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. 2020 Jul 6;10:11084. doi: 10.1038/s41598-020-67852-3

Association of maternal sleep before and during pregnancy with preterm birth and early infant sleep and temperament

Kazushige Nakahara 1,#, Takehiro Michikawa 2,#, Seiichi Morokuma 3,4,, Masanobu Ogawa 4, Kiyoko Kato 1,4, Masafumi Sanefuji 4,5, Eiji Shibata 6,7, Mayumi Tsuji 6,8, Masayuki Shimono 6,9, Toshihiro Kawamoto 6, Shouichi Ohga 5, Koichi Kusuhara 6,9; The Japan Environment and Children’s Study Group
PMCID: PMC7338358  PMID: 32632276

Abstract

This study aimed to investigate the association of maternal sleep before and during pregnancy with preterm birth, infant sleep and temperament at 1 month of age. We used the data of the Japan Environment and Children’s Study, a cohort study in Japan, which registered 103,099 pregnancies between 2011 and 2014. Participants were asked about their sleep before and during pregnancy, and the sleep and temperament of their newborns at 1 month of age. Preterm birth data were collected from medical records. Maternal sleep was not associated with preterm birth, but subjective sleep quality during pregnancy was associated with late preterm birth (birth at 34–36 weeks of gestation). For example, participants with extremely light subjective depth of sleep were more likely to experience preterm birth (RR = 1.19; 95% confidence interval [CI] = 1.04–1.35). Maternal sleep both before and during pregnancy seemed to be associated with infant sleep and temperament at 1 month of age. Infants, whose mothers slept for less than 6 hours before pregnancy, tended to cry intensely (RR = 1.15; 95% CI = 1.09–1.20). Maternal sleep problems before and during pregnancy were associated with preterm birth and child sleep problems and temperament.

Subject terms: Epidemiology, Risk factors

Introduction

In Japan, the average sleep duration is shorter than in other countries1, and it has become even shorter in recent years2. At the same time, the rate of preterm birth in Japan has increased3, as has the incidence of developmental disorders4.

Maternal short sleep duration and sleep-disordered breathing (SDB) are associated with increased preterm birth rates5,6. Furthermore, maternal SDB and apnea during pregnancy affects offspring’s development, manifesting as disrupted social skills and low reading test scores7,8.

However, no large-scale study has examined potential associations between sleep during pregnancy and offspring’s development. Additionally, the importance of maternal sleep during various periods of pregnancy remains unclear. Maternal short sleep and SDB increase inflammatory cytokine levels9,10, and maternal inflammation can cause preterm birth11,12 and developmental disorder13,14. Maternal obesity also increases inflammatory cytokines15,16, and a study reported that maternal pre-pregnancy body mass index (BMI) affects maternal inflammatory markers to a greater extent than does late pregnancy BMI17. Similarly, maternal sleep before pregnancy may also be more important for obstetric outcomes and offspring development than sleep during pregnancy.

In cases of neurodevelopmental disorders, including autism spectrum disorder (ASD), abnormalities of neurodevelopment, sleep, and temperament are observed in early infancy, such as a 1–4-month-old18,19. This study aimed to investigate the association of maternal sleep before and during pregnancy with preterm birth, infant sleep, and temperament at 1 month of age.

Results

The baseline characteristics of participants, along with available data on sleep duration before and during pregnancy, are shown in Table 1. The most commonly reported sleep duration was 7–8 h both before and during pregnancy.

Table 1.

Baseline characteristics of the participants in the Japan Environment and Children’s Study (2011–2014).

No. of womena Sleep duration during preconception (h) No. of womena Sleep duration during pregnancy (h)
< 6 6–7 7–8 8–9 9–10 > 10 < 6 6–7 7–8 8–9 9–10 > 10
(%) (%) (%) (%) (%) (%) (%) (%) (%) (%) (%) (%)
No. of women 87,106 6,028 17,260 29,350 21,521 8,830 4,117 86,358 4,305 12,948 26,769 24,491 12,166 5,679
Age at delivery (years)
 < 25 8,499 10.3 7.7 8.0 9.3 12.4 27.1 8,465 11.7 8.6 8.0 8.5 11.1 22.7
 25–29 24,039 25.5 26.8 27.6 27.9 28.7 30.3 23,838 25.4 26.3 27.2 27.7 28.6 31.6
 30–34 30,809 32.0 35.4 36.5 36.5 35.3 26.6 30,591 31.3 34.3 36.3 36.7 36.7 28.8
 ≥ 35 23,759 32.2 30.2 28.0 26.3 23.6 16.0 23,464 31.5 30.8 28.5 27.2 23.7 16.9
Smoking habits
 Never-smokers 50,646 52.8 60.3 60.4 58.4 55.8 46.4 50,269 53.7 59.5 60.1 59.1 56.7 50.3
 Ex-smokers who quit before pregnancy 20,358 20.7 21.7 23.0 24.7 26.1 24.8 20,184 21.3 21.8 22.7 24.0 25.6 24.6
 Smokers during early pregnancy 15,979 26.4 18.1 16.6 16.9 18.1 28.8 15,788 25.0 18.7 17.2 16.9 17.7 25.1
Alcohol consumption
 Never-drinkers 29,955 31.9 32.8 34.2 35.8 36.0 35.7 29,702 33.0 33.6 34.1 34.8 35.3 35.1
 Ex-drinkers who quit before pregnancy 16,233 17.1 16.7 17.8 19.7 22.5 21.7 15,767 17.9 16.2 17.6 18.4 20.7 21.1
 Drinkers during early pregnancy 40,885 51.1 50.5 48.0 44.6 41.5 42.7 40,859 49.2 50.2 48.4 46.8 44.0 43.9
Pre-pregnancy body mass index (kg/m2)
 < 18.5 14,045 15.8 16.1 16.0 16.2 15.8 18.0 13,969 16.9 15.9 16.0 15.8 16.7 17.6
 18.5–24.9 63,883 72.4 73.8 73.6 73.5 73.3 71.0 63,334 71.4 73.7 74.0 73.9 72.4 71.3
 ≥ 25.0 9,140 11.8 10.2 10.4 10.3 10.9 11.0 9,000 11.8 10.5 10.0 10.3 11.0 11.1
Parity
 0 37,911 57.8 57.6 47.3 32.1 24.1 41.0 37,640 55.3 57.0 48.7 36.5 29.1 44.0
 ≥ 1 48,900 42.2 42.4 52.7 67.9 75.9 59.0 48,407 44.7 43.0 51.3 63.5 70.9 56.0
Current history
 Diabetes or gestational diabetes 2,665 3.5 3.2 3.0 2.9 3.1 3.2 2,638 3.9 3.2 3.1 2.9 3.0 3.1
 Hypertensive disorders in pregnancy 2,759 4.5 3.7 3.2 2.7 2.4 3.0 2,618 4.0 3.6 3.1 2.8 2.6 2.6
 Intrauterine infection 612 1.0 0.8 0.7 0.6 0.5 0.8 554 0.7 0.8 0.7 0.6 0.5 0.6
History of preterm birth
 No 84,156 97.0 97.1 96.8 96.3 95.8 96.7 83,518 97.0 96.9 97.0 96.6 96.4 96.6
 Yes 2,934 3.1 3.0 3.2 3.7 4.2 3.3 2,799 3.1 3.1 3.0 3.4 3.7 3.4
Infertility treatment
 No 81,311 92.8 92.0 92.7 94.1 95.8 96.4 80,638 93.3 91.7 92.7 93.7 95.2 95.9
 Ovulation stimulation/artificial insemination by sperm from husband 3,158 3.9 4.4 3.9 3.4 2.5 2.1 3,109 3.8 4.4 3.9 3.5 2.8 2.5
 Assisted reproductive technology 2,609 3.3 3.6 3.5 2.6 1.8 1.6 2,553 2.9 3.9 3.4 2.8 2.0 1.7
Educational background, years
 < 13 30,964 40.4 32.9 33.8 35.4 40.1 54.2 31,045 42.6 34.9 33.4 34.7 37.8 48.9
 ≥ 13 54,926 59.6 67.1 66.2 64.6 59.9 45.8 54,986 57.4 65.1 66.6 65.3 62.2 51.1
Household income, million Japanese-yen/year
 < 6 58,726 71.3 69.5 71.1 74.6 79.3 86.1 58,763 73.9 69.6 70.3 73.1 77.6 84.9
 ≥ 6 21,569 28.7 30.5 28.9 25.4 20.8 14.0 21,590 26.1 30.4 29.7 26.9 22.4 15.1
Occupation in early pregnancy
 Administrative, managerial, professional, and engineering workers 20,047 22.0 26.3 25.5 22.9 17.1 9.7 19,798 20.2 24.7 25.7 24.4 19.6 12.9
 Clerical workers 14,816 18.8 21.4 19.6 14.8 10.0 6.9 14,580 17.7 21.2 19.7 16.3 12.3 8.9
 Sales and service workers 19,105 25.0 20.7 20.2 22.6 24.2 30.4 18,858 25.4 20.3 20.3 22.0 24.0 28.9
 Homemaker 24,024 22.3 22.0 25.3 30.6 38.8 39.8 23,688 24.2 23.8 25.1 28.2 34.5 36.1
 Others 8,472 11.8 9.6 9.4 9.2 9.9 13.2 8,360 12.5 10.1 9.2 9.2 9.6 13.2
Type of delivery
 Vaginal 70,776 79.8 81.1 81.2 82.0 82.3 81.8 70,603 81.9 81.4 81.6 81.9 82.9 82.4
 Caesarean 16,143 20.2 18.9 18.8 18.0 17.7 18.2 15,582 18.1 18.6 18.4 18.1 17.1 17.6
Postpartum depressive symptoms at 1 month after delivery assessed by the Edinburgh Postnatal Depression Scale
 Not depressive (score < 8) 72,482 82.2 85.2 86.3 87.2 86.7 80.7 72,137 80.1 84.7 86.0 87.3 87.1 82.7
 Depressive (score ≥ 9) 11,985 17.8 14.8 13.7 12.8 13.3 19.3 11,916 19.9 15.3 14.0 12.7 12.9 17.3
Small for gestational age
 No 80,106 92.3 92.2 92.5 92.6 92.8 92.8 79,496 92.7 92.5 92.6 92.7 92.6 92.6
 Yes 6,495 7.7 7.8 7.5 7.4 7.2 7.3 6,339 7.3 7.5 7.4 7.3 7.4 7.4
Infant sex
 Boys 44,592 51.1 51.0 51.0 51.4 51.6 51.6 44,161 51.1 51.1 50.9 50.9 52.4 50.9
 Girls 42,510 48.9 49.0 49.0 48.6 48.5 48.4 42,194 48.9 48.9 49.1 49.1 47.6 49.1

aSubgroup totals do not equal the overall number because of missing data.

Maternal sleep and preterm birth

Sleep duration and bedtime before and during pregnancy were not associated with preterm birth in this study (Table 2). However, very light sleep and very bad feeling when waking up during pregnancy were associated with late preterm birth in a multivariable model (RR for very light sleep vs. normal = 1.19, 95% CI = 1.04–1.35; RR for very bad feeling vs. normal = 1.31, 95% CI = 1.02–1.67) (Table 3).

Table 2.

Association between sleep during preconception and preterm birth in the Japan Environment and Children’s Study (2011–2014).

No. of participants Preterm births Maternal age-adjusted model Multivariable modela
No. % RR 95% CI RR 95% CI
Preterm birth
 Sleep time (h)
  < 6 6,028 288 4.8 1.08 0.95 1.22 1.04 0.92 1.17
  6–7 17,260 820 4.8 1.08 0.99 1.18 1.06 0.97 1.15
  7–8 29,350 1,283 4.4 Reference Reference
  8–9 21,521 922 4.3 0.99 0.91 1.07 1.00 0.92 1.09
  9–10 8,830 353 4.0 0.93 0.83 1.05 0.93 0.83 1.04
  > 10 4,117 177 4.3 1.04 0.89 1.22 1.00 0.85 1.16
 Bedtime
  21:00–24:00 58,425 2,582 4.4 Reference Reference
  24:00–03:00 26,187 1,157 4.4 1.02 0.95 1.09 1.00 0.94 1.08
  Other 2,494 104 4.2 0.99 0.81 1.19 0.91 0.75 1.11
Late preterm birth (34–36 weeks)
 Sleep time (h)
  < 6 5,973 233 3.9 1.10 0.95 1.26 1.07 0.93 1.22
  6–7 17,104 664 3.9 1.10 1.00 1.21 1.08 0.99 1.19
  7–8 29,091 1,024 3.5 Reference Reference
  8–9 21,352 753 3.5 1.01 0.92 1.11 1.02 0.93 1.12
  9–10 8,758 281 3.2 0.93 0.81 1.06 0.92 0.81 1.05
  > 10 4,080 140 3.4 1.03 0.86 1.22 0.98 0.82 1.17
 Bedtime
 21:00–24:00 57,925 2,082 3.6 Reference Reference
 24:00–03:00 25,962 932 3.6 1.02 0.94 1.10 1.02 0.94 1.10
 Other 2,471 81 3.3 0.96 0.77 1.19 0.89 0.71 1.11
Early preterm birth (23–33 weeks)
 Sleep time (h)
  < 6 5,795 55 1.0 1.02 0.76 1.36 0.92 0.69 1.22
  6–7 16,596 156 0.9 1.02 0.83 1.24 0.96 0.78 1.17
  7–8 28,326 259 0.9 Reference Reference
  8–9 20,768 169 0.8 0.90 0.74 1.09 0.93 0.77 1.13
  9–10 8,549 72 0.8 0.95 0.73 1.23 0.97 0.74 1.26
  > 10 3,977 37 0.9 1.10 0.78 1.55 1.05 0.73 1.49
 Bedtime
  21:00–24:00 56,343 500 0.9 Reference Reference
  24:00–03:00 25,255 225 0.9 1.03 0.88 1.21 0.97 0.82 1.14
  Other 2,413 23 1.0 1.15 0.75 1.75 1.01 0.66 1.54

CI, confidence interval; RR, relative risk.

aAdjusted for maternal age at delivery, smoking habits, alcohol consumption, pre-pregnancy body mass index, parity, current history of diabetes or gestational diabetes, hypertensive disorders in pregnancy and intrauterine infection, history of preterm birth, and infertility treatment.

Table 3.

Association between sleep during pregnancy and late preterm birth in the Japan Environment and Children’s Study (2011–2014).

No. of participants Preterm births Maternal age-adjusted model Multivariable modela
No. % OR 95% CI OR 95% CI
Sleep duration (h)
 < 6 4,305 169 3.9 1.11 0.94 1.30 1.09 0.93 1.28
 6–7 12,948 469 3.6 1.02 0.92 1.14 1.00 0.90 1.12
 7–8 26,769 944 3.5 Reference Reference
 8–9 24,491 882 3.6 1.03 0.94 1.12 1.04 0.95 1.14
 9–10 12,166 417 3.4 0.99 0.88 1.11 0.99 0.88 1.11
 > 10 5,679 196 3.5 1.03 0.89 1.20 1.01 0.87 1.18
Bedtime
 21:00–24:00 63,212 2,298 3.6 Reference Reference
 24:00–03:00 21,173 717 3.4 0.95 0.87 1.03 0.95 0.87 1.03
 Other 1,973 62 3.1 0.89 0.69 1.14 0.86 0.68 1.10
Depth of sleep
 Very light 6,135 266 4.3 1.21 1.06 1.38 1.19 1.04 1.35
 Light 36,158 1,293 3.6 1.00 0.93 1.09 1.01 0.94 1.09
 Normal 34,339 1,213 3.5 Reference Reference
 Deep 8,035 258 3.2 0.92 0.80 1.05 0.94 0.82 1.07
 Very deep 1,545 42 2.7 0.78 0.58 1.06 0.76 0.56 1.02
p for trend < 0.01b p for trend < 0.01b
Feeling when waking up in the morning
 Very bad 1,372 65 4.7 1.38 1.08 1.75 1.31 1.02 1.67
 Bad 17,875 629 3.5 1.01 0.92 1.10 1.01 0.92 1.10
 Normal 53,523 1,890 3.5 Reference Reference
 Good 11,868 428 3.6 1.02 0.92 1.13 1.05 0.94 1.16
 Very good 1,526 60 3.9 1.11 0.86 1.42 1.08 0.83 1.39
p for trend = 0.62b p for trend = 0.94b

CI, confidence interval; RR, relative risk.

aAdjusted for maternal age at delivery, smoking habits, alcohol consumption, pre-pregnancy body mass index, parity, current history of diabetes or gestational diabetes, hypertensive disorders in pregnancy and intrauterine infection, history of preterm birth, and infertility treatment.

bLinear trend in the association was tested by assignment of ordinal variables for the five categories.

Maternal sleep and infant sleep

Sleep duration and bed time before pregnancy were not associated with ≥ 5 nocturnal awakenings. However, both sleep duration and bed time were likely to be related with an infant’s tendency to sleep longer during the day than at night (Table 4).

Table 4.

Association between sleep before pregnancy and neonatal sleep in the Japan Environment and Children’s Study (2011–2014).

No. of participants Outcome Maternal age-adjusted model Multivariable modela
No. % RR 95% CI RR 95% CI
Five or more awakenings during the night
 Sleep time (h)
  < 6 5,455 355 6.5 1.02 0.91 1.14 1.07 0.96 1.20
  6–7 15,797 924 5.9 0.91 0.84 0.98 0.95 0.87 1.02
  7–8 27,051 1,733 6.4 Reference Reference
  8–9 19,855 1,316 6.6 1.04 0.97 1.11 1.00 0.93 1.07
  9–10 8,116 538 6.6 1.05 0.96 1.16 0.99 0.90 1.09
  > 10 3,683 225 6.1 1.03 0.90 1.17 0.98 0.86 1.13
 Bedtime
  21:00–24:00 53,841 3,488 6.5 Reference Reference
  24:00–03:00 23,870 1,450 6.1 0.96 0.90 1.02 1.05 0.98 1.12
  Other 2,246 153 6.8 1.13 0.96 1.32 1.17 1.00 1.37
Sleeping longer during the day than at night
 Sleep time (h)
  6 5,439 1,287 23.7 1.24 1.17 1.31 1.18 1.12 1.25
  6–7 15,734 3,401 21.6 1.14 1.09 1.18 1.10 1.06 1.15
  7–8 26,996 5,141 19.0 Reference Reference
  8–9 19,811 3,535 17.8 0.93 0.90 0.97 0.98 0.95 1.02
  9–10 8,088 1,349 16.7 0.87 0.82 0.92 0.94 0.89 1.00
  > 10 3,673 663 18.1 0.92 0.85 0.99 0.94 0.88 1.02
 Bedtime
  21:00–24:00 53,708 9,479 17,7 Reference Reference
  24:00–03:00 23,796 5,411 22.7 1.28 1.24 1.32 1.17 1.13 1.20
  Other 2,237 486 21.7 1.20 1.11 1.30 1.13 1.04 1.22

CI, confidence interval; RR, relative risk.

aAdjusted for maternal age at delivery, smoking habits, alcohol consumption, pre-pregnancy body mass index, gestational age at birth, parity, infertility treatment, infant sex, small for gestational age, type of delivery, and postpartum depressive symptoms.

In the M-T2, waking up ≥ 5 times during the night was associated with maternal light sleep and feeling bad at awakening during pregnancy. Sleeping longer during the day than at night was related not only to maternal short sleep duration but also to late bed time and feeling bad at awakening (Table 5).

Table 5.

Association between sleep during pregnancy and neonatal sleep in the Japan Environment and Children’s Study (2011–2014).

No. of participants No. of outcome Maternal age adjusted model Multivariable modela
% RR 95% CI RR 95% CI
Five or more awakenings during the night
 Sleep time (h)
  < 6 3,932 245 6.2 1.03 0.90 1.17 1.07 0.94 1.22
  6–7 11,999 764 6.4 1.04 0.96 1.13 1.07 0.98 1.16
  7–8 24,914 1,524 6.1 Reference Reference
  8–9 22,802 1,442 6.3 1.04 0.97 1.11 1.00 0.93 1.07
  9–10 11,320 801 7.1 1.17 1.08 1.27 1.10 1.01 1.20
  > 10 5,183 324 6.3 1.08 0.96 1.22 1.06 0.95 1.20
 Bedtime
  21:00–24:00 58,817 3,788 6.4 Reference Reference
  24:00–03:00 19,541 1,179 6.0 0.95 0.90 1.02 1.04 0.97 1.11
  Other 1,792 133 7.4 1.19 1.01 1.41 1.19 1.00 1.41
 Depth of sleep
  Very light 5,567 436 7.8 1.29 1.17 1.43 1.27 1.14 1.40
  Light 33,580 2,224 6.6 1.09 1.03 1.15 1.07 1.01 1.14
  Normal 31,909 1,929 6.1 Reference Reference
  Deep 7,510 418 5.6 0.92 0.83 1.02 0.94 0.85 1.04
  Very deep 1,450 84 5.8 0.98 0.79 1.21 1.00 0.81 1.24
p for trend < 0.01b p for trend < 0.01b
Feeling when waking up in the morning
  Very bad 1,240 112 9.0 1.52 1.27 1.81 1.53 1.28 1.84
  Bad 16,514 1,131 6.9 1.12 1.05 1.19 1.12 1.05 1.20
  Normal 49,715 3,073 6.2 Reference Reference
  Good 11,085 689 6.2 1.00 0.92 1.08 1.01 0.93 1.09
  Very good 1,422 81 5.7 0.92 0.74 1.14 0.95 0.76 1.17
p for trend < 0.01b p for trend < 0.01b
Sleeping longer during the day than at night
 Sleep time (h)
  < 6 3,914 915 23.4 1.19 1.12 1.27 1.16 1.09 1.24
  6–7 11,958 2,663 22.3 1.14 1.10 1.19 1.11 1.06 1.16
  7–8 24,868 4,843 19.5 Reference Reference
  8–9 22,738 4,147 18.2 0.94 0.90 0.97 0.97 0.94 1.01
  9–10 11,288 1,898 16.8 0.86 0.82 0.90 0.92 0.88 0.97
  > 10 5,167 964 18.7 0.93 0.88 0.99 0.96 0.90 1.03
Bedtime
  21:00–24:00 58,673 10,533 18.0 Reference Reference
  24:00–03:00 19,499 4,516 23.2 1.28 1.24 1.32 1.18 1.14 1.22
  Other 1,783 381 21.4 1.17 1.07 1.29 1.15 1.05 1.26
 Depth of sleep
  Very light 5,550 1,162 20.9 1.09 1.03 1.15 1.08 1.02 1.15
  Light 33,500 6,397 19.1 0.99 0.96 1.02 1.00 0.97 1.03
  Normal 31,812 6,139 19.3 Reference Reference
  Deep 7,489 1,427 19.1 0.99 0.94 1.04 0.96 0.92 1.02
  Very deep 1,448 286 19.8 1.02 0.91 1.13 0.99 0.89 1.10
p for trend = 0.15b p for trend = 0.02b
Feeling when waking up in the morning
 Very bad 1,237 300 24.1 1.24 1.12 1.37 1.21 1.09 1.34
 Bad 16,468 3,329 20.1 1.05 1.02 1.09 1.04 1.00 1.07
 Normal 49,582 9,472 19.0 Reference Reference
 Good 11,056 2,094 18.9 1.00 0.95 1.04 0.99 0.95 1.03
 Very good 1,416 258 18.1 0.95 0.84 1.06 0.93 0.83 1.05
p for trend < 0.01b p for trend < 0.01b

CI, confidence interval; RR, relative risk.

aAdjusted for maternal age at delivery, smoking habits, alcohol consumption, pre-pregnancy body mass index, gestational age at birth, parity, infertility treatment, infant sex, small for gestational age, type of delivery, and postpartum depressive symptoms.

bLinear trend in the association was tested by assignment of ordinal variables for the five categories.

In the subanalysis of participants who slept 7–9 h before pregnancy, maternal short sleep and bed time after midnight were associated with longer day sleeps. Similarly, in the group of participants who slept 7–9 h during pregnancy, maternal short sleep before pregnancy was associated with more awakenings during the night and longer day-time sleep durations (Table S1).

Maternal sleep and infant temperament

In the M-T1, sleeping < 7 h and going to bed after midnight were associated with infants with bad mood, frequent crying for long periods, and intense crying (Table 6).

Table 6.

Association between sleep during preconception and neonatal irritability in the Japan Environment and Children’s Study (2011–2014).

No. of participants Outcome Maternal age-adjusted model Multivariable modela
No. % RR 95% CI RR 95% CI
Bad mood
 Sleep time (h)
  < 6 5,603 469 8.4 1.33 1.21 1.47 1.12 1.01 1.23
  6–7 16,142 1,278 7.9 1.26 1.17 1.35 1.09 1.01 1.16
  7–8 27,584 1,735 6.3 Reference Reference
  8–9 20,238 966 4.8 0.76 0.70 0.82 0.97 0.90 1.05
  9–10 8,308 356 4.3 0.68 0.61 0.76 1.05 0.94 1.17
  > 10 3,804 239 6.3 1.00 0.87 1.14 1.17 1.02 1.33
 Bedtime
  21:00–24:00 54,935 2,803 5.1 Reference Reference
  24:00–03:00 24,434 2,084 8.5 1.68 1.59 1.77 1.12 1.06 1.19
  Other 2,310 156 6.8 1.35 1.15 1.57 1.10 0.94 1.29
Frequent crying, for long periods
 Sleep time (h)
  < 6 5,587 1,255 22.5 1.28 1.21 1.35 1.17 1.11 1.24
  6–7 16,093 3,332 20.7 1.18 1.14 1.23 1.09 1.05 1.13
  7–8 27,534 4,810 17.5 Reference Reference
  8–9 20,205 3,013 14.9 0.85 0.82 0.89 0.98 0.94 1.02
  9–10 8,299 1,066 12.8 0.74 0.69 0.78 0.91 0.86 0.97
  > 10 3,800 619 16.3 0.94 0.87 1.01 1.01 0.94 1.09
 Bedtime
  21:00–24:00 54,840 8,530 15.6 Reference Reference
  24:00–03:00 24,365 5,178 21.3 1.38 1.33 1.42 1.09 1.06 1.13
  Other 2,313 387 16.7 1.09 1.00 1.20 0.96 0.88 1.06
Intense crying
 Sleep time (h)
  < 6 5,592 1,448 25.9 1.30 1.23 1.36 1.15 1.09 1.20
  6–7 16,114 3,886 24.1 1.21 1.17 1.25 1.08 1.04 1.12
  7–8 27,546 5,490 19.9 Reference Reference
  8–9 20,201 3,234 16.0 0.80 0.77 0.84 0.97 0.93 1.01
  9–10 8,295 1,149 13.9 0.69 0.65 0.74 0.95 0.89 1.00
  > 10 3,800 671 17.7 0.88 0.81 0.94 0.98 0.91 1.06
 Bedtime
  21:00–24:00 54,833 9,350 17.1 Reference Reference
  24:00–03:00 24,402 6,082 24.9 1.46 1.42 1.51 1.07 1.04 1.10
  Other 2,313 446 19.3 1.14 1.04 1.24 0.97 0.89 1.05

CI, confidence interval; RR, relative risk.

aAdjusted for maternal age at delivery, smoking habits, alcohol consumption, pre-pregnancy body mass index, gestational age at birth, parity, infertility treatment, infant sex, small for gestational age, type of delivery, and postpartum depressive symptoms.

In the M-T2, we observed a relationship between bad mood and maternal short sleep, late bed time, light sleep, and feeling bad on awakening. Frequent crying for long periods was likely to be associated with short sleep, late bed time, light sleep, and feeling bad on awakening. Intense crying was also related to short sleep, late bed time, light sleep, and feeling bad on awakening (Table 7).

Table 7.

Association between sleep during pregnancy and neonatal temperament in the Japan Environment and Children’s Study (2011–2014).

No. of participants Outcome Maternal age-adjusted model Multivariable modela
No. % RR 95% CI RR 95% CI
Bad mood
 Sleep duration (h)
  < 6 4,049 373 9.2 1.40 1.26 1.56 1.22 1.09 1.36
  6–7 12,252 959 7.8 1.19 1.10 1.29 1.06 0.99 1.15
  7–8 25,432 1,671 6.6 Reference Reference
  8–9 23,266 1,215 5.2 0.79 0.74 0.85 0.97 0.91 1.04
  9–10 11,551 560 4.9 0.74 0.67 0.81 1.03 0.94 1.13
  > 10 5,343 301 5.6 0.85 0.76 0.96 0.95 0.85 1.07
 Bedtime
  21:00–24:00 60,030 3,214 5.4 Reference Reference
  24:00–03:00 20,013 1,759 8.8 1.64 1.55 1.74 1.15 1.09 1.22
  Other 1,850 106 5.7 1.08 0.89 1.30 0.96 0.79 1.16
 Depth of sleep
  Very light 5,740 480 8.4 1.47 1.33 1.61 1.46 1.32 1.61
  Light 34,277 2,172 6.3 1.11 1.05 1.18 1.14 1.07 1.21
  Normal 32,606 1,861 5.7 Reference Reference
  Deep 7,656 447 5.8 1.02 0.92 1.13 0.95 0.86 1.05
  Very deep 1,475 107 7.3 1.27 1.05 1.53 1.20 1.00 1.45
p for trend < 0.01b p for trend < 0.01b
Feeling when waking up in the morning
  Very bad 1,269 131 10.3 1.82 1.54 2.15 1.57 1.33 1.86
  Bad 16,920 1,353 8.0 1.41 1.32 1.50 1.29 1.21 1.37
  Normal 50,810 2,886 5.7 Reference Reference
  Good 11,265 612 5.4 0.96 0.88 1.04 0.92 0.85 1.01
  Very good 1,448 83 5.7 1.01 0.82 1.25 0.99 0.80 1.22
p for trend < 0.01b p for trend < 0.01b
Frequent crying, for long periods
 Sleep duration (h)
  < 6 4,036 898 22.3 1.24 1.16 1.32 1.15 1.08 1.22
  6–7 12,229 2,587 21.2 1.18 1.13 1.23 1.09 1.05 1.14
  7–8 25,373 4,543 17.9 Reference Reference
  8–9 23,209 3,609 15.6 0.87 0.84 0.90 0.96 0.93 1.00
  9–10 11,551 1,669 14.5 0.81 0.77 0.85 0.97 0.92 1.02
  > 10 5,333 862 16.2 0.91 0.85 0.97 0.97 0.91 1.04
 Bedtime
  21:00–24:00 59,915 9,559 16.0 Reference Reference
  24:00–03:00 19,970 4,253 21.3 1.34 1.30 1.39 1.09 1.05 1.13
  Other 1,846 356 19.3 1.22 1.11 1.34 1.15 1.04 1.26
 Depth of sleep
  Very light 5,727 1,194 20.9 1.27 1.20 1.35 1.24 1.18 1.31
  Light 34,222 6,148 18.0 1.10 1.07 1.14 1.11 1.07 1.14
  Normal 32,529 5,294 16.3 Reference Reference
  Deep 7,642 1,270 16.6 1.02 0.97 1.08 0.98 0.93 1.04
  Very deep 1,474 238 16.2 1.00 0.88 1.12 0.95 0.84 1.07
p for trend < 0.01b p for trend < 0.01b
Feeling when waking up in the morning
  Very bad 1,262 301 23.9 1.44 1.30 1.59 1.27 1.15 1.41
  Bad 16,880 3,515 20.8 1.25 1.21 1.30 1.17 1.13 1.21
  Normal 50,721 8,456 16.7 Reference Reference
  Good 11,243 1,668 14.8 0.89 0.85 0.93 0.88 0.84 0.92
  Very good 1,446 191 13.2 0.79 0.69 0.90 0.78 0.68 0.89
p for trend < 0.01b p for trend < 0.01b
Intense crying
 Sleep duration (h)
  < 6 4,043 1,053 26.1 1.25 1.18 1.33 1.15 1.08 1.21
  6–7 12,226 2,958 24.2 1.17 1.12 1.22 1.07 1.03 1.11
  7–8 25,404 5,256 20.7 Reference Reference
  8–9 23,224 3,941 17.0 0.82 0.79 0.85 0.95 0.92 0.99
  9–10 11,542 1,807 15.7 0.76 0.72 0.79 0.98 0.93 1.02
  > 10 5,327 946 17.8 0.85 0.80 0.91 0.94 0.88 1.00
 Bedtime
  21:00–24:00 59,939 10,555 17.6
  24:00–03:00 19,982 5,025 25.2 1.43 1.39 1.47 1.08 1.05 1.12
  Other 1,845 381 20.7 1.17 1.07 1.29 1.09 1.00 1.19
 Depth of sleep
  Very light 5,746 1,206 21.0 1.11 1.06 1.18 1.11 1.05 1.17
  Light 34,306 6,813 19.9 1.06 1.03 1.09 1.08 1.05 1.12
  Normal 32,669 6,129 18.8 Reference Reference
  Deep 7,664 1,545 20.2 1.07 1.02 1.13 1.02 0.97 1.07
  Very deep 1,481 294 19.9 1.05 0.95 1.17 1.00 0.91 1.11
p for trend < 0.01b p for trend < 0.01b
Feeling when waking up in the morning
  Very bad 1,266 302 23.9 1.28 1.16 1.42 1.16 1.05 1.28
  Bad 16,887 3,853 22.8 1.23 1.19 1.27 1.16 1.12 1.19
  Normal 50,737 9,417 18.6 Reference Reference
  Good 11,251 2,093 18.6 1.00 0.96 1.05 0.98 0.94 1.02
  Very good 1,445 255 17.7 0.95 0.85 1.06 0.93 0.83 1.04
p for trend < 0.01b p for trend < 0.01b

CI, confidence interval; RR, relative risk.

aAdjusted for maternal age at delivery, smoking habits, alcohol consumption, pre-pregnancy body mass index, gestational age at birth, parity, infertility treatment, infant sex, small for gestational age, type of delivery, and postpartum depressive symptoms.

bLinear trend in the association was tested by assignment of ordinal variables for the five categories.

In the subanalysis of participants who slept 7–9 h before pregnancy, maternal short sleep during pregnancy was associated with bad mood in infants. Similarly, in the group of participants who slept 7–9 h during pregnancy, maternal late bed time before pregnancy was associated with bad mood in infants (Table S2).

Discussion

This study investigated whether maternal sleep before and during pregnancy was associated with preterm birth, infants sleep and temperament at 1 month of age, using data from a nationwide large-scale cohort study.

In this study, preterm birth was only associated with the quality of maternal sleep during pregnancy. Previous studies reported an association between preterm birth and subjective maternal sleep quality9,20. Subjective sleep depth and mood on awakening may reflect maternal SDB or depression21,22, both of which are known to increase preterm birth rates6,20. Interventions to improve sleep depth and mood on awakening could reduce preterm birth rates.

Contrary to a previous meta-analysis in 20185, we found no association of sleep duration with preterm birth. One conceivable reason for this difference is the lower rate of preterm birth in Japan compared to other countries23,24.

This study also revealed an association of maternal sleep before and during pregnancy with infant sleep and temperament at 1 month of age. To our knowledge, no studies have previously reported similar findings. However, infant sleep disorders and temperament have been reported to increase maternal stress25 and relate to maternal anxiety disorder and depression26. As a result, it may lead to parenting abandonment and child abuse27. If maternal sleep before and during pregnancy could be addressed to improve infant sleep and temperament, maternal postpartum mental disease and child abuse could also be reduced.

Maternal sleep before pregnancy also seemed to be associated with some features of infant temperament and frequent night awakenings in the group of participants with adequate sleep duration (7–9 h) during pregnancy. The Centers for Disease Control and Prevention and the World Health Organization recently issued statements on the importance of preconception care28, without emphasising maternal sleep. We should probably pay more attention to maternal sleep not only during pregnancy but also before pregnancy.

This study had four major limitations. First, maternal obesity and depression may be confounding factors: both are associated with sleeping problems and can cause maternal inflammation29,30. Some epidemiological studies have also reported that maternal obesity and depression are associated with preterm birth and developmental disorders20,31. In this study, we showed an association between maternal sleep and preterm birth, infant sleeping problems, and temperament after adjustment for pre-pregnancy BMI and postpartum depressive symptoms. Maternal sleep may affect these outcomes. However, adjustment for maternal depression could be insufficient because depressive symptoms were investigated postpartum.

Second, information about maternal and infant sleeping problems and infant temperament were collected using a questionnaire.

Third, because of the observational study design, we were not able to demonstrate how maternal sleep affected outcomes. Evidence suggests that inflammatory response plays a role, due to maternal sleep disruption during pregnancy causing preterm birth and aberrant development of offspring; short maternal sleep duration and SDB increases inflammatory cytokine levels9,10. It is believed that maternal inflammation can cause preterm birth11,12 and developmental disorders, such as ASD13,14. However, this study did not analyse inflammatory markers.

Fourth, the large sample size might show a statistically significant difference even when the difference is small. Since there have been no similar reports to this work, further investigations of relationships between maternal sleep and offspring’s outcome are necessary.

In conclusion, maternal sleep problems before and during pregnancy were associated with preterm birth and infant sleep problems and temperament.

Methods

Research ethics

The study protocol was approved by the Ministry of Environment’s Institutional Review Board on Epidemiological Studies and by the Ethics Committee of all participating institutions: the National Institute for Environmental Studies that leads the JECS, the National Center for Child Health and Development, Hokkaido University, Sapporo Medical University, Asahikawa Medical College, Japanese Red Cross Hokkaido College of Nursing, Tohoku University, Fukushima Medical University, Chiba University, Yokohama City University, University of Yamanashi, Shinshu University, University of Toyama, Nagoya City University, Kyoto University, Doshisha University, Osaka University, Osaka Medical Center and Research Institute for Maternal and Child Health, Hyogo College of Medicine, Tottori University, Kochi University, University of Occupational and Environmental Health, Kyushu University, Kumamoto University, University of Miyazaki, and University of Ryukyu.. Written informed consent, which also included the follow-up study of children after birth, was obtained from all participants. All methods were performed in accordance with approved guidelines.

Study participants

Data used in this study were obtained from the Japan Environment and Children’s Study (JECS), an ongoing large-scale cohort study. The JECS elucidated environmental factors that affected children’s health and development and was designed to follow-up pregnant women until their newborns grow up to 13 years old. The participants were recruited between 2011 and 2014 in 15 regions throughout Japan, and the follow-up is carried out mainly by a self-administered questionnaire. The detailed protocol has been reported elsewhere32. The baseline profile of participants in the JECS was reported previously33. Participants answered a questionnaire about lifestyle and behaviour twice during pregnancy: at recruitment (early pregnancy, M-T1) and later during mid- and late-pregnancy (M-T2). Participants also answered a questionnaire about their newborns at 1 month after delivery (M-1m).

Of all 103,099 pregnancies, we excluded 14,845 pregnancies due to the following reasons: no delivery records (n = 2,321), prior participation in the study (n = 5,608), multiple pregnancy (n = 947), miscarriage or stillbirth (n = 1,427), congenital anomaly identified by 1 month old (n = 3,554), missing information on maternal age at delivery (n = 5), and no response to the questions related to sleep at both M-T1 and M-T2 (n = 983). The remaining 88,254 participants (87,106 with M-T1 data and 86,358 with M-T2 data) were included in the analysis of the association between maternal sleep and preterm birth. Then, we further excluded preterm or post-term deliveries (n = 4,113) and participants who did not respond to the questions related to the children’s sleep and temperament at M-1m (n = 1,307). (Fig. 1) Finally, 81,821 participants with M-T1 data and 82,038 participants with M-T2 data were included in the analysis of the association between maternal sleep and infant sleep and temperament.

Figure 1.

Figure 1

Flow chart representing the study population. M-T1: questionnaire administered at recruitment; M-T2: questionnaire administered during mid- and late-pregnancy; M-1m: questionnaire administered at 1 month after delivery.

Maternal sleep

In the M-T1 questionnaire, participants were asked about their sleep duration and bed time before pregnancy. We divided participants into six groups by sleep time: < 6 h, 6–7 h, 7–8 h, 8–9 h, 9–10 h, and > 10 h. Participants were also divided by bedtime: 9:00 p.m. to midnight, midnight to 3 a.m., and others.

In the M-T2 questionnaire, participants were asked about their sleep duration and bed time during pregnancy. The participants were divided into groups as described above for the M-T1. In addition, the M-T2 questionnaire included two more questions about sleep quality. One was, “How would you rate your average depth of sleep during the past month?” The other one was, “How would you rate your overall feeling when waking up in the morning during past month?” The answers to both questions were scored 1, 2, 3, 4, and 5, representing very light (bad), relatively light (bad), normal, relatively deep (good), and very deep (good), respectively.

Preterm birth

Information on gestational age at delivery was transferred from medical records. Preterm birth was defined as birth before 37 completed weeks of gestation. In the present study, 3,903 (4.4%) pregnant women had preterm births. We divided these women into two groups: the early preterm birth group (birth before 34 completed weeks of gestation) and the late preterm birth group (birth after 34 gestational weeks). There were 759 (0.9%) women in the early preterm birth group and 3,144 (3.6%) women in the late preterm birth group. In the analysis of association between maternal sleep during pregnancy and preterm birth, we selected only late preterm birth as an outcome because some participants in the early preterm birth group did not answer M-T2 questionnaire between 22 and 28 weeks gestational age. So, the available number of participants in the early preterm group was too small to analyse.

Outcome (infant sleep and temperament)

At 1 month after delivery, we assessed infant sleep and temperature using a parents-reported questionnaire (M-1m questionnaire). For infant sleep, participants were asked about sleep and wake times during a 24-h period for their newborns. In this analysis, we focused on two points. First, we analysed the number of nocturnal awakenings. We defined ≥ 5 awakenings as too many because a previous study reported that the average number of awakenings during the night (20:00 – 7:59) is 2.95 (range: 1.0–5.0) for 2-week-old infants34. Second, we analysed whether the infants slept longer during the day (08:00–19:59) or at night (20:00–7:59). We regarded longer sleeping times during the day than at night as unusual.

Also, the M-1m questionnaire included three questions about infant temperament. The first question was, “When you hold your baby, how often do you feel difficulty to hold your baby due to his/her fretting, crying, or throwing his/her head back?”; the answer options were “often,” “sometimes”, “seldom,” and “none.” Those who answered “often” were categorised as “bad mood.” The second question was, “How often and for how long does your baby cry?”; the answer options were “quite often and for long periods,” “sometimes and for short periods,” and “seldom and almost never.” Those who answered as “quite often and long” were categorised as “frequent crying, for long periods.” The third question was “Does your baby cry very hard sometimes no matter what you do to stop him/her?”; the answer options were “yes” and “no,” and those who answered “yes” were categorised as “intense crying”. These categories are the same as those in our previous study35.

Covariates

Information about maternal age at delivery, smoking habits, alcohol consumption, pre-pregnancy body mass index (BMI), parity, current history of diabetes, gestational diabetes, hypertensive disorder in pregnancy and intrauterine infection, history of preterm birth, gestational age at birth, infertility treatment, infant sex, type of delivery, small for gestational age and postpartum depressive symptoms were collected via self-administered questionnaires and/or medical records. Postpartum depressive symptoms were assessed using the Edinburgh Postnatal Depression Scale (EPDS), including in the questionnaire at 1 month after delivery36. According to previous studies37, participants with a score of 9 or more were categorized as having depressive symptoms.

Statistical analyses

We used the Poisson regression model with a robust error variance38 to explore the association of maternal sleep before and during pregnancy with each outcome and to estimate the relative risks (RRs) of each outcome and 95% confidence intervals (CIs). We initially adjusted for maternal age at delivery, and then further adjusted as follows. In the analysis of the association between maternal sleep and preterm birth, we adjusted for smoking habits (never-smokers, ex-smokers who quit before pregnancy, smokers during early pregnancy), alcohol consumption (never-drinkers, ex-drinkers who quit before pregnancy, drinkers during early pregnancy), pre-pregnancy BMI (< 18·5, 18·5–24·9, ≥ 25·0 kg m2), current history of diabetes or gestational diabetes (yes, no), hypertensive disorders in pregnancy (yes, no) and intrauterine infection (yes, no), parity (0, ≥ 1), history of preterm birth (yes, no) and infertility treatment (yes, no).

In the analysis of the association between maternal sleep and infant sleep or temperament, we adjusted for smoking habits, alcohol consumption, pre-pregnancy BMI, gestational age at birth (37, 38, 39, 40, and 41 weeks of gestation), infant sex (boys, girls), parity, infertility treatment, type of delivery (vaginal, caesarean section), small for gestational age infants (yes, no), and postpartum depressive symptoms (yes, no).

We performed a subanalysis of infant sleep or temperament in the participant groups that reported adequate sleep durations of 7–9 h both at M-T1 and M-T2 to evaluate how maternal sleep before and during pregnancy impacts the outcome of these parameters.

The dataset used for statistical analyses was the jecs-ag-20160424 dataset, which was released in June 2016, and revised in October 2016, along with the supplementary dataset jecs-ag-20160424-sp1. Stata version 14 (StataCorp LP, College Station, Texas, USA) was used for all analyses.

Supplementary information

Acknowledgements

We would like to express our gratitude to all the participants in this study and all the individuals involved in data collection. The Japan Environment and Children's Study was funded by the Ministry of the Environment, Japan. The findings and conclusions of this article are solely the responsibility of the authors and do not represent the official views of the Ministry of the Environment.

Author contributions

Study concept and design: S.M. Statistical analyses: T.M. Drafting of the manuscript and approval of the final content: K.N., S.M. and T.M. Critical revision of the manuscript for important intellectual content: all authors. Manuscript review: all authors.

Competing interests

The authors declare no competing interests.

Footnotes

The Study Group members are listed at the end of this article.

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

These authors contributed equally: Kazushige Nakahara and Takehiro Michikawa.

Contributor Information

Seiichi Morokuma, Email: morokuma@med.kyushu-u.ac.jp.

The Japan Environment and Children’s Study Group:

Michihiro Kamijima, Shin Yamazaki, Yukihiro Ohya, Reiko Kishi, Nobuo Yaegashi, Koichi Hashimoto, Chisato Mori, Shuichi Ito, Zentaro Yamagata, Hidekuni Inadera, Takeo Nakayama, Hiroyasu Iso, Masayuki Shima, Youichi Kurozawa, Narufumi Suganuma, and Takahiko Katoh

Supplementary information

is available for this paper at 10.1038/s41598-020-67852-3.

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