Morphological and morphokinetic associations with aneuploidy: a systematic review and meta-analysis.

IF 14.8 1区 医学 Q1 OBSTETRICS & GYNECOLOGY
Thomas Bamford, Amy Barrie, Sue Montgomery, Rima Dhillon-Smith, Alison Campbell, Christina Easter, Arri Coomarasamy
{"title":"Morphological and morphokinetic associations with aneuploidy: a systematic review and meta-analysis.","authors":"Thomas Bamford,&nbsp;Amy Barrie,&nbsp;Sue Montgomery,&nbsp;Rima Dhillon-Smith,&nbsp;Alison Campbell,&nbsp;Christina Easter,&nbsp;Arri Coomarasamy","doi":"10.1093/humupd/dmac022","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>A time lapse system (TLS) is utilized in some fertility clinics with the aim of predicting embryo viability and chance of live birth during IVF. It has been hypothesized that aneuploid embryos display altered morphokinetics as a consequence of their abnormal chromosome complement. Since aneuploidy is one of the fundamental reasons for IVF failure and miscarriage, attention has focused on utilizing morphokinetics to develop models to non-invasively risk stratify embryos for ploidy status. This could avoid or reduce the costs associated with pre-implantation genetic testing for aneuploidy (PGT-A). Furthermore, TLS have provided an understanding of the true prevalence of other dysmorphisms. Hypothetically, the incorporation of morphological features into a model could act synergistically, improving a model's discriminative ability to predict ploidy status.</p><p><strong>Objective and rationale: </strong>The aim of this systematic review and meta-analysis was to investigate associations between ploidy status and morphokinetic or morphological features commonly denoted on a TLS. This will determine the feasibility of a prediction model for euploidy and summarize the most useful prognostic markers to be included in model development.</p><p><strong>Search methods: </strong>Five separate searches were conducted in Medline, Embase, PubMed and Cinahl from inception to 1 July 2021. Search terms and word variants included, among others, PGT-A, ploidy, morphokinetics and time lapse, and the latter were successively substituted for the following morphological parameters: fragmentation, multinucleation, abnormal cleavage and contraction. Studies were limited to human studies.</p><p><strong>Outcomes: </strong>Overall, 58 studies were included incorporating over 40 000 embryos. All except one study had a moderate risk of bias in at least one domain when assessed by the quality in prognostic studies tool. Ten morphokinetic variables were significantly delayed in aneuploid embryos. When excluding studies using less reliable genetic technologies, the most notable variables were: time to eight cells (t8, 1.13 h, 95% CI: 0.21-2.05; three studies; n = 742; I2 = 0%), t9 (2.27 h, 95% CI: 0.5-4.03; two studies; n = 671; I2 = 33%), time to formation of a full blastocyst (tB, 1.99 h, 95% CI 0.15-3.81; four studies; n = 1640; I2 = 76%) and time to expanded blastocyst (tEB, 2.35 h, 95% CI: 0.06-4.63; four studies; n = 1640; I2 = 83%). There is potentially some prognostic potential in the degree of fragmentation, multinucleation persisting to the four-cell stage and frequency of embryo contractions. Reverse cleavage was associated with euploidy in this meta-analysis; however, this article argues that these are likely spurious results requiring further investigation. There was no association with direct unequal cleavage in an embryo that progressed to a blastocyst, or with multinucleation assessed on Day 2 or at the two-cell stage. However, owing to heterogeneous results and poor-quality evidence, associations between these morphological components needs to be investigated further before conclusions can be reliably drawn.</p><p><strong>Wider implications: </strong>This first systematic review and meta-analysis of morphological and morphokinetic associations with ploidy status demonstrates the most useful morphokinetic variables, namely t8, t9 and tEB to be included in future model development. There is considerable variability within aneuploid and euploid embryos making definitively classifying them impossible; however, it is feasible that embryos could be prioritized for biopsy. Furthermore, these results support the mechanism by which algorithms for live birth may have predictive ability, suggesting aneuploidy causes delayed cytokinesis. We highlight significant heterogeneity in our results secondary to local conditions and diverse patient populations, therefore calling for future models to be robustly developed and tested in-house. If successful, such a model would constitute a meaningful breakthrough when accessing PGT-A is unsuitable for couples.</p>","PeriodicalId":55045,"journal":{"name":"Human Reproduction Update","volume":"28 5","pages":"656-686"},"PeriodicalIF":14.8000,"publicationDate":"2022-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Reproduction Update","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/humupd/dmac022","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 14

Abstract

Background: A time lapse system (TLS) is utilized in some fertility clinics with the aim of predicting embryo viability and chance of live birth during IVF. It has been hypothesized that aneuploid embryos display altered morphokinetics as a consequence of their abnormal chromosome complement. Since aneuploidy is one of the fundamental reasons for IVF failure and miscarriage, attention has focused on utilizing morphokinetics to develop models to non-invasively risk stratify embryos for ploidy status. This could avoid or reduce the costs associated with pre-implantation genetic testing for aneuploidy (PGT-A). Furthermore, TLS have provided an understanding of the true prevalence of other dysmorphisms. Hypothetically, the incorporation of morphological features into a model could act synergistically, improving a model's discriminative ability to predict ploidy status.

Objective and rationale: The aim of this systematic review and meta-analysis was to investigate associations between ploidy status and morphokinetic or morphological features commonly denoted on a TLS. This will determine the feasibility of a prediction model for euploidy and summarize the most useful prognostic markers to be included in model development.

Search methods: Five separate searches were conducted in Medline, Embase, PubMed and Cinahl from inception to 1 July 2021. Search terms and word variants included, among others, PGT-A, ploidy, morphokinetics and time lapse, and the latter were successively substituted for the following morphological parameters: fragmentation, multinucleation, abnormal cleavage and contraction. Studies were limited to human studies.

Outcomes: Overall, 58 studies were included incorporating over 40 000 embryos. All except one study had a moderate risk of bias in at least one domain when assessed by the quality in prognostic studies tool. Ten morphokinetic variables were significantly delayed in aneuploid embryos. When excluding studies using less reliable genetic technologies, the most notable variables were: time to eight cells (t8, 1.13 h, 95% CI: 0.21-2.05; three studies; n = 742; I2 = 0%), t9 (2.27 h, 95% CI: 0.5-4.03; two studies; n = 671; I2 = 33%), time to formation of a full blastocyst (tB, 1.99 h, 95% CI 0.15-3.81; four studies; n = 1640; I2 = 76%) and time to expanded blastocyst (tEB, 2.35 h, 95% CI: 0.06-4.63; four studies; n = 1640; I2 = 83%). There is potentially some prognostic potential in the degree of fragmentation, multinucleation persisting to the four-cell stage and frequency of embryo contractions. Reverse cleavage was associated with euploidy in this meta-analysis; however, this article argues that these are likely spurious results requiring further investigation. There was no association with direct unequal cleavage in an embryo that progressed to a blastocyst, or with multinucleation assessed on Day 2 or at the two-cell stage. However, owing to heterogeneous results and poor-quality evidence, associations between these morphological components needs to be investigated further before conclusions can be reliably drawn.

Wider implications: This first systematic review and meta-analysis of morphological and morphokinetic associations with ploidy status demonstrates the most useful morphokinetic variables, namely t8, t9 and tEB to be included in future model development. There is considerable variability within aneuploid and euploid embryos making definitively classifying them impossible; however, it is feasible that embryos could be prioritized for biopsy. Furthermore, these results support the mechanism by which algorithms for live birth may have predictive ability, suggesting aneuploidy causes delayed cytokinesis. We highlight significant heterogeneity in our results secondary to local conditions and diverse patient populations, therefore calling for future models to be robustly developed and tested in-house. If successful, such a model would constitute a meaningful breakthrough when accessing PGT-A is unsuitable for couples.

形态学和形态动力学与非整倍体的关联:系统回顾和荟萃分析。
背景:一些生育诊所使用延时系统(TLS)来预测体外受精过程中胚胎活力和活产机会。据推测,非整倍体胚胎由于染色体补体异常而表现出形态动力学的改变。由于非整倍性是试管婴儿失败和流产的根本原因之一,人们关注的焦点是利用形态动力学建立模型来无创地分层胚胎的倍性状态。这可以避免或减少与非整倍体(PGT-A)植入前基因检测相关的费用。此外,TLS还提供了对其他畸形的真正流行的理解。假设形态学特征融入模型可以协同作用,提高模型预测倍性状态的判别能力。目的和理由:本系统综述和荟萃分析的目的是研究倍性状态与TLS上通常表示的形态动力学或形态特征之间的关系。这将确定整倍体预测模型的可行性,并总结在模型开发中包含的最有用的预后标记。检索方法:自成立至2021年7月1日,在Medline、Embase、PubMed和Cinahl中进行了五次独立检索。搜索词和词变体包括PGT-A、ploidy、morphokinetics和time lapse等,后者依次替换为以下形态学参数:片段化、多核化、异常卵裂和收缩。研究仅限于人体研究。结果:总的来说,58项研究纳入了超过40000个胚胎。当使用预后研究质量工具进行评估时,除一项研究外,所有研究在至少一个领域存在中等偏倚风险。10个形态动力学变量在非整倍体胚胎中显著延迟。当排除使用不太可靠的基因技术的研究时,最显著的变量是:8个细胞的时间(8,1.13 h, 95% CI: 0.21-2.05;三个研究;n = 742;I2 = 0%), t9 (2.27 h, 95% CI: 0.5-4.03;两项研究;n = 671;I2 = 33%),形成完整囊胚所需时间(tB, 1.99 h, 95% CI 0.15-3.81;四个研究;n = 1640;I2 = 76%)和囊胚膨大时间(tEB, 2.35 h, 95% CI: 0.06-4.63;四个研究;n = 1640;i2 = 83%)。在分裂程度、多核持续到四细胞阶段和胚胎收缩频率方面有潜在的一些预后潜力。在本荟萃分析中,反向切割与整倍体相关;然而,本文认为,这些可能是虚假的结果,需要进一步调查。在发育为囊胚的胚胎中,或在第2天或双细胞期评估的多核,与直接不均匀分裂没有关联。然而,由于结果异质性和证据质量差,这些形态学成分之间的关联需要进一步研究才能得出可靠的结论。更广泛的影响:这是第一次对形态和形态动力学与倍性状态关联的系统回顾和荟萃分析,证明了最有用的形态动力学变量,即t8、t9和tEB,将包括在未来的模型开发中。在非整倍体和整倍体胚胎中存在相当大的变异性,因此不可能对它们进行明确的分类;然而,胚胎优先进行活检是可行的。此外,这些结果支持活产算法可能具有预测能力的机制,表明非整倍体导致细胞分裂延迟。我们强调了我们的结果与当地条件和不同患者群体相关的显著异质性,因此要求未来的模型在内部进行强有力的开发和测试。如果成功,这种模式将在不适合夫妇使用PGT-A的情况下构成有意义的突破。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Human Reproduction Update
Human Reproduction Update 医学-妇产科学
CiteScore
28.80
自引率
1.50%
发文量
38
期刊介绍: Human Reproduction Update is the leading journal in its field, boasting a Journal Impact FactorTM of 13.3 and ranked first in Obstetrics & Gynecology and Reproductive Biology (Source: Journal Citation ReportsTM from Clarivate, 2023). It specializes in publishing comprehensive and systematic review articles covering various aspects of human reproductive physiology and medicine. The journal prioritizes basic, transitional, and clinical topics related to reproduction, encompassing areas such as andrology, embryology, infertility, gynaecology, pregnancy, reproductive endocrinology, reproductive epidemiology, reproductive genetics, reproductive immunology, and reproductive oncology. Human Reproduction Update is published on behalf of the European Society of Human Reproduction and Embryology (ESHRE), maintaining the highest scientific and editorial standards.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信