Next Article in Journal
A Systematic Review of Studies Examining Associations between Sleep Characteristics with Dietary Intake and Eating Behaviors during Pregnancy
Next Article in Special Issue
Diet and Exercise Exert a Differential Effect on Glucose Metabolism Markers According to the Degree of NAFLD Severity
Previous Article in Journal
Diosgenin Inhibits ROS Generation by Modulating NOX4 and Mitochondrial Respiratory Chain and Suppresses Apoptosis in Diabetic Nephropathy
Previous Article in Special Issue
Association of 24 h Behavior Rhythm with Non-Alcoholic Fatty Liver Disease among American Adults with Overweight/Obesity
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Association of Eating Pattern, Chronotype, and Social Jetlag: A Cross-Sectional Study Using Data Accumulated in a Japanese Food-Logging Mobile Health Application

1
Laboratory of Physiology and Pharmacology, School of Advanced Science and Engineering, Waseda University, Tokyo 162-0056, Japan
2
Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima 734-0037, Japan
3
Asken Inc., Tokyo 163-1408, Japan
*
Author to whom correspondence should be addressed.
Nutrients 2023, 15(9), 2165; https://doi.org/10.3390/nu15092165
Submission received: 8 March 2023 / Revised: 21 April 2023 / Accepted: 27 April 2023 / Published: 30 April 2023

Abstract

:
Chronotype (morningness–eveningness) and social jetlag (SJL; discrepancy in the sleep pattern between the weekday and weekend) are related to eating behavior and health. The association between sleep behavior and the daily macro- and micronutrient eating pattern of each meal (breakfast, lunch, and dinner) have not been discussed well and need more evidence. Here, meal pattern datasets of Japanese participants aged 20–59 years were obtained as averages over 1 month from the data stored in the food-logging app “Asken”. We allocated three groups for each chronotype and SJL. Multiple regression analyses revealed that morning chronotype and small SJL were associated with higher total daily intake of potassium, fiber, magnesium, phosphorus, and vitamin K. Breakfast energy intake and consumption of nutrients, including protein, lipid, carbohydrate, and minerals, were higher in the morning chronotype or small SJL. Lunch intake of potassium, cholesterol, fiber, magnesium, and vitamin K was also higher in the morning chronotype or small SJL. Dinner energy intake and nutrient intake of proteins, lipids, carbohydrates, sodium, and saturated fatty acids were lower in the morning chronotype or small SJL. The current data would help to establish a detailed reference for dietary intake which considers eating patterns over a day.

Graphical Abstract

1. Introduction

Chronotype (morningness–eveningness) describes different timings of comfortable living for individuals, and is determined by genetic, environmental, and social factors [1]. Those with the evening type tend to have a longer circadian clock period than those with the morning type do, and their daily rhythms are more easily delayed [2]. Genome-wide association studies revealed 351 single-nucleotide polymorphisms associated with chronotypes [3]. Evening individuals are forced to lead a morning lifestyle on workdays, owing to social restrictions, resulting in a discrepancy between their workdays and free days lifestyles. This weekly jetlag-induced problem is called “social jetlag” (SJL) [4]. Evening chronotypes and SJL are associated with obesity, lower academic achievement, depression, lower performance, and increased smoking habits [4,5,6]. Interventions for chronotypes and SJL prevent lifestyle-related diseases [7]; however, only a few intervention trials have been reported. The COVID-19 pandemic has delayed workday wake-up times and reduced SJL by prompting quarantining and working from home [8,9]. Although most Japanese participants in a study had increased body weight and decreased daily physical activity, associations with advances in sleep timing and weight loss and delays in sleep timing and weight gain were observed during the pandemic-related home quarantine in 2020 [8]. Improvements in sleep and daily performance have also been reported with a change to later school start times [10]. Thus, the individual characteristics of the circadian clock need to be carefully considered, and further cross-sectional and interventional research evidence on chronotype/SJL needs to be accumulated.
Evening chronotypes or people with SJL have higher breakfast skipping rates, and they consume more evening meals [11,12,13]. They also have irregular mealtimes, which are associated with obesity. Although eating patterns and nutritional contents related to chronotype have been reported, and studies have discussed the total daily amounts well, only a few studies have investigated meal contents [11,12,13]. According to a recent systematic review, eight studies indicated no difference in total daily macronutrient intake among chronotypes, and three studies revealed inconsistent differences in daily carbohydrate intake among chronotypes [14]. In addition, three studies have reported that morning chronotypes have higher macronutrient intake in the morning, and evening chronotypes have higher macronutrient intake in the evening [14]. Mito et al. reported that evening chronotype female students had a lower total daily intake of protein, calcium, magnesium, zinc, vitamins (D, riboflavin, and B6), and vegetables, and consumed more noodles [15]. In older women, the evening chronotype consumed less vitamin D, more bread, and more caffeinated beverages [16]. Yoshizaki et al. reported that higher SJL is related to a lower total daily energy intake, lower grain consumption, and higher sugar and confectionery consumption [17]. A previous study in Brazil revealed that the higher SJL group consumed more calories, saturated fat, and cholesterol during dinner; more protein, total fat, saturated fat, and cholesterol during lunch; and more total fat and saturated fat in morning snacks [18]. However, daily micronutrient eating patterns related to chronotype or SJL need to be investigated in a large sample size with a broad age range [14]. Therefore, this study aimed to examine the differences in eating patterns among chronotypes and SJL based on breakfast, lunch, and dinner meal data obtained from users of a Japanese food-logging mobile health application (mHealth app).

2. Materials and Methods

2.1. Ethical Considerations

This study was approved by the Ethics Review Committee on Research with Human Subjects at Waseda University (No. 2020-046), and was conducted in accordance with the guidelines of the Declaration of Helsinki. A cross-sectional study was designed, conducted, and analyzed according to the STROBE statement [19]. Informed consent was obtained from all individuals who participated in the study when they started using the app and answered the web survey. The participants completed the questionnaire anonymously to protect their privacy and maintain confidentiality.

2.2. Food-Logging mHealth App “Asken”

“Asken” is a popular Japanese food-logging and food-coaching mHealth app, downloaded by approximately over 7,329,000 users in May 2022 [20]. Self-reported food logs accumulated in the app have been deemed reliable for research purposes [21,22]. As most users (almost 95%) used this app for body weight reduction (evidence from another of our surveys for the same app users), and women may be more inclined to maintain their body shape than men, about 70% of the app users were women (evidence from the current data). Users can input ingredients, dishes and their portion sizes into the app. The app automatically calculates calorie intake and nutritional intake from food records by referencing the Standard Tables of Food Composition in Japan (Ministry of Education 2015). Detailed calculations of nutrient amounts using the food-logging mHealth app have been previously described [21,22]. The app also provides feedback on the value of nutrition intake based on the Dietary Intake Standards for the Japanese, as determined by the Ministry of Health, Labor, and Welfare [23].

2.3. Participants, and Data Inclusion and Exclusion

An online survey was conducted among Asken users at the end of January 2021. Amazon gift cards (500 Japanese yen) were offered to the participants in the lottery. We only set the age range (20–59 years), leaving out any disease information for inclusion and exclusion criteria in the online survey (6299 app users). We selected participants who recorded food logs for 10 or more days per month (848 people were excluded), reported their gender, and were non-shift workers (825 people were excluded). Finally, 4626 participants were included (3427 women and 1199 men, Table 1).

2.4. Dietary Data

The average dietary data during the 1-month period (January–February 2021) were used for the analysis. The current study used data on the energy and intake of 26 nutrients (protein, fat, carbohydrates, sodium, potassium, cholesterol, dietary fiber, saturated fatty acids, alcohol, calcium, magnesium, phosphorus, iron, zinc, and vitamins A, B1, B2, B3, B5, B6, B12, C, D, E, K, and folate) at breakfast, lunch, and dinner. Missing values in food logs were not included in the average calculation because we could not verify whether they were due to meal skipping or data omission. Although the food log includes a snack category, we did not use this data in the current analysis because of insufficient information on intake time. Because 99.7% of the data were included within 3× standard deviations of the distribution, the other 0.3% of the values were excluded as outliers in each category. The app also collected data on daily body weight, body fat percentage, step count, and time of food intake, if the users input the data or connected other health apps to the Asken.

2.5. Questionnaires

We asked participants to complete 50 questions, including 7 items on basic characteristics (age, self-reported gender, weight, height, prefecture of residence, shift work status, and regularity of lifestyle), 6 items on eating behavior, and 6 items on physical activity (a short version of the International Physical Activity Questionnaire) [24], subjective well-being, health, and physical fitness. For sleep behavior, we used the short version of the Munich Chrono Type Questionnaire to investigate sleep habits and chronotypes using 10 questions [25]. Some 8 items of the Athene Insomnia Scale (AIS) were used to assess sleep problems [26]. Breakfast or late-night snack frequency (days/week), subjective well-being, health, and physical fitness were assessed using a 5-step selection questionnaire: 1 = strongly disagree, 2 = disagree, 3 = neither agree nor disagree, 4 = agree, and 5 = strongly agree [27].

2.6. Grouping of Chronotype and SJL

To group chronotypes, mid-sleep on free days corrected for sleep debt accumulated during workdays (MSFsc) was used [1]. We divided the users into three groups based on MSFsc (morning: 3 < MSFsc; intermediate: 3 ≤ MSFsc < 5; evening: 5 ≤ MSFsc). SJL was calculated as the difference between the midpoints of sleep on workdays and free days. SJL was classified into three groups: small (SJL < 1 h), medium (1 h ≤ SJL < 2 h), and large SJL (SJL ≤ 3 h).

2.7. Statistical Analyses

Based on our previous findings from cross-sectional studies using food-logging app data [28], a power analysis was applied before the current experiment (G*Power, version 3.1.9, Heinrich-Heine-University, Düsseldorf, Germany). The analysis was conducted using SPSS software (version 27.0; IBM Corp., Armonk, NY, USA) (Faul et al. 2007). Data normality was analyzed using a Kolmogorov–Smirnov test. As most samples did not pass the normality test, a non-parametric analysis was used in this study. A Kruskal–Wallis test was conducted for multiple-sample statistics to understand the chronotype- or SJL-related general characteristics and eating behavior in women and men (Table 2, Table 3, Table 4 and Table 5). p < 0.001 by Kruskal–Wallis test with a coefficient of more than 0.2, or lower than −0.2 by Spearman’s correlation was considered a significant difference among groups. A multiple regression analysis (forced entry method) was conducted to determine the association between chronotype (1: morning, 2: intermediate, 3: evening) and SJL (1: small SJL, 2: medium SJL, 3: large SJL) and each nutriment intake in each meal timing, with confounding factors (age, gender, BMI, and total daily intake) (Table 6, Table 7, Table 8 and Table 9). Statistical significance was set at p < 0.001.

3. Results

3.1. Basic Characteristics

The general characteristics of the study group are indicated in Table 1. As described previously [28,29], the ratio of carbohydrate intake within the macronutrients in the current participants was lower than the Dietary Intake Standards for the Japanese, which is 50–65% carbohydrate in all ages. Interestingly, in a day, the carbohydrate ratio was higher at breakfast and lower at dinner.
Chronotype-dependent analyses are shown in Table 2 for women and Table 3 for men. Compared with morning types, evening types had a younger age; a later eating time for breakfast, lunch, and dinner; a more irregular lifestyle; larger SJL; and more frequent breakfast skipping in both women and men (Table 2 and Table 3; p < 0.001 by a Kruskal–Wallis test, with coefficient of more than 0.2 or lower than −0.2, Spearman’s correlation). In women, evening types also showed a later eating time for lunch and dinner. Based on only the Kruskal–Wallis test, evening types demonstrated higher body weight, smaller breakfast intake, bigger dinner, a larger standard deviation (SD) of eating time (suggesting irregularity in their daily eating times), more frequent night snacks, more sleep problems (measured by the AIS questionnaire) and lower scores for subjective health and well-being in women (Table 2).
As presented in Table 4 and Table 5, larger SJL demonstrated a later MSFsc in both genders. Based on only the Kruskal–Wallis test, larger SJL correlated with younger age, higher daily intake, bigger dinner, a later dinner time, larger SD of breakfast time, irregular lifestyle, more frequent breakfast-skipping, a higher AIS score, and lower subjective physical strength, health, and well-being in women (Table 4). Similar differences were seen in men (Table 5).

3.2. Chronotype/SJL Associated Eating Pattern

Multiple regression analyses were conducted to understand the association between eating patterns and chronotypes or SJL. Age, gender, body mass index (BMI), and total daily intake (kcal) were adjusted as confounding variables. For the total daily intake of each nutrient (Table 6), potassium, fiber, magnesium, phosphorus, and vitamin K were negatively associated with chronotype and SJL, suggesting that morning types or people with small SJL had more potassium, fiber, magnesium, phosphorus, and vitamin K in a day. The trend of each nutrient intake basically showed higher intake at breakfast and lower intake at dinner in the morning-type and small SJL group, compared with the evening-type and large SJL group (Tables S1 and S2).
At breakfast (Table 7), energy intake and many nutrients including proteins, lipids, carbohydrates, sodium, potassium, cholesterol, fiber, saturated fatty acid, calcium, magnesium, phosphorus, zinc, vitamin K, folate, and pantothenic acid were negatively associated with chronotype. Similar results were observed between breakfast eating patterns and SJL (Table 7). These results suggest that the morning chronotypes or those with small SJL eat more food during breakfast.
At lunch (Table 8), potassium, cholesterol, fiber, magnesium, and vitamin K levels demonstrated a common negative association with chronotype/SJL.
In contrast with breakfast intake, the dinner energy intake of each nutrient, including proteins, lipids, carbohydrates, sodium, and saturated fatty acids, were positively associated with chronotype or SJL (Table 9).

4. Discussion

In the present study, data from 1-month dietary records and web-based surveys were analyzed across a broad age distribution, and differences in eating patterns among chronotypes and SJL based on breakfast, lunch, and dinner meal were investigated. We obtained all the previously reported basic characteristics associated with chronotype/SJL [11,12,13]. We identified mealtimes, irregular mealtimes, breakfast/late-night snack intake frequency, exercise habits, and sleep problems related to chronotype and SJL. Systematic reviews revealed an association between chronotype and nutrient intake; however, the data were research-dependent, because of the research-specific differences in country, age, gender, and chronotype determination methodology [11,12,13,30,31]. In addition, the micronutrient eating pattern related to chronotype or SJL has not been investigated [14]. Here, we newly captured the daily eating patterns of 26 macro- and micronutrients at breakfast, lunch, and dinner against chronotype and SJL in a large sample size with a broad age range.
We identified lower total daily intakes of potassium, fiber, magnesium, phosphorus, and vitamin K in the evening types and large SJL group. Potassium controls fluid balance and blood pressure [32]. Dietary fiber intake is beneficial for the microbiome and good for immune function and cardiovascular function [33]. Magnesium, a cofactor in many enzymes for the cell function, is also beneficial for the muscle function, blood glucose control, and blood pressure regulation [34]. Phosphorus is a component of the cell membrane, nucleic acids, and ATP. Although higher intake of phosphorus has a negative impact on chronic kidney disease and cardiovascular disease, phosphorus is also an important essential mineral [35]. Vitamin K plays an important role in coagulation and bone metabolism [36]. Thus, compared with the evening-type and large SJL group, the morning-type and small SJL group showed a healthier dietary condition.
Some of the nutrients listed above were newly detected when compared with previous studies [14]. Sato-Mito et al. reported that among female university students, night owls had a lower intake of protein, calcium, magnesium, zinc, vitamins (D, riboflavin, and B6), and vegetables, and consumed more noodles [15]; their magnesium levels were consistent with our results. A higher SJL is associated with lower adherence to Mediterranean food, fruits, vegetables, and fiber, and a higher intake of fast food, sugar, confectionaries, and sweetened drinks [14,17,37,38,39]. Thus, since fruits and vegetables are rich in minerals and fiber, we can deduce that lower potassium, fiber, and magnesium intake might be a common feature of people with higher SJL.
The current study revealed the nutrient eating patterns of different chronotypes and levels of SJL. Breakfast energy intake and nutrient intake of proteins, lipids, carbohydrates, and minerals were positively associated with morning chronotype or small SJL, suggesting a bigger breakfast intake in people with the morning chronotype or small SJL. Lunch intake of potassium, cholesterol, fiber, magnesium, and vitamin K was also positively associated with the morning chronotype or small SJL. Dinner energy intake and nutrient intake of proteins, lipids, carbohydrates, sodium, and saturated fatty acids were negatively associated with the morning chronotype or small SJL. One study addressed eating patterns during each meal of the day, and reported that the large SJL group had more saturated fat and cholesterol intake at dinner and lunch among patients with obesity [18], which is consistent with the current data. A larger breakfast and smaller dinner were common eating behaviors related to the morning type and small SJL, a finding consistent with previous research [11,12,13]. Although causality could not be determined by the current and previous cross-sectional studies, the association between eating habits and chronotype can be explained by the food-entrained circadian clock, based on animal research [40]. Based on the phase–response curve of food stimulation of the circadian clock [41], breakfast consumption accelerates the morningness of the circadian clock, whereas dinner and evening meals promote a nocturnal shift in the internal clock. Foods/nutrients regulate the circadian clock in peripheral tissues through postprandial insulin secretion and insulin-induced acute changes in clock gene expression [42,43]. Therefore, higher insulin secretion owing to morning carbohydrate intake causes a shift in morningness. Magnesium and vitamin K, of which consumption is higher during breakfast in the morning-type and small SJL group, can also help insulin secretion/response and breakfast-induced phase advancement [44,45]. By contrast, higher carbohydrate intake at dinner or late at night may delay the sleep–wake cycle. In fact, dinner carbohydrates demonstrated stronger associations with MSFsc and SJL in the multiple regression analysis. Postprandial glucose at dinner can be inhibited directly by fiber intake at dinner, or by the second-meal effect of fiber intake at lunch or snack time [46,47]. This study identified an association between lunch fibers and morningness or small SJL, which may help reduce dinner-induced phase delay. In addition, fiber intake at breakfast enhances microbiota fermentation and increases short-chain fatty acid production, which accelerates food-induced circadian clock resetting in peripheral tissues [48]. Proteins have also been reported to be entrainment signals of clock gene expression through the IGF-1 pathway [49]. In the current study, dinner protein was related to eveningness, which might be due to protein-induced enhancement in the dinner-induced phase delay. In other words, morning protein promoted morningness. Recently, breakfast protein has been recognized as an important eating habit for maintaining muscle size in both human and mouse studies [50]. Daily physical activity and breakfast protein intake were higher in the morning chronotypes than in the evening chronotypes. Altogether, increasing morning protein levels, but not evening protein levels, is a good health intervention to prevent sarcopenia.
In this study, body weight was significantly different among chronotypes, but not SJL levels. Multiple regression analyses revealed a significant association between BMI and chronotype, but not SJL levels, adjusting for the confounding factors of age and gender (Table S3). However, the association between chronotype and SJL and body weight varies, with conflicting results shown in the literature [11]. SJL is associated with metabolic syndrome in Japanese workers [51]. However, the Chinese population did not indicate any association between BMI and SJL because of their daily napping culture and small SJL [52]. By contrast, Chinese adolescents with higher SJL (>2 h) had a higher BMI [53]. Another study suggested that shorter sleep duration was associated with higher carbohydrate and overall energy intake, and that SJL may be independently associated with increased appetite [54]. In addition, a study on SJL and eating styles in US adolescents predicted a tendency toward increased emotional eating and loss of control over food when SJL was greater [55]. Although no significant difference in the amount of food consumed per day was observed among the groups, the factors associated with the evening type with a higher body weight included a low breakfast and high dinner intake, low fiber throughout the day, a late dinner time, a higher nighttime snack frequency, and irregular mealtimes. These factors have been reported to be causal factors for increased weight [56]. Consuming large amounts of food late at night increases body weight [56]. Irregular eating times are associated with negative mood; “eating jetlag” (the difference in eating time between workdays and free days) was also associated with higher BMI and cardiovascular events [27,57,58]. Glucose tolerance is lower in the evening, and postprandial hyperglycemia is more likely to occur at dinner than at breakfast [59], which might be why the evening type is associated with higher body weight. Thus, evidence for an association between body weight and chronotype-related eating behavior is sufficient.
The limitations of our study included misclassification due to self-reporting, unmeasured and uncontrolled confounding factors, and unclear temporal ordering between variables. Dietary data were self-reported, and there is a possibility that errors and self-efficacy may have occurred. Although the current data included highly accurate food intake data collected across 1 month from a large number of samples of varying ages, research bias was present because 95% of the app users desired weight loss, and 70% of the app users were women. Nutrient data for snacks were not used in this study because the time information of snack intake was missing from the application. A more objective methodology, including actigraphy recordings and observation methods such as sleep diaries, is preferable. The cross-sectional study design limits the determination of causal links between all variables. The current study was conducted in winter, and seasonal effects should be considered [60]. Economic status, marital status, and occupation may also be confounding factors affecting the study, and future research should consider such attributes alongside the confounding factor of social background.

5. Conclusions

The current study revealed that people who were morning chronotypes or had small SJL had specific dietary conditions (higher potassium, fiber, magnesium, phosphorus, and vitamin K, with a bigger breakfast and smaller dinner amount) with regular eating and sleeping rhythms. This study provides information for future intervention studies addressing chronotype and SJL, and provides evidence-based personalized dietary suggestions. Since the Dietary Intake Standards for Japanese people do not include the reference intake for each meal (only including a daily total amount), the current data may help to establish a detailed reference intake that considers eating patterns across a day.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/nu15092165/s1, Table S1: Association between chronotype/SJL and % nutrient intake in the breakfast/total daily intake by multiple regression analyses, Table S2: Association between chronotype/SJL and % nutrient intake in dinner/total daily intake by multiple regression analyses, Table S3: Association between BMI and chronotype or SJL.

Author Contributions

Conceptualization, L.N., Y.T. and S.S.; methodology and data collection, L.N., T.S., S.M., M.K., A.T., N.A., M.M. and Y.T.; formal analysis, L.N. and Y.T.; writing—original draft preparation, L.N. and Y.T.; writing—review and editing, S.S.; visualization, L.N. and Y.T.; supervision, S.S.; funding acquisition, Y.T. and S.S. All authors have read and agreed to the published version of the manuscript.

Funding

This work was partially supported by the Japanese Society for the Promotion of Science under a Grant-in-Aid for Scientific Research (A, 19H01089 for S.S.; C, 21K11606 for Y.T.); by the Japan Science and Technology Agency under JST-Mirai Program (JMPJM120D5 for S.S.) and JST-FOREST Program (JPMJFR205G for Y.T.); and by the Foundation for Dietary Scientific Research under a research grant (May 2021 for Y.T.).

Institutional Review Board Statement

This study was approved by the Ethics Review Committee on Research with Human Subjects at Waseda University (No. 2020-046), and was conducted in accordance with the guidelines of the Declaration of Helsinki.

Informed Consent Statement

Informed consent was obtained from all individuals who participated in the study when they started using the app and answered the web survey. The participants completed the questionnaire anonymously to protect their privacy and maintain confidentiality.

Data Availability Statement

The data used in this study are the property of the company and will not be released to the public. However, the data will be provided to researchers, upon request, for research purposes.

Conflicts of Interest

A.T. and N.A. were full-time employees of asken Inc. M.M. is a corporate officer at asken Inc. The company’s policy was not involved in the study design, collection, analysis, interpretation of data, or the writing of the manuscript. The other authors report no conflict of interest.

References

  1. Roenneberg, T.; Merrow, M. The Circadian Clock and Human Health. Curr. Biol. 2016, 26, R432–R443. [Google Scholar] [CrossRef]
  2. Hida, A.; Kitamura, S.; Ohsawa, Y.; Enomoto, M.; Katayose, Y.; Motomura, Y.; Moriguchi, Y.; Nozaki, K.; Watanabe, M.; Aritake, S.; et al. In vitro circadian period is associated with circadian/sleep preference. Sci. Rep. 2013, 3, 2074. [Google Scholar] [CrossRef] [PubMed]
  3. Jones, S.E.; Lane, J.M.; Wood, A.R.; van Hees, V.T.; Tyrrell, J.; Beaumont, R.N.; Jeffries, A.R.; Dashti, H.S.; Hillsdon, M.; Ruth, K.S.; et al. Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms. Nat. Commun. 2019, 10, 343. [Google Scholar] [CrossRef]
  4. Roenneberg, T.; Allebrandt, K.V.; Merrow, M.; Vetter, C. Social jetlag and obesity. Curr. Biol. 2012, 22, 939–943. [Google Scholar] [CrossRef] [PubMed]
  5. Bauducco, S.; Richardson, C.; Gradisar, M. Chronotype, circadian rhythms and mood. Curr. Opin. Psychol. 2020, 34, 77–83. [Google Scholar] [CrossRef] [PubMed]
  6. Toscano-Hermoso, M.D.; Arbinaga, F.; Fernández-Ozcorta, E.J.; Gómez-Salgado, J.; Ruiz-Frutos, C. Influence of Sleeping Patterns in Health and Academic Performance Among University Students. Int. J. Environ. Res. Public Health 2020, 17, 2760. [Google Scholar] [CrossRef]
  7. Facer-Childs, E.R.; Middleton, B.; Skene, D.J.; Bagshaw, A.P. Resetting the late timing of ‘night owls’ has a positive impact on mental health and performance. Sleep Med. 2019, 60, 236–247. [Google Scholar] [CrossRef] [PubMed]
  8. Tahara, Y.; Shinto, T.; Inoue, K.; Roshanmehr, F.; Ito, A.; Michie, M.; Shibata, S. Changes in sleep phase and body weight of mobile health App users during COVID-19 mild lockdown in Japan. Int. J. Obes. 2021, 45, 2277–2280. [Google Scholar] [CrossRef]
  9. Korman, M.; Tkachev, V.; Reis, C.; Komada, Y.; Kitamura, S.; Gubin, D.; Kumar, V.; Roenneberg, T. Outdoor daylight exposure and longer sleep promote wellbeing under COVID-19 mandated restrictions. J. Sleep Res. 2022, 31, e13471. [Google Scholar] [CrossRef]
  10. Winnebeck, E.C.; Vuori-Brodowski, M.T.; Biller, A.M.; Molenda, C.; Fischer, D.; Zerbini, G.; Roenneberg, T. Later school start times in a flexible system improve teenage sleep. Sleep 2020, 43, zsz307. [Google Scholar] [CrossRef]
  11. Almoosawi, S.; Vingeliene, S.; Gachon, F.; Voortman, T.; Palla, L.; Johnston, J.D.; Van Dam, R.M.; Darimont, C.; Karagounis, L.G. Chronotype: Implications for Epidemiologic Studies on Chrono-Nutrition and Cardiometabolic Health. Adv. Nutr. 2019, 10, 30–42. [Google Scholar] [CrossRef] [PubMed]
  12. Mazri, F.H.; Manaf, Z.A.; Shahar, S.; Mat Ludin, A.F. The Association between Chronotype and Dietary Pattern among Adults: A Scoping Review. Int. J. Environ. Res. Public Health 2019, 17, 68. [Google Scholar] [CrossRef] [PubMed]
  13. Phoi, Y.Y.; Rogers, M.; Bonham, M.P.; Dorrian, J.; Coates, A.M. A scoping review of chronotype and temporal patterns of eating of adults: Tools used, findings, and future directions. Nutr. Res. Rev. 2021, 35, 112–135. [Google Scholar] [CrossRef] [PubMed]
  14. van der Merwe, C.; Münch, M.; Kruger, R. Chronotype Differences in Body Composition, Dietary Intake and Eating Behavior Outcomes: A Scoping Systematic Review. Adv. Nutr. 2022, 13, 2357–2405. [Google Scholar] [CrossRef] [PubMed]
  15. Sato-Mito, N.; Shibata, S.; Sasaki, S.; Sato, K. Dietary intake is associated with human chronotype as assessed by both morningness-eveningness score and preferred midpoint of sleep in young Japanese women. Int. J. Food Sci. Nutr. 2011, 62, 525–532. [Google Scholar] [CrossRef] [PubMed]
  16. Mito, N.; Fujimoto, E.; Sasaki, S.; The Three-Generation Study of Women on Diets and Health Study Group. Association of chronotype as assessed by the midpoint of sleep with the dietary intake and health-related quality of life for elderly Japanese women. J. Nutr. Sci. 2021, 10, e25. [Google Scholar] [CrossRef]
  17. Yoshizaki, T.; Togo, F. Objectively measured chronotype and social jetlag are associated with habitual dietary intake in undergraduate students. Nutr. Res. 2021, 90, 36–45. [Google Scholar] [CrossRef]
  18. Mota, M.C.; Silva, C.M.; Balieiro, L.C.T.; Gonçalves, B.F.; Fahmy, W.M.; Crispim, C.A. Association between social jetlag food consumption and meal times in patients with obesity-related chronic diseases. PLoS ONE 2019, 14, e0212126. [Google Scholar] [CrossRef]
  19. von Elm, E.; Altman, D.G.; Egger, M.; Pocock, S.J.; Gøtzsche, P.C.; Vandenbroucke, J.P. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: Guidelines for reporting observational studies. Lancet 2007, 370, 1453–1457. [Google Scholar] [CrossRef]
  20. Asken. Available online: https://en.asken.inc/ (accessed on 1 April 2023).
  21. Shimpo, M.; Fukkoshi, Y.; Akamatsu, R. Correlations between self-efficacy in resisting six temptations and dietary energy and macronutrient intake at each meal. Eat. Behav. 2014, 15, 563–566. [Google Scholar] [CrossRef]
  22. Shinozaki, N.; Murakami, K. Evaluation of the Ability of Diet-Tracking Mobile Applications to Estimate Energy and Nutrient Intake in Japan. Nutrients 2020, 12, 3327. [Google Scholar] [CrossRef] [PubMed]
  23. Sasaki, S. Dietary Reference Intakes for Japanese (2015): An Outline and Its Academic and Practical Significance. Nippon. Eiyo Shokuryo Gakkaishi 2017, 70, 53–59. [Google Scholar] [CrossRef]
  24. Craig, C.L.; Marshall, A.L.; Sjöström, M.; Bauman, A.E.; Booth, M.L.; Ainsworth, B.E.; Pratt, M.; Ekelund, U.; Yngve, A.; Sallis, J.F.; et al. International physical activity questionnaire: 12-country reliability and validity. Med. Sci. Sports Exerc. 2003, 35, 1381–1395. [Google Scholar] [CrossRef]
  25. Kitamura, S.; Hida, A.; Aritake, S.; Higuchi, S.; Enomoto, M.; Kato, M.; Vetter, C.; Roenneberg, T.; Mishima, K. Validity of the Japanese version of the Munich ChronoType Questionnaire. Chronobiol. Int. 2014, 31, 845–850. [Google Scholar] [CrossRef] [PubMed]
  26. Okajima, I.; Nakajima, S.; Kobayashi, M.; Inoue, Y. Development and validation of the Japanese version of the Athens Insomnia Scale. Psychiatry Clin. Neurosci. 2013, 67, 420–425. [Google Scholar] [CrossRef] [PubMed]
  27. Tahara, Y.; Makino, S.; Suiko, T.; Nagamori, Y.; Iwai, T.; Aono, M.; Shibata, S. Association between Irregular Meal Timing and the Mental Health of Japanese Workers. Nutrients 2021, 13, 2775. [Google Scholar] [CrossRef] [PubMed]
  28. Imamura, M.; Sasaki, H.; Shinto, T.; Tahara, Y.; Makino, S.; Kuwahara, M.; Tada, A.; Abe, N.; Michie, M.; Shibata, S. Association Between Na, K, and Lipid Intake in Each Meal and Blood Pressure. Front. Nutr. 2022, 9, 853118. [Google Scholar] [CrossRef]
  29. Shinto, T.; Makino, S.; Tahara, Y.; Nitta, L.; Kuwahara, M.; Tada, A.; Abe, N.; Michie, M.; Shibata, S. Relationship Between Protein Intake in Each Traditional Meal and Physical Activity: Cross-sectional Study. JMIR Public Health Surveill 2022, 8, e35898. [Google Scholar] [CrossRef]
  30. Fleig, D.; Randler, C. Association between chronotype and diet in adolescents based on food logs. Eat. Behav. 2009, 10, 115–118. [Google Scholar] [CrossRef]
  31. Maukonen, M.; Kanerva, N.; Partonen, T.; Kronholm, E.; Konttinen, H.; Wennman, H.; Männistö, S. The associations between chronotype, a healthy diet and obesity. Chronobiol. Int. 2016, 33, 972–981. [Google Scholar] [CrossRef]
  32. World Health Organization. Guideline: Sodium Intake for Adults and Children; World Health Organization: Geneva, Switzerland, 2012. [Google Scholar]
  33. Veronese, N.; Solmi, M.; Caruso, M.G.; Giannelli, G.; Osella, A.R.; Evangelou, E.; Maggi, S.; Fontana, L.; Stubbs, B.; Tzoulaki, I. Dietary fiber and health outcomes: An umbrella review of systematic reviews and meta-analyses. Am. J. Clin. Nutr. 2018, 107, 436–444. [Google Scholar] [CrossRef] [PubMed]
  34. Ross, A.; Caballero, B.H.; Cousins, R.J.; Tucker, K.L.; Ziegler, T.R. Modern Nutrition in Health and Disease, 11th ed.; Wolters Kluwer Health ADIS (ESP): London, UK, 2012. [Google Scholar]
  35. Chang, A.R.; Anderson, C. Dietary Phosphorus Intake and the Kidney. Annu. Rev. Nutr. 2017, 37, 321–346. [Google Scholar] [CrossRef] [PubMed]
  36. Salma; Ahmad, S.S.; Karim, S.; Ibrahim, I.M.; Alkreathy, H.M.; Alsieni, M.; Khan, M.A. Effect of Vitamin K on Bone Mineral Density and Fracture Risk in Adults: Systematic Review and Meta-Analysis. Biomedicines 2022, 10, 1048. [Google Scholar] [CrossRef] [PubMed]
  37. Zeron-Rugerio, M.F.; Cambras, T.; Izquierdo-Pulido, M. Social Jet Lag Associates Negatively with the Adherence to the Mediterranean Diet and Body Mass Index among Young Adults. Nutrients 2019, 11, 1756. [Google Scholar] [CrossRef]
  38. Mathew, G.M.; Hale, L.; Chang, A.M. Social jetlag, eating behaviours and BMI among adolescents in the USA. Br. J. Nutr. 2020, 124, 979–987. [Google Scholar] [CrossRef]
  39. Cetiner, O.; Yildirim, G.; Kalyoncu, Z.B. Social Jetlag Is Associated with the Frequency of Consumption of Sugar-Sweetened Beverages and a High BMI Percentile in Adolescents: Results of the Cross-Sectional Family Life, Activity, Sun, Health, and Eating (FLASHE) Study. J. Acad. Nutr. Diet 2021, 121, 1721–1731.e1. [Google Scholar] [CrossRef]
  40. Tahara, Y.; Shibata, S. Chronobiology and nutrition. Neuroscience 2013, 253, 78–88. [Google Scholar] [CrossRef]
  41. Hirao, A.; Nagahama, H.; Tsuboi, T.; Hirao, M.; Tahara, Y.; Shibata, S. Combination of starvation interval and food volume determines the phase of liver circadian rhythm in Per2::Luc knock-in mice under two meals per day feeding. Am. J. Physiol. Gastrointest Liver Physiol. 2010, 299, G1045–G1053. [Google Scholar] [CrossRef]
  42. Tahara, Y.; Otsuka, M.; Fuse, Y.; Hirao, A.; Shibata, S. Refeeding after fasting elicits insulin-dependent regulation of Per2 and Rev-erbα with shifts in the liver clock. J. Biol. Rhythms. 2011, 26, 230–240. [Google Scholar] [CrossRef]
  43. Crosby, P.; Hamnett, R.; Putker, M.; Hoyle, N.P.; Reed, M.; Karam, C.J.; Maywood, E.S.; Stangherlin, A.; Chesham, J.E.; Hayter, E.A.; et al. Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time. Cell 2019, 177, 896–909.e20. [Google Scholar] [CrossRef]
  44. Varsamis, N.A.; Christou, G.A.; Kiortsis, D.N. A critical review of the effects of vitamin K on glucose and lipid homeostasis: Its potential role in the prevention and management of type 2 diabetes. Hormones 2021, 20, 415–422. [Google Scholar] [CrossRef] [PubMed]
  45. de Sousa Melo, S.R.; Dos Santos, L.R.; da Cunha Soares, T.; Cardoso, B.E.P.; da Silva Dias, T.M.; Morais, J.B.S.; de Paiva Sousa, M.; de Sousa, T.G.V.; da Silva, N.C.; da Silva, L.D.; et al. Participation of Magnesium in the Secretion and Signaling Pathways of Insulin: An Updated Review. Biol. Trace. Elem. Res. 2022, 200, 3545–3553. [Google Scholar] [CrossRef] [PubMed]
  46. Kim, H.K.; Chijiki, H.; Nanba, T.; Ozaki, M.; Sasaki, H.; Takahashi, M.; Shibata, S. Ingestion of Helianthus tuberosus at Breakfast Rather Than at Dinner Is More Effective for Suppressing Glucose Levels and Improving the Intestinal Microbiota in Older Adults. Nutrients 2020, 12, 3035. [Google Scholar] [CrossRef]
  47. Kuwahara, M.; Kim, H.K.; Ozaki, M.; Nanba, T.; Chijiki, H.; Fukazawa, M.; Okubo, J.; Mineshita, Y.; Takahashi, M.; Shibata, S. Consumption of Biscuits with a Beverage of Mulberry or Barley Leaves in the Afternoon Prevents Dinner-Induced High, but Not Low, Increases in Blood Glucose among Young Adults. Nutrients 2020, 12, 1580. [Google Scholar] [CrossRef] [PubMed]
  48. Haraguchi, A.; Fukuzawa, M.; Iwami, S.; Nishimura, Y.; Motohashi, H.; Tahara, Y.; Shibata, S. Night eating model shows time-specific depression-like behavior in the forced swimming test. Sci. Rep. 2018, 8, 1081. [Google Scholar] [CrossRef]
  49. Ikeda, Y.; Kamagata, M.; Hirao, M.; Yasuda, S.; Iwami, S.; Sasaki, H.; Tsubosaka, M.; Hattori, Y.; Todoh, A.; Tamura, K.; et al. Glucagon and/or IGF-1 Production Regulates Resetting of the Liver Circadian Clock in Response to a Protein or Amino Acid-only Diet. EBioMedicine 2018, 28, 210–224. [Google Scholar] [CrossRef] [PubMed]
  50. Aoyama, S.; Kim, H.K.; Hirooka, R.; Tanaka, M.; Shimoda, T.; Chijiki, H.; Kojima, S.; Sasaki, K.; Takahashi, K.; Makino, S.; et al. Distribution of dietary protein intake in daily meals influences skeletal muscle hypertrophy via the muscle clock. Cell Rep. 2021, 36, 109336. [Google Scholar] [CrossRef]
  51. Islam, Z.; Akter, S.; Kochi, T.; Hu, H.; Eguchi, M.; Yamaguchi, M.; Kuwahara, K.; Kabe, I.; Mizoue, T. Association of social jetlag with metabolic syndrome among Japanese working population: The Furukawa Nutrition and Health Study. Sleep Med. 2018, 51, 53–58. [Google Scholar] [CrossRef]
  52. Zhang, Z.; Cajochen, C.; Khatami, R. Social Jetlag and Chronotypes in the Chinese Population: Analysis of Data Recorded by Wearable Devices. J. Med. Internet Res. 2019, 21, e13482. [Google Scholar] [CrossRef]
  53. Liang, F.; Fu, J.; Xu, Y.; Wang, Y.; Qiu, N.; Ding, K.; Zeng, J.; Moore, J.B.; Li, R. Associations of Social Jetlag with Dietary Behavior, Physical Activity and Obesity among Chinese Adolescents. Nutrients 2022, 14, 510. [Google Scholar] [CrossRef]
  54. Hall, W.L. The emerging importance of tackling sleep-diet interactions in lifestyle interventions for weight management. Br. J. Nutr. 2022, 128, 561–568. [Google Scholar] [CrossRef] [PubMed]
  55. Vrabec, A.; Yuhas, M.; Deyo, A.; Kidwell, K. Social jet lag and eating styles in young adults. Chronobiol. Int. 2022, 39, 1277–1284. [Google Scholar] [CrossRef] [PubMed]
  56. Flanagan, A.; Bechtold, D.A.; Pot, G.K.; Johnston, J.D. Chrono-nutrition: From molecular and neuronal mechanisms to human epidemiology and timed feeding patterns. J. Neurochem. 2021, 157, 53–72. [Google Scholar] [CrossRef] [PubMed]
  57. Zerón-Rugerio, M.F.; Hernáez, Á.; Porras-Loaiza, A.P.; Cambras, T.; Izquierdo-Pulido, M. Eating Jet Lag: A Marker of the Variability in Meal Timing and Its Association with Body Mass Index. Nutrients 2019, 11, 2980. [Google Scholar] [CrossRef] [PubMed]
  58. Makarem, N.; Sears, D.D.; St-Onge, M.P.; Zuraikat, F.M.; Gallo, L.C.; Talavera, G.A.; Castaneda, S.F.; Lai, Y.; Aggarwal, B. Variability in Daily Eating Patterns and Eating Jetlag Are Associated With Worsened Cardiometabolic Risk Profiles in the American Heart Association Go Red for Women Strategically Focused Research Network. J. Am. Heart Assoc. 2021, 10, e022024. [Google Scholar] [CrossRef] [PubMed]
  59. Takahashi, M.; Ozaki, M.; Kang, M.-I.; Sasaki, H.; Fukazawa, M.; Iwakami, T.; Lim, P.J.; Kim, H.-K.; Aoyama, S.; Shibata, S. Effects of Meal Timing on Postprandial Glucose Metabolism and Blood Metabolites in Healthy Adults. Nutrients 2018, 10, 1763. [Google Scholar] [CrossRef]
  60. Tanaka, N.; Okuda, T.; Shinohara, H.; Yamasaki, R.S.; Hirano, N.; Kang, J.; Ogawa, M.; Nishi, N.N. Relationship between Seasonal Changes in Food Intake and Energy Metabolism, Physical Activity, and Body Composition in Young Japanese Women. Nutrients 2022, 14, 506. [Google Scholar] [CrossRef]
Table 1. General characteristics of the study group.
Table 1. General characteristics of the study group.
WomenMen
N = 3427N = 1199
MeanSDMeanSD
Age (years old)40.910.545.69.3
Height (cm)158.75.6171.45.9
BMI (kg/m2)21.07.322.97.8
Weight (kg)58.111.074.113.7
Daily total energy intake (kcal)1652.9283.12068.9408.0
Breakfast energy intake (kcal)349.3124.7429.1154.1
Lunch energy intake (kcal)518.6119.8647.2145.5
Dinner energy intake (kcal)572.3163.8802.3200.3
Snacks energy (kcal)222.898.1263.3135.4
Daily totalProtein (%)17.24.017.25.9
Lipid (%)32.16.232.29.1
Carbohydrate (%)48.87.049.116.4
BreakfastProtein (%)17.56.917.68.1
Lipid (%)28.28.327.58.8
Carbohydrate (%)54.811.053.012.5
LunchProtein (%)16.94.316.14.7
Lipid (%)30.86.130.26.1
Carbohydrate (%)50.87.750.47.9
DinnerProtein (%)19.45.117.85.5
Lipid (%)33.76.632.37.0
Carbohydrate (%)42.69.340.610.2
% protein, lipids, and carbohydrates were calculated based on the total energy intake in each meal, or total daily intake (kcal).
Table 2. Basic characteristics of each chronotype among women.
Table 2. Basic characteristics of each chronotype among women.
MorningIntermediateEvening
(MSFsc < 3)
N = 950
(3 ≤ MSFsc < 5)
N = 1890
(5 ≤ MSFsc)
N = 587
Kruskal–Wallis TestSpearman’s
MeanSDMeanSDMeanSDpCorrelation Coefficient
Age (year)44.09.540.810.536.110.2<0.001−0.24
Height (cm)158.55.5158.85.6158.75.60.6580.01
BMI20.77.221.07.221.67.60.0020.06
Weight (kg)57.211.058.110.859.611.8<0.0010.07
Daily intake (kcal)1645.3276.31647.6277.81682.0308.50.1010.02
Breakfast intake (kcal)379.8122.8345.2119.2313.3133.7<0.001−0.18
Lunch intake (kcal)517.6116.9519.8116.5516.7134.40.8070.00
Dinner intake (kcal)547.3165.5570.7159.3617.9166.2<0.0010.13
Breakfast time (hh:mm)7:171:167:511:118:521:52<0.0010.37
Lunch time (hh:mm)12:171:0912:291:1313:031:35<0.0010.20
Dinner time (hh:mm)18:441:3219:071:1819:252:22<0.0010.24
SD of breakfast time (min)16.031.324.235.834.948.5<0.0010.14
SD of lunch time (min)12.727.718.531.230.241.4<0.0010.16
SD of dinner time (min)12.527.818.540.427.855.9<0.0010.11
Regularities in the rhythm of life (score)4.10.83.80.93.01.2<0.001−0.35
MSFsc (h)2.30.63.90.65.70.5<0.0010.90
SJL (h)0.60.50.90.71.10.8<0.0010.24
Frequency of breakfast (days/week)6.61.46.21.74.82.5<0.001−0.32
Frequency of late-night snack (days/week)1.82.71.92.62.12.6<0.0010.08
METs (total physical activity)34.144.427.534.727.540.50.008−0.05
AIS score4.13.34.43.35.03.6<0.0010.09
Physical strength (score)2.81.02.81.02.70.90.015−0.05
Health (score)3.70.93.70.93.40.9<0.001−0.10
Well-being (score)3.60.93.51.03.40.9<0.001−0.10
SD, standard deviation; BMI, body mass index; SJL, social jetlag; METs, metabolic equivalents; AIS, Athens Insomnia Scale; MSFsc, sleep-corrected midpoint of sleep on free days. p-values were calculated using the Kruskal–Wallis test. p < 0.001 was considered significant and is presented in bold font. A Spearman’s correlation coefficient of more than 0.2 or lower than −0.2 is presented in bold.
Table 3. Basic characteristics of each chronotype among men.
Table 3. Basic characteristics of each chronotype among men.
MorningIntermediateEvening
(MSFsc < 3)(3 ≤ MSFsc ≤ 5)(5 < MSFsc)
N = 475N = 588N = 136Kruskal–Wallis TestSpeaman’s
MeanSDMeanSDMeanSDpCorrelation Coefficient
Age (year old)48.08.244.79.540.99.9<0.001−0.23
Height (cm)171.25.9171.65.9171.76.00.4550.04
BMI22.57.523.07.824.18.20.0540.07
Weight (kg)72.812.774.413.377.317.60.0270.08
Daily intake (kcal)2061.1415.32084.5402.22028.9406.60.383−0.01
Breakfast intake (kcal)459.2149.2418.4147.2371.6177.0<0.001−0.18
Lunch intake (kcal)632.1145.9661.6144.1637.1145.10.0050.05
Dinner intake (kcal)794.9198.3808.0200.9803.4205.10.5860.03
Breakfast time (hh:mm)7:061:077:401:068:262:04<0.0010.34
Lunch time (hh:mm)12:160:5612:260:5512:511:17<0.0010.18
Dinner time (hh:mm)19:131:2219:301:1419:272:17<0.0010.14
SD of breakfast time (min)25.741.828.039.238.656.60.1000.06
SD of lunch time (min)16.233.920.332.029.445.70.0040.10
SD of dinner time (min)23.346.628.956.646.2107.10.1160.06
Regularities in the rhythm of life (score)4.10.83.90.83.21.2<0.001−0.22
MSFsc (h)2.10.63.80.55.70.5<0.0010.91
SJL (h)0.50.50.80.61.20.9<0.0010.32
Frequency of breakfast (days/week)6.41.66.21.85.32.4<0.001−0.20
Frequency of late night snack (days/week)2.02.92.22.82.92.9<0.0010.11
Mets (total physical activity)39.943.435.836.830.633.20.008−0.09
AIS score3.93.34.13.24.53.30.0470.07
Physical strength (score)3.11.03.00.93.01.00.328−0.04
Health (score)3.90.83.70.93.80.90.004−0.09
Well-being (score)3.60.93.50.93.31.00.008−0.08
SD: standard deviation; BMI: body mass index; SJL: social jetlag; Mets: metabolic equivalents; AIS: Athens Insomnia Scale; MSFsc: sleep-corrected midpoint of sleep in free days. p value was calculated using a Kruskal–Wallis test. p < 0.001 was considered as significant and shown in bold. Spearman’s correlation coefficient with more than 0.2 or lower than −0.2 was shown in bold.
Table 4. Basic characteristics of each SJL group among women.
Table 4. Basic characteristics of each SJL group among women.
Small SJLMedium SJLLarge SJL
(SJL < 1)
N = 2002
(1 ≤ SJL < 2)
N = 1138
(2 ≤ SJL)
N = 287
Kruskal–Wallis TestSpearman’s
MeanSDMeanSDMeanSDp ValueCorrelation Coefficient
Age (year)41.810.640.310.036.810.2<0.001−0.13
Height (cm)158.65.6158.75.7158.95.40.7240.01
BMI21.07.221.17.221.17.70.0840.04
Weight (kg)57.811.358.310.759.310.80.0190.05
Daily intake (kcal)1641.9285.51654.4275.31723.2287.6<0.0010.05
Breakfast intake (kcal)355.2125.4342.1120.5336.3134.10.002−0.06
Lunch intake (kcal)515.9120.1519.1116.4535.7130.10.0920.03
Dinner intake (kcal)560.5163.6581.2159.2619.0173.0<0.0010.09
Breakfast time (hh:mm)7.91.57.81.37.71.40.193−0.03
Lunch time (hh:mm)12.51.412.51.212.60.90.69−0.01
Dinner time (hh:mm)19.01.719.21.419.31.6<0.0010.10
SD of breakfast time (min)20.334.326.840.035.545.8<0.0010.09
SD of lunch time (min)18.230.819.435.722.533.70.1590.02
SD of dinner time (min)17.238.118.742.425.751.30.0320.03
Regularities in the rhythm of life (score)3.81.03.71.03.31.1<0.001−0.15
MSFsc (h)3.51.33.91.14.60.9<0.0010.28
SJL (h)0.40.31.30.32.30.4<0.0010.88
Frequency of breakfast (days/week)6.11.96.01.85.42.1<0.001−0.14
Frequency of late-night snack (days/week)1.92.72.02.71.92.50.0310.05
METs (total physical activity)29.737.928.034.031.657.80.547−0.02
AIS score4.33.34.53.45.23.6<0.0010.07
Physical strength (score)2.91.02.70.92.60.9<0.001−0.09
Health (score)3.70.93.60.93.50.9<0.001−0.06
Well-being (score)3.61.03.50.93.40.9<0.001−0.06
SD, standard deviation; BMI, body mass index; SJL, social jetlag; METs, metabolic equivalents; AIS, Athens Insomnia Scale; MSFsc, sleep-corrected midpoint of sleep on free days. p-values were calculated using the Kruskal–Wallis test. p < 0.001 was considered significant and is presented in bold font. A Spearman’s correlation coefficient of more than 0.2 or lower than −0.2 is presented in bold.
Table 5. Basic characteristics of each SJL group among men.
Table 5. Basic characteristics of each SJL group among men.
Small SJLIntermediate SJLLarge SJL
(SJL < 1)(1 ≤ SJL < 2)(2 ≤ SJL)
N = 780N = 348N = 71Kruskal–Wallis TestSpeaman’s
MeanSDMeanSDMeanSDp ValueCorrelation Coefficient
Age (year old)45.99.245.69.141.910.50.007−0.06
Height (cm)171.45.8171.56.2171.45.51.0000.00
BMI22.87.522.88.425.16.10.0160.06
Weight (kg)73.513.474.814.077.214.90.0620.06
Daily intake (kcal)2077.5394.42040.2431.52114.3433.00.541−0.01
Breakfast intake (kcal)437.3153.4413.9153.3413.9160.60.037−0.07
Lunch intake (kcal)647.0145.0650.8146.8630.9145.90.348−0.01
Dinner intake (kcal)799.7196.7804.5207.4820.8207.00.6840.02
Breakfast time (hh:mm)7:321:167:321:267:291:220.5530.03
Lunch time (hh:mm)12:240:5412:251:0212:341:270.2430.05
Dinner time (hh:mm)19:211:2519:261:4219:351:170.1050.06
SD of breakfast time (min)23.038.635.546.151.054.4<0.0010.17
SD of lunch time (min)17.634.022.935.127.838.8<0.0010.11
SD of dinner time (min)24.953.736.676.030.458.10.0300.08
Regularities in the rhythm of life (score)4.00.93.80.93.61.0<0.001−0.17
MSFsc (h)3.11.23.71.24.51.1<0.0010.32
SJL (h)0.30.31.30.32.40.5<0.0010.85
Frequency of breakfast (days/week)6.31.86.11.95.82.2<0.001−0.11
Frequency of late night snack (days/week)2.12.92.32.92.72.80.0710.06
Mets (total physical activity)37.738.833.136.445.953.20.004−0.06
AIS score3.83.04.53.64.63.80.0050.09
Physical strength (score)3.10.93.00.92.91.00.011−0.09
Health (score)3.90.83.60.93.80.8<0.001−0.15
Well-being (score)3.60.93.41.03.50.9<0.001−0.10
SD: standard deviation; BMI: body mass index; SJL: social jetlag; Mets: metabolic equivalents; AIS: Athens Insomnia Scale; MSFsc: sleep-corrected midpoint of sleep in free days. p value was calculated using a Kruskal–Wallis test. p < 0.001 was considered as significant and shown in bold. Spearman’s correlation coefficient with more than 0.2 or lower than −0.2 was shown in bold.
Table 6. Association between chronotype/SJL and daily total nutrient intake by multiple regression analyses.
Table 6. Association between chronotype/SJL and daily total nutrient intake by multiple regression analyses.
Dependent VariableIndependent Variable: ChronotypeIndependent Variable: SJL
Daily Total IntakeR2BMinMaxp ValueR2BMinMaxp Value
Energy0.255.19−2.4012.790.1800.2522.088.4535.710.002
Protein0.30−0.11−0.470.240.5230.30−0.85−1.48−0.220.008
Lipid0.540.290.050.540.0210.540.460.010.900.047
Carbohydrate0.590.21−0.571.000.5920.590.65−0.762.060.365
Sodium0.39−9.48−26.487.530.2750.3932.331.7962.880.038
Potassium0.14−40.24−53.90−26.59<0.0010.13−44.13−68.72−19.54<0.001
Cholesterol0.090.42−1.212.050.6130.09−1.88−4.811.040.207
Fiber0.08−0.49−0.62−0.36<0.0010.08−0.74−0.97−0.51<0.001
Saturated fatty acid0.390.100.010.190.0250.390.180.020.340.025
Alcohol0.09−0.29−0.48−0.100.0020.090.16−0.170.490.348
Calcium0.05−0.76−6.434.910.7930.05−14.15−24.33−3.960.006
Magnesium0.10−3.63−5.82−1.44<0.0010.10−7.41−11.34−3.48<0.001
Phosphorus0.31−14.26−18.98−9.54<0.0010.31−13.87−22.37−5.37<0.001
Iron0.010.03−0.110.170.6630.01−0.06−0.310.190.630
Zinc0.100.05−0.070.160.4260.10−0.06−0.260.140.570
Vitamin A0.029.40−5.2924.090.2100.02−6.28−32.6820.130.641
Vitamin D0.000.18−0.640.990.6700.001.31−0.162.770.080
Vitamin E0.000.540.011.070.0470.00−0.05−1.010.910.915
Vitamin K0.04−12.63−15.65−9.61<0.0010.03−17.14−22.59−11.70<0.001
Vitamin B10.010.200.030.360.0180.00−0.14−0.430.150.349
Vitamin B20.000.09−0.080.260.2910.00−0.16−0.460.140.297
Vitamin B30.030.10−0.420.620.7010.03−0.31−1.240.630.521
Vitamin B60.000.02−0.170.210.8100.00−0.09−0.430.260.627
Vitamin B120.00−0.07−0.990.850.8800.00−1.05−2.710.600.213
Folate0.02−3.41−8.111.290.1550.02−8.99−17.43−0.550.037
Vitamin B50.02−0.06−0.210.090.4270.02−0.34−0.61−0.070.014
Vitamin C0.008.350.0516.640.0490.0011.55−3.3626.450.129
Multiple regression analyses were conducted with each nutrient intake amount as a dependent variable and chronotype (1: morning, 2: intermediate, and 3: evening) or SJL (1: small SJL, 2: medium SJL, and 3: large SJL) as an independent variable in each calculation. Age, gender, BMI, and total daily intake were used as confounding factors. Significant p-values of the independent variable (chronotype or SJL) are presented in bold (p < 0.001).
Table 7. Association between chronotype /SJL and breakfast nutrient intake by multiple regression analyses.
Table 7. Association between chronotype /SJL and breakfast nutrient intake by multiple regression analyses.
Dependent VariableIndependent Variable: ChronotypeIndependent Variable: SJL
Brakfast IntakeR2BMinMaxp ValueR2BMinMaxp Value
Energy0.29−21.88−24.66−19.09<0.0010.26−14.82−19.89−9.75<0.001
Protein0.12−1.04−1.21−0.87<0.0010.100.010.000.01<0.001
Lipid0.19−0.71−0.83−0.59 <0.0010.17−0.51−0.73−0.30<0.001
Carbohydrate0.23−2.99−3.41−2.56 <0.0010.20−1.71−2.48−0.94<0.001
Sodium0.14−50.84−59.16−42.52 <0.0010.11−24.07−39.16−8.970.002
Potassium0.08−44.69−51.56−37.81 <0.0010.05 −39.94−52.36−27.52<0.001
Cholesterol0.06−6.71−7.83−5.59 <0.0010.03−4.87−6.90−2.83<0.001
Fiber0.04−0.41−0.48−0.34 <0.0010.02−0.42−0.55−0.30<0.001
Saturated fatty acid0.15−0.18−0.22−0.14 <0.0010.14−0.13−0.20−0.06<0.001
Alcohol0.05−0.02−0.02−0.01 <0.0010.04−0.01−0.030.000.058
Calcium0.03−8.87−11.96−5.79 <0.0010.03−6.70−12.24−1.1600.018
Magnesium0.05−4.74−5.85−3.63 <0.0010.04−4.53−6.53−2.53<0.001
Phosphorus0.13−19.15−21.56−16.75 <0.0010.09−14.67−19.07−10.26<0.001
Iron0.00−0.12−0.23−0.020.0230.00−0.03−0.220.160.752
Zinc0.04−0.10−0.16−0.05<0.0010.03−0.06−0.150.040.225
Vitamin A0.02−6.93−13.17−0.700.0290.020.03−11.1511.210.996
Vitamin D0.00−0.42−0.72−0.110.0080.00−0.24−0.800.310.388
Vitamin E0.00−0.24−0.570.090.1490.000.16−0.430.740.594
Vitamin K0.04−9.77−11.46−8.09<0.0010.02−9.57−12.63−6.52<0.001
Vitamin B10.00−0.04−0.130.060.4220.00−0.08−0.250.090.348
Vitamin B20.00−0.07−0.180.030.1600.00−0.09−0.280.090.318
Vitamin B30.01−0.40−0.71−0.100.0100.01−0.24−0.780.310.397
Vitamin B60.00−0.08−0.180.030.1510.00−0.14−0.330.050.137
Vitamin B120.00−0.07−0.450.310.7220.00−0.14−0.830.540.681
Folate0.01−5.75−8.60−2.90<0.0010.01−4.72−9.830.390.070
Vitamin B50.01−0.18−0.27−0.08<0.0010.01−0.22−0.39−0.050.013
Vitamin C0.002.82−1.807.430.2320.002.10−6.1810.370.620
Multiple regression analyses were conducted with each nutrient intake amount as a dependent variable and chronotype (1: morning, 2: intermediate, and 3: evening) or SJL (1: small SJL, 2: medium SJL, and 3: large SJL) as an independent variable in each calculation. Age, gender, BMI, and total daily intake were used as confounding factors. Significant p-values of the independent variable (chronotype or SJL) are presented in bold (p < 0.001).
Table 8. Association between chronotype /SJL and lunch nutrient intake by multiple regression analyses.
Table 8. Association between chronotype /SJL and lunch nutrient intake by multiple regression analyses.
Dependent VariableIndependent Variable: ChronotypeIndependent Variable: SJL
Lunch IntakeR2BMinMaxp ValueR2BMinMaxp Value
Energy0.46−2.67−5.12−0.220.0330.46−0.91−5.313.500.686
Protein0.18−0.21−0.36−0.070.0040.18−0.27−0.53−0.010.040
Lipid0.260.06−0.070.190.3550.260.03−0.200.260.808
Carbohydrate0.38−0.48−0.85−0.110.0100.38−0.09−0.750.570.791
Sodium0.23−6.71−15.632.210.1400.2310.58−5.4426.600.196
Potassium0.05−15.47−20.92−10.02<0.0010.04−17.32−27.10−7.53<0.001
Cholesterol0.03−2.02−2.99−1.06<0.0010.03−4.26−5.99−2.53<0.001
Fiber0.03−0.15−0.20−0.10<0.0010.03−0.23−0.32−0.14<0.001
Saturated fatty acid0.180.02−0.020.060.2800.18−0.01−0.070.060.895
Alcohol0.04−0.03−0.05−0.010.0040.030.00−0.040.040.883
Calcium0.02−0.35−1.961.270.6730.02−4.08−6.97−1.180.006
Magnesium0.05−1.48−2.14−0.81<0.0010.05−2.19−3.38−1.00<0.001
Phosphorus0.13−5.64−7.70−3.57<0.0010.12−5.60−9.32−1.890.003
Iron0.03−0.03−0.050.000.0570.03−0.06−0.10−0.010.015
Zinc0.05−0.03−0.060.010.1360.050.02−0.040.080.576
Vitamin A0.01−8.26−12.76−3.76<0.0010.00−6.00−14.102.090.146
Vitamin D0.000.22−0.160.600.2570.000.820.151.500.017
Vitamin E0.010.03−0.060.110.5510.01−0.07−0.220.080.375
Vitamin K0.01−2.87−4.02−1.72<0.0010.01−5.45−7.52−3.39<0.001
Vitamin B10.000.02−0.010.040.1770.000.01−0.040.050.711
Vitamin B20.000.02−0.010.050.2060.000.00−0.060.060.993
Vitamin B30.09−0.11−0.18−0.030.0050.08−0.09−0.220.040.191
Vitamin B60.000.01−0.020.040.4990.000.00−0.050.050.991
Vitamin B120.00−0.10−0.250.050.2050.00−0.16−0.430.110.247
Folate0.01−2.78−4.14−1.41<0.0010.01−3.83−6.27−1.380.002
Vitamin B50.03−0.02−0.050.000.0850.03−0.05−0.100.000.048
Vitamin C0.000.33−1.181.840.6710.00−1.39−4.111.320.314
Multiple regression analyses were conducted with each nutrient intake amount as a dependent variable and chronotype (1: morning, 2: intermediate, and 3: evening) or SJL (1: small SJL, 2: medium SJL, and 3: large SJL) as an independent variable in each calculation. Age, gender, body mass index, and total daily intake were used as confounding factors. Significant p-values of the independent variable (chronotype or SJL) are presented in bold (p < 0.001).
Table 9. Association between chronotype/SJL and dinner nutrient intake by multiple regression analyses.
Table 9. Association between chronotype/SJL and dinner nutrient intake by multiple regression analyses.
Dependent VariableIndependent Variable: ChronotypeIndependent Variable: SJL
Dinner IntakeR2BMinMaxp ValueR2BMinMaxp Value
Energy0.5515.7612.5518.98<0.0010.5516.5410.7222.36<0.001
Protein0.290.700.520.87<0.0010.280.640.330.96<0.001
Lipid0.330.630.470.79<0.0010.320.720.431.00<0.001
Carbohydrate0.372.672.213.12<0.0010.352.121.282.95<0.001
Sodium0.2341.6031.2251.99<0.0010.2243.0624.3361.78<0.001
Potassium0.129.242.4616.010.0080.12−0.64−12.7911.520.918
Cholesterol0.111.900.902.90<0.0010.112.200.413.990.016
Fiber0.090.060.000.110.0390.09−0.06−0.160.040.209
Saturated fatty acid0.270.170.120.22<0.0010.270.210.120.30<0.001
Alcohol0.09−0.34−0.51−0.17<0.0010.090.16−0.140.470.294
Calcium0.030.25−1.942.450.8210.03−1.53−5.472.410.447
Magnesium0.090.61−0.351.570.2100.09−0.35−2.071.380.694
Phosphorus0.226.634.069.20<0.0010.226.421.8011.040.006
Iron0.020.080.020.130.0090.020.09−0.010.190.092
Zinc0.050.090.020.160.0090.05−0.03−0.150.090.572
Vitamin A0.0115.063.9926.140.0080.001.88−18.0421.790.854
Vitamin D0.000.08−0.140.310.4680.000.16−0.250.570.444
Vitamin E0.000.260.050.460.0140.00−0.10−0.470.270.607
Vitamin K0.02−0.35−2.051.350.6880.02−1.90−4.951.160.223
Vitamin B10.000.080.020.140.0100.00−0.04−0.150.070.462
Vitamin B20.000.04−0.030.110.2170.00−0.08−0.210.040.205
Vitamin B30.010.430.140.710.0040.010.18−0.340.700.487
Vitamin B60.000.03−0.030.090.3530.00−0.03−0.150.080.556
Vitamin B120.000.17−0.540.880.6440.00−0.40−1.670.880.543
Folate0.021.69−0.163.540.0730.020.21−3.113.530.900
Vitamin B50.010.05−0.010.100.0930.01−0.02−0.120.080.741
Vitamin C0.001.49−1.974.940.3990.005.24−0.9611.440.098
Multiple regression analyses were conducted with each nutrient intake amount as a dependent variable and chronotype (1: morning, 2: intermediate, and 3: evening) or SJL (1, small SJL, 2: medium SJL, and 3: large SJL) as an independent variable in each calculation. Age, gender, body mass index, and total daily intake were used as confounding factors. Significant p-values of the independent variable (chronotype or SJL) are presented in bold (p < 0.001).
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Nitta, L.; Tahara, Y.; Shinto, T.; Makino, S.; Kuwahara, M.; Tada, A.; Abe, N.; Michie, M.; Shibata, S. Association of Eating Pattern, Chronotype, and Social Jetlag: A Cross-Sectional Study Using Data Accumulated in a Japanese Food-Logging Mobile Health Application. Nutrients 2023, 15, 2165. https://doi.org/10.3390/nu15092165

AMA Style

Nitta L, Tahara Y, Shinto T, Makino S, Kuwahara M, Tada A, Abe N, Michie M, Shibata S. Association of Eating Pattern, Chronotype, and Social Jetlag: A Cross-Sectional Study Using Data Accumulated in a Japanese Food-Logging Mobile Health Application. Nutrients. 2023; 15(9):2165. https://doi.org/10.3390/nu15092165

Chicago/Turabian Style

Nitta, Lyie, Yu Tahara, Takae Shinto, Saneyuki Makino, Mai Kuwahara, Ayako Tada, Nanako Abe, Mikiko Michie, and Shigenobu Shibata. 2023. "Association of Eating Pattern, Chronotype, and Social Jetlag: A Cross-Sectional Study Using Data Accumulated in a Japanese Food-Logging Mobile Health Application" Nutrients 15, no. 9: 2165. https://doi.org/10.3390/nu15092165

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop