Literature DB >> 32483686

Are ovarian response and pregnancy rates similar in selected FMR1 premutated and mutated patients undergoing preimplantation genetic testing?

Noemie Ranisavljevic1, Mathilde Hess2, Christel Castelli3,4, Marjolene Willems5, Alice Ferrieres-Hoa6, Anne Girardet7, Tal Anahory2.   

Abstract

PURPOSE: To assess if the ovarian response of FMR1 premutated women undergoing preimplantation genetic testing (PGT) for Fragile X syndrome is lower compared with fully mutated patients, due to their frequent premature ovarian failure.
METHODS: In a retrospective cohort study from January 2009 to March 2019, we compared PGT outcomes in 18 FMR1 premutated women and 12 fully mutated women and aimed to identify predictive factors of stimulation outcomes.
RESULTS: Eighty-six IVF/PGT-M cycles for FMR1 PGT were analyzed. Premutation and full mutation patients were comparable in terms of age, body mass index (BMI), basal FSH, antral follicular count, and cycle length. However, premutation carriers had significantly lower AMH (1.9 versus 4.0 ng/mL, p = 0.0167). Premutated patients required higher doses of FSH (2740 versus 1944 IU, p = 0.0069) but had similar numbers of metaphase II oocytes (7.1 versus 6.6, p = 0.871) and embryos (5.6 versus 4.9, p = 0. 554). Pregnancy rates (37.1% versus 13.3%, p = 0.1076) were not statistically different in both groups.
CONCLUSION: In spite of lower ovarian reserve and thanks to an increased total dose of FSH, FMR1 premutated selected patients seem to have similar ovarian response as fully mutated patients. Neither the number of CGG repeats in FMR1 gene nor FMR1 mutation status was good predictors of the number of retrieved oocytes.

Entities:  

Keywords:  Fragile X syndrome; IVF; Ovarian reserve; Ovarian stimulation; Preimplantation genetic testing

Mesh:

Substances:

Year:  2020        PMID: 32483686      PMCID: PMC7376994          DOI: 10.1007/s10815-020-01809-3

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  49 in total

1.  Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10-year experience.

Authors:  A Girardet; A Ishmukhametova; M Willems; C Coubes; S Hamamah; T Anahory; M Des Georges; M Claustres
Journal:  Clin Genet       Date:  2014-05-20       Impact factor: 4.438

2.  A marker X chromosome.

Authors:  H A Lubs
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

3.  Obstetrical and gynecological complications in fragile X carriers: a multicenter study.

Authors:  C E Schwartz; J Dean; P N Howard-Peebles; M Bugge; M Mikkelsen; N Tommerup; C Hull; R Hagerman; J J Holden; R E Stevenson
Journal:  Am J Med Genet       Date:  1994-07-15

4.  Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

Authors:  Y H Fu; D P Kuhl; A Pizzuti; M Pieretti; J S Sutcliffe; S Richards; A J Verkerk; J J Holden; R G Fenwick; S T Warren
Journal:  Cell       Date:  1991-12-20       Impact factor: 41.582

5.  The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosis.

Authors:  Guy Bibi; Mira Malcov; Yaron Yuval; Adi Reches; Dalit Ben-Yosef; Beni Almog; Ami Amit; Foad Azem
Journal:  Fertil Steril       Date:  2009-05-29       Impact factor: 7.329

6.  First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.

Authors:  A Girardet; S Hamamah; T Anahory; H Déchaud; P Sarda; B Hédon; J Demaille; M Claustres
Journal:  Mol Hum Reprod       Date:  2003-02       Impact factor: 4.025

7.  Predictors of ovarian response in women treated with corifollitropin alfa for in vitro fertilization/intracytoplasmic sperm injection.

Authors:  Nikolaos P Polyzos; Herman Tournaye; Luis Guzman; Michel Camus; Scott M Nelson
Journal:  Fertil Steril       Date:  2013-05-10       Impact factor: 7.329

8.  Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.

Authors:  R A M Buijsen; J A Visser; P Kramer; E A W F M Severijnen; M Gearing; N Charlet-Berguerand; S L Sherman; R F Berman; R Willemsen; R K Hukema
Journal:  Hum Reprod       Date:  2015-11-03       Impact factor: 6.918

9.  Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR.

Authors:  Mira Malcov; Tova Naiman; Dalit Ben Yosef; Ariella Carmon; Nava Mey-Raz; Ami Amit; Israel Vagman; Yuval Yaron
Journal:  Reprod Biomed Online       Date:  2007-04       Impact factor: 3.828

10.  Elevated levels of FMR1 mRNA in granulosa cells are associated with low ovarian reserve in FMR1 premutation carriers.

Authors:  Shai E Elizur; Oshrit Lebovitz; Sanaz Derech-Haim; Olga Dratviman-Storobinsky; Baruch Feldman; Jehoshua Dor; Raoul Orvieto; Yoram Cohen
Journal:  PLoS One       Date:  2014-08-25       Impact factor: 3.240

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