Fertility issues and pregnancy outcomes in Turner syndrome

被引:45
作者
Calanchini, Matilde [1 ,2 ]
Aye, Christina Y. L. [3 ,4 ]
Orchard, Elizabeth [5 ]
Baker, Kathy [6 ]
Child, Tim [4 ,6 ]
Fabbri, Andrea [2 ]
Mackillop, Lucy [3 ,4 ]
Turner, Helen E. [1 ]
机构
[1] Oxford Univ Hosp NHS Trust, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[2] Univ Roma Tor Vergata, CTO Hosp, Endocrinol & Metab Unit, Dept Syst Med, Rome, Italy
[3] Oxford Univ Hosp NHS Fdn Trust, Womens Ctr, Fetal Maternal Med Unit, Oxford, England
[4] Univ Oxford, Nuffield Dept Womens & Reprod Hlth, Oxford, England
[5] Oxford Univ Hosp NHS Trust, ACHD Cardiol, Oxford, England
[6] Inst Reprod Sci, Oxford Fertil, Oxford, England
关键词
Turner syndrome; pregnancy outcome; spontaneous pregnancy; aortic dissection; OOCYTE DONATION; CARDIOVASCULAR RISK; WOMEN; DISSECTION;
D O I
10.1016/j.fertnstert.2020.03.002
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To study fertility issues and pregnancy outcomes in Turner syndrome (TS). Design: Retrospective cohort study. Setting: Not applicable. Patient(s): One hundred fifty-six TS patients, median age 32 years, 23 mosaic 45,X/46,XX, 45,X/47,XXX, 45,X/46,XX/47,XXX. Intervention(s): None. Main Outcome Measure(s): Fertility choices, spontaneous pregnancy, and oocyte donation (OD) outcomes. Conditions associated with aortic dissection and poor pregnancy outcomes at preconception were considered. Pregnancy -related aortic dimension changes and the long-term impact of pregnancy on TS -related comorbidities were assessed. Results(s): In all, 13.5% had spontaneous pregnancies, resulting in a pregnancy with live birth in 18 patients (37 newborns); 16% considered OD, one adopted, and one underwent fertility preservation. Spontaneous pregnancy predictive factors were a karyotype with a second or third cell line with more than one X and spontaneous menarche. In all, 47.6% had miscarriages, two experienced preeclampsia, and two had gestational diabetes. One daughter was diag- nosed with TS in adulthood. Seven of 14 who attempted OD had a pregnancy with live birth; two of seven had gestational diabetes; 64.3% attempting OD had risk factors associated with poor pregnancy outcomes, including four who had double embryo transfer. Cardiac status at preconception was evaluated in 12 of 25 women who had a pregnancy. The aortic diameters during pregnancy increased. The aortic growth at sinuses was 0.51 ? 0.71 mm/year and at ascending aorta 0.67 ? 0.67 mm/year, reaching a signi ficant difference at sinuses compared with the growth in nulliparous TS. Among women who had a pregnancy, none experienced aortic dissection during and in the years after pregnancy. Conclusion(s): This study highlights the importance of a TS -dedicated multidisciplinary management of pregnancy, before and during pregnancy and in the postpartum period. (Fertil Steril (R) 2020;114:144-54. (C) 2020 by American Society for Reproductive Medicine.)
引用
收藏
页码:144 / 154
页数:11
相关论文
共 51 条
  • [31] Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review
    Martin, Richard J.
    Smith, Geoff
    Hughes, James
    Morrison, Patrick J.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (04) : 1029 - 1029
  • [32] Aortic dilatation and dissection in Turner syndrome
    Matura, Lea Ann
    Ho, Vincent B.
    Rosing, Douglas R.
    Bondy, Carolyn A.
    [J]. CIRCULATION, 2007, 116 (15) : 1663 - 1670
  • [33] A Spontaneous Pregnancy in a Patient with Turner Syndrome with 45,X/47,XXX Mosaicism: A Case Report and Review of the Literature
    Mavridi, Artemis
    Ntali, Georgia
    Theodora, Marianna
    Stamatelopoulos, Kimon
    Michala, Lina
    [J]. JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY, 2018, 31 (06) : 651 - 654
  • [34] Pregnancy outcome after oocyte donation in patients with Turner's syndrome and partial X monosomy
    Mercadal, B. Alvaro
    Imbert, R.
    Demeestere, I.
    Englert, Y.
    Delbaere, A.
    [J]. HUMAN REPRODUCTION, 2011, 26 (08) : 2061 - 2068
  • [35] Fertility counseling and preservation discussions for females with Turner syndrome in pediatric centers: practice patterns and predictors
    Morgan, Taylor L.
    Kapa, Hillary M.
    Crerand, Canice E.
    Kremen, Jessica
    Tishelman, Amy
    Davis, Shanlee
    Nahata, Leena
    [J]. FERTILITY AND STERILITY, 2019, 112 (04) : 740 - 748
  • [36] Increased prevalence of autoimmunity in Turner syndrome - influence of age
    Mortensen, K. H.
    Cleemann, L.
    Hjerrild, B. E.
    Nexo, E.
    Locht, H.
    Jeppesen, E. M.
    Gravholt, C. H.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2009, 156 (02) : 205 - 210
  • [37] Cardiovascular Phenotype in Turner Syndrome-Integrating Cardiology, Genetics, and Endocrinology
    Mortensen, Kristian H.
    Andersen, Niels H.
    Gravholt, Claus H.
    [J]. ENDOCRINE REVIEWS, 2012, 33 (05) : 677 - 714
  • [38] Physiological sex steroid replacement in premature ovarian failure: randomized crossover trial of effect on uterine volume, endometrial thickness and blood flow, compared with a standard regimen
    O'Donnell, R. L.
    Warner, P.
    Lee, R. J.
    Walker, J.
    Bath, L. E.
    Kelnar, C. J.
    Wallace, W. H. B.
    Critchley, H. O. D.
    [J]. HUMAN REPRODUCTION, 2012, 27 (04) : 1130 - 1138
  • [39] Fertility preservation in girls with Turner syndrome: limitations, current success and future prospects
    Oktay, Kutluk
    Bedoschi, Giuliano
    [J]. FERTILITY AND STERILITY, 2019, 111 (06) : 1124 - 1126
  • [40] Spontaneous pubertal development in Turner's syndrome
    Pasquino, AM
    Passeri, F
    Pucarelli, I
    Segni, M
    Municchi, G
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (06) : 1810 - 1813