High-resolution lifestyle profiling and metabolic subphenotypes of type 2 diabetes

IF 15.1 1区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Heyjun Park, Ahmed A. Metwally, Alireza Delfarah, Yue Wu, Dalia Perelman, Caleb Mayer, Curtis McGinity, Majid Rodgar, Alessandra Celli, Tracey McLaughlin, Emmanuel Mignot, Michael Snyder
{"title":"High-resolution lifestyle profiling and metabolic subphenotypes of type 2 diabetes","authors":"Heyjun Park, Ahmed A. Metwally, Alireza Delfarah, Yue Wu, Dalia Perelman, Caleb Mayer, Curtis McGinity, Majid Rodgar, Alessandra Celli, Tracey McLaughlin, Emmanuel Mignot, Michael Snyder","doi":"10.1038/s41746-025-01728-6","DOIUrl":null,"url":null,"abstract":"<p>Distinct metabolic susceptibilities (beta-cell dysfunction, insulin resistance (IR), and impaired incretin response) underlie type 2 diabetes (T2D). However, their relationships with habitual lifestyle behaviors are underexplored. This study integrated high-resolution lifestyle data from wearable devices, continuous glucose monitoring, and smartphone-based food logs with gold-standard physiological tests in 36 individuals at risk for T2D (ClinicalTrials.Gov; NCT03919877; 2019-04-18). Over 6400 timestamped records of diet, sleep, and physical activity were analyzed with in participants with measures of beta-cell function, tissue-specific IR (muscle, hepatic, adipose), and incretin response. We found that lifestyle timing and variability were strongly associated with metabolic subphenotypes: (1) eating timing was associated with muscle IR and incretin function; (2) irregular sleep correlated to IR and incretin function; and (3) Time-of-day effects of physical activity varied by subphenotype. These findings were validated in an independent cohort. Our results highlight novel physiological links between daily behaviors and metabolic risk, informing potential lifestyle modifications for T2D prevention.</p>","PeriodicalId":19349,"journal":{"name":"NPJ Digital Medicine","volume":"26 1","pages":""},"PeriodicalIF":15.1000,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NPJ Digital Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41746-025-01728-6","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0

Abstract

Distinct metabolic susceptibilities (beta-cell dysfunction, insulin resistance (IR), and impaired incretin response) underlie type 2 diabetes (T2D). However, their relationships with habitual lifestyle behaviors are underexplored. This study integrated high-resolution lifestyle data from wearable devices, continuous glucose monitoring, and smartphone-based food logs with gold-standard physiological tests in 36 individuals at risk for T2D (ClinicalTrials.Gov; NCT03919877; 2019-04-18). Over 6400 timestamped records of diet, sleep, and physical activity were analyzed with in participants with measures of beta-cell function, tissue-specific IR (muscle, hepatic, adipose), and incretin response. We found that lifestyle timing and variability were strongly associated with metabolic subphenotypes: (1) eating timing was associated with muscle IR and incretin function; (2) irregular sleep correlated to IR and incretin function; and (3) Time-of-day effects of physical activity varied by subphenotype. These findings were validated in an independent cohort. Our results highlight novel physiological links between daily behaviors and metabolic risk, informing potential lifestyle modifications for T2D prevention.

Abstract Image

2型糖尿病的高分辨率生活方式分析和代谢亚表型
不同的代谢敏感性(β细胞功能障碍,胰岛素抵抗(IR)和肠促胰岛素反应受损)是2型糖尿病(T2D)的基础。然而,它们与习惯生活方式行为的关系尚未得到充分探讨。该研究将来自可穿戴设备的高分辨率生活方式数据、连续血糖监测和基于智能手机的食物记录与金标准生理测试结合起来,对36名有T2D风险的个体进行了研究(ClinicalTrials.Gov;NCT03919877;2019-04-18)。研究人员分析了超过6400份有时间戳的饮食、睡眠和身体活动记录,并对参与者的β细胞功能、组织特异性IR(肌肉、肝脏、脂肪)和肠促胰岛素反应进行了测量。我们发现,生活方式的时间和可变性与代谢亚表型密切相关:(1)进食时间与肌肉IR和肠促胰岛素功能相关;(2)睡眠不规律与IR和肠促胰岛素功能相关;(3)身体活动的时间效应因亚表型而异。这些发现在一个独立的队列中得到了验证。我们的研究结果强调了日常行为和代谢风险之间的新生理联系,为预防糖尿病的潜在生活方式改变提供了信息。
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
CiteScore
25.10
自引率
3.30%
发文量
170
审稿时长
15 weeks
期刊介绍: npj Digital Medicine is an online open-access journal that focuses on publishing peer-reviewed research in the field of digital medicine. The journal covers various aspects of digital medicine, including the application and implementation of digital and mobile technologies in clinical settings, virtual healthcare, and the use of artificial intelligence and informatics. The primary goal of the journal is to support innovation and the advancement of healthcare through the integration of new digital and mobile technologies. When determining if a manuscript is suitable for publication, the journal considers four important criteria: novelty, clinical relevance, scientific rigor, and digital innovation.
×
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:604180095
Book学术官方微信