不同年龄段胸主动脉瘤和夹层致病变异的差异分析

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Shilei Luo, Fei Leng, He Zhao, Wei Li, Qiaochu Wang, Jun Guo
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引用次数: 0

摘要

目的利用全外显子组测序(WES)鉴定与斯坦福A型胸主动脉瘤和夹层(ATAAD)相关的基因变异,并分析不同发病年龄患者的阳性突变率。方法对62例散发性中国ATAAD患者(51-74岁)进行全外显子组测序,然后根据发病年龄与之前报道的73例TAAD患者(19-50岁)进行分组:≤35岁、36-45岁、46-55岁和>55岁。比较了不同组别中TAAD致病基因中致病/可能致病(P/LP)变异的患者比例。结果显示62 名患者的平均发病年龄为 57.66 岁。在8名患者的5个已知TAAD致病基因(FBN1、SMAD3、TGFBR2、TGFB2和MYLK)中发现了8个P/LP变异(2个新变异,6个以前描述过的)。各年龄组患者的 P/LP 变异阳性率分别为≤35岁为22.73%,36-45岁为32%,46-55岁为15.52%,>55岁为3.33%。36-45 岁组和 55 岁以上组之间存在显著差异(P = 0.0077)。结论诊断时年龄在 36-45 岁的 ATAAD 患者出现 P/LP 变异的几率更高,而年龄大于 55 岁的患者 P/LP 诊断率最低。因此,对 55 岁以下的 ATAAD 患者进行基因筛查是提高诊断率的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential Analysis of Pathogenic Variants in Thoracic Aortic Aneurysm and Dissection at Different Ages.

Objective: To identify genetic variants associated with Stanford A thoracic aortic aneurysm and dissection (ATAAD) using whole-exome sequencing (WES) and analyze positive mutation rates among patients of different onset ages. Methods: WES was performed on 62 sporadic Chinese ATAAD patients (51-74 years old), and then grouped based on onset age together with 73 previously reported TAAD patients (19-50 years old): ≤35, 36-45, 46-55, and >55 years. The proportion of patients with pathogenic/likely pathogenic (P/LP) variants in TAAD causal genes was compared across groups. Results: The average onset age of the 62 patients was 57.66 years. Eight P/LP variants were identified (two novel, six previously described) in five known TAAD causal genes (FBN1, SMAD3, TGFBR2, TGFB2, and MYLK) in eight individuals. P/LP variant positive rates among patients across age groups were: 22.73% for ≤35 years, 32% for 36-45 years, 15.52% for 46-55 years, and 3.33% for >55 years. Significant differences (p = 0.0077) were observed between 36-45 and >55 years group. Conclusions: ATAAD patients aged 36-45 years old at diagnosis had a higher chance of having a P/LP variant and patients >55 years old had the lowest P/LP diagnostic rate. Therefore, gene screening in ATAAD patients ≤55 years old is key to improved diagnostic rate.

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来源期刊
CiteScore
2.50
自引率
7.10%
发文量
63
审稿时长
1 months
期刊介绍: Genetic Testing and Molecular Biomarkers is the leading peer-reviewed journal covering all aspects of human genetic testing including molecular biomarkers. The Journal provides a forum for the development of new technology; the application of testing to decision making in an increasingly varied set of clinical situations; ethical, legal, social, and economic aspects of genetic testing; and issues concerning effective genetic counseling. This is the definitive resource for researchers, clinicians, and scientists who develop, perform, and interpret genetic tests and their results. Genetic Testing and Molecular Biomarkers coverage includes: -Diagnosis across the life span- Risk assessment- Carrier detection in individuals, couples, and populations- Novel methods and new instrumentation for genetic testing- Results of molecular, biochemical, and cytogenetic testing- Genetic counseling
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