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本文引用的文献

1
Key challenges for delivering clinical impact with artificial intelligence.人工智能实现临床影响的关键挑战。
BMC Med. 2019 Oct 29;17(1):195. doi: 10.1186/s12916-019-1426-2.
2
Prediction and Risk Stratification of Kidney Outcomes in IgA Nephropathy.IgA 肾病的肾脏结局预测和风险分层。
Am J Kidney Dis. 2019 Sep;74(3):300-309. doi: 10.1053/j.ajkd.2019.02.016. Epub 2019 Apr 25.
3
Machine Learning in Medicine.医学中的机器学习
N Engl J Med. 2019 Apr 4;380(14):1347-1358. doi: 10.1056/NEJMra1814259.
4
A machine learning approach to integrate big data for precision medicine in acute myeloid leukemia.一种用于整合大数据以实现急性髓系白血病精准医疗的机器学习方法。
Nat Commun. 2018 Jan 3;9(1):42. doi: 10.1038/s41467-017-02465-5.
5
Unintended consequences of machine learning in medicine?机器学习在医学领域的意外后果?
F1000Res. 2017 Sep 19;6:1707. doi: 10.12688/f1000research.12693.1. eCollection 2017.
6
Common pitfalls in statistical analysis: Logistic regression.统计分析中的常见陷阱:逻辑回归
Perspect Clin Res. 2017 Jul-Sep;8(3):148-151. doi: 10.4103/picr.PICR_87_17.
7
Oxford Classification of IgA nephropathy 2016: an update from the IgA Nephropathy Classification Working Group.牛津 IgA 肾病分类 2016 年更新:IgA 肾病分类工作组的报告。
Kidney Int. 2017 May;91(5):1014-1021. doi: 10.1016/j.kint.2017.02.003. Epub 2017 Mar 22.
8
Machine learning for prediction of all-cause mortality in patients with suspected coronary artery disease: a 5-year multicentre prospective registry analysis.机器学习用于预测疑似冠心病患者的全因死亡率:一项为期5年的多中心前瞻性登记分析。
Eur Heart J. 2017 Feb 14;38(7):500-507. doi: 10.1093/eurheartj/ehw188.
9
Intensive Supportive Care plus Immunosuppression in IgA Nephropathy.IgA 肾病的强化支持治疗加免疫抑制。
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10
New developments in the genetics, pathogenesis, and therapy of IgA nephropathy.IgA肾病的遗传学、发病机制及治疗方面的新进展。
Kidney Int. 2015 Nov;88(5):974-89. doi: 10.1038/ki.2015.252. Epub 2015 Sep 16.

可解释机器学习生存模型预测 IgA 肾病的长期肾脏结局。

An Interpretable Machine Learning Survival Model for Predicting Long-term Kidney Outcomes in IgA Nephropathy.

机构信息

Ping An Healthcare Technology, Beijing.

National Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China.

出版信息

AMIA Annu Symp Proc. 2021 Jan 25;2020:737-746. eCollection 2020.

PMID:33936448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8075445/
Abstract

IgA nephropathy (IgAN) is common worldwide and has heterogeneous phenotypes. Predicting long-term outcomes is important for clinical decision-making. As right-censored patients become common during the long-term follow-up, either excluding these patients from the cohort or labeling them as control will bias the risk estimation. Thus, we constructed a survival model using EXtreme Gradient Boosting for survival (XSBoost-Surv), to accurately predict the prognosis of IgAN patients by taking the time-to-event information into the modeling procedure. Shapley Additive exPlanations (SHAP) was employed to interpret the individual predicted result and the non-linear relationships between the predictors and outcome. Experiments on real-world data showed our model achieved superior discrimination performance over other conventional survival methods. By providing insights into the exact changes in risk induced by certain characteristics of the patients, this explainable and accurate survival model can help improve the clinical understanding of renal progression and benefit the therapies for the IgAN patients.

摘要

IgA 肾病(IgAN)在全球范围内较为常见,具有异质性表型。预测长期结局对于临床决策非常重要。由于在长期随访过程中,右删失患者变得较为常见,如果将这些患者从队列中排除或将其标记为对照,将导致风险估计出现偏差。因此,我们构建了一个使用极端梯度提升进行生存分析(XSBoost-Surv)的生存模型,通过将事件时间信息纳入建模过程,准确预测 IgAN 患者的预后。我们还使用 Shapley Additive exPlanations(SHAP)来解释个体预测结果以及预测因子与结局之间的非线性关系。在真实世界数据上的实验表明,我们的模型在判别性能上优于其他传统的生存方法。通过深入了解患者某些特征所引起的风险确切变化,这个可解释且准确的生存模型有助于提高对肾脏进展的临床认识,并为 IgAN 患者的治疗带来益处。