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Genetics of Atrial Fibrillation and Possible Implications for Ischemic Stroke

机译:心房颤动的遗传学及其对缺血性中风的可能意义

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Atrial fibrillation is the most common cardiac arrhythmia mainly caused by valvular, ischemic, hypertensive, and myopathic heart disease. Atrial fibrillation can occur in families suggesting a genetic background especially in younger subjects. Additionally recent studies have identified common genetic variants to be associated with atrial fibrillation in the general population. This cardiac arrhythmia has important public health implications because of its main complications: congestive heart failure and ischemic stroke. Since atrial fibrillation can result in ischemic stroke, one might assume that genetic determinants of this cardiac arrhythmia are also implicated in cerebrovascular disease. Ischemic stroke is a multifactorial, complex disease where multiple environmental and genetic factors interact. Whether genetic variants associated with a risk factor for ischemic stroke also increase the risk of a particular vascular endpoint still needs to be confirmed in many cases. Here we review the current knowledge on the genetic background of atrial fibrillation and the consequences for cerebrovascular disease.
机译:房颤是最常见的心律不齐,主要由瓣膜性,缺血性,高血压和肌病性心脏病引起。心房颤动可能发生在有遗传背景的家庭中,尤其是在年轻的受试者中。另外,最近的研究已经确定了普通人群中与房颤相关的常见遗传变异。由于其主要并发症:充血性心力衰竭和缺血性中风,这种心律不齐具有重要的公共卫生意义。由于心房颤动可导致缺血性中风,因此可以假设这种心律失常的遗传决定因素也与脑血管疾病有关。缺血性中风是一种多因素,复杂的疾病,其中多种环境和遗传因素相互作用。在许多情况下,仍需要确认与缺血性中风危险因素相关的遗传变异是否还会增加特定血管终点的风险。在这里,我们回顾了有关房颤的遗传背景和对脑血管疾病的后果的当前知识。

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