Polymorphism in vitamin D-binding protein as a genetic risk factor in the pathogenesis of endometriosis

J Clin Endocrinol Metab. 2011 Jan;96(1):E233-41. doi: 10.1210/jc.2010-1532. Epub 2010 Oct 27.


Context: Previous studies have implicated a deficiency in the inflammatory response in women who develop endometriosis. The specific immunological deficits have not been completely elucidated.

Objective: Our objective was to identify differences in protein expression in serum that might shed light on the pathophysiology of endometriosis.

Design and setting: This cross-sectional study of women undergoing laparoscopy between 2003 and 2005 took place at a university medical center.

Patients: Patients included consenting women age 18-49 yr undergoing surgery for pain and/or infertility or elective tubal ligation. Women with acute or chronic medical conditions were excluded.

Intervention: Blood was collected preoperatively.

Main outcome measure: Proteomic analysis of serum was done using two-dimensional difference gel electrophoresis.

Results: We found 25 protein spots with a significant difference in abundance between women with endometriosis and controls, including acute-phase proteins and complement components. The abundance of vitamin D-binding protein was higher in all endometriosis pools by a factor of approximately 3 compared with the control pool (P < 0.02). Analysis of specific allele products using nano-scale liquid chromatography-electrospray ionization-mass spectrometry indicated that it was the GC*2 allele product that was in greater concentration in serum pools, as well as in single validation samples, in women with endometriosis (P = 0.006). In contrast to the GC*1 allele product, which is readily converted to a potent macrophage factor (Gc protein-derived macrophage-activating factor), the GC*2 allele product undergoes practically no such conversion.

Conclusions: We speculate that the inability to sufficiently activate macrophages' phagocytotic function in those carrying the GC*2 polymorphism (more prevalent in endometriosis) may allow endometriotic tissues to implant in the peritoneal cavity. Future studies evaluating specific vitamin D-binding protein polymorphisms as a risk factor for endometriosis in larger populations of women are warranted.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Chromatography, Liquid
  • Cross-Sectional Studies
  • Electrophoresis, Gel, Two-Dimensional
  • Endometriosis / blood*
  • Endometriosis / etiology
  • Female
  • Humans
  • Mass Spectrometry
  • Polymorphism, Genetic*
  • Risk Factors
  • Vitamin D-Binding Protein / analysis
  • Vitamin D-Binding Protein / blood*


  • Vitamin D-Binding Protein