首页> 外文期刊>Human Genomics >Evaluation of a genetic risk score for severity of COVID-19 using human chromosomal-scale length variation
【24h】

Evaluation of a genetic risk score for severity of COVID-19 using human chromosomal-scale length variation

机译:使用人染色体尺度长度变化评估Covid-19严重程度的遗传风险评分

获取原文
       

摘要

The course of COVID-19 varies from asymptomatic to severe in patients. The basis for this range in symptoms is unknown. One possibility is that genetic variation is partly responsible for the highly variable response. We evaluated how well a genetic risk score based on chromosomal-scale length variation and machine learning classification algorithms could predict severity of response to SARS-CoV-2 infection. We compared 981 patients from the UK Biobank dataset who had a severe reaction to SARS-CoV-2 infection before 27 April 2020 to a similar number of age-matched patients drawn for the general UK Biobank population. For each patient, we built a profile of 88 numbers characterizing the chromosomal-scale length variability of their germ line DNA. Each number represented one quarter of the 22 autosomes. We used the machine learning algorithm XGBoost to build a classifier that could predict whether a person would have a severe reaction to COVID-19 based only on their 88-number classification. We found that the XGBoost classifier could differentiate between the two classes at a significant level (p?=?2?·?10?11) as measured against a randomized control and (p?=?3?·?10?14) as measured against the expected value of a random guessing algorithm (AUC = 0.5). However, we found that the AUC of the classifier was only 0.51, too low for a clinically useful test. Genetics play a role in the severity of COVID-19, but we cannot yet develop a useful genetic test to predict severity.
机译:Covid-19的过程从患者中无症状变化。症状症状的基础是未知的。一种可能性是遗传变异是对高度可变响应的部分原因。我们评估了基于染色体尺度长度变化和机器学习分类算法的遗传风险得分如何预测对SARS-COV-2感染的反应严重程度。我们将981名来自英国Biobank DataSet的患者进行了比较了对2020年4月27日之前对SARS-COV-2感染的严重反应,以对英国普通的BioBank人口绘制的类似年龄匹配的患者。对于每位患者,我们构建了88个数字的轮廓,其特征表征其种系DNA的染色体级长度变异性。每个数字代表22个常染素的四分之一。我们使用了机器学习算法XGBoost来构建一个分类器,该分类器可以预测仅基于其88号分类对Covid-19的严重反应。我们发现,XGBoost分类器可以以显着水平(p?=Δ2?····················10?11)区分两个类别,如针对随机控制的(P?= 3?3?10?10?14)测量随机猜测算法的预期值(AUC = 0.5)。然而,我们发现分类器的AUC仅为0.51,对于临床有用的测试,太低。遗传学在Covid-19的严重程度中发挥作用,但我们还无法制定有益的遗传测试来预测严重程度。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号