染色体易位携带者的生殖健康问题

Q4 Medicine
Yulia V. Shilenkova, A. Pendina, E. M. Fedorova, O. Efimova, O. Chiryaeva, L. Petrova, V. Dudkina, A. Tikhonov, A. Gzgzyan, O. Bespalova, I. Kogan
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引用次数: 0

摘要

背景:配偶中一方发生结构性染色体畸变是常见的多种生殖疾病,如不孕症、流产、辅助生殖技术尝试失败等。在这方面,预测一对特定夫妇的生育结果是一项极其困难的任务。要解决这一问题,需要考虑染色体易位类型和携带者性别等多种因素的影响。目的:评价一方为染色体易位携带者的夫妻生殖疾病的结构,这取决于其类型:罗伯逊型或互惠型,以及携带者的性别。材料与方法:在这项回顾性队列研究中,我们分析了100对夫妻的临床和记忆资料,其中一方是染色体易位携带者。夫妇们在2009年3月至2019年5月期间向生育中心提出申请。为了评估染色体易位类型和携带者性别的影响,我们进行了组间比较。结果:女性患者躯体病理与慢性妇科疾病比较分析,各组间差异无统计学意义(fisher精确检验,p < 0.05)。对按染色体易位类型(互惠型或罗伯逊型)和携带者性别划分的夫妇的生殖结果进行组间比较,发现了显著差异。携带男性易位携带者的夫妇原发性不孕症更常见,携带女性易位携带者的夫妇继发性不孕症更常见(fisher精确检验,p = 0.01)。女性携带反向或罗伯逊易位的夫妇的妊娠发生率明显更高,而且妊娠自然中断的几率也明显更高(2 = 13,29,df = 3, p = 0,004)。因此,携带染色体易位的女性流产的风险更大。结论:染色体易位类型和携带者性别对生殖障碍的性质有差异影响。携带染色体易位的女性增加了怀孕和自然终止的可能性。相比之下,在男性易位携带者的夫妇中,怀孕和流产的可能性都较低。因此,易位的类型和携带者的性别决定了个体的生殖障碍风险,包括不孕和流产,在计划、选择怀孕的开始方式和管理时应考虑到这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Issues in reproductive health in chromosome translocation carriers
BACKGROUND: It is common a wide range of reproductive disorders in couples with structural chromosome aberration in one of the partners, such as infertility, miscarriage, unsuccessful assisted reproductive technologies attempts. In this regard, predicting the reproductive outcome in a particular couple is an extremely difficult task. To solve it, it is necessary to consider the influence of many factors, including the type of chromosome translocation and the carriers sex. AIM: To evaluate the structure of reproductive disorders in couples where one of the partners was a chromosome translocation carrier, depending on its type: Robertsonian or reciprocal, and carriers sex. MATERIALS AND METHODS: In this retrospective cohort study, we analyzed the clinical and anamnestic data of 100 couples where one of the partners was a chromosome translocation carrier. Couples applied to fertility centers between March 2009 and May 2019. To assess the effect of the type of chromosomal translocation and carriers sex, we provided intergroup comparisons. RESULTS: Comparative analysis of somatic pathology and chronic gynecological diseases didnt reveal significant differences between groups of female patients (Fischers exact test, p 0,05). An intergroup comparison of reproductive outcomes in couples divided by the type of chromosome translocation: reciprocal or Robertsonian, and the carriers sex, detected significant differences. Primary infertility was significantly more often detected in couples with a male translocation carrier, secondary with a female carrier (Fishers exact test, p = 0,01). Pregnancy significantly more frequent occurred and, it was also significantly more often spontaneously interrupted in couples with a female carrying of reciprocal or Robertson translocation (2 = 13,29, df = 3, p = 0,004). Thus, a female carrying a chromosomal translocation is characterized by a greater risk of miscarriage. CONCLUSIONS: The chromosome translocation type and the carriers sex have a differential effect on the nature of reproductive disorders. Female carrying a chromosomal translocation increases the likelihood of both pregnancy and its spontaneous termination. In contrast, in couples with a male translocation carrier, the probability of both pregnancy and miscarriage is lower. Thus, the type of translocation and the carriers sex determine the individual risks of reproductive disorders, including infertility and miscarriage, which should be considered in the planning, choosing the method of onset and management of pregnancy.
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来源期刊
Journal of obstetrics and women's diseases
Journal of obstetrics and women's diseases Medicine-Obstetrics and Gynecology
CiteScore
0.40
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53
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