The effect of vitamin D3 supplementation on markers of cardiovascular health in hyperparathyroid, vitamin D insufficient women: a randomized placebo-controlled trial

Endocrine. 2018 Oct;62(1):182-194. doi: 10.1007/s12020-018-1659-4. Epub 2018 Jul 24.

Abstract

Purpose: Emerging data supports an association between parathyroid hormone (PTH) and aldosterone. It has been speculated, that potential adverse cardiovascular effects of vitamin D insufficiency may partly be caused by the development of secondary hyperparathyroidism with increased activity of the renin-angiotensin-aldosterone system (RAAS). We aimed to investigate the effect of normalizing vitamin D status and/or reducing PTH levels on RAAS activity and other markers of cardiovascular health.

Methods: In a double-blinded study during wintertime, we randomized 81 healthy postmenopausal women with secondary hyperparathyroidism (PTH > 6.9 pmol/l) and 25-hydroxy-vitamin D (25(OH)D) levels < 50 nmol/l to 12 weeks of treatment with vitamin D3 70 µg/day (2800 IU/day) or identical placebo. Markers of cardiovascular health were defined as changes in the plasma RAAS, glycated hemoglobin, lipids, and lipoproteins, blood pressure, vascular stiffness, heart rate, and cardiac conductivity.

Results: Compared to placebo, vitamin D3 treatment significantly increased plasma levels of 25(OH)D and 1,25(OH)2D by 230% (95% CI: 189-272%) and 58% (190-271%), respectively. Vitamin D3 treatment reduced PTH by 17% (11-23%), but did not reduce RAAS activity. Compared to placebo, vitamin D3 treatment increased plasma levels of high-density lipoproteins (HDL) by 4.6% (0.12-9.12%), but did not affect other measured indices.

Conclusions: Vitamin D3 supplementation normalized vitamin D levels and reduced PTH. The supplement increased levels of HDL, but had no effects on RAAS activity or other indices of cardiovascular health.

Keywords: Aldosterone; Blood pressure; Cholesterol; Parathyroid hormone; Renin-angiotensin-aldosterone system; Vitamin D.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Aged, 80 and over
  • Blood Pressure / drug effects
  • Blood Pressure / physiology
  • Cardiovascular System / drug effects*
  • Cardiovascular System / physiopathology
  • Cholecalciferol / administration & dosage
  • Cholecalciferol / therapeutic use*
  • Double-Blind Method
  • Female
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Hormone Replacement Therapy
  • Humans
  • Hyperparathyroidism / complications*
  • Hyperparathyroidism / physiopathology
  • Middle Aged
  • Treatment Outcome
  • Vascular Stiffness / drug effects
  • Vascular Stiffness / physiology
  • Vitamin D Deficiency / complications
  • Vitamin D Deficiency / drug therapy*
  • Vitamin D Deficiency / physiopathology

Substances

  • Cholecalciferol