Familial Aggregation of Aortic Valvular Stenosis: A Nationwide Study of Sibling Risk.

Andreas Martinsson, Xinjun Li, Bengt Zöller, Pontus Andell, Charlotte Andersson, Kristina Sundquist, J Gustav Smith
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引用次数: 20

Abstract

Background: Aortic valvular stenosis (AS) is the most common cause of cardiac valvular replacement surgery. During the last century, the pathogenesis of AS has undergone transitions in developed countries, from rheumatic heart disease to a degenerative calcific pathogenesis. Although a familial component has been described for a subset of cases with a bicuspid valve, data are limited on the overall familial aggregation of this disease.

Methods and results: Contemporary information on 6 117 263 Swedish siblings, of which 13 442 had a clinical diagnosis of AS, was collected from the nationwide Swedish Multi-Generation Register and the National Patient Register. A total of 4.8% of AS cases had a sibling history of AS. Having at least 1 sibling with AS was associated with a hazard ratio of 3.41 (95% confidence interval, 2.23-5.21) to be diagnosed with AS in an adjusted model. Individuals with >1 sibling with AS had an exceptionally high risk (hazard ratio, 32.84) but were uncommon (34 siblings from 11 sibships). In contrast, spouses of subjects with AS were only slightly more likely to be diagnosed with AS compared with subjects without spousal AS (hazard ratio 1.16 for husbands and 1.18 for wives).

Conclusions: A sibling history of clinically diagnosed AS was associated with increased risk of AS. Spouses of patients with AS only had a modest risk increase, suggesting that shared adult environmental factors contribute less to the development of AS than genetic factors.

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主动脉瓣狭窄的家族性聚集:一项全国同胞风险研究。
背景:主动脉瓣狭窄(AS)是心脏瓣膜置换术的最常见原因。在上个世纪,AS的发病机制在发达国家经历了从风湿性心脏病到退行性钙化发病机制的转变。尽管家族性因素已被描述为二尖瓣病例的一个子集,但该疾病的整体家族聚集性数据有限。方法和结果:从瑞典全国多代登记和国家患者登记中收集了6 117 263例瑞典兄弟姐妹的当代信息,其中13 442例临床诊断为AS。共有4.8%的AS病例有兄弟姐妹AS病史。在调整后的模型中,至少有一个兄弟姐妹患有AS,诊断为AS的风险比为3.41(95%可信区间为2.23-5.21)。有>1个兄弟姐妹患有AS的个体有异常高的风险(危险比,32.84),但不常见(来自11个兄弟姐妹的34个兄弟姐妹)。相反,与配偶没有患阿斯伯格综合症的人相比,患有阿斯伯格综合症的配偶被诊断为阿斯伯格综合症的可能性仅略高(丈夫的风险比为1.16,妻子的风险比为1.18)。结论:临床诊断为AS的兄弟姐妹病史与AS风险增加相关。AS患者的配偶只有适度的风险增加,这表明共同的成人环境因素对AS发展的影响小于遗传因素。
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来源期刊
Circulation: Cardiovascular Genetics
Circulation: Cardiovascular Genetics CARDIAC & CARDIOVASCULAR SYSTEMS-GENETICS & HEREDITY
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审稿时长
6-12 weeks
期刊介绍: Circulation: Genomic and Precision Medicine considers all types of original research articles, including studies conducted in human subjects, laboratory animals, in vitro, and in silico. Articles may include investigations of: clinical genetics as applied to the diagnosis and management of monogenic or oligogenic cardiovascular disorders; the molecular basis of complex cardiovascular disorders, including genome-wide association studies, exome and genome sequencing-based association studies, coding variant association studies, genetic linkage studies, epigenomics, transcriptomics, proteomics, metabolomics, and metagenomics; integration of electronic health record data or patient-generated data with any of the aforementioned approaches, including phenome-wide association studies, or with environmental or lifestyle factors; pharmacogenomics; regulation of gene expression; gene therapy and therapeutic genomic editing; systems biology approaches to the diagnosis and management of cardiovascular disorders; novel methods to perform any of the aforementioned studies; and novel applications of precision medicine. Above all, we seek studies with relevance to human cardiovascular biology and disease.
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