TY - JOUR
T1 - The effect of including cystatin C or creatinine in a cardiovascular risk model for asymptomatic individuals
AU - Ito, Hiroki
AU - Pacold, Ivan V.
AU - Durazo-Arvizu, Ramon
AU - Liu, Kiang
AU - Shilipak, Michael G.
AU - Goff, David C.
AU - Tracy, Russell P.
AU - Kramer, Holly
PY - 2011/10/15
Y1 - 2011/10/15
N2 - The authors studied the incremental value of adding serum cystatin C or creatinine to the Framingham risk score variables (FRSVs) for the prediction of incident cardiovascular disease (CVD) among 6,653 adults without clinical CVD utilizing the Multi-Ethnic Study of Atherosclerosis (2000-2008). CVD events included coronary heart disease, heart failure, stroke, and peripheral arterial disease. Variables were transformed to yield optimal prediction of 6-year CVD events in sex-stratified models with FRSVs alone, FRSVs + cystatin C, and FRSVs + creatinine. Risk prediction in the 3 models was assessed by using the C statistic, and net reclassification improvement was calculated. The mean ages were 61.9 and 64.6 years for individuals with and without diabetes, respectively. After 6 years of follow-up, 447 (7.2%) CVD events occurred. In the total cohort, no significant change in the C statistic was noted with FRSVs + cystatin C and FRSVs + creatinine compared with FRSVs alone, and net reclassification improvement for CVD risk was extremely small and not significant with the addition of cystatin C or creatinine to FRSVs. Similar findings were noted after stratifying by baseline presence of diabetes. In conclusion, the addition of cystatin C or serum creatinine to FRSVs does not improve CVD risk prediction among adults without clinical CVD.
AB - The authors studied the incremental value of adding serum cystatin C or creatinine to the Framingham risk score variables (FRSVs) for the prediction of incident cardiovascular disease (CVD) among 6,653 adults without clinical CVD utilizing the Multi-Ethnic Study of Atherosclerosis (2000-2008). CVD events included coronary heart disease, heart failure, stroke, and peripheral arterial disease. Variables were transformed to yield optimal prediction of 6-year CVD events in sex-stratified models with FRSVs alone, FRSVs + cystatin C, and FRSVs + creatinine. Risk prediction in the 3 models was assessed by using the C statistic, and net reclassification improvement was calculated. The mean ages were 61.9 and 64.6 years for individuals with and without diabetes, respectively. After 6 years of follow-up, 447 (7.2%) CVD events occurred. In the total cohort, no significant change in the C statistic was noted with FRSVs + cystatin C and FRSVs + creatinine compared with FRSVs alone, and net reclassification improvement for CVD risk was extremely small and not significant with the addition of cystatin C or creatinine to FRSVs. Similar findings were noted after stratifying by baseline presence of diabetes. In conclusion, the addition of cystatin C or serum creatinine to FRSVs does not improve CVD risk prediction among adults without clinical CVD.
KW - cardiovascular diseases
KW - creatinine
KW - cystatin C
KW - risk model
UR - http://www.scopus.com/inward/record.url?scp=80054062629&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=80054062629&partnerID=8YFLogxK
U2 - 10.1093/aje/kwr185
DO - 10.1093/aje/kwr185
M3 - Article
C2 - 21880578
AN - SCOPUS:80054062629
SN - 0002-9262
VL - 174
SP - 949
EP - 957
JO - American journal of epidemiology
JF - American journal of epidemiology
IS - 8
ER -