4.6 Article

Association of Cardiac Biomarkers With the Kansas City Cardiomyopathy Questionnaire in Patients With Chronic Kidney Disease Without Heart Failure

期刊

出版社

WILEY
DOI: 10.1161/JAHA.119.014385

关键词

cardiac biomarkers; heart failure; quality of life

资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases [U01DK060990, U01DK060984, U01DK061022, U01DK061021, U01DK061028, U01DK060980, U01DK060963, U01DK060902]
  2. Perelman School of Medicine at the University of Pennsylvania Clinical and Translational Science Award NIH/NCATS [UL1TR000003]
  3. Johns Hopkins University [UL1 TR-000424, GCRC M01 RR-16500, UL1TR000439]
  4. National Center for Advancing Translational Sciences (NCATS) component of the National Institutes of Health
  5. Michigan Institute for Clinical and Health Research (MICHR) [UL1TR000433]
  6. University of Illinois at Chicago CTSA [UL1RR029879, P20 GM109036]
  7. Kaiser Permanente NIH/National Center for Research Resources (NCRR) UCSF-Clinical AMP
  8. Translational Science Institute (CTSI) [UL1 RR-024131, R01 DK103612, R01 01DK104730]
  9. Roche Diagnostics
  10. NT-proBNP
  11. Northwest Kidney Centers

向作者/读者索取更多资源

BACKGROUND: The Kansas City Cardiomyopathy Questionnaire (KCCQ) is a measure of heart failure (HF) health status. Worse KCCQ scores are common in patients with chronic kidney disease (CKD), even without diagnosed heart failure (HF). Elevations in the cardiac biomarkers GDF-15 (growth differentiation factor--15), galectin--3, sST2 (soluble suppression of tumorigenesis--2), hsTnT (high--sensitivity troponin T), and NT--proBNP (N--terminal pro--B--type natriuretic peptide) likely reflect subclinical HF in CKD. Whether cardiac biomarkers are associated with low KCCQ scores is not known. METHODS AND RESULTS: We studied participants with CKD without HF in the multicenter prospective CRIC (Chronic Renal Insufficiency Cohort) Study. Outcomes included (1) low KCCQ score <75 at year 1 and (2) incident decline in KCCQ score to <75. We used multivariable logistic regression and Cox regression models to evaluate the associations between baseline cardiac biomarkers and cross--sectional and longitudinal KCCQ scores. Among 2873 participants, GDF-15 (adjusted odds ratio 1.42 per SD; 99% CI, 1.19-1.68) and galectin--3 (1.28; 1.12-1.48) were significantly associated with KCCQ scores <75, whereas sST2, hsTnT, and NT--proBNP were not significantly associated with KCCQ scores <75 after multivariable adjustment. Of the 2132 participants with KCCQ =75 at year 1, GDF-15 (adjusted hazard ratio, 1.36 per SD; 99% CI, 1.12-1.65), hsTnT (1.20; 1.01-1.44), and NT--proBNP (1.30; 1.08-1.56) were associated with incident decline in KCCQ to <75 after multivariable adjustment, whereas galectin--3 and sST2 did not have significant associations with KCCQ decline. CONCLUSIONS: Among participants with CKD without clinical HF, GDF-15, galectin--3, NT--proBNP, and hsTnT were associated with low KCCQ either at baseline or during follow--up. Our findings show that elevations in cardiac biomarkers reflect early symptomatic changes in HF health status in CKD patients.

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