Mailick Marsha R, Hong Jinkuk, Greenberg Jan, Smith Leann, Sherman Stephanie
Waisman Center, University of Wisconsin-Madison, Wisconsin.
Am J Med Genet B Neuropsychiatr Genet. 2014 Dec;165B(8):705-11. doi: 10.1002/ajmg.b.32277. Epub 2014 Oct 25.
In a sample of post-menopausal premutation carrier mothers of children with the full mutation of fragile X syndrome (n = 88), this study examined the co-occurrence of the reproductive and psychiatric phenotypes associated with FMR1 premutations. Mean age at menopause was 43.1 years, and 35.2% of premutation carriers reported cessation of menses prior to age 40 (premature ovarian failure), but only 18% of carriers had been medically diagnosed by a physician as having Fragile X-associated Primary Ovarian Insufficiency. There was a significant curvilinear association between CGG repeat length and age at menopause, with women who had mid-range repeats having the earliest menopause, similar to the pattern that has been found for the psychiatric phenotype of the FMR1 premutation.
在一组患有脆性X综合征完全突变的儿童的绝经后前突变携带者母亲样本(n = 88)中,本研究调查了与FMR1前突变相关的生殖和精神表型的共现情况。绝经的平均年龄为43.1岁,35.2%的前突变携带者报告在40岁之前月经停止(卵巢早衰),但只有18%的携带者被医生医学诊断为患有脆性X相关原发性卵巢功能不全。CGG重复长度与绝经年龄之间存在显著的曲线关联,中等重复长度的女性绝经最早,这与FMR1前突变的精神表型所发现的模式相似。