Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene

Author:

Quilichini Juliette1,Perol Sandrine2,Cuisset Laurence1,Grotto Sarah3,Fouveaut Corinne1,Barbot Jean Claude1,Verebi Camille1,Jordan Pénélope1,Héron Delphine4,Molina‐Gomes Denise5,Pipiras Eva6,Grynberg Michael7,Catteau‐Jonard Sophie8,Touraine Philippe9,Christin‐Maître Sophie10,Plu‐Bureau Geneviève2,El Khattabi Laila111,Bienvenu Thierry1ORCID

Affiliation:

1. Service de Médecine Génomique des maladies de système et d'organe APHP. Centre Université Paris Cité Paris France

2. Unité de gynécologie médicale APHP. Centre Université Paris Cité, Hôpital Cochin Port‐Royal Paris France

3. Maternité Port‐Royal APHP. Centre Université Paris Cité, Hôpital Cochin Paris France

4. Département de Génétique APHP. Sorbonne Université, Hôpital La Pitié‐Salpêtrière Paris France

5. Service de Biologie de la reproduction, Cytogénétique et Génétique Médicale, CHI Poissy‐Saint Germain Poissy France

6. Unité fonctionnelle de Médecine génomique et génétique clinique APHP. Université Sorbonne Paris Nord, Hôpital Jean Verdier Bondy France

7. Gynécologie médicale et médecine de la reproduction, Hôpital Jean Verdier Bondy France

8. Université de Lille CHU de Lille, Service de Gynécologie Médicale Lille France

9. Département d'Endocrinologie et médecine de la reproduction, APHP. Sorbonne Université, Pitié‐Salpêtrière Hospital, Center for Rare Endocrine and Gynecological Disorders Paris France

10. Service d'endocrinologie, diabétologie et médecine de la reproduction APHP. Sorbonne Université Paris France

11. Institut Cochin, INSERM U1016, team « From gametes to birth » Paris France

Abstract

AbstractFMR1 premutation female carriers are at risk of developing premature/primary ovarian insufficiency (POI) with an incomplete penetrance. In this study, we determined the CGG repeat size among 1095 women with diminished ovarian reserve (DOR) / POI and characterized the CGG/AGG substructure in 44 women carrying an abnormal FMR1 repeat expansion number, compared to a group of 25 pregnant women carrying an abnormal FMR1 CGG repeat size. Allelic complexity scores of the FMR1 gene were calculated and compared between the two groups. In the DOR/POI cohort, 2.1% of women presented with an intermediate repeat size and 1.9% with a premutation. Our results suggest that the risk of POI is highest in the mid‐range of CGG repeats. We observed that the allelic score is significantly higher in POI women compared to the pregnant women group (p‐value = 0.02). We suggest that a high allelic score due to more than 2 AGG interspersions in the context of an intermediate number of repetitions could favor POI. Larger studies are still needed to evaluate the relevance of this new tool for the determination of the individual risk of developing POI in women with abnormal number of CGG repeats.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Premature ovarian insufficiency;Nature Reviews Disease Primers;2024-09-12

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