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孤立性心房颤动的家族聚集性。

Familial aggregation in lone atrial fibrillation.

作者信息

Ellinor Patrick T, Yoerger Danita M, Ruskin Jeremy N, MacRae Calum A

机构信息

Cardiac Arrhythmia Service, Massachusetts General Hospital, 149 13th Street, 4th Floor, Charlestown, Boston, MA, 02129, USA.

出版信息

Hum Genet. 2005 Nov;118(2):179-84. doi: 10.1007/s00439-005-0034-8. Epub 2005 Nov 15.

Abstract

Atrial fibrillation (AF) is the most common clinical arrhythmia and a major risk factor for stroke. To investigate the role of genetic factors in a typical clinical population, we determined the extent of familial aggregation in patients with lone AF. To estimate the relative risk to family members, the prevalence of AF for each class of relative was compared to the prevalence in the comparable age and sex group from the general population. Family members had an increased relative risk of AF compared to the general population (risk ratio; 95% confidence intervals): sons (8.1; 2.0-32), daughters (9.5; 1.3-67), brothers (70; 47-102), sisters (34; 14-80), mothers (4.0; 2.5-6.5) and fathers (2.0; 1.2-3.6). Relatives of probands with lone AF are at a substantially increased risk of developing this arrhythmia suggesting a Mendelian genetic contribution to the etiology of this common trait.

摘要

心房颤动(AF)是最常见的临床心律失常,也是中风的主要危险因素。为了研究遗传因素在典型临床人群中的作用,我们确定了孤立性房颤患者的家族聚集程度。为了估计家庭成员的相对风险,将每类亲属的房颤患病率与来自普通人群的可比年龄和性别组的患病率进行了比较。与普通人群相比,家庭成员患房颤的相对风险增加(风险比;95%置信区间):儿子(8.1;2.0 - 32)、女儿(9.5;1.3 - 67)、兄弟(70;47 - 102)、姐妹(34;14 - 80)、母亲(4.0;2.5 - 6.5)和父亲(2.0;1.2 - 3.6)。孤立性房颤先证者的亲属患这种心律失常的风险大幅增加,这表明孟德尔遗传因素对这一常见特征的病因学有贡献。

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