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体外受精和卵胞浆内单精子注射受孕儿童的学龄期结局:一项使用全人群关联数据的因果推断分析。

School-age outcomes among IVF and ICSI-conceived children: a causal inference analysis using linked population-wide data.

作者信息

Kennedy Amber L, Hiscock Richard J, Vollenhoven Beverley J, Stern Catharyn J, Gurrin Lyle C, Osianlis Tiki, Kink Aleah, Walker Susan P, Cheong Jeanie L Y, Quach Jon L, Wilkinson David, McBain John, Green Mark P, Atkinson Jessica A, Agresta Franca, Baohm Susan P, Tong Stephen, Hastie Roxanne, Lindquist Anthea C

机构信息

Department of Obstetrics, Gynaecology and Newborn Health, University of Melbourne, Parkville, Melbourne, 3052, Australia.

Mercy Perinatal, Mercy Hospital for Women, Heidelberg, VIC, Australia.

出版信息

BMC Med. 2025 Apr 1;23(1):194. doi: 10.1186/s12916-025-03963-w.

Abstract

BACKGROUND

Use of intracytoplasmic sperm injection (ICSI) continues to increase as the most common mode of oocyte insemination during in vitro fertilisation (IVF), sometimes in the absence of clear indications (i.e. male factor infertility). Several studies suggest an increased risk of congenital abnormalities after ICSI. The association between the ICSI technique and long-term childhood development remains unclear.

METHODS

Our population-based study included singleton infants conceived via IVF and born between 2005 and 2013. The cohort included state-wide linked maternal and childhood administrative data from Victoria, Australia. The primary exposure was conception via ICSI (without severe male factor infertility), with those born following standard IVF as controls. Childhood development was examined using the Australian Early Development Census (AEDC), a broad assessment of childhood development across five domains of health and neurodevelopment performed in Australian schools every triennium at school entry (age 4-6 years). Our primary outcome used a validated global measure-developmental vulnerability-defined as scoring less than the 10th percentile in two or more of the five developmental domains (DV2). Causal inference methods were used to analyse observational data in a way that emulates a target randomised clinical trial. The adjustment variable set was determined a priori via a modified Delphi procedure. Given the use of observational data, there were missing data and inherent differences in the covariate profile between exposure cohorts. Multiple imputation, bootstrapping and doubly robust inverse probability weighted regression adjustment modelling was utilised to allow a causal interpretation of results.

RESULTS

Our cohort (N = 3656) included 1489 IVF and 2167 ICSI-conceived children. We found no causal effect of ICSI on the risk of AEDC-defined developmental vulnerability at school-entry age compared with children conceived via standard IVF; adjusted risk difference - 1.11% (95% CI - 4.23 to 2.01%) and adjusted risk ratio 0.90 (95% CI 0.68 to 1.21).

CONCLUSIONS

Our findings suggest that the use of ICSI in IVF cycles without severe male factor infertility does not increase the risk of early childhood developmental vulnerability among children in their first year of school. These findings provide important reassurance for current and prospective parents and clinicians alike.

摘要

背景

作为体外受精(IVF)期间最常见的卵母细胞授精方式,胞浆内单精子注射(ICSI)的使用持续增加,有时在没有明确指征的情况下(即男性因素不孕症)使用。多项研究表明,ICSI后先天性异常的风险增加。ICSI技术与儿童长期发育之间的关联仍不清楚。

方法

我们基于人群的研究纳入了2005年至2013年期间通过IVF受孕并出生的单胎婴儿。该队列包括来自澳大利亚维多利亚州的全州范围内关联的孕产妇和儿童管理数据。主要暴露因素是通过ICSI受孕(无严重男性因素不孕症),以标准IVF出生的婴儿作为对照。使用澳大利亚早期发展普查(AEDC)对儿童发育进行评估,这是一项对健康和神经发育五个领域的儿童发育进行的广泛评估,每三年在澳大利亚学校入学时(4至6岁)进行一次。我们的主要结局使用了一种经过验证的总体指标——发育易损性,定义为在五个发育领域中的两个或更多领域得分低于第10百分位数(DV2)。采用因果推断方法以模拟目标随机临床试验的方式分析观察性数据。通过改良的德尔菲程序预先确定调整变量集。鉴于使用的是观察性数据,暴露队列之间存在数据缺失和协变量特征的固有差异。采用多重填补、自助法和双重稳健逆概率加权回归调整模型,以便对结果进行因果解释。

结果

我们的队列(N = 3656)包括1489名IVF受孕儿童和2167名ICSI受孕儿童。我们发现,与通过标准IVF受孕的儿童相比,ICSI对入学年龄时AEDC定义的发育易损性风险没有因果效应;调整后的风险差异为 -1.11%(95% CI -4.23至2.01%),调整后的风险比为0.90(95% CI 0.68至1.21)。

结论

我们的研究结果表明,在没有严重男性因素不孕症的IVF周期中使用ICSI不会增加儿童入学第一年出现早期发育易损性的风险。这些发现为当前和未来的父母以及临床医生提供了重要的 reassurance。 (注:原文中“reassurance”未翻译,可能是因为其在医学语境中有特定含义,需结合上下文理解,此处保留英文供进一步参考,可根据实际情况补充合适的中文释义,比如“安心”等)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c222/11963277/5401aa423174/12916_2025_3963_Fig1_HTML.jpg

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