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产前诊断先天性心脏病的染色体分析及短期预后

Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease.

作者信息

Verbeke Marcellino, Hannes Laurens, Devriendt Koen, Van den Bogaert Kris, Cools Bjorn, De Catte Luc, Gewillig Marc, Breckpot Jeroen

机构信息

Department of Human Genetics, Catholic University Leuven, Leuven, Belgium.

Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.

出版信息

Sci Rep. 2025 Jan 31;15(1):3923. doi: 10.1038/s41598-025-88570-8.

Abstract

Congenital structural heart disease (CHD) is the leading cause of infant death from birth defects. Postnatal survival primarily depends on the type and severity of the defect. In addition, worse cardiac prognosis is observed when extra-cardiac anomalies (ECA) are associated. This retrospective chart review was aimed at finding markers for short-term outcome prediction of prenatally-diagnosed complex CHD, focusing in particular on the impact of CHD category, of CHD severity score and of prenatal or postnatal diagnosis of ECA or chromosomal anomalies on 4 primary outcomes: termination of pregnancy (TOP), intrauterine fetal demise, neonatal mortality and 1-year-survival rate. We reviewed medical files from 381 fetuses, presenting at our center between 2018 and 2021 with CHD for which prenatal advice by a pediatric cardiologist was sought. 341 fetuses met the inclusion criteria for the study. Twin pregnancies (7.62%; OR 4.76 (p < 0.001)) and pregnancies resulting from assisted reproductive technology (7.33%; OR 2.44 (p < 0.001)) were more prevalent compared to the general population. CHD categories and CHD severity scores, ranging from A (extremely high risk based on CHD or ECA type) to D (low risk), were assigned to each fetus. Prenatal or postnatal chromosomal microarray results were available for 232 fetuses (68%) and were abnormal in 30 (12.9%). Logistic regression analysis was used to determine significant predictors for the primary outcomes 'TOP', 'postnatal demise before the age of 1 month' and 'survival at the age of 1 year'. TOP was carried out significantly more with: prenatal genetic diagnosis, severity score A and severity score B. Interestingly, a prenatal genetic diagnosis was negatively correlated with pregnancy continuation, but it was not a significant predictor for postnatal mortality, while a postnatal diagnosis of a genetic disorder impacted early but not late postnatal mortality. In addition, postnatal mortality both before the age of 1 month or before the age of 1 year was significantly associated with lower postmenstrual age at birth, CHD severity score B and major ECA at birth. These results underscore the importance of genotyping and of accurate cardiac and extracardiac phenotyping for prognostication in fetuses with CHD.

摘要

先天性结构性心脏病(CHD)是出生缺陷导致婴儿死亡的主要原因。出生后的存活率主要取决于缺陷的类型和严重程度。此外,当合并心外异常(ECA)时,心脏预后更差。本回顾性病历审查旨在寻找产前诊断的复杂CHD短期预后预测指标,特别关注CHD类别、CHD严重程度评分以及产前或产后ECA或染色体异常诊断对四个主要结局的影响:终止妊娠(TOP)、宫内胎儿死亡、新生儿死亡率和1年生存率。我们回顾了2018年至2021年间在我们中心就诊的381例患有CHD并寻求儿科心脏病专家产前建议的胎儿的医疗档案。341例胎儿符合研究纳入标准。与普通人群相比,双胎妊娠(7.62%;比值比4.76(p<0.001))和辅助生殖技术妊娠(7.33%;比值比2.44(p<0.001))更为常见。为每个胎儿分配了CHD类别和CHD严重程度评分,范围从A(基于CHD或ECA类型的极高风险)到D(低风险)。232例胎儿(68%)可获得产前或产后染色体微阵列结果,其中30例(12.9%)异常。采用逻辑回归分析确定主要结局“TOP”、“1月龄前产后死亡”和“1岁时存活”的显著预测因素。TOP在以下情况发生得更为频繁:产前基因诊断、严重程度评分A和严重程度评分B。有趣的是,产前基因诊断与继续妊娠呈负相关,但不是产后死亡率的显著预测因素,而产后基因疾病诊断影响早期但不影响晚期产后死亡率。此外,1月龄前或1岁前的产后死亡率与出生时较低的月经后年龄、CHD严重程度评分B和出生时的主要ECA显著相关。这些结果强调了基因分型以及准确的心脏和心外表型分析对CHD胎儿预后评估的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc04/11785992/234a4720a12a/41598_2025_88570_Fig1_HTML.jpg

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