跳至主要内容
临床试验/NCT06783803
NCT06783803进行中(未招募)不适用

Application of Linkage Analysis in the Identification of Novel Hereditary Factors in Familial Aneurysms

IRCCS Policlinico S. Donato1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
20
试验地点
1
主要终点
DNA sequences in FTAAD

研究概览

简要总结

The aim of this study is to describe the effectiveness of the application of Linkage Analysis, compared to the standard procedures currently provided by the italian NHS, in the identification of thoracic aortic aneurysms and dissection (TAAD) transmission markers in individuals with familial TAAD.

详细描述

According to current guidelines, it is important to screen first-degree relatives of patients with familial thoracic aortic aneurysm and dissection (FTAAD) using imaging techniques in order to detect any undiagnosed or asymptomatic cases. The current diagnostic methods for FTAAD involve clinical and instrumental diagnosis. In addition to these methods, genetic analysis through DNA testing, using a blood sample has become an essential tool. The use of massive parallel sequencing (NGS) of multiple genes or the entire exome (Whole Exome Sequencing - WES) is considered the gold standard for genetic diagnosis of FTAAD. However, it should be noted that linkage studies are not currently included in the diagnostic protocols of the Italian National Health System, although they may be helpful in complex familial cases where DNA sequencing has not provided conclusive evidence.

研究设计

研究类型
Observational
观察模型
Family Based
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with ascending thoracic aortic aneurysms in the absence of a mutation identified by WES
  • •Subjects with small and medium artery aneurysms in the absence of a mutation identified by WES
  • •Relatives of individuals with ascending thoracic aortic aneurysms in the absence of a mutation identified by WES
  • •Relatives of individuals with ascending thoracic aortic aneurysms in the absence of a mutation identified by WES
  • •Signed informed consent

排除标准

  • •Subjects wit syndromic FTAAD with WES identified gene mutation
  • •Subjects wit non-syndromic FTAAD with WES identified gene mutation

结局指标

主要结局

DNA sequences in FTAAD

时间窗: 16 months

Identify those chromosome regions containing the DNA sequences responsible for each enrolled member of FTAAD families

次要结局

  • Mutations associated with Mendelian and monogenic diseases(24 months)

研究者

发起方
IRCCS Policlinico S. Donato
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alessandro Pini

Pincipal Investigator

IRCCS Policlinico S. Donato

研究点 (1)

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