13三体的死亡率模式和表型簇:一项来自日本的基于人群的研究。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Narumi Kato, Naho Morisaki, Akinori Moriichi
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引用次数: 0

摘要

13三体是继21三体和18三体之后第三种最常见的常染色体三体,它与婴儿死亡率非常高有关。然而,调查13型三体死亡原因的大规模研究仍然很少。因此,我们的目标是更好地了解死亡率模式。为此,利用来自生命统计数据库的日本人口死亡率数据(n = 4,230,092例死亡记录)开展了一项基于人口的研究;我们检查了早期死亡率,并根据共同发生的死亡原因的组合确定了表型亚组。我们确定了150名在2019年至2021年期间死亡的13号三体患者。心血管疾病与早期死亡率显著相关。使用基于死因分类主成分的k均值聚类,我们确定了三个不同的亚组:呼吸为主(19%)、心血管为主(64%)和多器官受累(17%)。心血管疾病为主的组在1岁前死亡率最高(83%,p = 0.001),而手术干预率在组间无显著差异。这些发现强调了表型异质性,可能支持13三体的个性化护理计划,并提供可能支持未来护理和决策的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population-Based Study From Japan.

Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large-scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns. To this end, a population-based study was conducted using Japanese population-based mortality data from the Vital Statistics Database (n = 4,230,092 death records); we examined early mortality and identified phenotypic subgroups based on combinations of co-occurring causes of death. We identified 150 individuals with trisomy 13 who died between 2019 and 2021. Cardiovascular disease was significantly associated with early mortality. Using K-means clustering based on principal components of cause-of-death categories, we identified three distinct subgroups: respiratory-dominant (19%), cardiovascular-dominant (64%), and multi-organ involvement (17%). The cardiovascular-dominant cluster showed the highest rate of death before age 1 (83%; p = 0.001), while surgical intervention rates did not significantly differ across clusters. These findings highlight phenotypic heterogeneity and may support individualized care planning for trisomy 13 and provide insights that may support future care and decision-making.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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