Associations of Ultraprocessed Food Intake, Wearable-Measured Lifestyle Factors, and Genetic Susceptibility With Incident Type 2 Diabetes

IF 9.3 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Diabetes Pub Date : 2026-09-17 DOI:10.2337/db26-0395
Wenxin Xu, Tong Chen, Wei Zhang, Collin Sakal, Xinyue Li
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Abstract

Growing evidence links ultraprocessed food (UPF) intake to type 2 diabetes (T2D) risk; however, whether reducing UPF consumption is associated with lower risk across genetic susceptibility strata and whether protective lifestyle factors are associated with lower risk among high UPF consumers remain uncertain. We studied 56,964 UK Biobank participants without diabetes at baseline. Diet was assessed using 24-h dietary records, and foods were classified according to the Nova system. Physical activity and sleep were measured by accelerometers for 7 consecutive days, and polygenic risk was derived from 424 T2D-associated single nucleotide polymorphisms. Multivariable Cox proportional hazards models and restricted cubic splines were used to estimate hazard ratios (HRs) and dose–response relationships. Each 10% higher UPF intake was associated with 7% higher T2D risk (HR 1.07 [95% CI 1.03, 1.12]). Dose–response analyses revealed a linear association with UPF intake and an L-shaped association with moderate to vigorous physical activity (MVPA; Pnonlinearity < 0.001). Among individuals with high genetic susceptibility, lower risk was observed with lower UPF intake (HR 0.65 [95% CI 0.49, 0.85]), higher total physical activity (0.79 [0.65, 0.97]), sufficient MVPA (0.67 [0.55, 0.81]), and adequate sleep (0.57 [0.39, 0.84]). In joint analyses, sufficient MVPA (HR 0.69 [95% CI 0.50, 0.96]) and adequate sleep (0.42 [0.24, 0.75]) were associated with lower risk among participants with high UPF intake and high genetic risk. Together, our findings show that healthier modifiable behaviors were associated with lower diabetes risk across genetic susceptibility strata, and wearable-derived evidence highlights MVPA and adequate sleep as behavioral targets among individuals with high UPF intake. Article Highlights Dietary intake, inactivity, poor sleep, and genetic risk may all contribute to diabetes risk, but their combined effects are unclear. Whether modifiable lifestyle factors are associated with diabetes risk across genetic risk strata and whether wearable-derived behaviors are associated with lower risk among individuals with high ultraprocessed food (UPF) intake remain uncertain. Lower UPF intake was associated with lower diabetes risk across all levels of genetic risk, and meeting moderate to vigorous physical activity targets and getting adequate sleep were associated with lower risk among individuals with high UPF intake. Wearable-derived behavioral targets may be practical solutions for reducing UPF-associated diabetes risk and supporting diabetes prevention.
超加工食品摄入、可穿戴测量的生活方式因素和遗传易感性与2型糖尿病的关系
越来越多的证据表明,超加工食品(UPF)摄入与2型糖尿病(T2D)风险有关;然而,减少UPF消费是否与遗传易感阶层的风险降低有关,以及保护性生活方式因素是否与高UPF消费者的风险降低有关,这些问题仍不确定。我们研究了56,964名基线时无糖尿病的英国生物银行参与者。使用24小时饮食记录对饮食进行评估,并根据Nova系统对食物进行分类。通过加速度计连续7天测量身体活动和睡眠,并从424个t2d相关的单核苷酸多态性中得出多基因风险。多变量Cox比例风险模型和限制三次样条用于估计风险比(hr)和剂量-反应关系。UPF摄入量每增加10%,T2D风险增加7% (HR 1.07 [95% CI 1.03, 1.12])。剂量-反应分析显示,与UPF摄入量呈线性关系,与中度至剧烈体力活动呈l型关系(MVPA;非线性&;lt; 0.001)。在高遗传易感性个体中,低UPF摄入量(HR 0.65 [95% CI 0.49, 0.85])、高总体力活动(0.79[0.65,0.97])、充足的MVPA(0.67[0.55, 0.81])和充足的睡眠(0.57[0.39,0.84])的风险较低。在联合分析中,在高UPF摄入量和高遗传风险的参与者中,充足的MVPA (HR 0.69 [95% CI 0.50, 0.96])和充足的睡眠(0.42[0.24,0.75])与较低的风险相关。总之,我们的研究结果表明,在遗传易感层中,更健康的可改变行为与较低的糖尿病风险相关,可穿戴设备衍生的证据强调,在高UPF摄入量的个体中,MVPA和充足的睡眠是行为目标。饮食摄入、缺乏运动、睡眠不足和遗传风险都可能导致糖尿病风险,但它们的综合影响尚不清楚。可改变的生活方式因素是否与遗传风险层的糖尿病风险相关,以及可穿戴设备衍生的行为是否与超加工食品(UPF)摄入量高的个体的较低风险相关,仍不确定。在所有遗传风险水平上,较低的UPF摄入量与较低的糖尿病风险相关,而在高UPF摄入量的个体中,达到中等到剧烈的体育活动目标和获得充足的睡眠与较低的风险相关。可穿戴行为目标可能是降低upf相关糖尿病风险和支持糖尿病预防的实用解决方案。
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来源期刊
Diabetes
Diabetes 医学-内分泌学与代谢
CiteScore
12.50
自引率
2.60%
发文量
1968
审稿时长
1 months
期刊介绍: Diabetes is a scientific journal that publishes original research exploring the physiological and pathophysiological aspects of diabetes mellitus. We encourage submissions of manuscripts pertaining to laboratory, animal, or human research, covering a wide range of topics. Our primary focus is on investigative reports investigating various aspects such as the development and progression of diabetes, along with its associated complications. We also welcome studies delving into normal and pathological pancreatic islet function and intermediary metabolism, as well as exploring the mechanisms of drug and hormone action from a pharmacological perspective. Additionally, we encourage submissions that delve into the biochemical and molecular aspects of both normal and abnormal biological processes. However, it is important to note that we do not publish studies relating to diabetes education or the application of accepted therapeutic and diagnostic approaches to patients with diabetes mellitus. Our aim is to provide a platform for research that contributes to advancing our understanding of the underlying mechanisms and processes of diabetes.
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