Examination of reproductive aging milestones among women who carry the FMRI premutation

被引:165
作者
Allen, E. G.
Sullivan, A. K.
Marcus, M.
Small, C.
Dominguez, C.
Epstein, M. P.
Charen, K.
He, W.
Taylor, K. C.
Sherman, S. L.
机构
[1] Emory Univ, Dept Human Genet, Atlanta, GA 30322 USA
[2] Emory Univ, Rollins Sch Publ Hlth, Dept Epidemiol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Dept Gynecol & Obstet, Atlanta, GA 30322 USA
关键词
FMRP; infertility; menopause; RNA toxic effect; trinucleotide;
D O I
10.1093/humrep/dem148
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: The fragile X premutation is characterized by a large CGG repeat track (55-199 repeats) in the 5' UTR of the FMR1 gene. This X-linked mutation leads to an increased risk for premature ovarian failure; interestingly, the association of repeat size with risk is non-linear. We hypothesize that the premutation-associated ovarian insufficiency is due to a diminished oocyte pool and examined reproductive aging milestones by repeat size group to determine if the same non-linear association is observed. METHODS: We analyzed cross-sectional reproductive history questionnaire data from 948 women with a wide range of repeat sizes. RESULTS: We have confirmed the nonlinear relationship among premutation carriers for ovarian insufficiency. The mid-range repeat size group (80-100 repeats), not the highest group, had an increased risk for: altered cycle traits (shortened cycle length, irregular cycles and skipped cycles), subfertility and dizygotic twinning. Smoking, a modifiable risk, decreased the reproductive lifespan of women with the premutation by about 1 year, similar to its effect on non-carriers. As expected, premutation carriers were found to be at an increased risk for osteoporosis. CONCLUSIONS: Possible molecular mechanisms to explain the non-linear repeat size risk for ovarian insufficiency are discussed.
引用
收藏
页码:2142 / 2152
页数:11
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