Exclusion of coding-region mutations in luteinizing hormone and follicle-stimulating hormone receptor genes as the cause of ovarian hyperstimulation syndrome

Fertil Steril. 2007 Mar;87(3):603-6. doi: 10.1016/j.fertnstert.2006.06.060. Epub 2006 Oct 30.

Abstract

Objective: To sequence the coding regions of the luteinizing hormone receptor (LHR) and follicle-stimulating hormone receptor (FSHR) genes to find out if polymorphisms in them are responsible for the severe form of ovarian hyperstimulation syndrome (OHSS) in Swedish patients.

Design: A mutation analysis of gonadotropin receptor genes from women undergoing gonadotropin treatment.

Setting: The Fertility Unit of Karolinska University Hospital Huddinge, Stockholm, Sweden.

Patient(s): A set of 10 well-characterized patients with severe OHSS, and 10 control women who did not develop OHSS after FSH stimulation. An additional 11 patients and 41 control women were screened for a two-amino-acid insertion in the first exon of the LHR gene.

Intervention(s): None.

Main outcome measure(s): Changes in the sequence of the receptor genes between patients and controls.

Result(s): No association was found between polymorphisms of the coding region of LHR or FSHR genes and the development of OHSS. Incidence of the two-amino-acid insertion in the first exon of the LHR gene was slightly higher in patients than in controls, but no statistically significant difference was seen.

Conclusion: LHR and FSHR coding polymorphisms are not a major cause of severe OHSS in Swedish patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Exons / genetics
  • Female
  • Gene Frequency
  • Humans
  • Iatrogenic Disease
  • Ovarian Hyperstimulation Syndrome / genetics*
  • Polymorphism, Genetic*
  • Receptors, FSH / genetics*
  • Receptors, LH / genetics*
  • Sweden

Substances

  • Receptors, FSH
  • Receptors, LH