Key result
In HIV-infected individuals without prior CVD, reduced kidney function and albuminuria were not independently associated with subclinical vascular disease assessed by carotid intima-medial thickness.
Why the study?
Is reduced kidney function or albuminuria independently associated with subclinical vascular disease (cIMT) in HIV-infected individuals without prior CVD?
Cross-Sectional (n=476)
Is reduced kidney function or albuminuria independently associated with subclinical vascular disease (cIMT) in HIV-infected individuals without prior CVD?
Reduced kidney function and albuminuria are not independently associated with subclinical atherosclerosis (cIMT) in HIV-infected patients without prior CVD, suggesting other mechanisms drive their cardiovascular risk.
Does not support kidney-based vascular risk stratification in HIV; leaves open alternative drivers of excess CVD.
BACKGROUND/AIMS: Reduced kidney function and albuminuria are associated with higher risk for cardiovascular disease (CVD) and mortality in HIV-infected individuals. We investigated whether reduced estimated glomerular filtration rate (eGFR) and albuminuria are associated with subclinical vascular disease, as assessed by carotid intima-medial thickness (cIMT). METHODS: Cross-sectional analysis of 476 HIV-infected individuals without clinical evidence of CVD enrolled in the Fat Redistribution and Metabolic Change in HIV infection (FRAM) study, using multivariable linear regression. eGFR(Cys) and eGFR(Cr) were calculated from cystatin C and creatinine levels. Albuminuria was defined as a positive urine dipstick (≥ 1+) or urine albumin-to-creatinine ratio ≥ 30 mg/g. Common and internal cIMT were measured by high-resolution B-mode ultrasound. RESULTS: In unadjusted analyses, eGFR(Cys) and eGFR(Cr) were strongly associated with com- mon and internal cIMT. Each 10 ml/min/1.73 m2 decrease in eGFR(Cys) and eGFR(cr) was associated with a 0.008 mm higher common cIMT (p = 0.003, p = 0.01) and a 0.024 and 0.029 mm higher internal cIMT (p = 0.003), respectively. These associations were eliminated after adjustment for age, gender, and race. Albuminuria showed little association with common or internal cIMT in all models. CONCLUSIONS: In HIV-infected individuals without prior CVD, reduced kidney function and albuminuria were not independently associated with subclinical vascular disease, as assessed by cIMT. These results suggest that research should focus on searching for novel mechanisms by which kidney disease confers cardiovascular risk in HIV-infected individuals.
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Jotwani et al. (2011) conducted a cross-sectional in HIV infection (n=476). Reduced estimated glomerular filtration rate (eGFR) and albuminuria was evaluated on Subclinical vascular disease assessed by common and internal carotid intima-medial thickness (cIMT). In HIV-infected individuals without prior CVD, reduced kidney function and albuminuria were not independently associated with subclinical vascular disease assessed by carotid intima-medial thickness.
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