Constructing a predictive model for live birth following fresh embryo transfer in antagonist protocol for polycystic ovary syndrome.

IF 3.2 3区 医学 Q2 GENETICS & HEREDITY
Suqin Zhu, Xiaojing Chen, Rongshan Li, Wenwen Jiang, Beihong Zheng, Yan Sun
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引用次数: 0

Abstract

Objective: The present research aims to assess the factors that influence live birth outcomes following fresh embryo transfers using antagonist protocols in individuals diagnosed with polycystic ovary syndrome (PCOS). Furthermore, it seeks to develop a predictive nomogram model to facilitate clinical decision-making and provide personalized treatment strategies.

Methods: This retrospective cohort research analyzed the clinical data of 1242 individuals having PCOS who went through fresh embryo transfers employing antagonist protocols and in vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) at Fujian Provincial Maternal and Child Health Hospital between January 2018 and December 2022. Individuals were assigned randomly to a modeling group (869 cases) and a validation group (373 cases) in a 7:3 ratio. The Boruta algorithm and multivariable logistic regression were utilized to identify independent risk factors linked to live births after transfer. A predictive nomogram was subsequently developed. The discriminatory power of the model and its accuracy were monitored by utilizing receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis.

Results: Multivariable logistic regression analysis identified several independent factors that influence live birth rates in fresh embryo transfer cycles for individuals having PCOS using antagonist protocols, including female age, body mass index (BMI), infertility duration, serum testosterone levels, progesterone levels at the time of human chorionic gonadotropin (hCG) injection, number of high-quality cleavage-stage embryos, type of embryo transferred, and the total number of embryos transferred. Based on these findings, a predictive nomogram was developed. The area under the ROC curve stood at 0.804 (95% confidence interval (CI), 0.775-0.833) for the modeling group and 0.807 (95% CI, 0.762-0.851) for the validation group. Calibration curves confirmed that the predictions of the nomogram closely matched the actual live birth outcomes. Decision curve analysis highlighted that the model provides significant net benefits for predicting live birth rates, with optimal performance across a probability range of 16.5 to 88.6%.

Conclusion: Independent factors, including female age, infertility duration, BMI, serum testosterone levels, progesterone levels on the day of hCG injection, and the number and type of high-quality cleavage-stage embryos transferred are pivotal in influencing live birth outcomes in fresh embryo transfer cycles under antagonist protocols in individuals with PCOS undergoing IVF/ICSI treatments. The predictive nomogram developed from these factors offers substantial predictive accuracy and clinical utility, providing a reliable basis for clinical prognosis, targeted interventions, and the development of personalized treatment plans.

Abstract Image

构建多囊卵巢综合征拮抗剂方案中新鲜胚胎移植后活产的预测模型。
研究目的本研究旨在评估影响多囊卵巢综合征(PCOS)患者使用拮抗剂方案进行新鲜胚胎移植后活产结果的因素。此外,本研究还试图开发一个预测性提名图模型,以促进临床决策并提供个性化治疗策略:这项回顾性队列研究分析了2018年1月至2022年12月期间福建省妇幼保健院采用拮抗剂方案和体外受精/卵胞浆内单精子注射(IVF/ICSI)进行鲜胚移植的1242名多囊卵巢综合征患者的临床数据。受试者按7:3的比例随机分配到建模组(869例)和验证组(373例)。利用 Boruta 算法和多变量逻辑回归来确定与转院后活产相关的独立风险因素。随后制定了预测提名图。利用接收者操作特征曲线(ROC)、校准曲线和决策曲线分析,对模型的判别能力及其准确性进行了监测:多变量逻辑回归分析确定了影响多囊卵巢综合症患者使用拮抗剂方案进行新鲜胚胎移植周期中活产儿率的几个独立因素,包括女性年龄、体重指数(BMI)、不孕症持续时间、血清睾酮水平、注射人绒毛膜促性腺激素(hCG)时的孕酮水平、优质分裂期胚胎数量、移植胚胎类型和移植胚胎总数。根据这些研究结果,绘制了预测提名图。建模组的 ROC 曲线下面积为 0.804(95% 置信区间 (CI),0.775-0.833),验证组的 ROC 曲线下面积为 0.807(95% 置信区间 (CI),0.762-0.851)。校准曲线证实,提名图的预测结果与实际活产结果非常吻合。决策曲线分析表明,该模型在预测活产率方面具有显著的净效益,在 16.5% 到 88.6% 的概率范围内具有最佳性能:包括女性年龄、不孕持续时间、体重指数、血清睾酮水平、注射 hCG 当天的孕酮水平以及移植的高质量裂解期胚胎的数量和类型在内的独立因素,对接受体外受精/卵子显微注射治疗的多囊卵巢综合征患者在拮抗剂方案下的新鲜胚胎移植周期中的活产结果具有关键影响。根据这些因素制定的预测提名图具有很高的预测准确性和临床实用性,为临床预后、针对性干预和制定个性化治疗方案提供了可靠的依据。
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来源期刊
CiteScore
5.70
自引率
9.70%
发文量
286
审稿时长
1 months
期刊介绍: The Journal of Assisted Reproduction and Genetics publishes cellular, molecular, genetic, and epigenetic discoveries advancing our understanding of the biology and underlying mechanisms from gametogenesis to offspring health. Special emphasis is placed on the practice and evolution of assisted reproduction technologies (ARTs) with reference to the diagnosis and management of diseases affecting fertility. Our goal is to educate our readership in the translation of basic and clinical discoveries made from human or relevant animal models to the safe and efficacious practice of human ARTs. The scientific rigor and ethical standards embraced by the JARG editorial team ensures a broad international base of expertise guiding the marriage of contemporary clinical research paradigms with basic science discovery. JARG publishes original papers, minireviews, case reports, and opinion pieces often combined into special topic issues that will educate clinicians and scientists with interests in the mechanisms of human development that bear on the treatment of infertility and emerging innovations in human ARTs. The guiding principles of male and female reproductive health impacting pre- and post-conceptional viability and developmental potential are emphasized within the purview of human reproductive health in current and future generations of our species. The journal is published in cooperation with the American Society for Reproductive Medicine, an organization of more than 8,000 physicians, researchers, nurses, technicians and other professionals dedicated to advancing knowledge and expertise in reproductive biology.
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