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

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Infertile women with diminished ovarian reserve exhibited a significantly higher prevalence of 35-44 FMR1 CGG repeats compared to the general female population, indicating an overrepresentation of these intermediate repeat counts in this patient group.

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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.

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MeSH descriptors

Fragile X Messenger Ribonucleoprotein 1 Infertility, Female Primary Ovarian Insufficiency Trinucleotide Repeats Adult Amenorrhea Amenorrhea Cohort Studies Female Follicle Stimulating Hormone Follicle Stimulating Hormone Fragile X Messenger Ribonucleoprotein 1 Humans Infertility, Female Intellectual Disability Intellectual Disability Primary Ovarian Insufficiency Primary Ovarian Insufficiency Prospective Studies Trinucleotide Repeats

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europepmc
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pubmed
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