Journal
AMERICAN JOURNAL OF KIDNEY DISEASES
Volume 72, Issue 3, Pages 419-428Publisher
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.ajkd.2018.03.026
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Funding
- National Heart, Lung and Blood Institute [T32DK069263]
- National Institute of Diabetes, Digestive, and Kidney Diseases [R01DK101720, K24 DK110427]
- National Institute on Aging (NIA) [5R01AG027002]
- University of Washington Nutrition and Obesity Research Center [P30DK035816]
- Intramural Research Program of the National Institutes of Health, NIA
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Rationale & Objectives: Lower 25-hydroxyvitamin D concentrations have been associated with risk for kidney function decline, heart failure, and mortality. However, 25-hydroxyvitamin D requires conversion to its active metabolite, calcitriol, for most biological effects. The associations of calcitriol concentrations with clinical events have not been well explored. Study Design: Case-cohort study. Setting& Participants: Well-functioning community-living older adults aged 70 to 79 years at inception who participated in the Health, Aging, and Body Composition (Health ABC) Study. Predictor: Serum calcitriol measured using positive ion electrospray ionization-tandem mass spectrometry. Outcomes: Major kidney function decline (>= 30% decline in estimated glomerular filtration rate from baseline), incident heart failure (HF), and all-cause mortality during 10 years of follow-up. Analytic Approach: Baseline calcitriol concentrations were measured in a random subcohort of 479 participants and also in cases with major kidney function decline [n = 397() and incident HF (n = 207) during 10 years of follow-up. Associations of serum calcitriol concentrations with these end points were evaluated using weighted Cox regression to account for the case-cohort design, while associations with mortality were assessed in the subcohort alone using unweighted Cox regression. Results: During 8.6 years of mean follow-up, 212 (44%) subcohort participants died. In fully adjusted models, each 1-standard deviation lower calcitriol concentration was associated with 30% higher risk for major kidney function decline (95% CI, 1.03-1.65; P = 0.03). Calcitriol was not significantly associated with incident HF (HR, 1.16; 95% CI, 0.94-1.47) or mortality (HR, 1.01; 95% CI, 0.81-1.26). We observed no significant interactions between calcitriol concentrations and chronic kidney disease status, baseline intact parathyroid or fibroblast factor 23 concentrations. Limitations: Observational study design, calcitriol measurements at a single time point, selective study population of older adults only of white or black race. Conclusions: Lower calcitriol concentrations are independently associated with kidney function decline in community-living older adults. Future studies will be needed to clarify whether these associations reflect lower calcitriol concentrations resulting from abnormal kidney tubule dysfunction or direct mechanisms relating lower calcitriol concentrations to more rapid loss of kidney function.
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