Elastin genetic point mutation and the risk of pelvic organ prolapse

N. Haya, I. Feferkorn, F. Fares, N. Azzam, R. Auslender, Y. Abramov

Research output: Contribution to journalArticlepeer-review

Abstract

Aim: A missense mutation in the elastin gene (g28197A > G) is associated with an increased risk for inguinal hernias. Due to the shared epidemiological and pathophysiological features between pelvic organ prolapse (POP) and inguinal hernias, the authors hypothesized that a similar association exists between elastin gene polymorphism and POP. Materials andMethods: Patients of Ashkenazi Jewish ori- gin with advanced (stage III-IV) POP (as assessed by POP-Q) and healthy controls were compared for the presence of the elastin gene g28197A > G missense mutation. Results: The missense mutation in the elastin gene was not found in neither the study or the control group. Conclusion: The elastin gene g28197A > G missense mutation was not found to be associated with an increased risk for POP.

Original languageEnglish
Pages (from-to)75-78
Number of pages4
JournalClinical and Experimental Obstetrics and Gynecology
Volume47
Issue number1
DOIs
StatePublished - 15 Feb 2020

Bibliographical note

Publisher Copyright:
©2020 Haya et al.

Keywords

  • Elastin
  • Genetic polymorphism
  • Pelvic organ prolapse
  • Point mutation

ASJC Scopus subject areas

  • Reproductive Medicine
  • Obstetrics and Gynecology

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