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Where culture meets genetics: Exploring Latina immigrants' lay beliefs of disease inheritance

机译:文化符合遗传学的地方:探索拉丁移民的界定疾病遗产

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摘要

As medical genetic services become a standard part of healthcare, it will become increasingly important to understand how individuals interpret and use genetic information. Exploring lay beliefs of disease inheritance that differ along cultural lines is one research strategy. The purpose of this study was to describe conceptualizations of disease inheritance held by members of the Latina immigrant population in the United States. Semi-structured interviews were employed to gather qualitative, exploratory data from 20 Latina immigrant women. All interviews were conducted in Spanish, and thematic analysis was used to analyze interview transcripts. Demographic and acculturation data were also collected and analyzed. The final sample was diverse in age, time lived in the United States, country of birth, and education level. From participant interviews, the authors identified one dominant model of disease inheritance to which most participants ascribed as well as two non-dominant models. The main model was characterized by a focus on the ability to modify an underlying disease risk, especially in the case of hereditary predisposition to common complex disease. Of the non-dominant models, one focused on genetic disease as extraordinary and less modifiable while the other placed less emphasis on the role of genes in health and greater emphasis on non-genetic factors. Across these models, participants expressed their uncertainty about their understanding of genetics. Many of the themes that arose from the interviews, including uncertainty in their own understanding of genetics, were similar to those seen in studies among other populations. Importantly, participants in this study demonstrated a lack of genetic fatalism, which may allay fears that explaining the role of genetics in common health conditions will reduce uptake of positive health behaviors. These findings have practice implications for healthcare providers communicating genetic information to Latina immigrants.
机译:随着医学基因服务成为医疗保健的标准组成部分,了解个人如何解读和使用基因信息将变得越来越重要。探索不同文化背景下疾病遗传的世俗信仰是一种研究策略。本研究的目的是描述美国拉丁裔移民群体成员持有的疾病遗传概念。采用半结构式访谈,从20名拉丁裔移民女性中收集定性、探索性数据。所有访谈均以西班牙语进行,主题分析用于分析访谈记录。还收集和分析了人口统计学和文化适应数据。最终的样本在年龄、在美国生活的时间、出生国和教育水平上存在差异。从参与者访谈中,作者确定了大多数参与者认为的一种显性疾病遗传模式,以及两种非显性疾病遗传模式。主要模型的特点是关注改变潜在疾病风险的能力,尤其是在遗传易感常见复杂疾病的情况下。在非显性模型中,一种侧重于遗传疾病,认为它非同寻常,不易修改,而另一种则不太强调基因在健康中的作用,而是更强调非遗传因素。在这些模型中,参与者表达了他们对遗传学理解的不确定性。采访中出现的许多主题,包括他们自己对遗传学理解的不确定性,与其他人群研究中看到的主题相似。重要的是,这项研究的参与者表现出缺乏遗传宿命论,这可能会减轻人们的担忧,即解释基因在常见健康状况中的作用会减少积极健康行为的吸收。这些发现对医疗保健提供者向拉丁裔移民传达基因信息具有实践意义。

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