Gersak Ksenija, Meden-Vrtovec Helena, Peterlin Borut
Department of Obstetrics and Gynaecology, Division of Medical Genetics, University Medical Centre, Ljubljana, Slovenia.
Hum Reprod. 2003 Aug;18(8):1637-40. doi: 10.1093/humrep/deg327.
Fragile X premutation carriers are at increased risk of premature ovarian failure (POF), which is usually defined as menopause before the age of 40 years.
We evaluated 83 women with sporadic premature ovarian failure, treated at the Department of Obstetrics and Gynaecology, University Medical Centre, Ljubljana, between 1991 and 2001. There was no family history of mental retardation in any of the patients. They were phenotypically normal and had normal female karyotype (46,XX), without a past history of pelvic surgery, chemotherapy or autoimmune diseases.
The premutation in the FRAXA locus was found in four of the women screened (4.8%; 95% confidence interval 1.9-11.7). This prevalence (1 in 21) was statistically significantly higher than expected in the female Caucasian population.
In this study we have confirmed an important association between FRAXA premutation and the pathogenesis of POF. This result has practical implications for genetic counselling and fertility treatment.
脆性X前突变携带者发生卵巢早衰(POF)的风险增加,卵巢早衰通常定义为40岁之前绝经。
我们评估了1991年至2001年间在卢布尔雅那大学医学中心妇产科接受治疗的83例散发性卵巢早衰女性。所有患者均无智力发育迟缓家族史。她们表型正常,具有正常的女性核型(46,XX),无盆腔手术、化疗或自身免疫性疾病病史。
在筛查的女性中有4例(4.8%;95%置信区间1.9 - 11.7)发现FRAXA位点存在前突变。这种患病率(21分之一)在统计学上显著高于白种女性人群的预期。
在本研究中,我们证实了FRAXA前突变与卵巢早衰发病机制之间的重要关联。这一结果对遗传咨询和生育治疗具有实际意义。