Role of Vitamin D in Patients with Heart Failure with Reduced Ejection Fraction

Am J Cardiovasc Drugs. 2019 Dec;19(6):541-552. doi: 10.1007/s40256-019-00357-1.

Abstract

Heart failure (HF) with reduced ejection fraction (HFrEF) presents as the severest phenotype on the spectrum of HF. Although great progress has been made with respect to its treatment over the past 3 decades, morbidity and mortality remain high, posing a big burden on human health. Recent evidence suggests vitamin D has a critical role in maintaining heart health through activation of the vitamin D receptor expressed in cardiomyocytes, and vitamin D deficiency may be implicated in the pathophysiology of HFrEF through activation of the renin-angiotensin system, impaired calcium handling, exaggerated inflammation, secondary hyperparathyroidism, pro-fibrotic properties, and proatherogenic potential. Additionally, epidemiological data disclosed that vitamin D deficiency is highly prevalent in patients with HFrEF and is associated with poor clinical outcomes. However, randomized control trials of vitamin D supplementation in HF, especially in HFrEF, have shown inconsistent results. Thus, this article aims to review the epidemiology, pathophysiology, and prognostic value of vitamin D deficiency in HF, with a special focus on randomized control trials associated with vitamin D supplementation in patients with HFrEF.

Publication types

  • Review

MeSH terms

  • Atrial Fibrillation / epidemiology
  • Atrial Fibrillation / physiopathology
  • Calcium / metabolism
  • Dietary Supplements
  • Extracellular Matrix / physiology
  • Fibrosis / epidemiology
  • Fibrosis / physiopathology
  • Heart Failure / epidemiology*
  • Heart Failure / physiopathology*
  • Humans
  • Hyperparathyroidism, Secondary / epidemiology
  • Hyperparathyroidism, Secondary / physiopathology
  • Inflammation Mediators / metabolism
  • Myocytes, Cardiac / metabolism
  • Prognosis
  • Renin-Angiotensin System / physiology
  • Severity of Illness Index
  • Stroke Volume / physiology
  • Vitamin D / metabolism
  • Vitamin D / therapeutic use
  • Vitamin D Deficiency / drug therapy
  • Vitamin D Deficiency / epidemiology*
  • Vitamin D Deficiency / physiopathology*

Substances

  • Inflammation Mediators
  • Vitamin D
  • Calcium