TY - JOUR
T1 - Kidney function estimated from serum creatinine and cystatin C and peripheral arterial disease in NHANES 1999-2002
AU - Selvin, Elizabeth
AU - Köttgen, Anna
AU - Coresh, Josef
N1 - Funding Information:
This research was supported by grants UO1 DK 053869, UO1 DK 067651, and UO1 DK 35073. Dr E.S. was supported by NIH/ NIDDK grant K01 DK076595. Dr A.K. was supported by a Fellowship from the German Research Foundation. Dr E.S. had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
PY - 2009/8
Y1 - 2009/8
N2 - AimsSerum cystatin C, a novel marker of kidney function, is reported to be superior to serum creatinine as a risk factor for atherosclerotic disease, but associations may vary across vascular beds.Methods and resultsA cross-sectional study of chronic kidney disease (CKD) and peripheral arterial disease (PAD) in 3089 adult participants aged 40+ from the 1999-2002 National Health and Nutrition Examination Survey (NHANES). Kidney function, assessed by estimated glomerular filtration rate (eGFR), was determined from serum creatinine and cystatin C using established equations. Peripheral arterial disease defined by an ankle brachial index <0.90. Glomerular filtration rate estimated using cystatin C was more strongly associated with PAD compared with eGFR using serum creatinine before and after multivariable adjustment. Further, after adjustment for cystatin C, kidney function based on serum creatinine was no longer significantly associated with PAD. However, cystatin C remained significantly associated with PAD even after adjustment for GFR estimated by serum creatinine. Compared with optimal kidney function (eGFRserum creatinine ≥60, eGFRcystatin C >90), the odds ratio for PAD was 3.11 (95 confidence interval 1.26-7.64) for preclinical CKD (eGFRserum creatinine ≥60, eGFRcystatin C <76.7) and 5.07 (3.01-8.52) for 'confirmed' CKD (eGFRserum creatinine <60, eGFRcystatin C <60).
AB - AimsSerum cystatin C, a novel marker of kidney function, is reported to be superior to serum creatinine as a risk factor for atherosclerotic disease, but associations may vary across vascular beds.Methods and resultsA cross-sectional study of chronic kidney disease (CKD) and peripheral arterial disease (PAD) in 3089 adult participants aged 40+ from the 1999-2002 National Health and Nutrition Examination Survey (NHANES). Kidney function, assessed by estimated glomerular filtration rate (eGFR), was determined from serum creatinine and cystatin C using established equations. Peripheral arterial disease defined by an ankle brachial index <0.90. Glomerular filtration rate estimated using cystatin C was more strongly associated with PAD compared with eGFR using serum creatinine before and after multivariable adjustment. Further, after adjustment for cystatin C, kidney function based on serum creatinine was no longer significantly associated with PAD. However, cystatin C remained significantly associated with PAD even after adjustment for GFR estimated by serum creatinine. Compared with optimal kidney function (eGFRserum creatinine ≥60, eGFRcystatin C >90), the odds ratio for PAD was 3.11 (95 confidence interval 1.26-7.64) for preclinical CKD (eGFRserum creatinine ≥60, eGFRcystatin C <76.7) and 5.07 (3.01-8.52) for 'confirmed' CKD (eGFRserum creatinine <60, eGFRcystatin C <60).
KW - Chronic kidney disease
KW - Cystatin C
KW - Epidemiology
KW - Glomerular filtration rate
KW - NHANES
KW - Peripheral arterial disease
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U2 - 10.1093/eurheartj/ehp195
DO - 10.1093/eurheartj/ehp195
M3 - Article
C2 - 19487236
AN - SCOPUS:68749099648
SN - 0195-668X
VL - 30
SP - 1918
EP - 1925
JO - European heart journal
JF - European heart journal
IS - 15
ER -