Literature DB >> 20149747

Effects of race/ethnicity on triple CGG counts in the FMR1 gene in infertile women and egg donors.

Norbert Gleicher1, Andrea Weghofer, David H Barad.   

Abstract

This cross-sectional cohort study investigated 385 females (344 infertile women and 41 oocyte donors), the numbers of CGG repeats on the FMR1 gene and differences between races/ethnicities. Traditional definitions of neuropsychiatric risks are classified as common, intermediate, premutation and full mutation ranges. Normal CGG count range was here, however, defined by box and whisker plot as 26-32 repeats (median 30). Distribution of abnormal outliers in CGG counts from this normal range was then compared between women of Caucasian, African and Asian descent. African and Asian women demonstrated a higher prevalence of two normal count alleles (65%) than Caucasians (54.3%; P=0.03). Caucasians demonstrated the highest rate of allele abnormalities (43.3%) and were the only race/ethnicity also demonstrating abnormalities in both FMR1 alleles. Asian women demonstrated significantly fewer low outlier counts than Caucasians (P=0.002) and Africans (P=0.03). This study, thus, suggests significant racial/ethnic differences in triple CGG counts on the FMR1 gene between races/ethnicities. Since CGG counts on FMR1 are associated with ovarian reserve, these findings may reflect potential differences between races/ethnicities in ovarian function and female fertility reported in the literature. Copyright (c) 2009 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 20149747     DOI: 10.1016/j.rbmo.2009.12.017

Source DB:  PubMed          Journal:  Reprod Biomed Online        ISSN: 1472-6483            Impact factor:   3.828


  22 in total

1.  Do BRCA1/2 mutations and low FMR1 alleles interact or not?

Authors:  Norbert Gleicher; Andrea Weghofer; David H Barad
Journal:  Eur J Hum Genet       Date:  2013-09-25       Impact factor: 4.246

2.  Distribution of the FMR1 gene in females by race/ethnicity: women with diminished ovarian reserve versus women with normal fertility (SWAN study).

Authors:  Lisa M Pastore; Steven L Young; Ani Manichaikul; Valerie L Baker; Xin Q Wang; Joel S Finkelstein
Journal:  Fertil Steril       Date:  2016-11-02       Impact factor: 7.329

3.  Defining ovarian reserve to better understand ovarian aging.

Authors:  Norbert Gleicher; Andrea Weghofer; David H Barad
Journal:  Reprod Biol Endocrinol       Date:  2011-02-07       Impact factor: 5.211

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

Authors:  Lisa M Pastore; Steven L Young; Valerie L Baker; Logan B Karns; Christopher D Williams; Lawrence M Silverman
Journal:  Reprod Sci       Date:  2012-05-10       Impact factor: 3.060

5.  Predictors and risk model development for menopausal age in fragile X premutation carriers.

Authors:  Marian A Spath; Ton B Feuth; Arie P T Smits; Helger G Yntema; Didi D M Braat; Chris M G Thomas; Ad Geurts van Kessel; Stephanie L Sherman; Emily G Allen
Journal:  Genet Med       Date:  2011-07       Impact factor: 8.822

6.  FMR1 genotype with autoimmunity-associated polycystic ovary-like phenotype and decreased pregnancy chance.

Authors:  Norbert Gleicher; Andrea Weghofer; Irene H Lee; David H Barad
Journal:  PLoS One       Date:  2010-12-16       Impact factor: 3.240

7.  Association of FMR1 genotypes with in vitro fertilization (IVF) outcomes based on ethnicity/race.

Authors:  Norbert Gleicher; Andrea Weghofer; Irene H Lee; David H Barad
Journal:  PLoS One       Date:  2011-04-15       Impact factor: 3.240

8.  The impact in older women of ovarian FMR1 genotypes and sub-genotypes on ovarian reserve.

Authors:  Norbert Gleicher; Andrea Weghofer; Ann Kim; David H Barad
Journal:  PLoS One       Date:  2012-03-16       Impact factor: 3.240

9.  Differences in ovarian aging patterns between races are associated with ovarian genotypes and sub-genotypes of the FMR1 gene.

Authors:  Norbert Gleicher; Ann Kim; Andrea Weghofer; David H Barad
Journal:  Reprod Biol Endocrinol       Date:  2012-09-10       Impact factor: 5.211

10.  BRCA1/2 mutations appear embryo-lethal unless rescued by low (CGG n<26) FMR1 sub-genotypes: explanation for the "BRCA paradox"?

Authors:  Andrea Weghofer; Muy-Kheng Tea; David H Barad; Ann Kim; Christian F Singer; Klaus Wagner; Norbert Gleicher
Journal:  PLoS One       Date:  2012-09-12       Impact factor: 3.240

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