Genetic testing in polygenic diseases. Atrial fibrillation, arterial hypertension and coronary artery disease

被引:1
作者
Trenkwalder, T. [1 ]
Kessler, T. [1 ]
Schunkert, H. [1 ,2 ]
机构
[1] Tech Univ Munich, Deutsch Herzzentrum Munchen, Klin Herz & Kreislauferkrankungen, Lazarettstr 36, D-80636 Munich, Germany
[2] Deutsch Zentrum Herz Kreislauf Forsch DZHK eV, Munich Heart Alliance, Munich, Germany
关键词
Genetic testing; Familial hypercholesterolemia; Familial atrial fibrillation; Monogenic hypertension; Coronary artery disease; GENOME-WIDE ASSOCIATION; ANGIOTENSIN-CONVERTING ENZYME; BLOOD-PRESSURE; CARDIOVASCULAR-DISEASE; GUANYLYL CYCLASE; RISK-FACTORS; CHOLESTEROL; LOCI; POLYMORPHISM; TRIGLYCERIDES;
D O I
10.1007/s00059-017-4576-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genetic testing plays an increasing role in cardiovascular medicine. Advances in technology and the development of novel and more affordable (high throughput) methods have led to the identification of genetic risk factors in research and clinical practice. Also, this progress has simplified the screening of patients and individuals at risk. In case of rare monogenic diseases, diagnostics, risk stratification, and, in some cases, treatment decisions have become easier. For common, polygenic cardiovascular diseases, the situation is more complex due to interaction of modifiable external risk factors and nonmodifiable factors like genetic predisposition. Over the last few years, it has been shown that multiple genes are involved in the pathophysiology of these cardiovascular diseases rather than one single gene. In the following article, we give an overview of the genetic risk factors in polygenic cardiovascular diseases as atrial fibrillation, arterial hypertension and coronary artery disease. Furthermore, we aim to illustrate in which cases genetic testing is recommended in these diseases.
引用
收藏
页码:440 / 448
页数:9
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