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首页> 外文期刊>Frontiers in Genetics >Corrigendum: Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example
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Corrigendum: Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example

机译:更正:将遗传风险简单,标准化地纳入针对复杂性状的非遗传风险预测工具中:以冠心病为例

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The original Figure 2 did not display the full sample risk report as described in the paper. Here we illustrate how one can convey personalized genetic risk to a patient and how the inclusion of the Genetic Risk Score changes the clinical interpretation of the individual's risk. Funding BG is supported by an NIH career development award K25DK097279. JK is supported by an American Heart Association, National Fellow to Faculty Award, 10FTF3360005. TA is supported by an NIH career development award K23DK088942. Your Risk Score Based on the traditional Framingham risk score, your risk of coronary heart disease over the next 10 years is approximately 5.5%. We tested for a total of 90 possible risks variants or alleles. Out of these 90, you carry 49 variants that are associated with higher risk. Your genetic profile puts you in the 89 percentile for risk. This means 89% of the general population have a genetic risk score more favorable than you and 11% have a genetic risk score less favorable than you. Based on the traditional Framingham risk score plus the genetic risk score, your risk of coronary heart disease over the next 10 years is approximately 7.6%. Your 10 year risk of coronary heart disease risk is ≥7.5% when considering your genetic risk. This information may be discussed with your physician in terms of what would be recommended as most appropriate management given your estimated risk. Conflict of interest statement The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
机译:原始图2并未显示本文所述的完整样本风险报告。在这里,我们说明了如何将个性化的遗传风险传达给患者,以及遗传风险评分的纳入如何改变个体风险的临床解释。 BG资金由NIH职业发展奖K25DK097279提供支持。 JK得到了美国心脏协会国家奖教金10FTF3360005的支持。 TA获得了美国国立卫生研究院职业发展奖K23DK088942的支持。您的风险评分根据传统的Framingham风险评分,在未来10年中,您患冠心病的风险约为5.5%。我们测试了总共90种可能的风险变体或等位基因。在这90个变量中,您携带49个与较高风险相关的变量。您的遗传特征使您处于89%的风险中。这意味着89%的普通人群的遗传风险得分比您好,而11%的遗传风险得分比您差。根据传统的Framingham风险评分加遗传风险评分,在未来10年中,您罹患冠心病的风险约为7.6%。考虑到遗传风险,您10年的冠心病风险为≥7.5%。鉴于您的估计风险,可以与您的医师讨论建议最合适的管理方法。利益冲突声明作者声明,这项研究是在没有任何商业或金融关系的情况下进行的,可以将其解释为潜在的利益冲突。

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