Department of Preventive Medicine and Public Health, School of Medicine, University of Valencia, 46010 Valencia, Spain.
CIBER Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Nutrients. 2023 Jan 30;15(3):708. doi: 10.3390/nu15030708.
Circadian rhythms regulate the sleep-wake and feeding-fasting cycles. Sleep and feeding constitute a complex cycle that is determined by several factors. Despite the importance of sleep duration and mealtimes for many obesity phenotypes, most studies on dietary patterns have not investigated the contribution of these variables to the phenotypes analyzed. Likewise, they have not investigated the factors related to sleep or mealtimes. Thus, our aims were to investigate the link between taste perception and eating/sleep patterns and to analyze the effect of the interactions between sleep/meal patterns and genetic factors on obesity phenotypes. We conducted a cross-sectional analysis on 412 adults from the Mediterranean population. We measured taste perception (bitter, sweet, salty, sour, and umami) and assessed sleep duration and waketime. The midpoint of sleep and social jetlag was computed. From the self-reported timing of meals, we estimated the eating window, eating midpoint, and eating jetlag. Adherence to the Mediterranean diet was measured with a validated score. Selected polymorphisms in the TAS2R38, CLOCK, and FTO genes were determined, and their associations and interactions with relevant phenotypes were analyzed. We found various associations between temporal eating, sleep patterns, and taste perception. A higher bitter taste perception was associated with an earlier eating midpoint ( = 0.001), breakfast time ( = 0.043), dinner time ( = 0.009), waketime ( < 0.001), and midpoint of sleep ( = 0.009). Similar results were observed for the bitter taste polymorphism TAS2R38-rs713598, a genetic instrumental variable for bitter perception, increasing the causality of the associations. Moreover, significant gene-sleep interactions were detected between the midpoint of sleep and the TAS2R38-rs713598 ( = 0.032), FTO-rs9939609 ( = 0.037), and CLOCK-rs4580704 ( = 0.004) polymorphisms which played a role in determining obesity phenotypes. In conclusion, our study provided more information on the sleep and mealtime patterns of the general Spanish Mediterranean population than on their main relationships. Moreover, we were able to show significant associations between taste perception, specifically bitter taste; sleep time; and mealtimes as well as an interaction between sleep time and several genetic variants linked to obesity phenotypes. However, additional research is needed to better characterize the causality and mechanisms behind these associations.
昼夜节律调节睡眠-觉醒和进食-禁食周期。睡眠和进食构成一个复杂的周期,由几个因素决定。尽管睡眠时间和进餐时间对许多肥胖表型很重要,但大多数关于饮食模式的研究并没有调查这些变量对所分析表型的贡献。同样,它们也没有调查与睡眠或进餐时间相关的因素。因此,我们的目的是研究味觉感知与进食/睡眠模式之间的联系,并分析睡眠/进餐模式与遗传因素之间的相互作用对肥胖表型的影响。我们对来自地中海人群的 412 名成年人进行了横断面分析。我们测量了味觉感知(苦、甜、咸、酸和鲜味),并评估了睡眠持续时间和醒来时间。计算了睡眠和社会时差的中点。根据自我报告的进餐时间,我们估计了进餐窗口、进餐中点和进餐时差。用经过验证的评分来衡量地中海饮食的依从性。确定了 TAS2R38、CLOCK 和 FTO 基因中的选定多态性,并分析了它们与相关表型的关联和相互作用。我们发现了时间进食、睡眠模式和味觉感知之间的各种关联。苦味感知较强与进食中点较早( = 0.001)、早餐时间( = 0.043)、晚餐时间( = 0.009)、醒来时间( < 0.001)和睡眠中点( = 0.009)相关。苦味味觉多态性 TAS2R38-rs713598 的结果类似,该多态性是苦味感知的遗传工具变量,增加了关联的因果关系。此外,还检测到睡眠中点与 TAS2R38-rs713598( = 0.032)、FTO-rs9939609( = 0.037)和 CLOCK-rs4580704( = 0.004)多态性之间存在显著的基因-睡眠相互作用,这些多态性在决定肥胖表型方面发挥了作用。总之,我们的研究提供了关于一般西班牙地中海人群的睡眠和进餐时间模式的更多信息,而不是它们的主要关系。此外,我们能够显示味觉感知(特别是苦味)、睡眠时间和进餐时间之间的显著关联,以及睡眠时间与几个与肥胖表型相关的遗传变异之间的相互作用。然而,需要进一步的研究来更好地描述这些关联背后的因果关系和机制。