Can the FMR1 (Fragile X) Gene Serve As Predictor of Response to Ovarian Stimulation?

被引:25
作者
Gleicher, Norbert [1 ,2 ,3 ]
Weghofer, Andrea [1 ,2 ,4 ]
Oktay, Kutluk [1 ,2 ,5 ]
Barad, David H. [1 ,2 ,6 ,7 ]
机构
[1] Ctr Human Reprod, New York, NY 10021 USA
[2] Fdn Reprod Med, New York, NY USA
[3] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT USA
[4] Univ Vienna, Sch Med, Dept Obstet & Gynecol, Vienna, Austria
[5] New York Med Coll, Dept Obstet & Gynecol, Valhalla, NY 10595 USA
[6] Albert Einstein Coll Med, Dept Epidemiol & Social Med, Bronx, NY 10467 USA
[7] Albert Einstein Coll Med, Dept Obstet Gynecol & Womens Hlth, Bronx, NY 10467 USA
关键词
Fragile X; FMR1; gene; premature ovarian senescence; ovarian aging; ovarian resistance; gonadotropins; ovarian stimulation; DEHYDROEPIANDROSTERONE SUPPLEMENTATION; REPEAT; PREMUTATION; FSH;
D O I
10.1177/1933719108328617
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Because triple GGG repeats on FMR1 correlate with anti-Mullerian hormone, repeats may also correlate with clinical outcomes. In 55 in vitro fertilization patients, repeats, corrected for gonadotropin dosage, were, therfore, correlated to oocytes. Patients were stratified by <35 and >= 35 repeats, and by age to <38 or >= 38 years. Less than 35 (but not >= 35) repeats demonstrated significantly lower anti-Mullerian hormone at ages >= 38 than at <38 years (P < .05). In >38 years, anti-Mullerian hormone was not affected by repeats. In <38 years, with <35 repeats (though not with >= 35), required significantly less gonadotropins than >= 38 (P < .05). In <38 years (though not >= 38), those with <35 repeats produced significantly more oocytes than women with >= 35 repeats (P = .006). In <38 years, retrieved oocytes were inversely related to repeats, adjusted for gonadotropin dosage (P = .03). This supports FMR1 testing as useful in fertility practice and suggests why response rates to increasing stimulation with gonadotropins may vary.
引用
收藏
页码:462 / 467
页数:6
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