Prenatal and Neonatal Factors Predicting Sleep Problems in Children Born Extremely Preterm or With Extremely Low Birthweight

Objective: Prematurely born children have been reported to have more sleep problems throughout childhood than children born at term. The aim of this study was to explore if prenatal or neonatal factors can predict sleep problems at age 11 years in children born extremely preterm (EPT).

Method: A prospective observational study of all infants who were born EPT in Norway in 1999 and 2000. Prenatal and neonatal data were collected by all Norwegian obstetric and pediatric departments. Parental questionnaire mapped sleep problems and sleep habits at the age of 11 years.

Results: Of the 372 eligible children, 221 participated. Of those, 28.1% snored, 27.5% had difficulty falling asleep or frequent awakenings and 17.2% suffered from daytime sleepiness. The mean sleep duration was 9.4 h (range 4.3–11.0 h). Smoking in pregnancy predicted snoring (odds ratio 4.3). Neonatal cerebral hemorrhage and being born small for gestational age predicted difficulty falling asleep or frequent awakenings (odds ratio 2.2 and 2.3). Other morbidities during pregnancy or the newborn period, gestational age or the burden of treatment in the neonatal intensive care unit did not predict sleep problems. None of the studied prenatal or neonatal factors predicted daytime sleepiness or sleep duration <9 h.

Conclusion: Of numerous prenatal and neonatal factors, only smoking during pregnancy, being born small for gestational age and cerebral hemorrhage predicted sleep problems at 11 years of age among these children born EPT.

Introduction

Premature birth in general is associated with an increased risk of experiencing neurodevelopmental impairments, mental health problems, limited respiratory and cardiovascular function and metabolic syndrome. These risks increase with decreasing gestational age (GA) at birth (1–3). Data on more subtle long-term consequences of extremely premature (EPT) birth, e.g., related to sleep, are just starting to emerge since survival after EPT is a relatively new phenomenon (4). Satisfactory sleep is an important part of children's development and quality of life (5), and in general, prematurely born children more commonly experience a variety of sleep problems (6–9, 35). Whether children born EPT are at particular risk is not well studied, but we have recently shown that children born EPT more often have sleep problems throughout childhood until 11 years of age than children born at term (10).

It is important to identify early risk factors for adverse outcomes in order to guide families, health care workers and other professionals who will share responsibilities for these children's development. It has been reported that preeclampsia (11), smoking in pregnancy (12), chorioamnonitis and multiple gestation (13) are associated with later sleep disordered breathing, i.e., conditions that provide unusual breathing patterns during sleep (14), in children born premature. However, whether prenatal or neonatal factors can predict other types of sleep problems, and particularly in children born EPT, have not been explored. Furthermore, it is unknown whether sleep problems in childhood or adolescence can be linked to prematurity per se or to specific prenatal and neonatal factors, such as intrauterine growth restriction or treatment and complications during their stay in the neonatal intensive care unit (NICU), e.g., assisted ventilation and cerebral and respiratory morbidities. Since such morbidities as well as EPT per se are associated with a number of later neurodevelopmental and respiratory difficulties (15–17), our hypothesis was that early life experiences may also have a significant impact on specific sleep related problems in children born EPT. Our aim was, therefore, to explore to what extent prenatal or neonatal factors may predict specific sleep problems at 11 years of age.

Materials and Methods

Population

The study population was a national cohort of all children born EPT (n = 372) in Norway in 1999 and 2000. EPT was defined as gestational age (GA) <28 completed weeks or birthweight (BW) <1,000 g. The children were prospectively followed from birth and were assessed for sleep problems at 11 years of age. The parents gave written informed consent.

Prenatal and Neonatal Factors

All obstetric and pediatric departments in Norway participated, and the study was coordinated by the Medical Birth Registry of Norway (MBRN). Local obstetricians and neonatologists recorded data on maternal health, pregnancy, delivery and diagnoses and treatments in the NICU, and the MBRN provided additional information. Being born small for gestational age (SGA) was defined as birthweight below 10th percentile (18). Details on the definitions of diseases, complications and treatment in the NICU have been published (19, 20). All infants had repeated cerebral ultrasound scans and examinations by ophthalmologists during the hospital stay. An illness severity score which is an index of early disease severity (21) was calculated for each child. It was computed from three components of the Clinical Risk Index for babies namely, the lowest and highest fractional oxygen requirements and the largest base deficit during the first 12 h of life (22). In order to explore whether extensive medical treatment at the NICU would predict sleep problems, we created a variable that identified children who had received at least one of three common extensive medical treatments; mechanical ventilation >40 days, necrotizing enterocolitis or ≥ four courses of antibiotic treatment.

Sleep Problems and Sleep Habits at 11 Years of Age

Current sleep problems were assessed by parental report, i.e., whether their child had difficulty falling asleep or frequent awakenings, snored, gasped for air or stopped breathing when asleep, and if the child had trouble breathing at night. They were also asked if the child had daytime sleepiness. The response options to these questions were “Not true,” “Partly true,” and “Absolutely true.” In our analyses, the variables “Partly true” and “Absolutely true” were merged. Sleep habits were measured by the following items: At what time their child went to bed and got up on weekdays, how long time it took from going to bed until falling asleep (sleep onset latency) and how long time the child was awake during the night after sleep onset. We calculated total sleep duration as time in bed minus sleep onset latency and time awake after sleep onset. In accordance with recently published guidelines, recommended sleep duration at 11 years was defined as 9–11 h (23).

Statistical Analyses

For each specific sleep outcome variable (yes or no), the predictors were compared as means and standard deviations (SD) or as proportions using Student's t-tests, Chi-square tests or Fisher's exact tests, as appropriate. Odds ratios and 95% confidence intervals (CI) were calculated both unadjusted and after adjusting for sex, single parenthood and maternal education (dichotomized as less than a 3-year college education or not) in logistic regression analyses. Significance level was set at α-level 0.05.

Ethics

The study was approved by the Regional Committee on Medical Research Ethics (2009-2271) and the Norwegian Data Inspectorate. The parents gave written informed consent in accordance with the Declaration of Helsinki.

Results

Sample Characteristics

Of 372 eligible children, sleep data were available for 221 (59%) at 11 years. The mothers answered the questionnaire in 64.7% (n = 139) of the cases, the fathers in 3.7% (n = 8), both parents in 30.7% (n = 66) and the child's foster mother in 0.9% (n = 2). The sociodemographic, prenatal and neonatal characteristics are listed in Table 1. The significant differences in family background and demographic characteristics between those with and without sleep data were a higher proportion of girls (50 vs. 39%, p = 0.049) and of mothers with higher education registered during the pregnancy (48 vs. 34%, p = 0.009) among those with sleep data.

TABLE 1

Table 1. Characteristics of the 221 children who were born extremely preterm^a in Norway in 1999–2000 and participated in the follow-up at 11 years of age.

Sleep Problems and Sleep Habits in EPT Children

Difficulty falling asleep or frequent awakenings was reported for 27.5%, snoring for 28.1% and daytime sleepiness for 17.2% of the children (Table 2). Only three children had breathing problems and two gasped for air when asleep (Table 2). Predictors of these outcomes were, therefore, not examined, but four of these five children also snored and were thereby included in the group of snorers. The mean time in bed was 10.2 h (SD = 0.5 h; range 9.0–12.0 h) and the mean sleep duration 9.4 h (SD = 1.0 h; range 4.3–11.0 h). The sleep duration was within the recommended 9–11 h for 75.3% of the children, within 7–8 h (possibly adequate) for 22.3 % and <7 h (less than recommended) for 2.4% of the children. None of the children slept more than recommended. There were no significant differences in the prevalence of difficulty falling asleep or frequent awakenings (27.2 vs. 28.0%, p = 0.9), snoring (26.2 vs. 34.0%, p = 0.3), daytime sleepiness (18.8 vs. 12.2%, p = 0.4) or sleep duration <9 h (78.2 vs. 66.7%, p = 0.1) at the age of 11 years between the groups of children born before GA 28 weeks and those born with GA 28–32 weeks.

TABLE 2

Table 2. Prevalence of parent reported sleep problems at age 11 years in children born extremely preterm^a in Norway in 1999–2000.

Prenatal and Neonatal Predictors of Sleep Problems

Being born SGA and neonatal cerebral hemorrhage (subependymal/ intraventricular hemorrhage) were the only prenatal and neonatal factors that significantly predicted difficulty falling asleep or frequent awakenings, i.e., 43% of SGA vs. 25% (p = 0.014) of non-SGA children, and 42% of children with cerebral hemorrhage vs. 24% of those without hemorrhage (p = 0.012, Table 3). The respective odds ratios (95% CI) were 2.3 (1.2–4.4) and 2.3 (1.2–4.6) and did not differ after adjustments for sex, single parenthood and maternal education (Table 3). When restricting analyses to children with GA ≤27, SGA still predicted difficulty falling asleep or frequent awakenings (p = 0.001) (data not shown).

TABLE 3

Table 3. Prenatal and neonatal factors predicting difficulty falling asleep or frequent awakenings at 11 years of age among children born extremely preterm^a.

Smoking, both during early and end of pregnancy, significantly predicted snoring, i.e., 37 vs. 14% (p = 0.001) for early and 24 vs. 8% (p = 0.017) for late pregnancy. The respective odds ratios (95% CI) were 3.5 (1.6–7.7) and 3.4 (1.2–9.6) and did not differ significantly after adjustments (Table 4). The predictive value of intrauterine cigarette exposures for later snoring remained unchanged after including the parents' current smoking habits and the child's body mass index at 11 years in the adjusted analysis (data not shown).

TABLE 4

Table 4. Prenatal and neonatal factors predicting snoring at 11 years of age among children born extremely preterm^a.

There were no statistically significant predictors of sleep duration <9 h or daytime sleepiness (data not shown). None of the factors related to the severity of early lung disease, such as treatment modalities and duration of treatment for lung disease, severity of bronchopulmonary dysplasia, or extensive medical treatment in the NICU predicted sleep problems at the age of 11 years (Tables 3, 4).

Discussion

In this national cohort of children born EPT we found that 28.1% snored, 27.5% had difficulty falling asleep or frequent awakenings, 17.2% experienced daytime sleepiness and 24.7% did not get the recommended sleep duration. Smoking was the only predictor of snoring, and SGA birth and neonatal cerebral hemorrhage were the only predictors of difficulty falling asleep and frequent awakenings.

Our hypothesis was that several early life experiences in children born EPT would affect sleep at 11 years of age, in particular long term consequences related to early cerebral and respiratory morbidity. The limited significance of early events and exposures was remarkable, in particular the lack of association with the extensive and intrusive treatments that the EPT infants encounter. Similarly, studies have suggested that such neonatal exposures did not predict psychiatric disorders in EPT children (24, 25). Sleep and mental health are closely linked and these studies should therefore be seen in context (26).

Our finding that smoking in pregnancy was a predictor of snoring is in agreement with a Finnish study that examined young adults who had a birth weight <1,500 g (12). Furthermore, a study of children born at term also found that smoking in pregnancy predicted childhood snoring (27). Combined, these studies may suggest that exposure to smoking in pregnancy has a negative effect on respiratory function independent of GA at birth, but that the stresses of prematurity may have an additive effect. The most frequent movement of the fetus during the second trimester is sucking (28). It is hypothesized that sucking is central for oral-facial growth and that extreme premature birth disturbs this process and thereby affects the development of both oral facial anatomy and muscular tone. This may contribute to pediatric sleep related breathing disorders, i.e., snoring (29). It is also a possibility that smoking in pregnancy may affect later physiological regulation, including sleep regulation (30, 31).

The prevalence of snoring (28.1%) in our EPT population was markedly higher than the prevalence of 7.5% in a meta-analysis of parent reported snoring in unselected children aged 0–18 years (32). Rosen et al. found that 21% of children who were born at a mean GA of 31 weeks compared to 14% of children born at term snored at the age of 8–11 years (p = 0.0049) (6). Together, these data may suggest that the prevalence of snoring increases with decreasing GA. The high prevalence of snoring in our study was unrelated to most pre-and neonatal factors suggesting that the general stresses of extra-uterine life of EPT birth may explain the excess risk. Reversed causality may also be a factor since studies have shown that sleep apnea in pregnant women may increase the risk of spontaneous premature birth (33). Sleep apnea and snoring are associated (34) which may imply a genetic predisposition. We were not able to explore this possibility since we had no information on snoring or other sleep disorders in the parents. Snoring can be a symptom or possibly a precursor of sleep disordered breathing (34).

Previous studies have shown that children born prematurely have an increased risk of sleep disordered breathing in childhood (35) and as an adult (12), and that they may also be particularly vulnerable to the negative sequelae of sleep disordered breathing in childhood (36). In general, sleep disordered breathing in childhood is a risk factor for impaired neurocognitive performance, behavioral problems, externalizing symptoms and inattention (37–42). The American Academy of Pediatrics therefore suggests that all children should be screened for snoring, and that high-risk patients should be referred to a specialist (43). The prevalence of sleep disordered breathing during childhood in children born EPT is unknown, but may be high judged from the high prevalence of snoring. Our findings indicate that snoring is a significant problem in preterm born children, and underline that more studies are needed to map the explicit risks and possible consequences of this condition in children born EPT.

To our knowledge, our findings that neonatal cerebral hemorrhage and SGA birth predicted difficulty falling asleep or frequent awakenings at 11 years of age are novel. Wang et al. found no association between neonatal risk factors, including grade III–IV intraventricular hemorrhage, and restless sleep in children born EPT at the age of 18–22 months (44). However, our findings were not unexpected since both cerebral hemorrhage and SGA are known risk factors for adverse neurodevelopmental outcomes (16, 45), and since we previously reported that a variety of sleep problems are more prevalent in EPT children with neurodevelopmental disabilities (10). Previous studies show that to be SGA add to the risk for several types of morbidity for EPT children (46). The fact that we found that SGA predicts difficulty falling asleep or frequent awakenings at the age of 11 years confirms this group‘s increased vulnerability. Difficulty falling asleep or frequent awakenings was reported in 27.5% of the EPT children in our cohort as opposed to a prevalence of 12.7% in an unselected cohort of 11–13 year-old Norwegian children (47). A previous study using polysomnography also reported increased number of awakenings in children born prematurely (GA <32weeks) compared to children born at term (7).

According to the parents, 17.2% of the EPT children suffered from daytime sleepiness. Rosen et al. found a lower prevalence in children born premature and no difference between the premature and a reference group born at term (6 vs. 7%) (6). However, their children were more mature at birth (mean gestational age 31 weeks) compared to our cohort. In another population-based unselected study of American children the parent-reported prevalence of daytime sleepiness was 15% (48), which is similar to what we found. Daytime sleepiness may therefore not be a problem related to extreme prematurity. This notion is strengthened by our findings that none of the prenatal or neonatal factors predicted daytime sleepiness.

None of the prenatal and neonatal factors predicted less than recommended sleep duration. Sleeping less than recommended is shown to have several negative consequences for children (49, 50) and, in adults, long sleep duration is also associated with poor health (51). We previously reported that the EPT children have longer sleep duration than a control group (10). However, in that report we used a slightly different definition of sleep duration, where we did not take into account time awake during nightly awakenings.

Strengths of this study included the national longitudinal population-based design of the EPT cohort. The limited response rate at follow-up was a weakness, as in most population based follow-up studies. This can lead to selection bias, but we have previously shown that the assessed children were probably representative of all the survivors at 11 years of age (52). It would have been desirable to compare the prevalence of sleep problems in our EPT group with that of children born at term. Unfortunately, we had no control group for comparison. In our previous study, we used a control group to compare the prevalence of sleep problems in childhood (10). Unfortunately, the questions that form the basis of the present article were not included in the questionnaire to this control group. However, the main intention of the study was not to map the prevalence of sleep problems, but to explore which factors may predict sleep problems in children born EPT. The majority of these factors are unique to children born EPT, and not relevant for a control group.

We did not ask the children themselves about their sleep. It may be difficult for parents of 11 year old children to answer some of the questions, for example, nightly awakenings and daytime sleepiness. Another limitation relates to the many prenatal and neonatal factors that were included in the analyses. We did not adjust for multiple testing (type 1 errors), thus the results need to be interpreted with caution. We adjusted for single parenthood, maternal education and sex in all our analyses, and in addition for the parents' smoking habits and the child's BMI at 11 years of age when exploring predictive factors for snoring. We may, however, have overlooked other clinically significant confounders.

Conclusions

Our main finding was that a multitude of factors related to morbidity and treatment in the prenatal or neonatal period did not predict sleep problems at age 11 years in children born EPT. Smoking in pregnancy predicted snoring, and SGA birth and neonatal cerebral hemorrhage predicted difficulty falling asleep or frequent awakenings.

Data Availability Statements

According to the approvals granted for this study by The Regional Committee on Medical Research Ethics and The Norwegian Data Inspectorate, the data files are to be stored properly and in line with the Norwegian Law of Privacy Protection. The data file is not made publically available as this might compromise the respondents' privacy, particularly as some of our participating centers are small and the number of extremely preterm births very limited. Moreover, the data file is currently used by other researchers in our group to prepare future research papers. A subset of the data file with anonymized data may be made available to interested researchers upon reasonable request to Thomas Halvorsen (thomas.halvorsen@helse-bergen.no) and providing permission from The Norwegian Data Inspectorate and the other members of our research group.

Author Contributions

KS secured the data set, contributed to the design of the study and to the analysis strategy, carried out all the analyses and drafted the initial manuscript. TM coordinated and supervised data collection for the extremely premature children and contributed to the design of the study and to the analysis strategy. MH, SF, IE, TH, and BB contributed to the design of the study and to the analysis strategy. All authors revised the manuscript and approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

Funding

This research was supported by the Norwegian Extra Foundation for Health and Rehabilitation through the Premature Society.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The reviewer RS and handling Editor declared their shared affiliation.

Acknowledgments

Parts of the results are previously presented as a poster at the congress World Sleep 2017 in Prague, Czech Republic.

References

1. Bhutta AT, Cleves MA, Casey PH, Cradock MM, Anand KJ. Cognitive and behavioral outcomes of school-aged children who were born preterm: a meta-analysis. JAMA (2002) 288:728–37. doi: 10.1001/jama.288.6.728

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Aarnoudse-Moens CS, Weisglas-Kuperus N, Van Goudoever JB, Oosterlaan J. Meta-analysis of neurobehavioral outcomes in very preterm and/or very low birth weight children. Pediatrics (2009) 124:717–28. doi: 10.1542/peds.2008-2816

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Raju TNK, Buist AS, Blaisdell CJ, Moxey-Mims M, Saigal S. Adults born preterm: a review of general health and system-specific outcomes. Acta Paediatr. (2017) 106:1409–37. doi: 10.1111/apa.13880

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Johnson S, Marlow N. Charting the survival, health and development of extremely preterm infants: EPICure and beyond. Paediatr Child Health (2016) 26:498–504. doi: 10.1016/j.paed.2016.08.003

CrossRef Full Text | Google Scholar

5. Dewald JF, Meijer AM, Oort FJ, Kerkhof GA, Bogels SM. The influence of sleep quality, sleep duration and sleepiness on school performance in children and adolescents: a meta-analytic review. Sleep Med Rev. (2010) 14:179–89. doi: 10.1016/j.smrv.2009.10.004

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Rosen CL, Larkin EK, Kirchner HL, Emancipator JL, Bivins SF, Surovec SA, et al. Prevalence and risk factors for sleep-disordered breathing in 8- to 11-year-old children: association with race and prematurity. J Pediatr. (2003) 142:383–9. doi: 10.1067/mpd.2003.28

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Hagmann-Von Arx P, Perkinson-Gloor N, Brand S, Albert D, Holsboer-Trachsler E, Grob A, et al. In school-age children who were born very preterm sleep efficiency is associated with cognitive function. Neuropsychobiology (2014) 70:244–52. doi: 10.1159/000369026

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Hibbs AM, Storfer-Isser A, Rosen C, Ievers-Landis CE, Taveras EM, Redline S. Advanced sleep phase in adolescents born preterm. Behav Sleep Med. (2014) 12:412–24. doi: 10.1080/15402002.2013.825838

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Marcus CL, Meltzer LJ, Roberts RS, Traylor J, Dix J, D'ilario J, et al. Long-term effects of caffeine therapy for apnea of prematurity on sleep at school age. Am J Respir Crit Care Med. (2014) 190:791–9. doi: 10.1164/rccm.201406-1092OC

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Stangenes KM, Fevang SK, Grundt J, Donkor HM, Markestad T, Hysing M, et al. Children born extremely preterm had different sleeping habits at 11 years of age and more childhood sleep problems than term-born children. Acta Paediatr. (2017) 106:1966–72. doi: 10.1111/apa.13991

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Hibbs AM, Johnson NL, Rosen CL, Kirchner HL, Martin R, Storfer-Isser A, et al. Prenatal and neonatal risk factors for sleep disordered breathing in school-aged children born preterm. J Pediatr. (2008) 153:176–82. doi: 10.1016/j.jpeds.2008.01.040

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Paavonen EJ, Strang-Karlsson S, Raikkonen K, Heinonen K, Pesonen AK, Hovi P, et al. Very low birth weight increases risk for sleep-disordered breathing in young adulthood: the helsinki study of very low birth weight adults. Pediatrics (2007) 120:778–84. doi: 10.1542/peds.2007-0540

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Tapia IE, Shults J, Doyle LW, Nixon GM, Cielo CM, Traylor J, et al. Perinatal risk factors associated with the obstructive sleep apnea syndrome in school-aged children born preterm. Sleep (2016) 39:737–42. doi: 10.5665/sleep.5618

PubMed Abstract | CrossRef Full Text | Google Scholar

14. American Academy of SleepMedicine. The International Classification of Sleep Disorders. 3rd ed. Darien, CT (2014).

15. Roksund OD, Clemm H, Heimdal JH, Aukland SM, Sandvik L, Markestad T, et al. Left vocal cord paralysis after extreme preterm birth, a new clinical scenario in adults. Pediatrics (2010) 126:e1569–77. doi: 10.1542/peds.2010-1129

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Leversen KT, Sommerfelt K, Ronnestad A, Kaaresen PI, Farstad T, Skranes J, et al. Prediction of neurodevelopmental and sensory outcome at 5 years in Norwegian children born extremely preterm. Pediatrics (2011) 127:e630–8. doi: 10.1542/peds.2010-1001

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Vollsaeter M, Roksund OD, Eide GE, Markestad T, Halvorsen T. Lung function after preterm birth: development from mid-childhood to adulthood. Thorax (2013) 68:767–76. doi: 10.1136/thoraxjnl-2012-202980

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Skjaerven R, Gjessing HK, Bakketeig LS. Birthweight by gestational age in Norway. Acta Obstet Gynecol Scand. (2000) 79:440–9. doi: 10.1080/j.1600-0412.2000.079006440.x

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Markestad T, Kaaresen PI, Ronnestad A, Reigstad H, Lossius K, Medbo et al. Early death, morbidity, and need of treatment among extremely premature infants. Pediatrics (2005) 115:1289–98. doi: 10.1542/peds.2004-1482

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Westby Wold SH, Sommerfelt K, Reigstad H, Ronnestad A, Medbo S, Farstad T, et al. Neonatal mortality and morbidity in extremely preterm small for gestational age infants: a population based study. Arch Dis Child Fetal Neonatal Ed. (2009) 94:F363–7. doi: 10.1136/adc.2009.157800

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Baumer JH, Wright D, Mill T. Illness severity measured by CRIB score: a product of changes in perinatal care? Arch Dis Child Fetal Neonatal Ed. (1997) 77:F211–5. doi: 10.1136/fn.77.3.F211

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Scottish Neonatal Consultants Collaborative Study Group and the International Neonatal Network ' Collaborative Study Group and the International Neonatal Network. CRIB (clinical risk index for babies), mortality, and impairment after neonatal intensive care. Lancet (1995) 345:1020–2. doi: 10.1016/S0140-6736(95)90758-0

PubMed Abstract | CrossRef Full Text

23. Hirshkowitz M, Kaitlynwhiton P, Albert S, Alessi C, Bruni O, Doncarlos L, et al. National Sleep Foundation's updated sleep duration recommendations: final report. Sleep Health (2015) 1:233–43. doi: 10.1016/j.sleh.2015.10.004

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Johnson S, Hollis C, Kochhar P, Hennessy E, Wolke D, Marlow N. Psychiatric disorders in extremely preterm children: longitudinal finding at age 11 years in the EPICure study. J Am Acad Child Adolesc Psychiatry (2010) 49:453–63. doi: 10.1097/00004583-201005000-00006

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Fevang SKE, Hysing M, Sommerfelt K, Elgen I. Mental health assessed by the Strengths and Difficulties Questionnaire for children born extremely preterm without severe disabilities at 11 years of age: a Norwegian, national population-based study. Eur Child Adolesc Psychiatry (2017) 26:1523–31. doi: 10.1007/s00787-017-1007-x

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Krystal AD. Psychiatric disorders and sleep. Neurol Clin. (2012) 30:1389–1413. doi: 10.1016/j.ncl.2012.08.018

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Li S, Jin X, Yan C, Wu S, Jiang F, Shen X. Habitual snoring in school-aged children: environmental and biological predictors. Respir Res. (2010) 11:144. doi: 10.1186/1465-9921-11-144

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Kurjak A, Stanojevic M, Andonotopo W, Scazzocchio-Duenas E, Azumendi G, Carrera JM. Fetal behavior assessed in all three trimesters of normal pregnancy by four-dimensional ultrasonography. Croat Med J. (2005) 46:772–80.

PubMed Abstract | Google Scholar

29. Huang YS, Guilleminault C. Pediatric obstructive sleep apnea and the critical role of oral-facial growth: evidences. Front Neurol. (2012) 3:184. doi: 10.3389/fneur.2012.00184

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Zhang L, Samet J, Caffo B, Punjabi NM. Cigarette smoking and nocturnal sleep architecture. Am J Epidemiol. (2006) 164:529–37. doi: 10.1093/aje/kwj231

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Schuetze P, Eiden RD, Colder CR, Gray TR, Huestis MA. Physiological regulation in cigarette exposed infants: an examination of potential moderators. Neurotoxicol Teratol. (2011) 33:567–74. doi: 10.1016/j.ntt.2011.07.004

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Lumeng JC, Chervin RD. Epidemiology of pediatric obstructive sleep apnea. Proc Am Thorac Soc. (2008) 5:242–52. doi: 10.1513/pats.200708-135MG

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Felder JN, Baer RJ, Rand L, Jelliffe-Pawlowski LL, Prather AA. Sleep disorder diagnosis during pregnancy and risk of preterm birth. Obstet Gynecol. (2017) 130:573–81. doi: 10.1097/AOG.0000000000002132

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Bhattacharyya N. Sleep and health implications of snoring: a populational analysis. Laryngoscope (2015) 125:2413–6. doi: 10.1002/lary.25346

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Ross KR, Redline S. Sleep outcomes in children born prematurely. In: Respiratory Outcomes in Preterm Infants, Hibbs A, Muhlebach M. editors. Cham: Respiratory Medicine. Humana Press (2017) 161–79.

Google Scholar

36. Emancipator JL, Storfer-Isser A, Taylor HG, Rosen CL, Kirchner HL, Johnson NL, et al. Variation of cognition and achievement with sleep-disordered breathing in full-term and preterm children. Arch Pediatr Adolesc Med. (2006) 160:203–10. doi: 10.1001/archpedi.160.2.203

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Gozal D. Sleep-disordered breathing and school performance in children. Pediatrics (1998) 102:616–20. doi: 10.1542/peds.102.3.616

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Gozal D, Pope DW Jr. Snoring during early childhood and academic performance at ages thirteen to fourteen years. Pediatrics (2001) 107:1394–9. doi: 10.1542/peds.107.6.1394

PubMed Abstract | CrossRef Full Text | Google Scholar

39. O'brien LM, Gozal D. Behavioural and neurocognitive implications of snoring and obstructive sleep apnoea in children: facts and theory. Paediatr Respir Rev. (2002) 3:3–9. doi: 10.1053/prrv.2002.0177

PubMed Abstract | CrossRef Full Text | Google Scholar

40. O'brien LM, Mervis CB, Holbrook CR, Bruner JL, Klaus CJ, Rutherford J, et al. Neurobehavioral implications of habitual snoring in children. Pediatrics (2004) 114:44–9. doi: 10.1542/peds.114.1.44

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Halbower AC, Mahone EM. Neuropsychological morbidity linked to childhood sleep-disordered breathing. Sleep Med Rev. (2006) 10:97–107. doi: 10.1016/j.smrv.2005.10.002

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Beebe DW, Rausch J, Byars KC, Lanphear B, Yolton K. Persistent snoring in preschool children: predictors and behavioral and developmental correlates. Pediatrics (2012) 130:382–9. doi: 10.1542/peds.2012-0045

PubMed Abstract | CrossRef Full Text | Google Scholar

43. American Academy of Pediatrics. Section on Pediatric Pulmonology and Subcommittee on Obstructive Sleep Apnea, Syndrome Clinical practice guideline: diagnosis and management of childhood obstructive sleep apnea syndrome. Pediatrics (2002) 109:704–12.

PubMed Abstract

44. Wang K, Difiore JM, Martin RJ, Rosen CL, Hibbs AM. Markers for severity of illness associated with decreased snoring in toddlers born ELGA. Acta Paediatr. (2013) 102:e39–43. doi: 10.1111/apa.12033

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Lekic T, Klebe D, Poblete R, Krafft PR, Rolland WB, Tang J, et al. Neonatal brain hemorrhage (NBH) of prematurity: translational mechanisms of the vascular-neural network. Curr Med Chem. (2015) 22:1214–38. doi: 10.2174/0929867322666150114152421

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Bardin C, Zelkowitz P, Papageorgiou A. Outcome of small-for-gestational age and appropriate-for-gestational age infants born before 27 weeks of gestation. Pediatrics (1997) 100:E4. doi: 10.1542/peds.100.2.e4

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Sivertsen B, Harvey AG, Pallesen S, Hysing M. Trajectories of sleep problems from childhood to adolescence: a population-based longitudinal study from Norway. J Sleep Res. (2017) 26:55–63. doi: 10.1111/jsr.12443

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Calhoun SL, Vgontzas AN, Fernandez-Mendoza J, Mayes SD, Tsaoussoglou M, Basta M, et al. Prevalence and risk factors of excessive daytime sleepiness in a community sample of young children: the role of obesity, asthma, anxiety/depression, and sleep. Sleep (2011) 34:503–7. doi: 10.1093/sleep/34.4.503

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Cappuccio FP, Taggart FM, Kandala NB, Currie A, Peile E, Stranges S, et al. Meta-analysis of short sleep duration and obesity in children and adults. Sleep (2008) 31:619–26. doi: 10.1093/sleep/31.5.619

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Gruber R, Cassoff J, Frenette S, Wiebe S, Carrier J. Impact of sleep extension and restriction on children's emotional lability and impulsivity. Pediatrics (2012) 130:e1155–61. doi: 10.1542/peds.2012-0564

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Cappuccio FP, Miller MA. Sleep and cardio-metabolic disease. Curr Cardiol Rep. (2017) 19:110. doi: 10.1007/s11886-017-0916-0

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Fevang SK, Hysing M, Markestad T, Sommerfelt K. Mental health in children born extremely preterm without severe neurodevelopmental disabilities. Pediatrics (2016) 137:e20153002. doi: 10.1542/peds.2015-3002

PubMed Abstract | CrossRef Full Text | Google Scholar