Oktay Kutluk, Bedoschi Giuliano, Berkowitz Karen, Bronson Richard, Kashani Banafsheh, McGovern Peter, Pal Lubna, Quinn Gwendolyn, Rubin Karen
Department of Obstetrics and Gynecology, Laboratory of Molecular Reproduction and Fertility Preservation, New York Medical College, Valhalla, New York; Innovation Institute for Fertility Preservation and In Vitro Fertilization, New York, New York.
Department of Obstetrics and Gynecology, Laboratory of Molecular Reproduction and Fertility Preservation, New York Medical College, Valhalla, New York; Innovation Institute for Fertility Preservation and In Vitro Fertilization, New York, New York.
J Pediatr Adolesc Gynecol. 2016 Oct;29(5):409-416. doi: 10.1016/j.jpag.2015.10.011. Epub 2015 Oct 17.
In this article we review the existing fertility preservation options for women diagnosed with Turner syndrome and provide practical guidelines for the practitioner. Turner syndrome is the most common sex chromosome abnormality in women, occurring in approximately 1 in 2500 live births. Women with Turner syndrome are at extremely high risk for primary ovarian insufficiency and infertility. Although approximately 70%-80% have no spontaneous pubertal development and 90% experience primary amenorrhea, the remainder might possess a small residual of ovarian follicles at birth or early childhood. The present challenge is to identify these women as early in life as is possible, to allow them to benefit from a variety of existing fertility preservation options. To maximize the benefits of fertility preservation, all women with Turner syndrome should be evaluated by an expert as soon as possible in childhood because the vast majority will have their ovarian reserve depleted before adulthood. Cryopreservation of mature oocytes and embryos is a proven fertility preservation approach, and cryopreservation of ovarian tissue is a promising technique with a growing number of live births, but remains investigational. Oocyte cryopreservation has been performed in children with Turner syndrome as young as 13 years of age and ovarian tissue cryopreservation in affected prepubertal children. However, current efficacy of these approaches is unknown in this cohort. For those who have already lost their ovarian reserve, oocyte or embryo donation and adoption are strategies that allow fulfillment of the desire for parenting. For those with Turner syndrome-related cardiac contraindications to pregnancy, use of gestational surrogacy allows the possibility of biological parenting using their own oocytes. Alternatively, gestational surrogacy can serve to carry pregnancy resulting from the use of donor oocytes or embryos, if needed.
在本文中,我们回顾了针对被诊断为特纳综合征的女性现有的生育力保存选择,并为从业者提供实用指南。特纳综合征是女性中最常见的性染色体异常疾病,约每2500例活产中就有1例发生。患有特纳综合征的女性原发性卵巢功能不全和不孕的风险极高。虽然约70%-80%的患者没有自然青春期发育,90%经历原发性闭经,但其余患者在出生时或幼儿期可能仍残留少量卵巢卵泡。目前的挑战是尽早在生命早期识别这些女性,使她们能够从现有的各种生育力保存选择中获益。为了使生育力保存的益处最大化,所有特纳综合征女性应在童年期尽早由专家进行评估,因为绝大多数患者在成年前卵巢储备就会耗尽。成熟卵母细胞和胚胎的冷冻保存是一种已被证实的生育力保存方法,卵巢组织冷冻保存是一种有前景的技术,活产数量不断增加,但仍处于研究阶段。在年仅13岁的特纳综合征儿童中已进行了卵母细胞冷冻保存,在受影响的青春期前儿童中进行了卵巢组织冷冻保存。然而,这些方法在该队列中的当前疗效尚不清楚。对于那些已经失去卵巢储备的患者,卵母细胞或胚胎捐赠以及领养是实现为人父母愿望的策略。对于那些因特纳综合征相关心脏疾病而有妊娠禁忌的患者,使用妊娠代孕可以让她们有可能使用自己的卵母细胞实现亲生育儿。或者,如果需要,妊娠代孕可以用于孕育使用捐赠卵母细胞或胚胎后的妊娠。