A Study of IL-1β, MMP-3, TGF-β1, and GDF5 Polymorphisms and Their Association with Primary Frozen Shoulder in a Chinese Han Population

Biomed Res Int. 2017:2017:3681645. doi: 10.1155/2017/3681645. Epub 2017 Jun 6.

Abstract

Primary frozen shoulder (PFS) is a common condition of uncertain etiology that is characterized by shoulder pain and restriction of active and passive glenohumeral motions. The pathophysiology involves chronic inflammation and fibrosis of the joint capsule. Single nucleotide polymorphisms (SNPs) at IL-1β, MMP3, TGF-β1, and GDF5 have been associated with risk of a variety of inflammatory diseases; however, no studies have examined these SNPs with susceptibility to PFS. We investigated allele and genotype frequencies of rs1143627 at IL-1β, rs650108 at MMP-3, rs1800469 at TGF-β1, and rs143383 at GDF5 in 42 patients with PFS and 50 healthy controls in a Chinese Han population. Serum samples from both cohorts were evaluated to determine the expression levels of IL-1β. We found that the IL-1β rs1143627 CC genotype was associated with a decreased risk of PFS compared to the TT genotype (P = 0.022) and that serum IL-1β was expressed at a significantly higher level in the PFS cohort compared to that found in the control group (P < 0.001). Our findings indicated no evidence of an association between rs650108, rs1800469, or rs143383 and PFS. IL-1β is associated with susceptibility to PFS and may have a role in its pathogenesis in a Chinese Han population.

Publication types

  • Clinical Trial

MeSH terms

  • Asian People / ethnology
  • Asian People / genetics
  • Bursitis / ethnology
  • Bursitis / genetics*
  • China / ethnology
  • Female
  • Genetic Predisposition to Disease*
  • Growth Differentiation Factor 5 / genetics*
  • Humans
  • Interleukin-1beta / genetics*
  • Male
  • Matrix Metalloproteinase 3 / genetics*
  • Middle Aged
  • Polymorphism, Single Nucleotide*

Substances

  • GDF5 protein, human
  • Growth Differentiation Factor 5
  • IL1B protein, human
  • Interleukin-1beta
  • MMP3 protein, human
  • Matrix Metalloproteinase 3