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Characterizing the Genetic Influences on Risk Aversion

机译:表征遗传对风险规避的影响

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摘要

Risk aversion has long been cited as an important factor in retirement decisions, investment behavior, and health. Some of the heterogeneity in individual risk tolerance is well understood, reflecting age gradients, wealth gradients, and similar effects, but much remains unexplained. This study explores genetic contributions to heterogeneity in risk aversion among older Americans. Using over 2 million genetic markers per individual from the U.S. Health and Retirement Study, I report results from a genome-wide association study (GWAS) on risk preferences using a sample of 10,455 adults. None of the single-nucleotide polymorphisms (SNPs) are found to be statistically significant determinants of risk preferences at levels stricter than 5 × 10~(-8). These results suggest that risk aversion is a complex trait that is highly polygenic. The analysis leads to upper bounds on the number of genetic effects that could exceed certain thresholds of significance and still remain undetected at the current sample size. The findings suggest that the known heritability in risk aversion is likely to be driven by large numbers of genetic variants, each with a small effect size.
机译:长期以来,人们一直将规避风险作为退休决策,投资行为和健康状况的重要因素。人们对个人风险承受能力的某些异质性已经很好地理解,反映了年龄梯度,财富梯度和类似的影响,但很多原因尚无法解释。这项研究探讨了遗传因素对老年美国人风险规避的异质性的影响。我使用美国健康与退休研究中的每个人使用了超过200万个遗传标记,我报告了一项全基因组关联研究(GWAS)关于风险偏好的研究,该研究使用了10,455名成年人作为样本。没有发现单核苷酸多态性(SNPs)在高于5×10〜(-8)的水平上是风险偏好的统计学显着决定因素。这些结果表明,风险规避是一个高度多基因的复杂特征。分析得出的遗传效应数量上限可能超过某些重要的阈值,但在当前样本量下仍未被发现。这些发现表明,风险规避的已知遗传力很可能是由大量遗传变异驱动的,每个遗传变异的效应大小都很小。

著录项

  • 来源
    《Social Biology》 |2014年第2期|185-198|共14页
  • 作者

    AMAL HARRATI;

  • 作者单位

    Department of Demography, University of California, Berkeley, Berkeley, California, USA,UC Berkeley, Department of Demography, 2232 Piedmont Avenue, Berkeley, CA 94720, USA;

  • 收录信息 美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:45:02

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