Effects of Vitamin D Supplementation on Renin and Aldosterone Concentrations in Patients with Advanced Heart Failure: The EVITA Trial
Autor: | Cornelius Knabbe, Jens Dreier, Jochen Börgermann, Uwe Fuchs, Jan Gummert, Jana B. Ernst, Ioanna Gouni-Berthold, Heiner K. Berthold, Sylvana Prokop, Joachim Kuhn, Stefan Pilz, Armin Zittermann |
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Rok vydání: | 2018 |
Předmět: |
medicine.medical_specialty
Article Subject Endocrinology Diabetes and Metabolism Reference range 030204 cardiovascular system & hematology lcsh:Diseases of the endocrine glands. Clinical endocrinology Plasma renin activity law.invention 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Endocrinology Randomized controlled trial law Internal medicine Renin–angiotensin system Vitamin D and neurology Medicine 030212 general & internal medicine lcsh:RC648-665 Aldosterone Vitamin d supplementation Endocrine and Autonomic Systems business.industry medicine.disease chemistry Heart failure business Research Article |
Zdroj: | International Journal of Endocrinology, Vol 2018 (2018) International Journal of Endocrinology |
ISSN: | 1687-8345 1687-8337 |
Popis: | Objective. 1,25-Dihydroxyvitamin D (1,25([OH]2D) is considered to be a negative endogenous regulator of the renin-angiotensin-aldosterone system (RAAS), but the effect of vitamin D supplementation on the RAAS is inconclusive. Design. In this prespecified secondary analysis of a randomized controlled trial, we assessed in 165 patients with heart failure (vitamin D group: n=83; placebo group: n=82) the effect of three years of vitamin D supplementation with 4000 IU daily on parameters of the RAAS (renin and aldosterone) and on circulating 1,25(OH)2D, plasma phosphate, and fibroblast growth factor (FGF)-23. We assessed age- and baseline-adjusted between-group differences at study termination. Results. Almost all patients were under treatment with beta-blockers, inhibitors of the RAAS, and diuretics. Initially, the frequency of concentrations above the laboratory-specific reference range (renin: >23.9 mIU/L; aldosterone: >232 ng/L) in the vitamin D and placebo group was 87.7% and 92.7%, respectively (renin), and 24.1% and 32.5%, respectively (aldosterone). Vitamin D increased adjusted 1,25(OH)2D concentrations significantly (mean treatment effect and 95% CI: 18.3 pmol/L,7.3 to 29.3 pmol/L; P<0.001) but had no significant effects on phosphate (0.18 mmol/L, −0.00 to 0.35 mmol/L; P=0.051), FGF-23 (685 RU/mL, −213 to 1585 RU/mL; P=0.134), renin (312 mIU/L, −279 to 902 ng/L; P=0.298), or aldosterone (−0.19 ng/L, −5.09 to 4.70 ng/L; P=0.938). Vitamin D supplementation was, however, associated with an increase in renin concentrations in the subgroup with baseline 25-hydroxyvitamin D below 30 nmol/L (n=67; 1365 mIU/, 343 to 2386 mIU/L; P=0.010). Conclusions. In patients with advanced heart failure treated according to evidence-based guidelines, vitamin D supplementation did not significantly influence parameters of the RAAS in the entire study cohort but was associated with an increase in plasma renin concentrations in the subgroup with low baseline 25-hydroxyvitamin D concentrations. |
Databáze: | OpenAIRE |
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