Your browser doesn't support javascript.
loading
Correlation of normal-range FMR1 repeat length or genotypes and reproductive parameters.
Maslow, Bat-Sheva L; Davis, Stephanie; Engmann, Lawrence; Nulsen, John C; Benadiva, Claudio A.
Afiliación
  • Maslow BS; Division of Reproductive Endocrinology and Infertility, University of Connecticut School of Medicine, 2 Batterson Park Rd, Farmington, CT, 06032, USA.
  • Davis S; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH, 45229, USA.
  • Engmann L; Division of Reproductive Endocrinology and Infertility, University of Connecticut School of Medicine, 2 Batterson Park Rd, Farmington, CT, 06032, USA.
  • Nulsen JC; Division of Reproductive Endocrinology and Infertility, University of Connecticut School of Medicine, 2 Batterson Park Rd, Farmington, CT, 06032, USA.
  • Benadiva CA; Division of Reproductive Endocrinology and Infertility, University of Connecticut School of Medicine, 2 Batterson Park Rd, Farmington, CT, 06032, USA. benadiva@uchc.edu.
J Assist Reprod Genet ; 33(9): 1149-55, 2016 Sep.
Article en En | MEDLINE | ID: mdl-27189053
ABSTRACT

PURPOSE:

This study aims to ascertain whether the length of normal-ranged CGG repeats on the FMR1 gene correlates with abnormal reproductive parameters.

METHODS:

We performed a retrospective, cross-sectional study of all FMR1 carrier screening performed as part of routine care at a large university-based fertility center from January 2011 to March 2014. Correlations were performed between normal-range FMR1 length and baseline serum anti-Müllerian hormone (AMH), cycle day 3 follicle stimulating hormone (FSH), ovarian volumes (OV), antral follicle counts (AFC), and incidence of diminished ovarian reserve (DOR), while controlling for the effect of age.

RESULTS:

Six hundred three FMR1 screening results were collected. One subject was found to be a pre-mutation carrier and was excluded from the study. Baseline serum AMH, cycle day 3 FSH, OV, and AFC data were collected for the 602 subjects with normal-ranged CGG repeats. No significant difference in median age was noted amongst any of the FMR1 repeat genotypes. No significant correlation or association was found between any allele length or genotype, with any of the reproductive parameters or with incidence of DOR at any age (p > 0.05). However, subjects who were less than 35 years old with low/low genotype were significantly more likely to have below average AMH levels compared to those with normal/normal genotype (RR 3.82; 95 % CI 1.38-10.56).

CONCLUSIONS:

This large study did not demonstrate any substantial association between normal-range FMR1 repeat lengths and reproductive parameters.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Expansión de Repetición de Trinucleótido / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Reserva Ovárica Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: J Assist Reprod Genet Asunto de la revista: GENETICA / MEDICINA REPRODUTIVA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Expansión de Repetición de Trinucleótido / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Reserva Ovárica Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: J Assist Reprod Genet Asunto de la revista: GENETICA / MEDICINA REPRODUTIVA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos