Circadian meal timing is heritable and associated with insulin sensitivity

Janna Vahlhaus, Beeke Peters, Silke Hornemann, Anne-Cathrin Ost, Michael Kruse, Andreas Busjahn, Andreas F.H. Pfeiffer, Olga Pivovarova-Ramich
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Abstract

Background: Although the contribution of the circadian clock to metabolic regulation is widely recognized, the role of meal timing in glucose metabolism and diabetes risk remains insufficiently studied. This study aimed (i) to investigate the link between individual circadian meal timing pattern and glucose homeostasis and (ii) to explore the contribution of genetic and environmental factors to meal timing parameters. Methods: In the German NUtriGenomic Analysis in Twins (NUGAT) cohort, which includes 92 adult twins, glucose metabolism parameters were assessed using fasting samples and the oral glucose tolerance test (OGTT). Parameters of meal timing pattern (meal timing itself, daily calorie distribution, and meal number) were extracted from five-day food records. Circadian eating timing was determined relative to the individual’s chronotype (MSFsc) assessed by the Munich chronotype questionnaire. The heritability of meal timing components was estimated using the ACE model. Results: Multiple meal timing components showed associations with glucose metabolism parameters. Most associations were found for the calorie midpoint defined as the time point at which 50% of daily calories were consumed. Indices of insulin sensitivity, ISI Stumvoll (β = 0.334, p = 2.9 x 10-4) and HOMA-IR (β = -0.276, p = 0.007), as well as fasting insulin levels were significantly associated with the circadian caloric midpoint even after the model adjustment for gender, age, energy intake, and sleep duration. BMI and waist circumference also demonstrated robust associations with circadian caloric midpoint. High or moderate heritability was shown for all meal timing components. Meal timing pattern was also strongly related to individual sleep timing and chronotype, both of which also showed a marked genetic impact. Conclusion: Circadian meal timing is associated with insulin sensitivity and shows significant genetic influences, sharing a common genetic architecture with sleep behaviour. Shifting the main calorie intake to earlier circadian time might protect against diabetes, although this could be challenging due to the high heritability of meal timing components.
昼夜进餐时间可遗传并与胰岛素敏感性有关
背景:尽管昼夜节律对代谢调节的贡献已得到广泛认可,但对进餐时间在糖代谢和糖尿病风险中的作用的研究仍然不足。本研究旨在(i)研究个体昼夜进餐时间模式与葡萄糖稳态之间的联系;(ii)探讨遗传和环境因素对进餐时间参数的影响。研究方法在德国 NUtriGenomic Analysis in Twins(NUGAT)队列(包括 92 对成年双胞胎)中,使用空腹样本和口服葡萄糖耐量试验(OGTT)评估葡萄糖代谢参数。从五天的饮食记录中提取了进餐时间模式参数(进餐时间本身、每日卡路里分布和进餐次数)。昼夜节律进食时间是根据慕尼黑时间型问卷评估的个人时间型(MSFsc)确定的。用 ACE 模型估计了进餐时间成分的遗传率。结果显示多个进餐时间成分与葡萄糖代谢参数有关。其中,卡路里中点与血糖代谢参数的关系最为密切,卡路里中点被定义为摄入50%每日卡路里的时间点。胰岛素敏感性指数、ISI Stumvoll(β = 0.334,p = 2.9 x 10-4)和 HOMA-IR (β = -0.276,p = 0.007)以及空腹胰岛素水平与昼夜热量中点有显著关联,即使在对性别、年龄、能量摄入和睡眠时间进行模型调整后也是如此。体重指数(BMI)和腰围也与昼夜热量中点密切相关。所有进餐时间成分都显示出高度或中度遗传性。进餐时间模式还与个人的睡眠时间和时间型密切相关,这两者也显示出明显的遗传影响。结论昼夜进餐时间与胰岛素敏感性有关,并显示出显著的遗传影响,与睡眠行为具有共同的遗传结构。将主要热量摄入时间提前到昼夜节律时间可能会预防糖尿病,但由于进餐时间的遗传率较高,这可能具有挑战性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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