Vitamin D Metabolism Genes Are Differentially Methylated in Individuals with Chronic Knee Pain

Lifestyle Genom. 2023;16(1):98-105. doi: 10.1159/000529823. Epub 2023 Feb 28.

Abstract

Introduction: Recent evidence suggests that vitamin D may interact with the epigenome and play a role in the pain experience. In order for proper functioning to occur, there must be an adequate level of vitamin D present, made possible by enzymatic reactions that allow vitamin D to be biologically active. The purpose of this study was to explore the epigenetic landscape of genes involved in vitamin D metabolism in individuals with and without chronic knee pain.

Methods: Community-dwelling individuals recruited as part of a larger study focused on knee pain provided demographic, clinical, and pain-related information, as well as an intravenous blood sample to determine DNA methylation levels at CpG sites.

Results: There were differences in DNA methylation between those with and without pain in genes that code for enzymes related to vitamin D metabolism: CYP27B1 (1-α-hydroxylase). There was also hypermethylation on the gene that codes for the vitamin D receptor (VDR).

Conclusions: The presence of chronic pain is associated with epigenetic modifications in genes responsible for the expression of enzymes involved in vitamin D metabolism and cellular function. These results lay groundwork in understanding the mechanism underlying the association between vitamin D and chronic pain.

Keywords: Epigenetics; Pain; Vitamin D; Vitamin D receptor.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase* / genetics
  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase* / metabolism
  • Chronic Pain* / genetics
  • DNA Methylation
  • Epigenesis, Genetic
  • Humans
  • Vitamin D / metabolism
  • Vitamins

Substances

  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase
  • Vitamin D
  • Vitamins