INSERM UMR 1231, Equipe 'Génétique des Anomalies du Développement', Université de Bourgogne Franche-Comté, Dijon, France.
Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement, Centre Hospitalier Universitaire de Dijon Bourgogne, Dijon, France.
Ultrasound Obstet Gynecol. 2022 Apr;59(4):532-542. doi: 10.1002/uog.23715. Epub 2022 Mar 10.
To describe clinical and molecular findings in a French multicenter cohort of fetuses with prenatal diagnosis of congenital abnormality and suspicion of a localized overgrowth disorder (LOD) suggestive of genetic variants in the PI3K-AKT-mTOR signaling pathway.
We analyzed retrospectively data obtained between 1 January 2013 and 1 May 2020 from fetuses with brain and/or limb overgrowth referred for molecular diagnosis of PI3K-AKT-mTOR pathway genes by next-generation sequencing (NGS) using pathological tissue obtained by fetal autopsy. We also assessed the diagnostic yield of amniotic fluid.
During the study period, 21 subjects with LOD suspected of being secondary to a genetic variant of the PI3K-AKT-mTOR pathway were referred for analysis. Of these, 17 fetuses had brain overgrowth, including six with isolated megalencephaly (MEG) and 11 with hemimegalencephaly (HMEG). Of the six with MEG, germline variants were identified in four cases, in either PIK3R2, AKT3 or MTOR, and a postzygotic PIK3R2 variant was found in the other two cases. Of the 11 with HMEG, a postzygotic PIK3CA variant was found in three fetuses with extracerebral features of PIK3CA-related overgrowth spectrum, and in seven fetuses with isolated HMEG. No pathogenic variant was identified in the 11 case with HMEG. Four fetuses with limb overgrowth also had one or more lymphatic malformations (LM) and harbored a postzygotic PIK3CA variant. NGS on cultured amniocytes performed in 10 cases, of which nine had been found positive on analysis of pathological fetal tissue, showed variants in four, in either PIK3CA, PIK3R2 or AKT3.
Isolated MEG or HMEG may lead to identification of genetic variants in the PI3K-AKT-mTOR signaling pathway. Cases of limb overgrowth and LM or isolated HMEG are likely associated with PIK3CA variants. © 2021 International Society of Ultrasound in Obstetrics and Gynecology.
描述法国多中心队列中产前诊断为先天性异常并疑似局部过度生长障碍(LOD)的胎儿的临床和分子发现,这些胎儿的 LOD 提示遗传变异存在于 PI3K-AKT-mTOR 信号通路中。
我们回顾性分析了 2013 年 1 月 1 日至 2020 年 5 月 1 日期间因疑似 PI3K-AKT-mTOR 通路基因遗传变异而通过下一代测序(NGS)进行分子诊断的脑和/或肢体过度生长胎儿的数据,这些胎儿的病理组织均通过胎儿尸检获得。我们还评估了羊水的诊断效果。
在研究期间,21 名疑似 LOD 的胎儿被转介进行 PI3K-AKT-mTOR 通路基因分析,这些胎儿的 LOD 怀疑是由遗传变异引起的。其中 17 名胎儿有脑过度生长,包括 6 名单纯巨脑畸形(MEG)和 11 名偏侧巨脑畸形(HMEG)。在 6 名 MEG 患者中,4 例存在 PIK3R2、AKT3 或 MTOR 的种系变异,另外 2 例存在 PIK3R2 的合子后变异。在 11 名 HMEG 患者中,3 名有脑外 PIK3CA 相关过度生长谱特征的胎儿存在 PIK3CA 的合子后变异,7 名单纯 HMEG 患者存在 PIK3CA 的合子后变异。在 11 名 HMEG 患者中未发现致病性变异。4 名肢体过度生长的胎儿还存在一个或多个淋巴管畸形(LM),并携带 PIK3CA 的合子后变异。
单纯 MEG 或 HMEG 可能导致 PI3K-AKT-mTOR 信号通路的遗传变异被识别。肢体过度生长和 LM 或单纯 HMEG 可能与 PIK3CA 变异相关。 © 2021 年国际妇产科超声学会。