Application of Linkage Analysis in the Identification of Novel Hereditary Factors in Familial Aneurysms
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
Alessandro Pini
Pincipal Investigator
IRCCS Policlinico S. Donato
