Department of Molecular Medicine, Aarhus University Hospital, Aarhus N, Denmark; Department of Gynaecology and Obstetrics, Aarhus University Hospital, Aarhus N, Denmark.
Department of Molecular Medicine, Aarhus University Hospital, Aarhus N, Denmark; Department of Endocrinology, Aarhus University Hospital, Aarhus, Denmark.
Ann Endocrinol (Paris). 2022 Aug;83(4):244-249. doi: 10.1016/j.ando.2022.06.001. Epub 2022 Jun 18.
Turner syndrome (TS) is tightly associated with hypergonadotropic hypogonadism and ovarian dysgenesis, typically resulting in infertility in the great majority of patients. Therefore females with TS are usually treated with female sex steroids from 11-12years of age until the normal age of natural menopause of around 53-54years of age. Infertility is rated among females with TS as a distressing concern and a detractor from a good quality of life. Options for motherhood for females with TS has expanded during recent years. Originally, only adoption was an option, unless of course for the small minority of TS females that still has ovarian function and are capable of achieving pregnancy through normal means. Oocyte donation has become the mainstream option in many countries and seems to work well, especially if patients have been treated with optimal estrogen and gestagen for a prolonged time before the intervention. It comes with an increased risk of cardiovascular complications and TS oocyte donation pregnancies are viewed as high risk pregnancies necessitating increased vigilance. Oocyte cryopreservation of own oocytes is also becoming an option in a select group of TS and has special challenges. Ovarian tissue cryopreservation is a promising new techniques that has been applied successfully in children with cancer. Currently, several trials are running around the world evaluating this techniques in TS. The genetics and genomics behind the ovarian dysgenesis seen in TS is not understood, but new studies have elucidated global changes in DNA methylation and RNA expression in blood from persons with TS and it is likely that similar changes are present in the ovaries. We still, however, need more thorough research to fully uncover the genetic background of ovarian failure in TS. Gene expression studies and methylation analysis from ovarian TS tissues still needs to be performed.
特纳综合征(TS)与促性腺激素性性腺功能减退症和卵巢发育不良密切相关,通常导致绝大多数患者不孕。因此,TS 女性通常在 11-12 岁时开始接受女性性激素治疗,直到正常自然绝经年龄约为 53-54 岁。不孕是 TS 女性关注的焦点问题之一,会降低生活质量。近年来,TS 女性实现母性的选择有所增加。最初,只有收养是一种选择,除非极少数仍具有卵巢功能且能够通过正常方式怀孕的 TS 女性。供卵已成为许多国家的主流选择,效果似乎很好,尤其是对于在干预前已接受最佳雌激素和孕激素治疗延长时间的患者。但供卵妊娠也会带来心血管并发症风险增加的问题,并且 TS 供卵妊娠被视为高危妊娠,需要加强监护。在选择的 TS 患者群体中,自身卵母细胞的卵母细胞冷冻保存也成为一种选择,并且具有特殊的挑战。卵巢组织冷冻保存是一种很有前途的新技术,已成功应用于患有癌症的儿童。目前,全世界正在进行几项临床试验,评估该技术在 TS 中的应用。导致 TS 中卵巢发育不良的遗传和基因组学尚未被理解,但新的研究已经阐明了 TS 患者血液中 DNA 甲基化和 RNA 表达的整体变化,并且很可能在卵巢中也存在类似的变化。然而,我们仍然需要更全面的研究来充分揭示 TS 中卵巢衰竭的遗传背景。仍需要对卵巢 TS 组织进行基因表达研究和甲基化分析。