- Yaffe, Kristine;
- Kurella‐Tamura, Manjula;
- Ackerson, Lynn;
- Hoang, Tina D;
- Anderson, Amanda H;
- Duckworth, Mark;
- Go, Alan S;
- Krousel‐Wood, Marie;
- Kusek, John W;
- Lash, James P;
- Ojo, Akinlolu;
- Robinson, Nancy;
- Sehgal, Ashwini R;
- Sondheimer, James H;
- Steigerwalt, Susan;
- Townsend, Raymond R
Objectives
To determine the association between cognition and levels of cystatin C in persons with chronic kidney disease (CKD).Design
Prospective observational study.Setting
Chronic Renal Insufficiency Cohort Cognitive Study.Participants
Individuals with a baseline cognitive assessment completed at the same visit as serum cystatin C measurement (N = 821; mean age 64.9, 50.6% male, 48.6% white).Measurements
Levels of serum cystatin C were categorized into tertiles; cognitive function was assessed using six neuropsychological tests. Scores on these tests were compared across tertiles of cystatin C using linear regression and logistic regression to examine the association between cystatin C level and cognitive performance (1 standard deviation difference from the mean).Results
After multivariable adjustment for age, race, education, and medical comorbidities in linear models, higher levels of cystatin C were associated with worse cognition on the modified Mini-Mental State Examination, Buschke Delayed Recall, Trail-Making Test Part (Trails) A and Part B, and Boston Naming (P < .05 for all). This association remained statistically significant for Buschke Delayed Recall (P = .01) and Trails A (P = .03) after additional adjustment for estimated glomerular filtration rate (eGFR). The highest tertile of cystatin C was associated with greater likelihood of poor performance on Trails A (odds ratio (OR) = 2.17, 95% confidence interval (CI) = 1.16-4.06), Trails B (OR = 1.89, 95% CI = 1.09-3.27), and Boston Naming (OR = 1.85, 95% CI = 1.07-3.19) than the lowest tertile after multivariate adjustment in logistic models.Conclusion
In individuals with CKD, higher serum cystatin C levels were associated with worse cognition and greater likelihood of poor cognitive performance on attention, executive function, and naming. Cystatin C is a marker of cognitive impairment and may be associated with cognition independent of eGFR.