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Volume 51, Issue 6, Pages 914-924 (June 2008)


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Cystatin C and Creatinine in an HIV Cohort: The Nutrition for Healthy Living Study

Clara Y. Jones, MD, MPH1Corresponding Author Informationemail address, Camille A. Jones, MD, MPH2, Ira B. Wilson, MD, MSc13, Tamsin A. Knox, MD1, Andrew S. Levey, MD3, Donna Spiegelman, PhD4, Sherwood L. Gorbach, MD1, Frederick Van Lente, PhD5, Lesley A. Stevens, MD, MS3

Received 11 July 2007; accepted 3 January 2008. published online 06 May 2008.

Background

Human immunodeficiency virus (HIV)-infected persons have an increased risk of chronic kidney disease (CKD). Serum creatinine level may underestimate the prevalence of CKD in subjects with decreased lean body mass or liver disease. Level of serum cystatin C, an alternative kidney function marker, is independent of lean body mass.

Study Design

Cross-sectional.

Setting & Participants

250 HIV-infected subjects on highly active antiretroviral therapy in the Nutrition for Healthy Living (NFHL) cohort; 2,628 National Health and Nutrition Examination Survey (NHANES) 2001-2002 subjects.

Predictors & Outcomes

Comparison of serum creatinine levels in NFHL to those in NHANES subjects; comparison of CKD in NFHL subjects ascertained using serum creatinine versus cystatin C levels.

Measurements

Standardized serum creatinine, serum cystatin C, glomerular filtration rate (GFR) estimated from serum creatinine and cystatin C levels.

Results

Creatinine levels were lower in NFHL than NHANES subjects despite greater rates of hepatitis, diabetes, and drug use (mean difference, −0.18 mg/dL; P < 0.001 adjusted for age, sex, and race). Of NFHL subjects, only 2.4% had a creatinine-based estimated GFR less than 60 mL/min/1.73 m2, but 15.2% had a cystatin-based estimated GFR less than 60 mL/min/1.73 m2.

Limitations

GFR was estimated rather than measured. Other factors in addition to GFR may affect creatinine and cystatin C levels. Measurements of proteinuria were not available.

Conclusions

Serum creatinine levels may overestimate GFRs in HIV-infected subjects. Kidney disease prevalence may be greater than previously appreciated.

1 Tufts University School of Medicine, Boston, MA

2 University of Arkansas School for Medical Sciences, Little Rock, AR

3 Tufts-New England Medical Center, Boston, MA

4 Harvard School of Public Health, Boston, MA

5 Cleveland Clinic, Cleveland, OH.

Corresponding Author InformationAddress correspondence to Clara Y. Jones, MD, MPH, Tufts University School of Medicine, 200 Harrison Ave, Posner 415, Boston, MA 02111.

 Because an author of this manuscript is an editor for AJKD, the peer-review and decision-making processes were handled entirely by an Associate Editor (Haiyan Wang, MD, Peking University) who served as Acting Editor-in-Chief. Details of the journal's procedures for potential editor conflicts are given in the Editorial Policies section of the AJKD website.

 Originally published online as doi:10.1053/j.ajkd.2008.01.027 on May 2, 2008.

PII: S0272-6386(08)00585-4

doi:10.1053/j.ajkd.2008.01.027


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