Prediction of progression from pre‐diabetes to diabetes: Development and validation of a machine learning model

逻辑回归 机器学习 人工智能 糖尿病 医学 数据集 队列 预测建模 计算机科学 内科学 内分泌学
作者
Avivit Cahn,Avi Shoshan,Tal Sagiv,Rachel Yesharim,Ran Goshen,Varda Shalev,Itamar Raz
出处
期刊:Diabetes-metabolism Research and Reviews [Wiley]
卷期号:36 (2): e3252-e3252 被引量:98
标识
DOI:10.1002/dmrr.3252
摘要

Abstract Aims Identification, a priori, of those at high risk of progression from pre‐diabetes to diabetes may enable targeted delivery of interventional programmes while avoiding the burden of prevention and treatment in those at low risk. We studied whether the use of a machine‐learning model can improve the prediction of incident diabetes utilizing patient data from electronic medical records. Methods A machine‐learning model predicting the progression from pre‐diabetes to diabetes was developed using a gradient boosted trees model. The model was trained on data from The Health Improvement Network (THIN) database cohort, internally validated on THIN data not used for training, and externally validated on the Canadian AppleTree and the Israeli Maccabi Health Services (MHS) data sets. The model's predictive ability was compared with that of a logistic‐regression model within each data set. Results A cohort of 852 454 individuals with pre‐diabetes (glucose ≥ 100 mg/dL and/or HbA1c ≥ 5.7) was used for model training including 4.9 million time points using 900 features. The full model was eventually implemented using 69 variables, generated from 11 basic signals. The machine‐learning model demonstrated superiority over the logistic‐regression model, which was maintained at all sensitivity levels – comparing AUC [95% CI] between the models; in the THIN data set (0.865 [0.860,0.869] vs 0.778 [0.773,0.784] P < .05), the AppleTree data set (0.907 [0.896, 0.919] vs 0.880 [0.867, 0.894] P < .05) and the MHS data set (0.925 [0.923, 0.927] vs 0.876 [0.872, 0.879] P < .05). Conclusions Machine‐learning models preserve their performance across populations in diabetes prediction, and can be integrated into large clinical systems, leading to judicious selection of persons for interventional programmes.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
shy完成签到,获得积分10
1秒前
2秒前
zf发布了新的文献求助10
2秒前
传奇3应助LGZ采纳,获得10
2秒前
坚定雁桃完成签到,获得积分10
3秒前
jackie完成签到,获得积分20
3秒前
3秒前
ganjqly完成签到,获得积分10
3秒前
3秒前
lhy发布了新的文献求助10
4秒前
SciGPT应助刻苦若冰采纳,获得30
4秒前
做好人难完成签到,获得积分10
4秒前
5秒前
6秒前
fifi关注了科研通微信公众号
6秒前
汉堡包应助明朗采纳,获得10
6秒前
小吉完成签到 ,获得积分10
7秒前
烟花应助屁屁驴采纳,获得10
7秒前
暴龙战士图图完成签到,获得积分10
7秒前
Limengjie完成签到,获得积分10
7秒前
顾矜应助叫滚滚采纳,获得20
8秒前
zqee完成签到,获得积分10
8秒前
轻松碧玉完成签到,获得积分20
9秒前
拥月亮发布了新的文献求助10
9秒前
9秒前
蔷薇泡沫发布了新的文献求助10
10秒前
123完成签到,获得积分10
11秒前
11秒前
Crystal发布了新的文献求助10
11秒前
李健的小迷弟应助Cici采纳,获得10
12秒前
12秒前
doudou完成签到,获得积分10
12秒前
12秒前
lhy完成签到,获得积分10
13秒前
丁可心完成签到 ,获得积分10
13秒前
Ava应助123123采纳,获得10
15秒前
15秒前
LGZ发布了新的文献求助10
15秒前
jason完成签到 ,获得积分10
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Feldspar inclusion dating of ceramics and burnt stones 1000
What is the Future of Psychotherapy in a Digital Age? 801
The Psychological Quest for Meaning 800
Digital and Social Media Marketing 600
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5982854
求助须知:如何正确求助?哪些是违规求助? 7379224
关于积分的说明 16029500
捐赠科研通 5123126
什么是DOI,文献DOI怎么找? 2749301
邀请新用户注册赠送积分活动 1719404
关于科研通互助平台的介绍 1625603