FERTILITY AND PARENTING OPTIONS IN TURNER SYNDROME - A REVIEW OF CURRENT POTENTIAL AND LIMITATIONS
Abstract
Turner syndrome (TS) is a chromosomal disorder with a prevalence of 1 in 2,500 live births. The most common karyotype is 45.X, however, mosaic karyotypes are also present and are associated with a milder presentation of the syndrome. The main symptoms faced by patients with TS include growth deficiency, cardiovascular disorders, and reproductive disorders, including premature ovarian failure (POI). Fertility disorders are mainly due to the presence of dysgenetic gonads, which negatively affect the development of secondary sexual characteristics. Changes in the ovarian cells, including stunted follicle development, abnormal morphology, and follicle atresia, are also a significant problem. Measurements of FSH, LH, and AMH, which appear to be the most stable parameters of ovarian reserve, play an important role in the diagnosis of POI. Due to the fertility disorders in TS, spontaneous pregnancies are achieved in less than 6% of women. Among the fertility preservation methods in patients with preserved ovarian reserve are oocyte cryopreservation or cryopreservation of ovarian tissue, while oocyte donation is the method of choice when ovarian reserve is depleted. For women desiring offspring with contraindications to pregnancy, surrogacy or adoption are alternatives. Pregnancy in TS is associated with many risks for both the mother and the fetus. Patients should be managed by a specialised team experienced in the management of women with TS, including cardiac assessment, both preconceptional and postconceptional. This review discusses the available parenting methods for patients with TS, taking into account recent literature.
References
Turner, H. H. (1938). A syndrome of infantilism, congenital webbed neck, and cubitus valgus. Endocrinology, 23(5), 566–574. https://doi.org/10.1210/endo-23-5-566
Gravholt, C. H., Viuff, M., Just, J., et al. (2023). The changing face of Turner syndrome. Endocrine Reviews, 44(1), 33-69. https://doi.org/10.1210/endrev/bnac016
Tuke, M. A., Ruth, K. S., Wood, A. R., et al. (2019). Mosaic Turner syndrome shows reduced penetrance in an adult population study. Genetics in Medicine, 21(4), 877-886. https://doi.org/10.1038/s41436-018-0271-6
Schoemaker, M. J., Swerdlow, A. J., Higgins, C. D., et al.; United Kingdom Clinical Cytogenetics Group. (2008). Mortality in women with Turner syndrome in Great Britain: A national cohort study. The Journal of Clinical Endocrinology & Metabolism, 93(12), 4735-4742. https://doi.org/10.1210/jc.2008-1049
Papp, C., Beke, A., Mezei, G., et al. (2006). Prenatal diagnosis of Turner syndrome: Report on 69 cases. Journal of Ultrasound in Medicine, 25(6), 711-720. https://doi.org/10.7863/jum.2006.25.6.711
Gravholt, C. H., Andersen, N. H., Christin-Maitre, S., et al. (2024). Clinical practice guidelines for the care of girls and women with Turner syndrome. European Journal of Endocrinology, 190(6), G53-G151. https://doi.org/10.1093/ejendo/lvae050
Bryman, I., Sylvén, L., Berntorp, K., et al. (2011). Pregnancy rate and outcome in Swedish women with Turner syndrome. Fertility and Sterility, 95(8), 2507-2510. https://doi.org/10.1016/j.fertnstert.2010.12.039
Gravholt, C. H. (2005). Clinical practice in Turner syndrome. Nature Clinical Practice Endocrinology & Metabolism, 1(1), 41-52. https://doi.org/10.1038/ncpendmet0024
Cameron-Pimblett, A., La Rosa, C., King, T. F. J., et al. (2017). The Turner syndrome life course project: Karyotype-phenotype analyses across the lifespan. Clinical Endocrinology, 87(5), 532-538. https://doi.org/10.1111/cen.13394
Viuff, M., & Gravholt, C. H. (2022). Turner syndrome and fertility. Annales d’Endocrinologie, 83(4), 244-249. https://doi.org/10.1016/j.ando.2022.06.001
Visser, J. A., Hokken-Koelega, A. C., Zandwijken, G. R., et al. (2013). Anti-Müllerian hormone levels in girls and adolescents with Turner syndrome are related to karyotype, pubertal development and growth hormone treatment. Human Reproduction, 28(7), 1899-1907. https://doi.org/10.1093/humrep/det089
Plociennik, L., Nelson, S. M., Łukaszuk, A., et al. (2018). Age-related decline in AMH is assay dependent limiting clinical interpretation of repeat AMH measures across the reproductive lifespan. Gynecological Endocrinology, 34(2), 115-119. https://doi.org/10.1080/09513590.2017.1358708
Weenen, C., Laven, J. S., Von Bergh, A. R., et al. (2004). Anti-Müllerian hormone expression pattern in the human ovary: Potential implications for initial and cyclic follicle recruitment. Molecular Human Reproduction, 10(2), 77-83. https://doi.org/10.1093/molehr/gah015
Lunding, S. A., Aksglaede, L., Anderson, R. A., et al. (2015). AMH as predictor of premature ovarian insufficiency: A longitudinal study of 120 Turner syndrome patients. The Journal of Clinical Endocrinology & Metabolism, 100(7), E1030-E1038. https://doi.org/10.1210/jc.2015-1621
Visser, J. A., Hokken-Koelega, A. C., Zandwijken, G. R., et al. (2013). Anti-Müllerian hormone levels in girls and adolescents with Turner syndrome are related to karyotype, pubertal development and growth hormone treatment. Human Reproduction, 28(7), 1899-1907. https://doi.org/10.1093/humrep/det089
Nadesapillai, S., van der Velden, J., Braat, D., et al. (2021). The challenge of defining predictive parameters for fertility preservation counseling in young females with Turner syndrome. Acta Obstetricia et Gynecologica Scandinavica, 100(6), 1155-1156. https://doi.org/10.1111/aogs.14094
Chon, S. J., Umair, Z., & Yoon, M. S. (2021). Premature ovarian insufficiency: Past, present, and future. Frontiers in Cell and Developmental Biology, 9, 672890. https://doi.org/10.3389/fcell.2021.672890
Negreiros, L. P., Bolina, E. R., & Guimarães, M. M. (2014). Pubertal development profile in patients with Turner syndrome. Journal of Pediatric Endocrinology & Metabolism, 27(9-10), 845-849. https://doi.org/10.1515/jpem-2013-0256
Pasquino, A. M., Passeri, F., Pucarelli, I., et al. (1997). Spontaneous pubertal development in Turner's syndrome. Italian Study Group for Turner's Syndrome. The Journal of Clinical Endocrinology & Metabolism, 82(6), 1810-1813. https://doi.org/10.1210/jcem.82.6.3970
Ye, M., Yeh, J., Kosteria, I., et al. (2020). Progress in fertility preservation strategies in Turner syndrome. Frontiers in Medicine, 7, 3. https://doi.org/10.3389/fmed.2020.00003
Fukami, M. (2023). Ovarian dysfunction in women with Turner syndrome. Frontiers in Endocrinology, 14, 1160258. https://doi.org/10.3389/fendo.2023.1160258
Hreinsson, J. G., Otala, M., Fridström, M., et al. (2002). Follicles are found in the ovaries of adolescent girls with Turner's syndrome. The Journal of Clinical Endocrinology & Metabolism, 87(8), 3618-3623. https://doi.org/10.1210/jcem.87.8.8753
Reynaud, K., Cortvrindt, R., Verlinde, F., et al. (2004). Number of ovarian follicles in human fetuses with the 45,X karyotype. Fertility and Sterility, 81(4), 1112-1119. https://doi.org/10.1016/j.fertnstert.2003.12.011
Mamsen, L. S., Charkiewicz, K., Anderson, R. A., et al. (2019). Characterization of follicles in girls and young women with Turner syndrome who underwent ovarian tissue cryopreservation. Fertility and Sterility, 111(6), 1217-1225.e3. https://doi.org/10.1016/j.fertnstert.2019.02.003
Ramage, K., Grabowska, K., Silversides, C., et al. (2020). Maternal, pregnancy, and neonatal outcomes for women with Turner syndrome. Birth Defects Research, 112(14), 1067-1073. https://doi.org/10.1002/bdr2.1739
Bernard, V., Donadille, B., Zenaty, D., et al. (2016). Spontaneous fertility and pregnancy outcomes amongst 480 women with Turner syndrome. Human Reproduction, 31(4), 782-788. https://doi.org/10.1093/humrep/dew012
Cauldwell, M., Steer, P. J., Adamson, D., et al. (2022). Pregnancies in women with Turner syndrome: A retrospective multicentre UK study. BJOG, 129(5), 796-803. https://doi.org/10.1111/1471-0528.17025
Calanchini, M., Aye, C. Y. L., Orchard, E., et al. (2020). Fertility issues and pregnancy outcomes in Turner syndrome. Fertility and Sterility, 114(1), 144-154. https://doi.org/10.1016/j.fertnstert.2020.03.002
Quenby, S., Gallos, I. D., Dhillon-Smith, R. K., et al. (2021). Miscarriage matters: The epidemiological, physical, psychological, and economic costs of early pregnancy loss. Lancet, 397(10285), 1658-1667. https://doi.org/10.1016/S0140-6736(21)00682-6
Yaron, Y., Ochshorn, Y., Amit, A., et al. (1996). Patients with Turner's syndrome may have an inherent endometrial abnormality affecting receptivity in oocyte donation. Fertility and Sterility, 65(6), 1249-1252.
Porcu, E., Cipriani, L., & Damiano, G. (2023). Reproductive health in Turner's syndrome: From puberty to pregnancy. Frontiers in Endocrinology, 14, 1269009. https://doi.org/10.3389/fendo.2023.1269009
Gravholt, C. H., Andersen, N. H., Conway, G. S., et al. (2017). Clinical practice guidelines for the care of girls and women with Turner syndrome: Proceedings from the 2016 Cincinnati International Turner Syndrome Meeting. European Journal of Endocrinology, 177(3), G1-G70. https://doi.org/10.1530/EJE-17-0430
Practice Committee of the American Society for Reproductive Medicine. (2012). Increased maternal cardiovascular mortality associated with pregnancy in women with Turner syndrome. Fertility and Sterility, 97(2), 282-284. https://doi.org/10.1016/j.fertnstert.2011.11.049
Porcu, E., Cipriani, L., Dirodi, M., et al. (2022). Successful pregnancies, births, and children development following oocyte cryostorage in female cancer patients during 25 years of fertility preservation. Cancers, 14(6), 1429. https://doi.org/10.3390/cancers14061429
Solé, M., Santaló, J., Boada, M., et al. (2013). How does vitrification affect oocyte viability in oocyte donation cycles? A prospective study to compare outcomes achieved with fresh versus vitrified sibling oocytes. Human Reproduction, 28(8), 2087-2092. https://doi.org/10.1093/humrep/det242
Nadesapillai, S., Mol, F., Broer, S. L., et al. (2023). Reproductive outcomes of women with Turner syndrome undergoing oocyte vitrification: A retrospective multicenter cohort study. Journal of Clinical Medicine, 12(20), 6502. https://doi.org/10.3390/jcm12206502
Talaulikar, V. S., Conway, G. S., Pimblett, A., et al. (2019). Outcome of ovarian stimulation for oocyte cryopreservation in women with Turner syndrome. Fertility and Sterility, 111(3), 505-509. https://doi.org/10.1016/j.fertnstert.2018.11.010
Strypstein, L., Van Moer, E., Nekkebroeck, J., et al. (2022). First live birth after fertility preservation using vitrification of oocytes in a woman with mosaic Turner syndrome. Journal of Assisted Reproduction and Genetics, 39(2), 543-549. https://doi.org/10.1007/s10815-022-02420-4
Donnez, J., & Dolmans, M. M. (2015). Ovarian cortex transplantation: 60 reported live births brings the success and worldwide expansion of the technique towards routine clinical practice. Journal of Assisted Reproduction and Genetics, 32(8), 1167-1170. https://doi.org/10.1007/s10815-015-0544-9
Borgström, B., Hreinsson, J., Rasmussen, C., et al. (2009). Fertility preservation in girls with Turner syndrome: Prognostic signs of the presence of ovarian follicles [published correction appears in The Journal of Clinical Endocrinology & Metabolism, 94(4), 1478]. The Journal of Clinical Endocrinology & Metabolism, 94(1), 74-80. https://doi.org/10.1210/jc.2008-0708
Schleedoorn, M. J., Fleischer, K., Braat, D., et al. (2022). Why Turner patients with 45, X monosomy should not be excluded from fertility preservation services. Reproductive Biology and Endocrinology, 20(1), 143. https://doi.org/10.1186/s12958-022-01015-z
Peek, R., Schleedoorn, M., Smeets, D., et al. (2019). Ovarian follicles of young patients with Turner's syndrome contain normal oocytes but monosomic 45,X granulosa cells. Human Reproduction, 34(9), 1686-1696. https://doi.org/10.1093/humrep/dez135
Peek, R., Nadesapillai, S., Thi Nguyen, T. Y., et al. (2023). Assessment of folliculogenesis in ovarian tissue from young patients with Turner syndrome using a murine xenograft model. Fertility and Sterility, 120(2), 371-381. https://doi.org/10.1016/j.fertnstert.2023.04.008
Khastgir, G., Abdalla, H., Thomas, A., et al. (1997). Oocyte donation in Turner's syndrome: An analysis of the factors affecting the outcome. Human Reproduction, 12(2), 279-285. https://doi.org/10.1093/humrep/12.2.279
Press, F., Shapiro, H. M., Cowell, C. A., et al. (1995). Outcome of ovum donation in Turner's syndrome patients. Fertility and Sterility, 64(5), 995-998.
Stoop, D., Baumgarten, M., Haentjens, P., et al. (2012). Obstetric outcome in donor oocyte pregnancies
Mercadal, B. A., Imbert, R., Demeestere, I., et al. (2011). Pregnancy outcome after oocyte donation in patients with Turner’s syndrome and partial X monosomy. Human Reproduction, 26(8), 2061–2068. https://doi.org/10.1093/humrep/der166
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