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Fragile X‐associated primary ovarian insufficiency: evidence for additional genetic contributions to severity
Author(s) -
Hunter Jessica Ezzell,
Epstein Michael P.,
Tinker Stuart W.,
Charen Krista H.,
Sherman Stephanie L.
Publication year - 2008
Publication title -
genetic epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.301
H-Index - 98
eISSN - 1098-2272
pISSN - 0741-0395
DOI - 10.1002/gepi.20329
Subject(s) - fmr1 , menopause , fragile x syndrome , premature ovarian failure , allele , genetics , population , biology , body mass index , medicine , gene , endocrinology , environmental health
The fragile X mental retardation gene ( FMR1 ) contains a CGG repeat sequence in its 5′ untranslated region that can become unstable and expand in length from generation to generation. Alleles with expanded repeats in the range of ∼55–199, termed premutation alleles, are associated with an increased risk for fragile‐X‐associated primary ovarian insufficiency (FXPOI). However, not all women who carry the premutation develop FXPOI. To determine if additional genes could explain variability in onset and severity, we used a random‐effects Cox proportional hazards model to analyze age at menopause on 680 women from 225 families who have a history of fragile X syndrome and 321 women from 219 families from the general population. We tested for the presence of a residual additive genetic effect after adjustment for FMR1 repeat length, race, smoking, body mass index, and method of ascertainment. Results showed significant familial aggregation of age at menopause with an estimated additive genetic variance of 0.55–0.96 depending on the parameterization of FMR1 repeat size and definition of age at menopause ( P ‐values ranging between 0.0002 and 0.0027). This is the first study to analyze familial aggregation of FXPOI. This result is important for proper counseling of women who carry FMR1 premutation alleles and for guidance of future studies to identify additional genes that influence ovarian insufficiency. Genet. Epidemiol . 2008. © 2008 Wiley‐Liss, Inc.