Development and validation of a diabetes risk prediction model with individualized preventive intervention effects.

IF 5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Byron Jaeger, Ramon Casanova, Yitbarek Demesie, Jeanette Stafford, Brian Wells, Michael P Bancks
{"title":"Development and validation of a diabetes risk prediction model with individualized preventive intervention effects.","authors":"Byron Jaeger, Ramon Casanova, Yitbarek Demesie, Jeanette Stafford, Brian Wells, Michael P Bancks","doi":"10.1210/clinem/dgaf250","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Type 2 diabetes risk prediction models lack the option to predict risk conditional on initiating different preventive interventions. Our objective was to develop and validate a diabetes risk prediction model with individualized preventive intervention effects among racially diverse populations.</p><p><strong>Methods: </strong>The derivation cohort included participants in the Diabetes Prevention Program (DPP) trial randomized to placebo, metformin, or intensive lifestyle intervention (N=2640). A risk prediction model for incident diabetes was developed using Cox proportional hazards regression using clinically available predictors: sex, glycated hemoglobin, fasting plasma glucose (FPG), body mass index (BMI), triglycerides, and intervention. To create individualized intervention effects, pairwise interactions between intervention and age, FPG, and BMI were included. The discrimination, calibration, and net benefit of the model's 3-year predictions for incident diabetes were internally validated within the DPP and externally validated among participants with prediabetes in the Multi-Ethnic Study of Atherosclerosis (MESA; N=2104).</p><p><strong>Results: </strong>In DPP and MESA, mean (standard deviation) age was 51 years (11) and 64 (10) and 67% and 50% of participants were women, respectively. The mean C-statistic was 0.71 (95% confidence interval [CI]: 0.68, 0.74) in DPP and 0.86 (95% CI: 0.83, 0.88) in MESA. The optimal preventive intervention (lowest 3-year risk) was lifestyle for 86% and 97% of DPP and MESA participants, respectively, and metformin for the remaining. Model performance was similar across race/ethnicity groups.</p><p><strong>Conclusion: </strong>This is the first study to develop and validate a diabetes risk prediction model with individualized preventive intervention effects which may improve clinical decision-making and diabetes prevention.</p>","PeriodicalId":50238,"journal":{"name":"Journal of Clinical Endocrinology & Metabolism","volume":" ","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Endocrinology & Metabolism","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1210/clinem/dgaf250","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Type 2 diabetes risk prediction models lack the option to predict risk conditional on initiating different preventive interventions. Our objective was to develop and validate a diabetes risk prediction model with individualized preventive intervention effects among racially diverse populations.

Methods: The derivation cohort included participants in the Diabetes Prevention Program (DPP) trial randomized to placebo, metformin, or intensive lifestyle intervention (N=2640). A risk prediction model for incident diabetes was developed using Cox proportional hazards regression using clinically available predictors: sex, glycated hemoglobin, fasting plasma glucose (FPG), body mass index (BMI), triglycerides, and intervention. To create individualized intervention effects, pairwise interactions between intervention and age, FPG, and BMI were included. The discrimination, calibration, and net benefit of the model's 3-year predictions for incident diabetes were internally validated within the DPP and externally validated among participants with prediabetes in the Multi-Ethnic Study of Atherosclerosis (MESA; N=2104).

Results: In DPP and MESA, mean (standard deviation) age was 51 years (11) and 64 (10) and 67% and 50% of participants were women, respectively. The mean C-statistic was 0.71 (95% confidence interval [CI]: 0.68, 0.74) in DPP and 0.86 (95% CI: 0.83, 0.88) in MESA. The optimal preventive intervention (lowest 3-year risk) was lifestyle for 86% and 97% of DPP and MESA participants, respectively, and metformin for the remaining. Model performance was similar across race/ethnicity groups.

Conclusion: This is the first study to develop and validate a diabetes risk prediction model with individualized preventive intervention effects which may improve clinical decision-making and diabetes prevention.

具有个体化预防干预效果的糖尿病风险预测模型的建立与验证。
目的:2型糖尿病风险预测模型缺乏在启动不同预防干预措施的条件下预测风险的选项。我们的目的是在不同种族的人群中建立并验证具有个体化预防干预效果的糖尿病风险预测模型。方法:衍生队列包括糖尿病预防计划(DPP)试验的参与者,随机分为安慰剂、二甲双胍或强化生活方式干预组(N=2640)。使用临床可用的预测因子:性别、糖化血红蛋白、空腹血糖(FPG)、体重指数(BMI)、甘油三酯和干预,采用Cox比例风险回归建立了糖尿病发生的风险预测模型。为了创造个性化的干预效果,纳入了干预与年龄、FPG和BMI之间的两两相互作用。在DPP内部验证了该模型对糖尿病事件3年预测的鉴别、校准和净效益,并在多种族动脉粥样硬化研究(MESA;N = 2104)。结果:DPP和MESA的平均(标准差)年龄分别为51岁(11岁)和64岁(10岁),67%和50%的参与者为女性。DPP的平均c统计量为0.71(95%可信区间[CI]: 0.68, 0.74), MESA的平均c统计量为0.86(95%可信区间[CI]: 0.83, 0.88)。DPP和MESA参与者的最佳预防干预(最低3年风险)分别为86%和97%的生活方式,其余为二甲双胍。不同种族/民族的模型表现相似。结论:本研究首次建立并验证了具有个体化预防干预效果的糖尿病风险预测模型,可提高临床决策水平和糖尿病预防水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信