中国先天性膈疝婴儿并发出生缺陷的模式:一项基于全国医院的监测研究。

IF 1.6 4区 医学 Q4 DEVELOPMENTAL BIOLOGY
Zhi-Yu Chen, Wen-Li Xu, Yu-Yang Gao, Wen-Yan Li, Zhen Liu, Jia-Yuan Zhou, Li Dai
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引用次数: 0

摘要

背景:先天性膈疝(CDH)婴儿同时发生出生缺陷的情况仍未得到充分研究。目的:本研究旨在阐明中国人群中并发缺陷的复杂模式。材料和方法:我们分析了来自中国出生缺陷监测网络(2007-2019)的CDH病例,这些病例至少伴有一种额外的缺陷,但没有综合征诊断。调整后的观察到的预期患病率(O/E)比值被计算为所有二到五种组合,以识别与CDH共同发生的缺陷比预期的更频繁的模式。结果:在1235例CDH合并其他出生缺陷的病例中,调整后O/E比值最高的前30位组合包括肌肉骨骼、心血管、中枢神经系统、面部和肾脏缺陷。心血管缺陷占76.7%,其次是中枢神经系统缺陷(23.3%)和肌肉骨骼缺陷(20.0%)。合并多指畸形和并指畸形的调整后O/E比值最高,为5963.37(95%可信区间:5960.00 ~ 5966.73)。讨论:骨骼肌畸形与CDH的关系可从流行病学、胚胎学和发病机制等方面加以解释。心血管和CDH共同发生的机制可能涉及共同途径的破坏。结论:我们的分析描述了CDH婴儿出生缺陷的共同发生模式,并揭示了几个值得注意的模式。观察到的模式可以指导进一步的研究,并增强我们对多种缺陷的发育机制的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patterns of Co-Occurring Birth Defects in Chinese Infants With Congenital Diaphragmatic Hernia: A National Hospital-Based Surveillance Study.

Background: The landscape of co-occurring birth defects among infants with congenital diaphragmatic hernia (CDH) remains underexplored.

Aims: This study aims to elucidate the complex patterns of co-occurring defects in Chinese population.

Materials and methods: We analyzed cases from the Chinese Birth Defects Monitoring Network (2007-2019) with CDH that presented along with at least one additional defect but without a syndromic diagnosis. Adjusted observed-to-expected prevalence (O/E) ratios were calculated for all two- to five-way combinations to discern patterns of co-occurring defects with CDH more frequently than expected by chance.

Results: Among 1235 CDH cases associated with other birth defects, the top 30 combinations with the highest adjusted O/E ratios included musculoskeletal, cardiovascular, central nervous system, facial, and renal defects. Cardiovascular defects were involved in 76.7% of the top combinations, followed by central nervous system (23.3%) and musculoskeletal defects (20.0%). The combination of polydactyly and syndactyly anomalies exhibited the highest adjusted O/E ratio of 5963.37 (95% confidence interval: 5960.00-5966.73).

Discussion: The relationship between musculoskeletal malformation and CDH may be explained from the aspects of epidemiology, embryology and pathogenesis. And mechanisms for the co-occurrence of cardiovascular and CDH may involve disruption of common pathways.

Conclusion: Our analyses describe the co-occurrence patterns of birth defects in CDH infants and reveal several noteworthy patterns. The observed patterns can guide further study and enhance our comprehension understanding of the developmental mechanisms underlying multiple defects.

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来源期刊
Birth Defects Research
Birth Defects Research Medicine-Embryology
CiteScore
3.60
自引率
9.50%
发文量
153
期刊介绍: The journal Birth Defects Research publishes original research and reviews in areas related to the etiology of adverse developmental and reproductive outcome. In particular the journal is devoted to the publication of original scientific research that contributes to the understanding of the biology of embryonic development and the prenatal causative factors and mechanisms leading to adverse pregnancy outcomes, namely structural and functional birth defects, pregnancy loss, postnatal functional defects in the human population, and to the identification of prenatal factors and biological mechanisms that reduce these risks. Adverse reproductive and developmental outcomes may have genetic, environmental, nutritional or epigenetic causes. Accordingly, the journal Birth Defects Research takes an integrated, multidisciplinary approach in its organization and publication strategy. The journal Birth Defects Research contains separate sections for clinical and molecular teratology, developmental and reproductive toxicology, and reviews in developmental biology to acknowledge and accommodate the integrative nature of research in this field. Each section has a dedicated editor who is a leader in his/her field and who has full editorial authority in his/her area.
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