Microalbuminuria in HIV Disease

Colleen Hadigan(National Institute of Allergy and Infectious Diseases), Elizabeth Edwards, Alice Rosenberg(Science Applications International Corporation (United States)), Julia Purdy, Estee Fleischman, Lilian Howard(National Institute of Diabetes and Digestive and Kidney Diseases), JoAnn M. Mican(National Institutes of Health), Karmini Sampath(National Institute of Diabetes and Digestive and Kidney Diseases), Akinbowale Oyalowo(National Institute of Diabetes and Digestive and Kidney Diseases), Antoinette Johnson(National Institute of Diabetes and Digestive and Kidney Diseases), Alexandra Adler(National Institute of Diabetes and Digestive and Kidney Diseases), Catherine Rehm, Margo Smith(MedStar Washington Hospital Center), Leon Lai(MedStar Washington Hospital Center), Jeffrey B. Kopp(National Institute of Diabetes and Digestive and Kidney Diseases)
American Journal of Nephrology
January 1, 2013
Cited by 43Open Access
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Abstract

BACKGROUND/AIMS: Microalbuminuria is a marker for early kidney disease and cardiovascular risk. The purposes of this study were to determine the prevalence of microalbuminuria in an HIV-infected clinic population, to test the predictive value of a single urine albumin/creatinine ratio (ACR) to identify persistent microalbuminuria and to examine covariates of microalbuminuria. METHODS: We conducted a prospective cohort study of HIV-infected subjects (n = 182) without proteinuria (urine protein/creatinine ratio ≥0.5 g/g), elevated serum creatinine, diabetes, or chronic inflammatory conditions. Subjects completed three research visits within 9 months. Microalbuminuria was defined as the geometric mean ACR of 25-355 mg/g for females and 17-250 mg/g for males. RESULTS: The prevalence of microalbuminuria was 14%. The negative predictive value of a single urine ACR determination was 98%, whereas the positive predictive value was only 74%. Microalbuminuria was similar among Black (15%) and non-Black (14%) subjects (p = 0.8). Subjects with microalbuminuria were more likely to have hypertension (p = 0.02) and metabolic syndrome (p = 0.03). While duration of HIV infection and the level of HIV viremia were similar between groups, those with microalbuminuria were more likely to have a CD4 count <200 cells/μl (p = 0.0003). In a multivariate logistic regression analysis, the only significant independent predictors of microalbuminuria were low CD4 count (p = 0.018) and current ritonavir exposure (p = 0.04). CONCLUSION: The prevalence of microalbuminuria in an HIV-infected clinic population was similar to earlier reports, and was associated with hypertension and impaired immune function. A single normal ACR determination effectively excludes microalbuminuria, whereas an elevated ACR requires confirmation.


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