CGG repeat length and AGG interruptions as indicators of fragile X–associated diminished ovarian reserve

Jovana Lekovich, Limor Man, Kangpu Xu, Chelsea Canon, Debra Lilienthal, Joshua D. Stewart, Nigel Pereira, Zev Rosenwaks, Jeannine Gerhardt

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Purpose: Fragile X premutation (PM) carriers may experience difficulties conceiving a child probably due to fragile X–associated diminished ovarian reserve (FXDOR). We investigated which subgroups of carriers with a PM are at higher risk of FXDOR, and whether the number of AGG interruptions within the repeat sequence further ameliorates the risk. Methods: We compared markers of ovarian reserve, including anti-Müllerian hormone, antral follicle count, and number of oocytes retrieved between different subgroups of patients with a PM. Results: We found that carriers with midrange repeats size (70–90 CGG) demonstrate significantly lower ovarian reserve. Additionally, the number of AGG interruptions directly correlated with parameters of ovarian reserve. Patients with longer uninterrupted CGG repeats post–AGG interruptions had the lowest ovarian reserve. Conclusion: This study connects AGG interruptions and certain CGG repeat length to reduced ovarian reserve in carriers with a PM. A possible explanation for our findings is the proposed gonadotoxicity of the FMR1 transcripts. Reduction of AGG interruptions could increase the likelihood that secondary RNA structures in the FMR1 messenger RNA are formed, which could cause cell dysfunction within the ovaries. These findings may provide women with guidance regarding their fertility potential and accordingly assist with their family planning.

Original languageEnglish
Pages (from-to)957-964
Number of pages8
JournalGenetics in Medicine
Volume20
Issue number9
DOIs
StatePublished - 1 Sep 2018
Externally publishedYes

Keywords

  • AGG interruptions
  • FMR1 RNA toxicity
  • fragile X permutation
  • fragile X–associated diminished ovarian reserve
  • genetic counseling

ASJC Scopus subject areas

  • Genetics(clinical)

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