Key result
Rapid annual decline (>5%) in cystatin C-derived estimated glomerular filtration rate was associated with a 51% higher relative risk of subsequent coronary artery calcium (RR 1.51) compared to stable kidney function.
Why the study?
Does an annual decline in eGFRcys increase the risk of subsequent coronary artery calcium in young and middle-aged adults with preserved kidney function?
Cohort (n=3,070)
Yes
Does an annual decline in eGFRcys increase the risk of subsequent coronary artery calcium in young and middle-aged adults with preserved kidney function?
In young and middle-aged adults with preserved kidney function, an annual decline in eGFRcys is an independent risk factor for subsequent coronary artery calcium development.
Rapid eGFRcys decline may flag higher CAC risk in preserved function; leaves open whether monitoring alters prevention in young adults.
Whether kidney dysfunction is associated with coronary artery calcium (CAC) in young and middle-aged adults who have a cystatin C-derived estimated glomerular filtration rate (eGFRcys) greater than 60 mL/min/1.73 m(2) is unknown. In the Coronary Artery Risk Development in Young Adults (CARDIA) cohort (recruited in 1985 and 1986 in Birmingham, Alabama; Chicago, Illinois; Minneapolis, Minnesota; and Oakland, California), we examined 1) the association of eGFRcys at years 10 and 15 and detectable CAC over the subsequent 5 years and 2) the association of change in eGFRcys and subsequent CAC, comparing those with stable eGFRcys to those whose eGFRcys increased (>3% annually over 5 years), declined moderately (3%-5%), or declined rapidly (>5%). Generalized estimating equation Poisson models were used, with adjustment for age, sex, race, educational level, income, family history of coronary artery disease, diabetes, body mass index, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and tobacco use. Among 3,070 participants (mean age 35.6 (standard deviation, 4.1) years and mean eGFRcys 106.7 (standard deviation, 18.5) mL/min/1.73 m(2)), 529 had detectable CAC. Baseline eGFRcys was not associated with CAC. Moderate eGFRcys decline was associated with a 33% greater relative risk of subsequent CAC (95% confidence interval: 5, 68; P = 0.02), whereas rapid decline was associated with a 51% higher relative risk (95% confidence interval: 10, 208; P = 0.01) in adjusted models. In conclusion, among young and middle-aged adults with eGFRcys greater than 60 mL/min/1.73 m(2), annual decline in eGFRcys is an independent risk factor for subsequent CAC.
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Bansal et al. (2013) conducted a cohort in Preserved kidney function (n=3,070). Rapid annual decline in eGFRcys (>5%) vs. Stable eGFRcys (±3% annual change) was evaluated on Detectable coronary artery calcium (CAC score >0) (RR 1.51, 95% CI 1.10-2.08, p=0.01). Rapid annual decline (>5%) in cystatin C-derived estimated glomerular filtration rate was associated with a 51% higher relative risk of subsequent coronary artery calcium (RR 1.51) compared to stable kidney function.
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