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Article

Early Childhood Diet in Relation to Toddler Nighttime Sleep Duration Trajectories

1
Departments of Nutritional Sciences & Neurology, University of Michigan, Ann Arbor, MI 48109, USA
2
University of Michigan, Ann Arbor, MI 48109, USA
3
Department of Nutritional Sciences, University of Michigan, Ann Arbor, MI 48109, USA
4
Department of Community and Preventive Dentistry, College of Dentistry, University of Iowa, Iowa City, IA 52242, USA
5
Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA 15260, USA
6
Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15260, USA
7
Departments of Psychology and Dental Public Health & Professional Practice, Center for Oral Health Research in Appalachia, West Virginia University, Morgantown, WV 26506, USA
8
Clinical and Translational Science, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15260, USA
9
Center of Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI 48109, USA
*
Author to whom correspondence should be addressed.
Nutrients 2022, 14(15), 3059; https://doi.org/10.3390/nu14153059
Submission received: 20 June 2022 / Revised: 19 July 2022 / Accepted: 21 July 2022 / Published: 26 July 2022
(This article belongs to the Collection Dietary Nutrient Intake and Sleep)

Abstract

:
The objective of this study was to evaluate whether dietary habits at age 2 associate with sleep duration trajectories through age 5 in children from north and central Appalachia. A total of 559 children from the Center for Oral Health Research in Appalachia (COHRA) cohort 2 were followed via caregiver phone interviews up to six times between ages 2 and 5. Exposures included data from the year 2 interview: sleep habits, household and demographic characteristics, meal patterns and consumption frequencies of fruits, vegetables, water, juice, milk, and soda. Sleep duration trajectories were identified using group-based trajectory models from ages 2 to 5. Three distinct nightly sleep duration trajectories were identified: short, increasing duration (4.5% of the study population); steady, 9 h of sleep (37.3%); and longer, slightly decreasing sleep duration (58.2%). Using multinomial logistic models that accounted for confounders, children with consistent meal patterns (i.e., meals and snacks at same time every day) and with higher fruit and vegetable consumption were more likely to follow the longer duration sleep trajectory compared to the steady sleep trajectory. In contrast, children who drank milk more frequently at age 2 were less likely to be in the longer duration sleep trajectory than the steady sleep trajectory.

Graphical Abstract

1. Introduction

Sleep is fundamental for growth and development in young children. Children who do not get adequate sleep for their age are more likely to have lower cognitive development, increased behavioral issues, and higher body weight than those who do get adequate sleep [1,2,3]. At 2 years of age, toddlers are recommended to get 11–14 h of sleep each day (combining nighttime and daytime naps), and by ages 3–5, the recommendation is 10–13 h [4]. Sleep patterns change throughout childhood; therefore, examination of sleep trajectories may be more informative than sleep duration at any one age. Indeed, it is common for children to experience brief periods of problematic sleep [5], but short sleep duration and sleep problems that persist over time are likely more indicative of negative health outcomes [6]. To illustrate, a short sleep duration trajectory from ages 2 through 5/6 within a cohort of French children was associated with hyperactivity/inattention for boys [1]. Among girls, those in the “changing sleep” category had higher hyperactivity/inattention scores. In a cohort of Canadian children, short sleep trajectories from ages 3 months to 2 years were associated with lower cognitive development [2]. Finally, another Canadian cohort study showed that persistent short sleep duration from early to mid-childhood was associated with poor receptive vocabulary during middle childhood [7] and with overweight/obesity [3].
The establishment of bedtime routines has been linked to longer nighttime sleep duration in children [8,9]. Daytime activities and routines are also important for nighttime sleep; for example, lower physical activity and higher screen time during the day have been associated with shorter nighttime sleep [10]. Diet also plays a key role in nighttime sleep. First, meal patterns and timing are known to be important circadian timekeepers (zeitgebers) [11]. Thus, consistent, predictable schedules of eating could be associated with more consistent naptimes and bedtimes and subsequently longer overall duration of sleep. Second, higher diet quality has been consistently linked with better sleep quality and/or longer sleep duration in both adults [12] and children [13,14,15]. Whereas most studies in children are cross-sectional, one study of French children found that a “processed and fast food” diet pattern and a “baby food” diet pattern were associated with a short sleep duration trajectory from age 2 to 5/6 years [16].
Disparities in sleep health exist across race/ethnicity groups and in lower- versus higher-income groups in adults and children [17]. The Appalachian region of the US is marked by high rates of poverty in some areas, and higher risk of multiple disease outcomes in both children and adults [18]. Yet, child sleep has not been well-described within this population. Here, we fill this gap using results from a longitudinal investigation of Appalachian children by the Center for Oral Health Research in Appalachia (COHRA), a study originally designed to examine factors influencing oral health. Specifically, we aimed to examine baseline dietary habits in relation to prospective nighttime sleep duration trajectories.

2. Materials and Methods

Study Population: The study sample included 559 children who were involved in the Center for Oral Health Research in Appalachia (COHRA) COHRA2 study [19], a longitudinal investigation designed to collect data on expectant mothers and their babies from pregnancy through the early years of the child’s life. Participants were enrolled in sites in Pennsylvania and West Virginia on a rolling basis between 2012 and 2018 during mothers’ pregnancy, and they and their child were followed at regular intervals. The present study includes child dietary data at 2 years of age and sleep data from ages 2 through 5.5, which was collected as a part of follow-up caregiver phone interviews that occurred approximately every 6 months (a total of eight possible follow-ups in this analysis). Of the 563 children who were enrolled in the study at 2 years of age, 559 of them had dietary and sleep data collected at least once. The study protocol was approved by the institutional review boards (IRB) at the University of Pittsburgh and West Virginia.
Exposure: During 30-to-45-min interviews conducted by the University Center for Social & Urban Research (UCSUR; http://ucsur.pitt.edu/, accessed on 19 June 2020), caregivers were asked about children’s dietary intake within the last 7 days including typical meal pattern (i.e., whether meals are consumed on a consistent time schedule), fruit consumption, vegetable consumption, water, milk, 100% juice, and soda/pop. Response options for meal patterns were “meals and snacks at about the same time most days”, “meals and snacks at different times most days”, or “snacking throughout the day with few (if any) meals”. For individual foods, response options for frequency of intake were never or once, every few days, once a day, and several times a day. For this study, we used only the dietary information collected at the 2-year-old interview. This decision was made based on the conceptualization of the research question and due to data sparsity in some of the follow-up interviews.
Outcome: At each phone interview, caregivers were asked about their child’s sleep habits, including nighttime and daytime sleep and presence of sleep problems (yes/no). Daytime sleep duration was defined to be the typical duration of child’s sleep from 7 a.m. to 7 p.m.; nightly sleep duration was the typical duration of child’s sleep from 7 p.m. to 7 a.m. The exact sleep questions were “how much time does your child spend in sleep during the night between 7 in the evening and 7 in the morning?”, “How much time does your child spend in sleep during the day between 7 in the morning and 7 in the evening?”, and “Do you consider your child’s sleep a problem?”. For sleep problems, response options were not a problem at all, a small problem, a very serious problem, and don’t know. Although sleep recommendations for this age group include all sleep within a 24-h period (i.e., nighttime sleep + naps), we decided a priori to focus on nighttime sleep duration, given that circadian-related mechanisms between diet and sleep may operate more strongly at night when melatonin levels are highest.
Confounders: Potential confounders were identified a priori from the literature and included the following variables collected at the 2-year-old follow-up: age in months, ever breastfed (yes/no), whether the child attended daycare, sleep problem (yes/no), mother’s age at birth, gestational week at delivery, child sex, vaginal delivery (yes/no), birth weight (kg), household income, and maternal education.

Statistical Analysis

Sleep trajectories were identified using a STATA plug-in for group-based trajectory models (command “traj”). The number and shape of trajectories (linear, quadratic, or cubic) were identified based on model fit statistics (Bayesian information criterion), as outlined previously [20]. Briefly, the trajectory model was built by adding trajectories one at a time, and the linear, quadratic, and cubic functions were tested for each trajectory. To choose the more appropriate model fit at each step, the BIC values for the more complex model were compared to the simpler model using previously established guidelines for weak, moderate, or strong evidence in support of the more complex model. The number of trajectories to retain was also informed by previous literature on child sleep and interpretability (i.e., it is recommended that each trajectory represents approximately 5% of the sample or greater). Each child was assigned to one of the trajectories based on the group trajectory for which they had the highest probability of membership. Children did not need to have sleep data at every follow-up visit in order to be assigned to a trajectory. The majority of participants (84%) had at least three data points for sleep, and exclusion of participants with fewer than three data points did not alter findings.
To examine associations between potential confounders and sleep trajectories, we estimated means ± SD of continuous confounders (proportions for categorical variables) according to sleep trajectory category. To evaluate the primary research question, we used multinomial logistic regression models to compute adjusted odds of nightly sleep duration trajectories according to categories of baseline eating behaviors and adjusted for child’s age, household income, delivery method, mother’s age at birth, and maternal education (variables that were associated with sleep trajectories).

3. Results

At baseline, children were on average (±SD) 2.0 ± 0.1 years of age; 54% were male. The average nighttime sleep duration at baseline was 9.8 ± 1.5 h, and average daytime duration was 2.1 ± 1.0 h. Children were followed four times on average, over a median of 2.3 (1.1, 3.5) years. By the end of the follow-up period, children averaged 5.5 ± 0.1 years of age, had an average nighttime sleep duration of 9.6 ± 1.2 h, and average daytime duration of 0.5 ± 0.9 h. Three distinct nightly sleep duration trajectories were identified (Figure 1): (1) short, increasing duration (short duration); (2) steady, 9 h of sleep (steady), and (3) longer, slightly decreasing duration (longer duration).
The short duration group represented 4.5% of the sample and averaged 6.5 ± 1.5 h of sleep at night at baseline, increasing to 7.0 ± 0.7 h of nightly sleep at follow-up. The steady group represented over a third of the sample (37.3%) and averaged right around 9 h at night consistently over time. The longer duration group represented the majority, starting with 10.6 ± 1.0 h of sleep and declined slightly to 10.2 ± 0.7 h by follow-up. Children in the longer duration trajectory (considered as optimal sleep health) were more likely to have been delivered vaginally, to live in higher-income households, and to have mothers with higher education than those in the other groups. In addition, mothers of children in the short duration group were much more likely to report that their child had a sleep problem (44% vs. 16% and 15%, respectively) (Table 1).
Baseline dietary habits were related to sleep duration trajectories (Table 2 and Table 3). After accounting for confounders, children with non-habitual meal patterns (i.e., meals and snacks not taken at same time every day) were more likely to follow the steady trajectory compared to the longer duration trajectory (optimal sleep health). To illustrate, children who ate meals and snacks at different times each day rather than at the same time each day were two times as likely to be in the steady group versus the longer duration trajectory (95% CI 1.1, 3.5; Table 3). Similarly, children who drank milk more frequently at 2 years of age were 1.9 (95% CI 1.0 to 3.5) times more likely to be in the steady trajectory than the longer duration trajectory. In contrast, children with higher fruit and vegetable consumption were more likely to be in the longer duration trajectory than the steady trajectory. Children who consumed fruits or vegetables several times per day were 0.35 (95% CI 0.188, 0.69) and 0.47 (95% CI 0.27, 0.80) times less likely to be in the steady trajectory compared to the longer duration trajectory, respectively.
In sensitivity analyses, we evaluated potential confounding by sleep problems and by maternal depression scores (CES-D scale) and found that estimates were not appreciably altered. In addition, we considered the possibility of correlations among the dietary variables. Fruit and vegetable consumption were the only variables with moderate correlation (r = 0.4). The inclusion of both of these variables in one model resulted in an attenuation of the association between vegetable consumption and longer sleep duration trajectory.

4. Discussion

Within this cohort of young children from north and north-central Appalachia, we found that inconsistent mealtimes, higher milk consumption, and lower fruit and vegetable consumption were each associated with a shorter sleep nighttime duration trajectory over time.
An inconsistent mealtime was related to shorter nighttime sleep. To illustrate, children with meals and snacks at different times every day were over twice as likely to be in a shorter sleep duration trajectory. To our knowledge, this finding has not been reported previously. However, there are several potential mechanisms that might explain this association. First is the content of snacks versus meals. Reports from NHANES have shown that toddlers who consume more snacks consume more calories overall, and these calories are high in carbohydrates and discretionary items with added sugar and sodium [21]. In contrast, toddlers that consume more family meals have higher-quality diets [22]. In turn, higher quality diets have been associated with better sleep among toddlers. Within our dataset, the toddlers who had a snacking pattern also had higher caregiver-reported intakes of chips, desserts, candies, and less fruit. A second explanation could be related to the timing itself. Eating is one regulator of circadian rhythm; thus, keeping a consistent meal schedule would likely reinforce a consistent bedtime and wake time schedule, which is an important aspect of achieving optimal sleep. In adults, inconsistent meal timing is closely aligned with inconsistent sleep timing [23] and to poor cardiometabolic health [24]. One potential mechanism linking meal and sleep times to each other and to metabolic health is through alteration of circadian clock gene expression [25,26]. A third explanation for the association we observed between inconsistent mealtimes and nighttime sleep duration is that there are other behaviors related to snacking behaviors (i.e., confounders), such as higher screen time [27] or lower physical activity, which have each been related to shorter sleep duration in this age group. Household and family-level characteristics also very likely play a role in achieving both consistent meal patterns and consistent nighttime routines.
Beyond the consistency of meals and snacks, we also found that individual foods were associated with nighttime sleep duration. Specifically, we found that higher fruit and vegetable consumption were associated with longer sleep duration. This finding is consistent with some other studies in toddlers [13,14]. In a French mother–child cohort, a higher score on a “fruits and vegetables” dietary pattern was associated with longer sleep duration among girls [13]. In addition, a study among preschoolers from low-SES households in the US found that higher adherence to a “vegetables, healthy proteins and sides” pattern was associated with less variability of sleep duration from weekends to weekdays and a later timing of sleep (i.e., later bedtimes and/or wake times) [14]. Fruits and vegetables have also been related to better sleep quality among adolescents and adults [28]. One possible explanation is the antioxidant content, which promotes lower inflammation and has been associated with better sleep health [29]. An alternative explanation is that fiber-rich diets high in fruits and vegetables are related to lower consumption of other foods that may hinder sleep, such as saturated fat [30].
The only drink associated with sleep duration was milk, such that more-frequent consumption of milk was associated with shorter sleep duration. This finding is in contrast with a recent report among Mexican adolescents, where milk and 100% juice were each associated with better sleep health (either longer duration or earlier timing), and soda was associated with shorter sleep duration [31]. It is unclear why milk was associated with shorter sleep trajectories in this study, although it is worth pointing out that we did not have information on the quantity of beverages consumed or the time of day that they were consumed. Further, the fat and added sugar content of the milk was not ascertained. Of note, although it was not statistically significantly related, higher consumption of soda was associated with the shorter sleep duration trajectory in the expected direction [32].
Almost one-third of this sample of toddlers (31%) did not achieve the recommended sleep duration for their age, and 16% of caregivers reported that their child had problems with sleep. This is consistent with national averages of children ages 1–5 based on the US National Survey of Children’s Health (33% for children 1–2 years old and 35% for 3–5 year-olds) [33]. The maternal and household correlates of sleep duration trajectories are also worth mentioning. Older mothers and those with vaginal deliveries had children with longer sleep duration trajectories. This is in line with a perinatal study among 619 mother–infant pairs, which found that lower maternal education, prenatal depression, and emergency cesarean birth were associated with shorter infant sleep duration at 3 months [34].
This study has a number of strengths, including a longitudinal design with up to eight follow-ups. Further, with an understudied population of children in the Appalachia region of the US, the findings represent a unique contribution to the literature. There are also limitations to consider. The sleep information was parent-reported rather than being an objective assessment. Diet and meal patterns were also parent-reported, and we did not have detailed information on when each type of beverage or food was consumed throughout the day. Furthermore, the diet questionnaire was not a semi-quantitative food frequency questionnaire, which would have provided the typical number of servings consumed for each food and the total energy intake. Thus, we could not investigate whether the amount of each food or drink was related to sleep. Power was also an issue, especially when trying to make comparisons between the shortest sleep duration category with the other sleep trajectories. We also did not have complete dietary data over the follow-up period in order to evaluate changes in diet over time. There were likely some unmeasured confounders, including screen time and physical activity of the children.

5. Conclusions

In summary, we found several baseline dietary correlates of shorter nighttime sleep duration trajectories among toddlers living in households in Appalachia. Namely, inconsistent timing of meals was related to shorter sleep duration over time. Further, higher intake of milk was associated with shorter sleep duration while higher intake of fruits and vegetables related to longer sleep duration. Ultimately, intervention studies that evaluate the impact of meal modifications (both timing and content) in early childhood are needed to evaluate the causal nature of diet and sleep during this developmental period.

Author Contributions

Conceptualization, E.C.J. and W.Z.; formal analysis, E.C.J.; writing—original draft preparation, E.C.J. and W.Z.; writing—review and editing, E.C.J., W.Z., A.D.J., T.A.M., K.N., J.R.S., D.W.M., M.L.M. and B.F.; funding acquisition, B.F., M.L.M. and D.W.M. All authors have read and agreed to the published version of the manuscript.

Funding

This work was funded by the National Institute of Dental and Craniofacial Research (NIDCR), grant number R01-DE014899. Jansen was supported by NHLBI K01HL151673 during the course of the study.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Boards of the University of Pittsburgh (FWA# FWA00006790); IRB approval #’s CR19080178-001 and CR19110013-002) and West Virginia University (FWA# FWA00005078, IRB approval #1411480509A022).

Informed Consent Statement

Written informed consent was obtained from participants.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Reynaud, E.; Forhan, A.; Heude, B.; Charles, M.A.; Plancoulaine, S. Night-sleep Duration Trajectories and Behavior in Preschoolers: Results from a Prospective Birth Cohort Study. Behav. Sleep Med. 2021, 19, 445–457. [Google Scholar] [CrossRef] [PubMed]
  2. Smithson, L.; Baird, T.; Tamana, S.K.; Lau, A.; Mariasine, J.; Chikuma, J.; Lefebvre, D.L.; Subbarao, P.; Becker, A.B.; Turvey, S.E.; et al. Shorter sleep duration is associated with reduced cognitive development at two years of age. Sleep Med. 2018, 48, 131–139. [Google Scholar] [CrossRef] [PubMed]
  3. Touchette, É.; Petit, D.; Tremblay, R.E.; Boivin, M.; Falissard, B.; Genolini, C.; Montplaisir, J.Y. Associations between sleep duration patterns and overweight/obesity at age 6. Sleep 2008, 31, 1507–1514. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Hirshkowitz, M.; Whiton, K.; Albert, S.M.; Alessi, C.; Bruni, O.; DonCarlos, L.; Hazen, N.; Herman, J.; Katz, E.S.; Kheirandish-Gozal, L.; et al. National Sleep Foundation’s sleep time duration recommendations: Methodology and results summary. Sleep Health J. Natl. Sleep Found. 2015, 1, 40–43. [Google Scholar] [CrossRef]
  5. Singareddy, R.; Moole, S.; Calhoun, S.; Vocalan, P.; Tsaoussoglou, M.; Vgontzas, A.N.; Bixler, E.O. Medical Complaints Are More Common in Young School-Aged Children with Parent Reported Insomnia Symptoms. J. Clin. Sleep Med. 2009, 5, 549. [Google Scholar] [CrossRef] [Green Version]
  6. Williamson, A.A.; Mindell, J.A.; Hiscock, H.; Quach, J. Longitudinal sleep problem trajectories are associated with multiple impairments in child well-being. J. Child Psychol. Psychiatry 2020, 61, 1092–1103. [Google Scholar] [CrossRef]
  7. Seegers, V.; Touchette, E.; Dionne, G.; Petit, D.; Seguin, J.R.; Montplaisir, J.; Vitaro, F.; Falissard, B.; Boivin, M.; Tremblay, R.E. Short persistent sleep duration is associated with poor receptive vocabulary performance in middle childhood. J. Sleep Res. 2016, 25, 325–332. [Google Scholar] [CrossRef] [Green Version]
  8. Shetty, J.; Newton, A.; Reid, G. Parenting Practices, Bedtime Routines, and Consistency: Associations with Pediatric Sleep Problems. J. Pediatr. Psychol. 2022, 47, 49–58. [Google Scholar] [CrossRef]
  9. Zhang, Z.; Sousa-Sá, E.; Pereira, J.R.; Okely, A.D.; Feng, X.; Santos, R. Correlates of Sleep Duration in Early Childhood: A Systematic Review. Behav. Sleep Med. 2020, 19, 407–425. [Google Scholar] [CrossRef]
  10. Janssen, X.; Martin, A.; Hughes, A.R.; Hill, C.M.; Kotronoulas, G.; Hesketh, K.R. Associations of screen time, sedentary time and physical activity with sleep in under 5s: A systematic review and meta-analysis. Sleep Med. Rev. 2020, 49, 101226. [Google Scholar] [CrossRef]
  11. Ribas-Latre, A.; Eckel-Mahan, K. Interdependence of nutrient metabolism and the circadian clock system: Importance for metabolic health. Mol. Metab. 2016, 5, 133–152. [Google Scholar] [CrossRef] [PubMed]
  12. Jansen, E.C.; Prather, A.; Leung, C.W. Associations between sleep duration and dietary quality: Results from a nationally-representative survey of US adults. Appetite 2020, 153, 104748. [Google Scholar] [CrossRef] [PubMed]
  13. Plancoulaine, S.; Lioret, S.; Regnault, N.; Heude, B.; Charles, M.A. Gender-specific factors associated with shorter sleep duration at age 3 years. J. Sleep Res. 2015, 24, 610–620. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Jansen, E.C.; Peterson, K.E.; Lumeng, J.C.; Kaciroti, N.; LeBourgeois, M.K.; Chen, K.; Miller, A.L. Associations between Sleep and Dietary Patterns among Low-Income Children Attending Preschool. J. Acad. Nutr. Diet. 2019, 119, 1176–1187. [Google Scholar] [CrossRef] [PubMed]
  15. Ward, A.L.; Reynolds, A.N.; Kuroko, S.; Fangupo, L.J.; Galland, B.C.; Taylor, R.W. Bidirectional associations between sleep and dietary intake in 0–5 year old children: A systematic review with evidence mapping. Sleep Med. Rev. 2020, 49, 101231. [Google Scholar] [CrossRef]
  16. Plancoulaine, S.; Reynaud, E.; Forhan, A.; Lioret, S.; Heude, B.; Charles, M.-A.; Annesi-Maesano, I.; Bernard, J.; Botton, J.; Dargent-Molina, P.; et al. Night sleep duration trajectories and associated factors among preschool children from the EDEN cohort. Sleep Med. 2018, 48, 194–201. [Google Scholar] [CrossRef] [Green Version]
  17. Adam, E.K.; Snell, E.K.; Pendry, P. Sleep timing and quantity in ecological and family context: A nationally representative time-diary study. J. Fam. Psychol. 2007, 21, 4–19. [Google Scholar] [CrossRef] [Green Version]
  18. Hendryx, M. Poverty and Mortality Disparities in Central Appalachia: Mountaintop Mining and Environmental Justice. J. Health Dispar. Res. Pract. 2012, 4, 6. Available online: https://digitalscholarship.unlv.edu/jhdrp/vol4/iss3/6 (accessed on 12 October 2021).
  19. Neiswanger, K.; McNeil, D.W.; Foxman, B.; Govil, M.; Cooper, M.E.; Weyant, R.J.; Shaffer, J.R.; Crout, R.J.; Simhan, H.N.; Beach, S.R.; et al. Oral health in a sample of pregnant women from Northern Appalachia (2011–2015). Int. J. Dent. 2015, 2015, 469376. [Google Scholar] [CrossRef] [Green Version]
  20. Andruff, H.; Carraro, N.; Thompson, A.; Gaudreau, P. Latent Class Growth Modelling: A Tutorial. Tutor. Quant. Methods Psychol. 2009, 5, 11–24. [Google Scholar] [CrossRef]
  21. Kachurak, A.; Bailey, R.L.; Davey, A.; Dabritz, L.; Fisher, J.O. Daily snacking occasions, snack size, and snack energy density as predictors of diet quality among us children aged 2 to 5 years. Nutrients 2019, 11, 1440. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Verhage, C.L.; Gillebaart, M.; van der Veek, S.M.C.; Vereijken, C.M.J.L. The relation between family meals and health of infants and toddlers: A review. Appetite 2018, 127, 97–109. [Google Scholar] [CrossRef] [PubMed]
  23. 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] [Green Version]
  24. Makarem, N.; Sears, D.D.; St-Onge, M.; 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]
  25. Jansen, E.C.; Dolinoy, D.; Peterson, K.E.; O’Brien, L.M.; Chervin, R.D.; Cantoral, A.; Tellez-Rojo, M.M.; Solano-Gonzalez, M.; Goodrich, J. Adolescent sleep timing and dietary patterns in relation to DNA methylation of core circadian genes: A pilot study of Mexican youth. Epigenetics 2020, 16, 894–907. [Google Scholar] [CrossRef]
  26. Lopez-Minguez, J.; Gómez-Abellán, P.; Garaulet, M. Circadian rhythms, food timing and obesity. Proc. Nutr. Soc. 2016, 75, 501–511. [Google Scholar] [CrossRef] [Green Version]
  27. Loth, K.A.; Tate, A.; Trofholz, A.; Fisher, J.O.; Miller, L.; Neumark-Sztainer, D.; Berge, J. Ecological momentary assessment of the snacking environments of children from racially/ethnically diverse households. Appetite 2020, 145, 104497. [Google Scholar] [CrossRef]
  28. Jansen, E.C.; She, R.; Rukstalis, M.; Alexander, G.L. Changes in fruit and vegetable consumption in relation to changes in sleep characteristics over a 3-month period among young adults. Sleep Health 2021, 7, 345–352. [Google Scholar] [CrossRef]
  29. Godos, J.; Ferri, R.; Caraci, F.; Cosentino, F.I.I.; Castellano, S.; Shivappa, N.; Hebert, J.R.; Galvano, F.; Grosso, G. Dietary inflammatory index and sleep quality in Southern Italian Adults. Nutrients 2019, 11, 1324. [Google Scholar] [CrossRef] [Green Version]
  30. St-Onge, M.P.; Roberts, A.; Shechter, A.; Choudhury, A.R. Fiber and saturated fat are associated with sleep arousals and slow wave sleep. J. Clin. Sleep Med. 2016, 12, 19–24. [Google Scholar] [CrossRef] [Green Version]
  31. Jansen, E.C.; Corcoran, K.; Perng, W.; Dunietz, G.L.; Cantoral, A.; Zhou, L.; Téllez-Rojo, M.M.; Peterson, K.E. Relationships of beverage consumption and actigraphy-assessed sleep parameters among urban-dwelling youth from Mexico. Public Health Nutr. 2021, 25, 1844–1853. [Google Scholar] [CrossRef] [PubMed]
  32. Chaput, J.-P.; Tremblay, M.S.; Katzmarzyk, P.T.; Fogelholm, M.; Hu, G.; Maher, C.; Maia, J.; Olds, T.; Onywera, V.; Sarmiento, O.L.; et al. Sleep patterns and sugar-sweetened beverage consumption among children from around the world. Public Health Nutr. 2018, 21, 2385–2393. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Wheaton, A.G. Short Sleep Duration Among Infants, Children, and Adolescents Aged 4 Months–17 Years—United States, 2016–2018. MMWR Morb. Mortal. Wkly. Rep. 2021, 70, 1315–1321. [Google Scholar] [CrossRef] [PubMed]
  34. Kim, Y.; Bird, A.; Peterson, E.; Underwood, L.; Morton, S.M.B.; Grant, C.C. Maternal Antenatal Depression and Early Childhood Sleep: Potential Pathways Through Infant Temperament. J. Pediatr. Psychol. 2020, 45, 203–217. [Google Scholar] [CrossRef]
Figure 1. Trajectories of nightly sleep duration from age 2 years to age 5.5 years; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018; 1—short duration; 2—steady; 3—longer duration.
Figure 1. Trajectories of nightly sleep duration from age 2 years to age 5.5 years; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018; 1—short duration; 2—steady; 3—longer duration.
Nutrients 14 03059 g001
Table 1. Summary of sociodemographic and household characteristics according to trajectories of nightly sleep duration over childhood; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018, with sleep data from age 2 years to age 5.5 years.
Table 1. Summary of sociodemographic and household characteristics according to trajectories of nightly sleep duration over childhood; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018, with sleep data from age 2 years to age 5.5 years.
Nightly Sleep Duration Trajectories
Group 1
Short Duration
n = 25 1
Group 2
Steady
n = 201 1
Group 3
Longer Duration
n = 333 1
p 3
Baseline nightly sleep duration6.5 (1.5) 28.9 (1.1)10.6 (1.0)0.0001
Daytime nap duration2.9 (1.9)2.2 (1.2)2.0 (0.8)0.10
Age, months2.00 (0.07)2.00 (0.06)1.99 (0.06)0.79
Breastfeeding, any0.480.390.390.65
Daycare attendance0.440.440.510.29
Sleep problem (any at all)0.440.160.150.001
Mother’s age at birth28.3 (6.2)29.7 (5.6)30.6 (4.4)0.02
Gestational week at delivery39.6 (1.1)39.4 (1.4)39.5 (1.3)0.76
Male sex0.520.500.570.28
Vaginal delivery0.600.660.780.005
Birth weight, kg3.38 (0.41)3.42 (0.50)3.49 (0.46)0.19
Household income <0.0001
$0–14,9990.240.210.08
$15,000–34,9990.360.220.11
$35,000–49,9990.160.110.16
$50,000–74,9990.160.180.15
$75,000–99,9990.080.130.23
$100,000 or more00.140.27
Maternal education <0.0001
8th grade-completed high school0.120.520.36
Some college/Associate’s0.070.510.42
Bachelor’s degree0.020.260.72
Graduate degree00.230.77
1 Largest sample sizes shown. Some individual variables have smaller sample sizes. 2 Values represent means (SD) for continuous characteristics and proportions for categorical characteristics. 3 p values from Kruskal–Wallis tests for continuous variables and chi-squared tests for categorical variables.
Table 2. Eating behaviors at age 2 by to trajectories of nightly sleep duration over childhood; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018, with sleep data followed from age 2 years to age 5.5 years.
Table 2. Eating behaviors at age 2 by to trajectories of nightly sleep duration over childhood; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018, with sleep data followed from age 2 years to age 5.5 years.
Nightly Sleep Duration Trajectories,
Percentage in Each Category
%Short DurationSteadyLonger Duration
Typical meal pattern
  Meals and snacks at same time every day81.13.7731.9364.30
  Meals and snacks at different times every day14.07.6952.5639.74
  Snacking throughout the day, few meals4.97.4151.8540.74
p value <0.0001
Fruit consumption
  Never to every few days9.47.6957.6934.62
  Once per day19.28.4148.6042.99
  Several times per day71.43.0229.4767.51
p value <0.0001
Vegetable consumption
  Never to every few days17.82.0251.5246.46
  Once per day37.88.1033.3358.57
  Several times per day44.42.4331.5865.99
p value <0.0001
Water
  Never or once in last week3.814.2947.6238.1
  Every few days 3.45.2673.6821.05
  Once a day14.08.9741.0350.00
  Several times a day78.93.1732.8863.95
p value <0.0001
Milk
  Never or once in last week14.05.1324.3670.51
  Every few days 5.66.4535.4858.06
  Once a day14.91.2037.3561.45
  Several times a day65.74.938.1556.95
p value 0.239
Juice
  Never or once in last week42.82.0931.8066.11
  Every few days18.66.7334.6258.65
  Once a day19.56.4231.1962.39
  Several times a day19.05.6651.8942.45
p value 0.001
Soda
  Never or once in last week93.74.0134.7361.26
  At least every few days6.311.4354.2934.29
p value 0.637
Table 3. Adjusted odd ratios of nightly children’s sleep duration trajectories according to eating behaviors at age 2; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018, with sleep data followed from age 2 years to age 5.5 years.
Table 3. Adjusted odd ratios of nightly children’s sleep duration trajectories according to eating behaviors at age 2; 559 children enrolled in Center for Oral Health Research in Appalachia Cohort 2 between 2012 and 2018, with sleep data followed from age 2 years to age 5.5 years.
Short Duration vs. Longer Duration, OR (95% CI) 1pSteady vs.
Longer Duration,
OR (95% CI) 1
p
Typical meal pattern
  Meals and snacks at same time every dayReference Reference
  Meals and snacks at different times every day1.89 (0.65, 5.49)0.241.98 (1.12, 3.52)0.02
  Snacking throughout the day, few meals2.23 (0.41, 12.09)0.352.08 (0.83, 5.18)0.12
Fruit consumption
  Never to every few daysReference Reference
  Once per day0.91 (0.23, 3.63)0.900.65 (0.31, 1.40)0.27
  Several times per day0.38 (0.10, 1.40)0.150.35 (0.18, 0.69)0.002
Vegetable consumption
  Never to every few daysReference Reference
  Once per day4.64 (0.97, 22.19)0.060.59 (0.34, 1.03)0.06
  Several times per day1.15 (0.21, 6.26)0.870.47 (0.27, 0.80)0.006
Water
  Never or once in last weekReference Reference
  Every few days 1.16 (0.08, 17.08)0.913.87 (0.82, 18.19)0.09
  Once a day0.71 (0.13, 3.78)0.690.79 (0.26, 2.47)0.69
  Several times a day0.30 (0.06, 1.40)0.130.65 (0.23, 1.86)0.42
Milk
  Never or once in last weekReference Reference
  Every few days 1.66 (0.25, 11.18)0.601.93 (0.73, 5.11)0.19
  Once a day0.29 (0.03, 2.83)0.291.82 (0.87, 3.82)0.11
  Several times a day0.99 (0.30, 3.31)0.991.89 (1.03, 3.50)0.04
Juice
  Never or once in last weekReference Reference
  Every few days2.55 (0.73, 8.88)0.141.04 (0.61, 1.77)0.90
  Once a day1.58 (0.45, 5.61)0.480.67 (0.38, 1.16)0.15
  Several times a day1.75 (0.47, 6.53)0.411.58 (0.92, 2.73)0.10
Soda
  Never or once in last weekReference Reference
  At least every few days2.44 (0.64, 9.37)0.191.89 (0.81, 4.43)0.14
1 From multinomial logistic regression models and adjusted for child’s age, household income, delivery method, maternal age at birth, and maternal education. All factors examined in separate models.
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Jansen, E.C.; Zhao, W.; Jones, A.D.; Marshall, T.A.; Neiswanger, K.; Shaffer, J.R.; McNeil, D.W.; Marazita, M.L.; Foxman, B. Early Childhood Diet in Relation to Toddler Nighttime Sleep Duration Trajectories. Nutrients 2022, 14, 3059. https://doi.org/10.3390/nu14153059

AMA Style

Jansen EC, Zhao W, Jones AD, Marshall TA, Neiswanger K, Shaffer JR, McNeil DW, Marazita ML, Foxman B. Early Childhood Diet in Relation to Toddler Nighttime Sleep Duration Trajectories. Nutrients. 2022; 14(15):3059. https://doi.org/10.3390/nu14153059

Chicago/Turabian Style

Jansen, Erica C., Wentong Zhao, Andrew D. Jones, Teresa A. Marshall, Katherine Neiswanger, John R. Shaffer, Daniel W. McNeil, Mary L. Marazita, and Betsy Foxman. 2022. "Early Childhood Diet in Relation to Toddler Nighttime Sleep Duration Trajectories" Nutrients 14, no. 15: 3059. https://doi.org/10.3390/nu14153059

APA Style

Jansen, E. C., Zhao, W., Jones, A. D., Marshall, T. A., Neiswanger, K., Shaffer, J. R., McNeil, D. W., Marazita, M. L., & Foxman, B. (2022). Early Childhood Diet in Relation to Toddler Nighttime Sleep Duration Trajectories. Nutrients, 14(15), 3059. https://doi.org/10.3390/nu14153059

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