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存在心血管疾病风险:有或没有已知遗传易感性人群的认知和预防行为。

Being at risk for cardiovascular disease: perceptions and preventive behavior in people with and without a known genetic predisposition.

机构信息

Department of Public and Occupational Health, EMGO+ Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.

出版信息

Psychol Health Med. 2012;17(5):511-21. doi: 10.1080/13548506.2011.644246. Epub 2012 Feb 24.

DOI:10.1080/13548506.2011.644246
PMID:22360457
Abstract

This study compares and explains differences in perceptions of cardiovascular disease (CVD) risk and preventive behaviors in people with and without a known genetic predisposition to CVD. A cross-sectional study using two samples was performed. The first sample (genetic predisposition; n = 51) consisted of individuals recently diagnosed with familial hypercholesterolemia (FH) through DNA testing. The second sample (no genetic predisposition; n = 49) was recruited among patients with CVD-risk profiles based on family history of CVD, cholesterol levels, and blood pressure, registered at general practices. Participants filled out a postal questionnaire asking about their perceived risk, causal attributions (i.e. genetic and lifestyle), and about perceived efficacy and adoption of preventive behavior (i.e. medication adherence and adoption of a healthy diet and being sufficiently active). Perceived comparative risk, genetic attributions of CVD, and perceived efficacy of medication were higher in the "genetic predisposition" sample than in the "no genetic predisposition" sample. The samples did not differ on lifestyle attributions, efficacy of a healthy lifestyle, or preventive behavior. Individual differences in perceived risk, genetic attributions, perceived efficacy of medication, and adoption of a healthy lifestyle were best explained by family history of CVD. Our findings suggest that in people diagnosed with a single gene disorder characterized by a family disease history such as FH, family disease history may be more important than DNA information in explaining perceptions of and responses to risk.

摘要

本研究比较并解释了具有已知心血管疾病(CVD)遗传易感性和无遗传易感性的人群对 CVD 风险和预防行为的看法的差异。采用了横断面研究设计,使用了两个样本。第一个样本(遗传易感性;n=51)由通过 DNA 测试最近被诊断为家族性高胆固醇血症(FH)的个体组成。第二个样本(无遗传易感性;n=49)是从根据家族史、胆固醇水平和血压在普通诊所登记的 CVD 风险患者中招募的。参与者填写了一份邮寄问卷,询问他们对风险的感知、因果归因(即遗传和生活方式),以及对预防行为的感知效果和采用情况(即药物依从性和采用健康饮食和足够的活动)。在“遗传易感性”样本中,对比较风险、CVD 的遗传归因以及药物治疗效果的感知要高于“无遗传易感性”样本。两个样本在生活方式归因、健康生活方式的效果或预防行为方面没有差异。感知风险、遗传归因、药物治疗效果和采用健康生活方式的个体差异最好用 CVD 的家族史来解释。我们的研究结果表明,在被诊断为具有 FH 等家族病史的单一基因疾病的人群中,家族病史在解释对风险的感知和反应方面可能比 DNA 信息更重要。

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