4.0 Article

Cystatin C level as a marker of kidney function in human immunodeficiency virus infection - The FRAM study

Journal

ARCHIVES OF INTERNAL MEDICINE
Volume 167, Issue 20, Pages 2213-2219

Publisher

AMER MEDICAL ASSOC
DOI: 10.1001/archinte.167.20.2213

Keywords

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Funding

  1. NCRR NIH HHS [M01 RR000865, M01 RR000054, M01 RR 00865, M01 RR 00083, M01 RR000036, M01 RR 00054, M01 RR 00052, M01 RR000052, M01 RR000051, M01 RR000083, M01 RR 00636, M01 RR 00051, M01 RR 00036] Funding Source: Medline
  2. NHLBI NIH HHS [R01 HL 74814, R01 HL 073208-01, R01 HL073208, R01 HL 53359, R01 HL074814] Funding Source: Medline
  3. NIDDK NIH HHS [DK 02724-01A1, R01 DK 57508, R01 DK 066488-01, R01 DK066488, K23 DK002724, R01 DK057508] Funding Source: Medline

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Background: Although studies have reported a high prevalence of end-stage renal disease in human immunodeficiency virus (HIV)-infected individuals, little is known about moderate impairments in kidney function. Cystatin C measurement may be more sensitive than creatinine for detecting impaired kidney function in persons with HIV. Methods: We evaluated kidney function in the Fat Redistribution and Metabolic Change in HIV Infection (FRAM) cohort, a representative sample of 1008 HIV-infected persons and 290 controls from the Coronary Artery Risk Development in Young Adults (CARDIA) study in the United States. Results: Cystatin C level was elevated in HIV-infected individuals; the mean +/- SD cystatin C level was 0.92 +/- 0.22 mg/L in those infected with HIV and 0.76 +/- 0.15 mg/L in controls (P < .001). In contrast, both mean creatinine levels and estimated glomerular filtration rates appeared similar in HIV-infected individuals and controls (0.87 +/- 0.21 vs 0.85 +/- 0.19 mg/dL [to convert to micromoles per liter, multiply by 88.4] [P=.35] and 110 +/- 26 vs 106 +/- 23 mL/min/ 1.73 m(2) [P=.06], respectively). Persons with HIV infection were more likely to have a cystatin C level greater than 1.0 mg/L (OR, 9.8; 95% confidence interval, 4.4-22.0 [P < .001]), a threshold demonstrated to be associated with increased risk for death and cardiovascular and kidney disease. Among participants with HIV, potentially modifiable risk factors for kidney disease, hypertension, and low high-density lipoprotein concentration were associated with a higher cystatin C level, as were lower CD4 lymphocyte count and coinfection with hepatitis C virus (all P < .001). Conclusions: Individuals infected with HIV had substantially worse kidney function when measured by cystatin C level compared with HIV-negative controls, whereas mean creatinine levels and estimated glomerular filtration rates were similar. Cystatin C measurement could be a useful clinical tool to identify HIV-infected persons at increased risk for kidney and cardiovascular disease.

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