Vitamin D Treatment Attenuates Heart Apoptosis After Coronary Artery Bypass Surgery: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial

J Cardiovasc Pharmacol Ther. 2020 Jul;25(4):338-345. doi: 10.1177/1074248420920495. Epub 2020 Apr 23.

Abstract

Background: Vitamin D plays an important role in immune system and in the regulation of inflammatory cytokines. Coronary artery bypass graft (CABG) with cardiopulmonary bypass (CPB) is associated with an extensive inflammatory response. The aim of this study is to examine the effect of vitamin D treatment on the apoptosis and inflammatory changes developed after CABG.

Methods: This trial was conducted on 70 patients undergoing CABG with CPB. Patients were randomly administered either in placebo or in the group of orally consuming 150 000 IU vitamin D daily for 3 consecutive days before surgery. The right atrium sample was taken to assess caspases 2, 3, and 7 activity using immunohistochemistry method. The serum level of interleukin-10 (IL-10) and insulin-like growth factor 1 (IGF-1) were compared at intervals.

Results: The average number of positive cells for caspases 2 and 3 were less in vitamin D group (P = .006 and P < .001, respectively). There was an increase in serum levels of IL-10 after 3 days from vitamin D treatment before surgery (vitamin D group = 4.4 ± 4.9 ng/mL and control group = 1 ± 0.5 ng/mL, P = .001). After operation, IL-10 increased in both groups, higher level in vitamin D group (P < .001). The comparison of serum IGF-1 showed significant difference after 3 days (P = .006) and remained higher in vitamin D group after CPB (P < .001).

Conclusions: These findings suggest the apoptosis rate after CPB can be reduced by vitamin D. Vitamin D treatment may improve the inflammatory status before and after surgery. Further studies are needed to confirm the antiapoptotic property of vitamin D and clinical implication.

Keywords: apoptosis; cardiopulmonary bypass; coronary artery disease; insulin-like growth factor 1; interleukin-10; vitamin D.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Apoptosis / drug effects*
  • Biomarkers / blood
  • Cardiopulmonary Bypass / adverse effects*
  • Caspases / metabolism
  • Coronary Artery Bypass / adverse effects*
  • Dietary Supplements* / adverse effects
  • Double-Blind Method
  • Female
  • Heart Atria / drug effects*
  • Heart Atria / metabolism
  • Heart Atria / pathology
  • Humans
  • Inflammation Mediators / blood
  • Insulin-Like Growth Factor I / metabolism
  • Interleukin-10 / blood
  • Iran
  • Male
  • Middle Aged
  • Time Factors
  • Treatment Outcome
  • Vitamin D / administration & dosage*
  • Vitamin D / adverse effects

Substances

  • Biomarkers
  • IGF1 protein, human
  • IL10 protein, human
  • Inflammation Mediators
  • Interleukin-10
  • Vitamin D
  • Insulin-Like Growth Factor I
  • Caspases