A Randomized, Controlled Trial of Vitamin D Supplementation on Cardiovascular Risk Factors, Hormones, and Liver Markers in Women with Polycystic Ovary Syndrome

Nutrients. 2019 Jan 17;11(1):188. doi: 10.3390/nu11010188.

Abstract

Polycystic ovary syndrome (PCOS) increases the risk of metabolic syndrome and non-alcoholic-fatty-liver disease (NAFLD). Vitamin D supplementation may exert positive effects on liver biochemistry in patients with NAFLD; however, its effects on PCOS are unknown. This randomized, double-blind, placebo-controlled study explored the effect of vitamin D supplementation on cardiovascular risk factors (high-sensitivity C-reactive protein (hs-CRP), weight, body mass index (BMI), lipid profile, glucose levels, insulin levels, the homeostatic model assessment-insulin resistance (HOMA-IR), hormones (free androgen index (FAI), testosterone, sex hormone binding globulin (SHBG), and liver markers (alanine aminotransferase (ALT), hyaluronic acid (HA), N-terminal pro-peptide of type III procollagen (PIIINP), tissue inhibitor of metallo-proteinases-1 (TIMP-1), and the enhanced liver fibrosis (ELF) score). Forty women with PCOS were recruited and randomized to vitamin D (3200 IU) or placebo daily for 3 months. All outcomes were measured at baseline and 3 months follow-up (FU). Greater increases in vitamin D levels were shown in the supplementation group (vitamin D, baseline: 25.6 ± 11.4 nmol/L, FU: 90.4 ± 19.5 nmol/L vs. placebo, baseline: 30.9 ± 11.1 nmol/L, FU: 47.6 ± 20.5 nmol/L, p < 0.001). Between groups comparisons (% baseline change) revealed significant differences in ALT (p = 0.042) and a weak effect indicating a greater reduction in the HOMA-IR in the vitamin D group (p = 0.051). No further between group differences were seen in other cardiovascular risk factor, liver markers, or hormones. This study supports beneficial effects of vitamin D supplementation on liver markers and modest improvements in insulin sensitivity in vitamin D deficient women with PCOS.

Keywords: cardiovascular risk factors; hormones; liver markers; polycystic ovary syndrome; vitamin D.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Alanine Transaminase / metabolism
  • Biomarkers / blood*
  • Blood Glucose / metabolism
  • Body Mass Index
  • C-Reactive Protein / metabolism
  • Cardiovascular Diseases / blood
  • Cardiovascular Diseases / prevention & control*
  • Cholesterol / blood
  • Dietary Supplements*
  • Double-Blind Method
  • Female
  • Humans
  • Hyaluronic Acid / blood
  • Insulin / blood
  • Insulin Resistance
  • Liver / metabolism
  • Middle Aged
  • Polycystic Ovary Syndrome / blood*
  • Risk Factors
  • Sex Hormone-Binding Globulin / metabolism
  • Testosterone / blood
  • Tissue Inhibitor of Metalloproteinase-1 / blood
  • Triglycerides / blood
  • Vitamin D / administration & dosage*
  • Vitamin D / blood
  • Vitamin D Deficiency / blood
  • Vitamin D Deficiency / drug therapy
  • Young Adult

Substances

  • Biomarkers
  • Blood Glucose
  • Insulin
  • Sex Hormone-Binding Globulin
  • TIMP1 protein, human
  • Tissue Inhibitor of Metalloproteinase-1
  • Triglycerides
  • Vitamin D
  • Testosterone
  • Hyaluronic Acid
  • C-Reactive Protein
  • Cholesterol
  • Alanine Transaminase