The impact of FMR1 gene mutations on human reproduction and development: a systematic review

J Assist Reprod Genet. 2016 Sep;33(9):1135-47. doi: 10.1007/s10815-016-0765-6. Epub 2016 Jul 18.

Abstract

Purpose: This is a comprehensive review of the literature in this field attempting to put the FMR1 gene and its evaluation into context, both in general and for the reproductive health audience.

Methods: Online database search of publications with systematic review of all papers relevant to ovarian reserve and assisted reproduction was done.

Results: Relevant papers were identified and assessed, and an attempt was made to understand, rationalize and explain the divergent views in this field of study. Seminal and original illustrations were employed.

Conclusions: FMR1 is a highly conserved gene whose interpretation and effect on outcomes remains controversial in the reproductive health setting. Recent re-evaluations of the commonly accepted normal range have yielded interesting tools for possibly explaining unexpected outcomes in assisted reproduction. Fragile X investigations should perhaps become more routinely assessed in the reproductive health setting, particularly following a failed treatment cycle where oocyte quality is thought to be a contributing factor, or in the presence of a surprise finding of diminished ovarian reserve in a young patient.

Keywords: Assisted reproductive technology; FMR1; Fragile X; Genetics; Reproduction; Testing.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Female
  • Fragile X Mental Retardation Protein / genetics*
  • Humans
  • Mutation
  • Ovarian Reserve / genetics*
  • Reproduction / genetics*
  • Reproductive Techniques, Assisted*

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein