首页> 外文期刊>Journal of genetic counseling >Longitudinal Interviews of Couples Diagnosed with Diminished Ovarian Reserve Undergoing Fragile X Premutation Testing
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Longitudinal Interviews of Couples Diagnosed with Diminished Ovarian Reserve Undergoing Fragile X Premutation Testing

机译:经易碎X预突变测试诊断为卵巢储备减少的夫妇的纵向访谈

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About 10 % of infertile/subfertile women are diagnosed with diminished ovarian reserve (DOR), of which< 5 % will become pregnant spontaneously. Fragile X (FMR1) genetic testing may provide a reason for her early ovarian aging and/or have reproductive implications. Seven women with DOR (genetic study subset) and the male partners of six of these women were separately interviewed about the experience of being asked to undergo this unanticipated genetic test. Three interviews were conducted (before, within 1 week after, and 3 months after learning the test results). None of the participants carried the FMR1 premutation (largest FMR1 allele 27–50 CGG repeats). For women, their pregnancy-seeking journey was long and exhausting. Women understood the reproductive implications of carrying the FMR1 premutation, and hoped for a negative result. Being offered a genetic test caused women to pause and re-think their future reproductive plans. Husbands viewed the infertility journey as filled with unknowns, of which the genetic test results would be one more puzzle piece. The expense of fertility testing/treatment was mentioned by both spouses, though more notably by husbands. The introduction of a possible genetic cause of infertility, with additional potential health consequences for future biological children, caused women to re-think their quest for pregnancy. In contrast, the genetic test was viewed as an additional source of information for their husbands as opposed to raising concern regarding potential reproductive ramifications.
机译:大约10%的不育/不育妇女被诊断出卵巢储备(DOR)减少,其中<5%会自然怀孕。易碎X(FMR1)基因检测可能为她的卵巢早衰提供了原因和/或对生殖有影响。分别采访了七名患有DOR(遗传研究子集)的女性和其中六名女性的男性伴侣,以了解他们被要求接受这项意外的基因测试的经历。进行了三个访谈(在学习测试结果之前,之后的1周内和之后的3个月内)。没有参与者进行FMR1突变(最大的FMR1等位基因27–50 CGG重复)。对于女性而言,她们的寻求怀孕旅程漫长而费力。妇女了解携带FMR1突变对生殖的影响,并希望取得阴性结果。被提供基因测试导致女性停顿并重新考虑其未来的生殖计划。丈夫认为不育之旅充满了未知数,其中的基因检测结果将是另一个难题。夫妻双方都提到了生育力测试/治疗的费用,尽管丈夫尤其如此。可能的不育遗传原因的引入,以及对未来生孩子的健康的潜在潜在影响,促使妇女重新考虑寻求怀孕的机会。相反,基因测试被视为丈夫的另一信息来源,而不是引起人们对潜在生殖后果的关注。

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