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Onco-fertility and personalized testing for potential for loss of ovarian reserve in patients undergoing chemotherapy: proposed next steps for development of genetic testing to predict changes in ovarian reserve

机译:在进行化疗的患者卵巢储备损失潜力的卵反生能力和个性化测试:提出了遗传检测的下一步,以预测卵巢储备的变化

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Women of reproductive age undergoing chemotherapy face the risk of irreversible ovarian insufficiency. Current methods of ovarian reserve testing do not accurately predict future reproductive potential for patients undergoing chemotherapy. Genetic markers that more accurately predict the reproductive potential of each patient undergoing chemotherapy would be critical tools that would be useful for evidence-based fertility preservation counselling. To assess the possible approaches to take to develop personalized genetic testing for these patients, we review current literature regarding mechanisms of ovarian damage due to chemotherapy and genetic variants associated with both the damage mechanisms and primary ovarian insufficiency. The medical literature point to a number of genetic variants associated with mechanisms of ovarian damage and primary ovarian insufficiency. Those variants that appear at a higher frequency, with known pathways, may be considered as potential genetic markers for predictive ovarian reserve testing. We propose developing personalized testing of the potential for loss of ovarian function for patients with cancer, prior to chemotherapy treatment. There are advantages of using genetic markers complementary to the current ovarian reserve markers of AMH, antral follicle count and day 3 FSH as predictors of preservation of fertility after chemotherapy. Genetic markers will help identify upstream pathways leading to high risk of ovarian failure not detected by present clinical markers. Their predictive value is mechanism-based and will encourage research towards understanding the multiple pathways contributing to ovarian failure after chemotherapy.
机译:经历化疗的生殖年龄的妇女面临不可逆的卵巢功能不全的风险。目前的卵巢储备测试方法不准确地预测经过化疗的患者的未来生殖潜力。遗传标记更准确地预测经历化疗的每位患者的生殖潜力将是对基于证据的生育保存咨询有用的关键工具。为了评估为这些患者制定个性化遗传学检测的可能方法,我们审查了当前有关卵巢损伤机制,由于损伤机制和原发性卵巢功能不全相关的化疗和遗传变异。医学文献指向许多与卵巢损伤机制相关的遗传变异,原发性卵巢功能不全。具有已知途径的较高频率的那些变体可以被认为是用于预测卵巢储备测试的潜在遗传标记。在化疗治疗之前,我们建议开发对癌症患者的卵巢功能丧失的个性化测试。使用遗传标记与当前卵巢储备标志物互补的遗传标记,AMH,Antral卵泡计数和第3天FSH作为化疗后生育能力的预测因素。遗传标记将有助于识别上游途径,导致目前临床标记未检测到未检测到的卵巢衰竭的高风险。他们的预测价值是基于机制的,并鼓励研究化疗后有助于卵巢衰竭的多种途径。

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