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利用深度学习对原始肺量计图进行慢性阻塞性肺疾病推断可识别新的基因位点并改进风险模型。

Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models.

作者信息

Cosentino Justin, Behsaz Babak, Alipanahi Babak, McCaw Zachary R, Hill Davin, Schwantes-An Tae-Hwi, Lai Dongbing, Carroll Andrew, Hobbs Brian D, Cho Michael H, McLean Cory Y, Hormozdiari Farhad

机构信息

Google Health AI, Palo Alto, CA, USA.

Google Health AI, Cambridge, MA, USA.

出版信息

Nat Genet. 2023 May;55(5):787-795. doi: 10.1038/s41588-023-01372-4. Epub 2023 Apr 17.

Abstract

Chronic obstructive pulmonary disease (COPD), the third leading cause of death worldwide, is highly heritable. While COPD is clinically defined by applying thresholds to summary measures of lung function, a quantitative liability score has more power to identify genetic signals. Here we train a deep convolutional neural network on noisy self-reported and International Classification of Diseases labels to predict COPD case-control status from high-dimensional raw spirograms and use the model's predictions as a liability score. The machine-learning-based (ML-based) liability score accurately discriminates COPD cases and controls, and predicts COPD-related hospitalization without any domain-specific knowledge. Moreover, the ML-based liability score is associated with overall survival and exacerbation events. A genome-wide association study on the ML-based liability score replicates existing COPD and lung function loci and also identifies 67 new loci. Lastly, our method provides a general framework to use ML methods and medical-record-based labels that does not require domain knowledge or expert curation to improve disease prediction and genomic discovery for drug design.

摘要

慢性阻塞性肺疾病(COPD)是全球第三大死因,具有高度遗传性。虽然COPD在临床上是通过对肺功能汇总指标应用阈值来定义的,但定量易感性评分在识别遗传信号方面更具效力。在此,我们基于噪声自我报告和国际疾病分类标签训练一个深度卷积神经网络,以从高维原始肺量图预测COPD病例对照状态,并将模型预测用作易感性评分。基于机器学习(ML)的易感性评分能够准确区分COPD病例和对照,且无需任何特定领域知识即可预测与COPD相关的住院情况。此外,基于ML的易感性评分与总体生存率和病情加重事件相关。一项基于ML易感性评分的全基因组关联研究重复了现有的COPD和肺功能基因座,还鉴定出67个新基因座。最后,我们的方法提供了一个通用框架,用于使用ML方法和基于病历的标签,无需领域知识或专家整理即可改善疾病预测和用于药物设计的基因组发现。

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