Early meal timing attenuates high polygenic risk of obesity

IF 4.7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Obesity Pub Date : 2025-07-20 DOI:10.1002/oby.24319
R De la Peña-Armada, María Rodríguez-Martín, Hassan S. Dashti, Ana Isabel Cascales, Frank A. J. L. Scheer, Richa Saxena, Marta Garaulet
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Abstract

Objective

We examined whether meal timing is associated with long-term weight-loss maintenance and whether meal timing interacts with a genome-wide polygenic score (PRS-BMI) on body weight-related outcomes. We then examined the interaction of meal timing with 97 BMI-related single-nucleotide polymorphisms on obesity outcome.

Methods

Participants (N = 1195, mean age 41.07 [SD 12.68] years, female 80.8%, baseline mean BMI 31.32 [SD 5.53] kg/m2) were adults with overweight or obesity from the Obesity, Nutrigenetics, Timing, and Mediterranean (ONTIME) study. We developed a PRS-BMI to assess the genetic risk for obesity and estimated the timing of the midpoint of meal intake. We also calculated the success in long-term weight-loss maintenance after a dietary obesity treatment (at least 3 years). Linear regression analyses were performed for association and interaction assessments.

Results

Each hour of delay in meal timing was associated with 2.2% higher long-term body weight (β [SE] = 2.177% [1.067%]; p = 0.042) (i.e., with lower weight-loss maintenance following dietary obesity treatment). There was a significant interaction between meal timing and PRS-BMI (p = 0.008); BMI increased by more than 2 kg/m2 for every hour of delay in meal timing in individuals with high PRS-BMI (β [SE] = 2.208 [0.502] kg/m2; p = 1.0E-5), whereas no associations were evident for those with lower genetic risk.

Conclusions

Meal timing is associated with weight-loss maintenance and may influence the association between obesity genetics and BMI. Findings underscore the importance of personalized obesity management.

Abstract Image

早进餐可以降低肥胖的多基因风险。
目的:我们研究了进餐时间是否与长期减肥维持有关,以及进餐时间是否与体重相关结果的全基因组多基因评分(PRS-BMI)相互作用。然后,我们研究了进餐时间与97个bmi相关的单核苷酸多态性对肥胖结果的相互作用。方法:参与者(N = 1195,平均年龄41.07 [SD 12.68]岁,女性80.8%,基线平均BMI 31.32 [SD 5.53] kg/m2)为肥胖、营养遗传学、时间和地中海(ONTIME)研究中超重或肥胖的成年人。我们开发了一种PRS-BMI来评估肥胖的遗传风险,并估计膳食摄入中点的时间。我们还计算了饮食性肥胖治疗(至少3年)后长期减肥维持的成功率。对关联和相互作用进行线性回归分析。结果:进餐时间每延迟1小时,长期体重增加2.2% (β [SE] = 2.177% [1.067%];P = 0.042)(即,饮食肥胖治疗后的减肥维持时间较低)。进餐时间与PRS-BMI之间存在显著交互作用(p = 0.008);高PRS-BMI人群进餐时间每延迟1小时,BMI增加2 kg/m2以上(β [SE] = 2.208 [0.502] kg/m2;p = 1.0E-5),而遗传风险较低的人群则无明显关联。结论:进餐时间与减肥维持有关,并可能影响肥胖遗传学和BMI之间的关系。研究结果强调了个性化肥胖管理的重要性。
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来源期刊
Obesity
Obesity 医学-内分泌学与代谢
CiteScore
11.70
自引率
1.40%
发文量
261
审稿时长
2-4 weeks
期刊介绍: Obesity is the official journal of The Obesity Society and is the premier source of information for increasing knowledge, fostering translational research from basic to population science, and promoting better treatment for people with obesity. Obesity publishes important peer-reviewed research and cutting-edge reviews, commentaries, and public health and medical developments.
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