跳至主要内容
临床试验/NCT04513054
NCT04513054招募中不适用

Is There a Genetic Predisposition for Acute Stress-induced (Takotsubo) Cardiomyopathy: The GENETIC Study

University of Aberdeen2 个研究点 分布在 1 个国家目标入组 700 人开始时间: 2019年3月12日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
700
试验地点
2
主要终点
Genome Wide Association Study

研究概览

简要总结

Acute stress-induced (takotsubo) cardiomyopathy or broken heart syndrome presents like a heart attack, classically is triggered by intense emotional or physical stress and can have serious health consequences. In the current study the investigators wish to establish whether there is a genetic predisposition making certain people more susceptible to this condition. This could also have implications for their families.

详细描述

Acute stress-induced (takotsubo) cardiomyopathy presents like a myocardial infarct, is triggered by intense emotional or physical stress, and can have catastrophic and potentially fatal consequences. Despite data linking takotsubo cardiomyopathy with conditions that have a recognized genetic predisposition (such as mental health and neurological problems), a systematic and comprehensive characterisation of the genetic-epidemiologic factors in takotsubo is lacking. The researchers propose to further investigate this disorder by collecting blood from probands and characterising the genotype of patients with takotsubo cardiomyopathy in a large scale, nationwide genome wide association study. The investigators will also archive DNA for identification of future candidate genetic variants. Ultimately, understanding the underlying predisposition of this poorly understood neuro-psycho-cardiac disorder is essential if we are to move this field forward.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • All patients who have been diagnosed with Takotsubo cardiomyopathy in Scotland between 2010 to date.
  • Familial cases elsewhere in the world who would be willing to participate.

排除标准

  • Unwillingness to participate

结局指标

主要结局

Genome Wide Association Study

时间窗: At baseline

Genome Wide Association Study to search for susceptibility variants

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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