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通过辅助生殖技术受孕的 Beckwith-Wiedemann 综合征患者的临床和分子特征。

Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques.

机构信息

Department of Public Health and Pediatric Sciences, University of Torino, Torino, Italy.

Research Laboratory of Medical Cytogenetics and Molecular Genetics, IRCCS Istituto Auxologico Italiano, Milan, Italy.

出版信息

Clin Genet. 2022 Oct;102(4):314-323. doi: 10.1111/cge.14193. Epub 2022 Jul 21.

DOI:10.1111/cge.14193
PMID:35842840
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9545072/
Abstract

The prevalence of Beckwith-Wiedemann spectrum (BWSp) is tenfold increased in children conceived through assisted reproductive techniques (ART). More than 90% of ART-BWSp patients reported so far display imprinting center 2 loss-of-methylations (IC2-LoM), versus 50% of naturally conceived BWSp patients. We describe a cohort of 74 ART-BWSp patients comparing their features with a cohort of naturally conceived BWSp patients, with the ART-BWSp patients previously described in literature, and with the general population of children born from ART. We found that the distribution of UPD(11)pat was not significantly different in ART and naturally conceived patients. We observed 68.9% of IC2-LoM and 16.2% of mosaic UPD(11)pat in our ART cohort, that strongly differ from the figure reported in other cohorts so far. Since UPD(11)pat likely results from post-fertilization recombination events, our findings allows to hypothesize that more complex molecular mechanisms, besides methylation disturbances, may underlie BWSp increased risk in ART pregnancies. Moreover, comparing the clinical features of ART and non-ART BWSp patients, we found that ART-BWSp patients might have a milder phenotype. Finally, our data show a progressive increase in the prevalence of BWSp over time, paralleling that of ART usage in the last decades.

摘要

贝克威思-威德曼综合征(BWSp)的患病率在通过辅助生殖技术(ART)受孕的儿童中增加了十倍。迄今为止,报道的超过 90%的 ART-BWSp 患者显示印迹中心 2 缺失甲基化(IC2-LoM),而自然受孕的 BWSp 患者为 50%。我们描述了一组 74 名 ART-BWSp 患者,将他们的特征与一组自然受孕的 BWSp 患者、文献中描述的 ART-BWSp 患者以及通过 ART 出生的儿童的一般人群进行了比较。我们发现,ART 和自然受孕患者的 UPD(11)pat 分布没有显著差异。我们在 ART 队列中观察到 68.9%的 IC2-LoM 和 16.2%的镶嵌 UPD(11)pat,与迄今为止其他队列报告的数字有很大不同。由于 UPD(11)pat 可能是受精后重组事件的结果,我们的发现表明,除了甲基化紊乱之外,可能还有更复杂的分子机制导致 ART 妊娠中 BWSp 风险增加。此外,比较 ART 和非 ART BWSp 患者的临床特征,我们发现 ART-BWSp 患者的表型可能更轻微。最后,我们的数据显示,BWSp 的患病率随着时间的推移呈逐渐增加的趋势,与过去几十年中 ART 的使用情况平行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d47/9545072/e2c21ce19ee2/CGE-102-314-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d47/9545072/8127c4fe7119/CGE-102-314-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d47/9545072/e2c21ce19ee2/CGE-102-314-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d47/9545072/8127c4fe7119/CGE-102-314-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d47/9545072/e2c21ce19ee2/CGE-102-314-g001.jpg

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Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance.
Nat Rev Dis Primers. 2023 Jun 29;9(1):33. doi: 10.1038/s41572-023-00443-4.
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