Elevated prevalence of 35-44 FMR1 trinucleotide repeats in women with diminished ovarian reserve

Reprod Sci. 2012 Nov;19(11):1226-31. doi: 10.1177/1933719112446074. Epub 2012 May 10.

Abstract

Introduction: Fragile X premutations are associated with primary ovarian insufficiency when the patient presents with amenorrhea, but the fragile X mental retardation 1 (FMR1) CGG repeat count among cycling women with low ovarian reserve (diminished ovarian reserve [DOR]) is not yet established.

Patients and methods: Sixty-two infertile DOR patients were recruited from 4 US private and academic fertility centers.

Results: The prevalence of 35-44 FMR1 CGG repeats was 14.5%. Compared with the general female population estimate from the literature, infertile women with DOR were more likely to have 35-44 FMR1 CGG repeats (14.5% and 3.9%, respectively, P = .0003). Similar findings were noted by 5-repeat bandwidth: 35-39 CGG repeats (9.7% DOR vs 3.2% comparison, P = .012) or 40-44 CGG repeats (4.8% DOR vs 0.7% comparison, P = .024).

Conclusions: These data suggest that CGG repeats of 35-44 may be markedly overrepresented in women with DOR, whereas the current FMR1 reference range indicates that there is no clinical phenotype with <45 CGG repeats.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Amenorrhea / genetics
  • Cohort Studies
  • Female
  • Follicle Stimulating Hormone / blood
  • Fragile X Mental Retardation Protein / genetics*
  • Humans
  • Infertility, Female / genetics*
  • Intellectual Disability / genetics
  • Primary Ovarian Insufficiency / blood
  • Primary Ovarian Insufficiency / genetics*
  • Prospective Studies
  • Trinucleotide Repeats / genetics*

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein
  • Follicle Stimulating Hormone