Association between vitamin D and endometriosis: a systematic review

Hormones (Athens). 2020 Jun;19(2):109-121. doi: 10.1007/s42000-019-00166-w. Epub 2019 Dec 21.

Abstract

Background: Endometriosis is one of the most common gynecological diseases of reproductive age, with a prevalence of 5-10% and grave consequences for quality of life and fertility. Vitamin D (vit D), a classic regulator of plasma calcium concentration and skeleton mineralization, is also an effective modulator of the immune system. Several studies suggest that immunologic properties attributed to vit D along with vit D receptor (VDR) expression in reproductive tissues may be involved in the pathogenesis of endometriosis.

Objective: To systematically review the literature for the association between components of vit D metabolism and endometriosis.

Materials and methods: A systematic review of the literature published in the Medline and Cochrane Central databases was conducted for original research articles on humans, published in any language.

Results: Twenty-one studies were included in the systematic review. Among them, 12 examined the relationship of endometriosis with vit D metabolites, eight with vit D-binding protein (VDBP), three with VDR polymorphisms, and two with vit D regulatory enzymes. There are discrepancies between the outcomes of the available literature publications.

Conclusions: This is a systematic attempt to collect, evaluate, and present the known data on the association between vit D and endometriosis. Given the heterogeneity and the diversity of the present studies, more research is required to elucidate the association between vit D and endometriosis.

Keywords: 1,25(OH)2D; 1α-hydroxylase; 25(OH)D; 25(ΟΗ)D3 endometriosis; 25α-hydroxylase; Vitamin D; Vitamin D receptor; Vitamin D–binding protein.

Publication types

  • Systematic Review

MeSH terms

  • Endometriosis / enzymology
  • Endometriosis / metabolism*
  • Female
  • Humans
  • Receptors, Calcitriol / genetics
  • Receptors, Calcitriol / metabolism*
  • Vitamin D / metabolism*
  • Vitamin D-Binding Protein / metabolism*

Substances

  • GC protein, human
  • Receptors, Calcitriol
  • Vitamin D-Binding Protein
  • Vitamin D