Epidemiology Collaboration formula and the Modification of Diet in Renal Disease equation, and proteinuria were the primary exposures of interest.
Results:
Mean eGFR was significantly lower in the patients compared with controls (68.4 vs. 103.2 ml/min per 1.73 m, P < 0.001 by Chronic Kidney Disease Epidemiology Collaboration formula and 69.0 vs. 103.1 ml/min per 1.73 m, P < 0.001 by Modification of Diet in Renal Disease equation). In univariate analysis, an eGFR of less than 60 ml/min per 1.73 m was associated with a 15.9-fold increased odds of a CVE compared with an eGFR of at least 60 ml/min per 1.73 m (P < 0.001). In multivariate analysis, a 10 ml/min per 1.73 m decrease in eGFR was associated with a 20% increased odds of a CVE (odds ratio 1.2, 95% confidence interval 1.1-1.4). The prevalence of proteinuria in the patients was approximately twice that of controls (51 vs. 25%, P < 0.001). Proteinuria was associated with CVEs both in univariate and multivariate analyses (odds ratio 3.6, 95% confidence interval 1.9-7.0 and odds ratio 2.2, 95% confidence interval 1.1-4.8, respectively). Traditional cardiovascular risk factors, such as history of previous CVEs, diabetes mellitus, and dyslipidemia, along with low CD4 cell counts were also found as significant predictors of risk of CVEs.
Conclusion:
Our study shows a significant independent association between decreased kidney function and increased risk of CVE in HIV-1-infected patients.
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