Literature DB >> 30226007

Night Shift Work Before and During Pregnancy and Offspring Weight Outcomes Through Adolescence.

Susanne Strohmaier1,2, Elizabeth E Devore1, Celine Vetter1,3, Stacey Missmer4,5, A Heather Eliassen1,5, Bernard Rosner1, Janet Rich-Edwards1,5, Alison E Field6, Eva S Schernhammer1,2,5.   

Abstract

OBJECTIVE: This study aimed to investigate associations between maternal history of rotating night shift nursing work before pregnancy and number of night shifts worked during pregnancy with offspring weight outcomes from early life through adolescence.
METHODS: More than 4,000 children, enrolled in the second phase of the Growing Up Today Study between 2004 and 2013, and their mothers participating in the Nurses' Health Study II were included in our analyses.
RESULTS: Children of women with and without a history of rotating night shift work before pregnancy were similar in birth weight and body size at age 5. However, for mothers with night shift work before pregnancy, their children had a modestly elevated risk of having overweight or obesity (relative risk = 1.11; 95% CI: 1.02-1.21), which was stronger for persistently having overweight or obesity during adolescence and early adulthood. Longer duration of rotating night shift work was not associated with any of these weight outcomes. Weight outcomes of children of women with versus without night shift work during pregnancy were similar, regardless of frequency of night shifts worked during pregnancy (all P > 0.09).
CONCLUSIONS: Overall, nurses' night shift work before or during pregnancy did not affect offspring weight outcomes. Future larger studies should explore these associations in more detail.
© 2018 The Obesity Society.

Entities:  

Mesh:

Year:  2018        PMID: 30226007      PMCID: PMC6146398          DOI: 10.1002/oby.22267

Source DB:  PubMed          Journal:  Obesity (Silver Spring)        ISSN: 1930-7381            Impact factor:   5.002


Introduction

Childhood and adolescent overweight and obesity have become a major public health concern in the United States and globally (1). Apart from childhood obesity's more immediate comorbidities, such as hyperinsulinemia, poor glucose tolerance, and increased risk for type 2 diabetes and hypertension, it can also lead to an increased risk of heart disease and certain cancers later in life (2). Although environmental and behavioral factors, such as parental socioeconomic status and children's sedentary behavior, have been established as major determinants of childhood obesity (3), growing evidence has suggested that several childhood and even adulthood health outcomes are, at least in part, programmed during pregnancy (4). Specifically, the maternal environment during pregnancy could influence fetal development and programming through alterations in the intrauterine environment (5). Night shift work and the resulting disruption of social and biological rhythms have been linked to higher risk of several chronic diseases (6, 7, 8) as well as epigenetic alterations (9); in addition, night shift work during pregnancy has been linked to an increased risk of spontaneous abortions (10) and preterm delivery (11). Emerging evidence from animal models has suggested that maternal circadian disruption can also induce long‐term metabolic changes in the offspring (12, 13, 14). For example, exposing pregnant rats to reversals of the photoperiod twice every week throughout gestation and for the first week after birth showed no effect on litter size or birth weight; however, the progeny had an increased risk of adiposity, hyperleptinemia, and altered glucose metabolism in adulthood (13). Despite the high prevalence of shift work among US women during pregnancy (15), little is known about the potential health implications of preconception shift work and night shift work during pregnancy on offspring later in life. We therefore aimed to provide insights regarding the association of preconception night shift work history and shift work during pregnancy with offspring weight outcomes during childhood and adolescence using existing data from mother‐child pairs participating in the Nurses' Health Study II (NHS II) and the second phase of the Growing Up Today Study (GUTS2).

Methods

Study population

The present study included mothers who were enrolled in NHS II and their children who participated in GUTS2. NHS II is an ongoing prospective cohort study of US female nurses, which was established in 1989 when 116,430 female nurses aged 25 to 42 years responded to mailed questionnaires regarding their lifestyle, reproductive factors, and medical history. Follow‐up questionnaires are mailed biennially to these nurses to update information on various risk factors and occurrence of major diseases. GUTS2 began in 2004 when NHS II participants who had previously reported to have children born between 1987 and 1995 were asked whether their children could participate in a follow‐up study. After receiving maternal consent, invitation letters and questionnaires were sent to 17,280 children; 10,918 children returned their completed questionnaire. Follow‐up questionnaires were sent to these children in 2006, 2008, 2011, and 2013 to update information on health, lifestyle factors, and growth indicators. This study was approved by the Human Subjects Committees at the Brigham and Women's Hospital and the Harvard T.H. Chan School of Public Health (Boston, Massachusetts). Returning the self‐administered questionnaires was taken to imply informed consent in both cohorts.

Ascertainment of night shift work among mothers

Mother's history of rotating night shift before pregnancy

The NHS II baseline questionnaire queried number of years having worked rotating night shifts (defined as “at least three nights per month in addition to working days or evenings in the respective month”). This information was updated in 1991 and 1993 to capture changes since the previous questionnaire and then again in 2001 to capture changes between 1993 and 1995 (the latest possible year of conception). Based on the return date of the respective NHS II questionnaire and birth date of the GUTS2 participant, we calculated the cumulative number of years a mother had worked rotating night shifts before conception for children born in 1989 or later.

Mother's night shift work exposure during pregnancy

On the 2001 NHS II questionnaire, participants were asked whether they had experienced at least one pregnancy since 1993, had worked as a nurse during the most recent pregnancy, and would be willing to answer a supplemental questionnaire focused on occupational activities and exposures during this pregnancy. A supplement´l questionnaire that queried shift work information among other occupational exposures during the most recent pregnancy since 1993 was mailed to those participants who answered “yes” to all three questions. Women were asked to report usual working schedules and average number of night shifts per month for each trimester of pregnancy, with the following response options: none, one to two nights per month, three to four nights per month, two to three nights per week, and four or more nights per week.

Ascertainment of weight outcomes among offspring

Information on offspring birth weight was obtained from the 2009 GUTS2 mothers' questionnaire. Recall of offspring birth weight has been found to have excellent validity (16). On the baseline questionnaire in 2004, GUTS2 participants (age range 9‐15 years) were asked to recall their body size at age 5 by selecting one of eight pictograms (“somatotypes”) that would most accurately represent their body shape at that age (ranging from 1, most lean, to 8, most severe obesity). Correlations between recalled somatotypes and BMI measured at approximately the same ages have ranged from 0.53 to 0.75 among studies of adults (17). We created a binary outcome splitting at the median value of the distribution and defined larger than median body sizes as cases. Information on weight and height was self‐reported on each GUTS2 questionnaire. To classify the offspring as having normal weight, overweight, or obesity, we used age‐and sex‐specific cutoffs from the International Obesity Task Force (18) for participants aged 18 years or younger. Beyond age 18, overweight and obesity were defined using standard World Health Organization cutoffs (i.e., BMI [kilograms per meter squared] 25.0‐29.9 as overweight; BMI > 30 as obesity). We defined participants as cases if they were classified as having either overweight or obesity at any given time during follow‐up. Additionally, we defined participants as persistently having overweight or obesity if they were classified as having overweight or obesity at three consecutive questionnaire cycles. Figure 1 displays a timeline of exposure and outcomes assessments.
Figure 1

Timeline of exposure and outcome assessments in NHSII and GUTS2 cohorts.

Timeline of exposure and outcome assessments in NHSII and GUTS2 cohorts.

Ascertainment of covariates

Maternal age at delivery was derived calculating the difference between a mother's birth date and that of her child. We utilized maternal dietary information assessed by the well‐validated Willett food frequency questionnaire (19), using information from the 1991 NHS II questionnaire to calculate the Alternative Healthy Eating Index (AHEI) (20). Physical activity was assessed in 1989 and derived as metabolic equivalent hours per week (21). Smoking status and BMI were queried biannually, and we selected the most recent value prior to conception of the first included child. Maternal chronotype was assessed in 2009. As a proxy for socioeconomic status, we used husband's education, which was assessed in 1999. Information on the number of previous pregnancies, mode of delivery, pregnancy‐related hypertension, preeclampsia, gestational age at delivery, and pregnancy multiplicity was extracted from the lifetime pregnancy assessment in 2009. We approximated pregnancy‐related weight gain by taking the difference of the first BMI reported after delivery and the last recorded BMI before conception. From the occupational supplemental questionnaire, we had trimester‐specific information on smoking behavior, alcohol consumption, coffee consumption, and frequency of activities involving lifting or moving a physical load of 25 lb or more during pregnancy. Offspring Tanner stage of pubertal development was determined in 2004 on the GUTS2 baseline questionnaire, using a validated scale of pubic hair illustrations (22). Tanner stage ranges from 1 to 5, with stage 1 indicating prepubescence and stage 5 indicating maturity. Offspring sedentary behavior was summarized by the sum of the hours per week spent watching television, using the computer, surfing on the Internet, and reading or doing homework over the past year, as reported in 2004. Detailed cutoffs used in all analyses are presented in the footnotes of Tables 1 and 2.
Table 1

Adjusted mean differences and relative risks for offspring weight outcomes through childhood and adolescence according to maternal rotating night shift work history before pregnancy using data from GUTS2 from 2004 to 2013, restricted to singleton full‐term births

History of rotating night shift work
Never worked rotating night shifts <3 years 3‐5 years ≥6 years P trend Ever worked rotating night shifts
MD in offspring birth weight (g)
Participants1,4581,3059644162,685
MD 95% CI MD 95% CI MD 95% CI MD 95% CI
Basic modela 0 (reference)10.68−26.33 to 47.690.98−39.06 to 41.03−7.80−65.11 to 49.510.794.41−27.48 to 36.30
MV model 1b 0 (reference)12.16−24.54 to 48.874.73−34.55 to 44.02−1.43−59.29 to 56.430.997.51−23.89 to 38.92
MV model 2c 0 (reference)10.33−26.26 to 49.912.39−36.85 to 41.64−6.28−63.84 to 51.270.855.06−26.32 to 36.44
RR of offspring's somatotype at age 5 being larger than the median
Cases/participants628/1,631584/1,451437/1,103186/4741,207/3,028
RR 95% CI RR 95% CI RR 95% CI RR 95% CI
Basic modela 1 (reference)1.040.95 to 1.141.020.93 to 1.131.010.89 to 1.150.821.030.95 to 1.11
MV model 1b 1 (reference)1.030.94 to 1.121.020.92 to 1.121.010.88 to 1.150.871.020.95 to 1.10
MV model 2c 1 (reference)1.020.94 to 1.121.010.92 to 1.121.000.88 to 1.140.971.020.94 to 1.10
RR of offspring having overweight or obesity at any time between 2004 and 2013 d
Cases/participants523/1,667523/1,494394/1,125168/4871,085/3,106
RR 95% CI RR 95% CI RR 95% CI RR 95% CI
Basic modela 1 (reference)1.101.00 to 1.221.111.00 to 1.241.080.94 to 1.250.111.101.01 to 1.20
MV model 1b 1 (reference)1.111.01 to 1.231.121.01 to 1.251.070.92 to 1.230.141.111.02 to 1.21
MV model 2c 1 (reference)1.111.00 to 1.221.100.99 to 1.231.030.89 to 1.180.311.091.00 to 1.19
RR of offspring persistently having overweight or obesity e
Cases/participants114/1,667124/1,494103/1,12537/487264/3,106
RR 95% CI RR 95% CI RR 95% CI RR 95% CI
Basic modela 1 (reference)1.190.92 to 1.541.351.04 to 1.761.070.74 to 1.550.131.230.99 to 1.53
MV model 1b 1 (reference)1.220.95 to 1.581.391.06 to 1.801.040.71 to 1.520.171.251.00 to 1.56
MV model 2c 1 (reference)1.210.94 to 1.551.331.02 to 1.730.960.67 to 1.400.311.210.97 to 1.51
MD in offspring BMI (kg/m2) using n=15,008 repeated measurements, 2004‐2013
Observations5,3094,6743,5281,4879,689
MD 95% CI MD 95% CI MD 95% CI MD 95% CI
Basic modela,f 0 (reference)0.04−0.20 to 0.290.22−0.04 to 0.490.530.17 to 0.89<0.010.18−0.03 to 0.39
MV model 1b 0 (reference)0.07−0.18 to 0.310.26−0.01 to 0.520.490.13 to 0.85<0.010.20−0.01 to 0.41
MV model 2c 0 (reference)0.03−0.21 to 0.260.20−0.06 to 0.450.33−0.02 to 0.670.030.13−0.01 to 0.41

Abbreviations: CI, confidence interval; MD, mean difference; MV, multivariable model; RR, relative risk.

Adjusted for offspring gender (boy/girl) and gestational age ≥ 42 weeks (yes/no).

Additionally adjusted for maternal age at pregnancy, smoking status before pregnancy (never, current, past), alternative healthy eating score (quintiles), physical activity (MET‐hours/week; quintiles), husband's education (less than 2 years of college, 4 years of college, graduate school), parity (nulliparity, 1, 2, or 3+ previous pregnancies).

Additionally adjusted for BMI before pregnancy (<25, 25‐29, ≥30 kg/m2).

Overweight and obesity status defined according to age‐ and sex‐specific cutoffs from International Obesity Task Force.

Persistently having overweight or obesity was defined as falling into that category in three consecutive follow‐up cycles.

All models are additionally adjusted for age at BMI measurement.

Table 2

Adjusted mean differences and relative risks for offspring weight outcomes through childhood and adolescence by categories of average number of night shifts worked per month during pregnancy using data from GUTS2 from 2004 to 2013 restricted to singleton, full‐term births (n = 545)

Average number of night shifts/ month
None <3 nights/month 3‐9 nights/month ≥10 nights/month P trend Any number nights/month
MD in offspring birth weight (g)
Participants35239173591
MD 95% CI MD 95% CI MD 95% CI MD 95% CI
Basic modela 0 (reference)−54.19−209.96 to 101.58−203.53−432.97 to 25.92−46.27−210.25 to 117.700.23−79.04−187.53 to 29.45
MV model 1b 0 (reference)−54.48−215.12 to 106.17−231.85−463.36 to −0.3318.94−146.85 to 184.730.58−57.76−170.10 to 54.58
MV model 2c 0 (reference)−64.28−225.75 to 97.19−223.23−456.26 to 9.8019.51−146.50 to 185.510.60−59.64−172.11 to 52.82
RR of offspring's somatotype at age 5 being larger than the median
Cases/participants159/41716/438/2110/4534/109
RR 95% CI RR 95% CI RR 95% CI RR 95% CI
Basic modela 1 (reference)0.950.64 to 1.421.010.57 to 1.780.590.34 to 1.040.080.820.60 to 1.11
MV model 1b 1 (reference)0.960.62 to 1.471.030.60 to 1.780.590.33 to 1.040.090.820.60 to 1.12
MV model 2c 1 (reference)0.960.63 to 1.481.060.61 to 1.840.590.33 to 1.050.100.820.60 to 1.13
RR of offspring having overweight or obesity at any time between 2004 and 2013 d
Cases/participants156/43112/434/2113/4529/109
RR 95% CI RR 95% CI RR 95% CI RR 95% CI
Basic modela 1 (reference)0.750.46 to 1.210.540.22 to 1.330.820.51 to 1.310.190.740.53 to 1.03
MV model 1b 1 (reference)0.760.45 to 1.290.510.20 to 1.270.800.49 to 1.290.160.730.51 to 1.03
MV model 2c 1 (reference)0.800.48 to 1.350.530.21 to 1.370.780.48 to 1.250.140.740.52 to 1.05
MD in offspring BMI (kg/m2) using n=1,632 repeated measurements, 2004‐2013
Observations1,30612064142326
MD 95% CI MD 95% CI MD 95% CI MD 95% CI
Basic modela,e 0 (reference)0.24−0.85 to 1.32−0.27−1.78 to 1.23−0.02−1.07 to 1.030.880.03−0.69 to 0.75
MV model 1b 0 (reference)0.21−0.91 to 1.34−0.54−2.08 to 1.00−0.21−1.29 to 0.870.56−0.11−0.86 to 0.64
MV model 2c 0 (reference)0.45−0.64 to 1.54−0.26−1.75 to 1.24−0.31−1.35 to 0.730.53−0.01−0.74 to 0.72

Abbreviations: CI, confidence interval; MD, mean difference; MV, multivariable model; RR, relative risk.

Adjusted for offspring gender (boy/girl) and gestational age ≥ 42 weeks (yes/no).

Additionally adjusted for maternal age at pregnancy, smoking status before pregnancy (never, current, past), alternative healthy eating score (quintiles), physical activity (MET‐hours /week; quintiles), husband's education (less than 2 years of college, 4 years of college, graduate school), parity (nulliparity, 1, 2, or 3+ previous pregnancies), history of rotating night shift work (never, <3 years, 3‐5 years, ≥6 years).

Additionally adjusted for BMI before pregnancy (<25, 25‐29, ≥30 kg/m2).

Overweight and obesity status defined according to age‐ and sex‐specific cutoffs from International Obesity Task Force.

All models are additionally adjusted for age at BMI measurement.

Adjusted mean differences and relative risks for offspring weight outcomes through childhood and adolescence according to maternal rotating night shift work history before pregnancy using data from GUTS2 from 2004 to 2013, restricted to singleton full‐term births Abbreviations: CI, confidence interval; MD, mean difference; MV, multivariable model; RR, relative risk. Adjusted for offspring gender (boy/girl) and gestational age ≥ 42 weeks (yes/no). Additionally adjusted for maternal age at pregnancy, smoking status before pregnancy (never, current, past), alternative healthy eating score (quintiles), physical activity (MET‐hours/week; quintiles), husband's education (less than 2 years of college, 4 years of college, graduate school), parity (nulliparity, 1, 2, or 3+ previous pregnancies). Additionally adjusted for BMI before pregnancy (<25, 25‐29, ≥30 kg/m2). Overweight and obesity status defined according to age‐ and sex‐specific cutoffs from International Obesity Task Force. Persistently having overweight or obesity was defined as falling into that category in three consecutive follow‐up cycles. All models are additionally adjusted for age at BMI measurement. Adjusted mean differences and relative risks for offspring weight outcomes through childhood and adolescence by categories of average number of night shifts worked per month during pregnancy using data from GUTS2 from 2004 to 2013 restricted to singleton, full‐term births (n = 545) Abbreviations: CI, confidence interval; MD, mean difference; MV, multivariable model; RR, relative risk. Adjusted for offspring gender (boy/girl) and gestational age ≥ 42 weeks (yes/no). Additionally adjusted for maternal age at pregnancy, smoking status before pregnancy (never, current, past), alternative healthy eating score (quintiles), physical activity (MET‐hours /week; quintiles), husband's education (less than 2 years of college, 4 years of college, graduate school), parity (nulliparity, 1, 2, or 3+ previous pregnancies), history of rotating night shift work (never, <3 years, 3‐5 years, ≥6 years). Additionally adjusted for BMI before pregnancy (<25, 25‐29, ≥30 kg/m2). Overweight and obesity status defined according to age‐ and sex‐specific cutoffs from International Obesity Task Force. All models are additionally adjusted for age at BMI measurement.

Statistical analysis

Mother's history of rotating night shift exposure before conception

As preconception history of rotating night shift work could be assessed only after 1989, we excluded the 4,721 children conceived before 1989 from the original cohort of 10,918 children. Among the remainder born after 1989, we further excluded twins and triplets (195 children, 87 mothers), children who were not born full term (less than 37 weeks) (1,182 children, 1,001 mothers), and mother‐child pairs with missing exposure information (7 children, 6 mothers), leaving 4,813 children born to 4,044 mothers that made up our analytic sample. Out of these, 91% had a least two measurements of BMI at different time points. We used generalized estimating equation regression models specifying an exchangeable correlation structure with appropriate link functions (to account for within‐sibling correlation in outcomes) to estimate mean differences and 95% confidence intervals (CIs) in offspring birth weight, comparing none versus any number of years of rotating night shift work as well as across four data‐driven categories of cumulative years of rotating night shift work before conception (none, < 3 years, 3‐5 years, and ≥ 6 years). We calculated relative risks (RR) and 95% CIs of offspring overweight and/or obesity and larger than median somatotype at age 5. We considered women without a history of rotating night shift work as the reference group. If the log‐binomial model did not converge, we approximated RRs using Poisson models with robust variance estimators (23). To utilize all available repeated measurements of offspring BMI, we applied linear mixed effects models with random intercepts and an unstructured covariance structure, which permit description of individual BMI trajectories across age and provide explicit tests for changes in BMI with age (24). In these analyses, we included terms for the exposure, covariates, offspring age, and the interaction of BMI and offspring age to evaluate differences in change in BMI over time across exposure groups. In basic models, we adjusted for offspring sex, gestational age, and offspring age at baseline where appropriate (basic model). We then considered the inclusion of several sets of potential confounding variables. First, we added maternal lifestyle characteristics (multivariate [MV] model 1), including smoking status before pregnancy, AHEI score, physical activity, husband's education, and parity. The addition of pregnancy‐related factors, including preeclampsia gestational hypertension or diabetes, type of delivery, or change in maternal BMI before and after pregnancy, did not markedly change effect estimates for shift work; therefore, these variables were not retained in the model. Lastly, we additionally adjusted for maternal BMI before pregnancy (MV model 2). For analyses assessing associations between night shift work during pregnancy and weight outcomes in the offspring, we identified all GUTS2 participants whose mothers had completed the supplemental pregnancy questionnaire between 2001 and 2003, resulting in 621 mother‐child pairs with available information on pregnancy behaviors coupled with outcome information on the matching GUTS2 child. Of these, only full‐term pregnancies were considered eligible (n = 549). After further removal of mother‐child pairs with missing exposure information, 545 matching pairs were left for these analyses, of which 89% had at least two repeated BMI measurements. Using trimester‐specific information on shift work frequency from the supplemental questionnaire, we calculated the average number of night shifts per month throughout the entire pregnancy and created four categories (none, ≤ 2, 3‐9, and ≥ 10 night shifts per month); we also created the category of any number of night shifts per month. We used standard generalized linear models with appropriate link functions (linear or log‐binomial/Poisson) and added covariates following a similar approach as described above; we added history of night shift work to MV model 1. We also considered maternal pregnancy‐related lifestyle factors (smoking behavior, alcohol consumption, coffee consumption, heavy lifting during first trimester), but we did not retain these variables in our main models because they did not alter our estimates (data not shown). Because previous studies have found maternal BMI before pregnancy (25) to be one of the strongest predictors of offspring obesity during adolescence, in addition to adjustment for maternal BMI, we assessed effect modification for offspring weight outcomes by maternal BMI before pregnancy. Maternal chronotype has also been found to potentially interact with work schedules in determining a person's disease risk (26, 27, 28); therefore, we examined whether associations were different in children born to mothers with reportedly different chronotypes. In all analyses, missing indicators were created for missing covariate values. P values for interactions were obtained by testing the significance of multiplicative interaction terms in multivariable regression models. All statistical tests were two‐sided and were considered statistically significant at P < 0.05. All analyses were conducted using SAS version 9.4 (SAS Institute, Cary, North Carolina).

Results

Mother's history of rotating night shift work before pregnancy

The 4,044 mothers were on average 33.4 (SD = 3.6) years old when they gave birth to the children included in this analysis, and 65% of them reported ever having worked night shifts. At enrollment in GUTS2 in 2004, children were on average 11.7 (SD = 1.2) years old. Overall, there were only modest differences in terms of maternal and offspring characteristics according to history of night shift work before pregnancy (Table 3). Mothers who had worked night shifts for 6 years or more prior to conception of the first considered child were older, more likely to be past or current smokers, more adherent to a healthy diet (AHEI), and more physically active compared with women with no history of working night shifts. Also, offspring born to mothers with longer shift work history were more likely to be delivered by Cesarean section compared with those born to mothers without a history of shift work.
Table 3

Maternal and offspring characteristics by rotating night shift work history before pregnancy for 4,044 mothers of a total of 4,813 children born between 1989 and 1995 enrolled in GUTS2

History of rotating night shift work
Characteristic Never worked rotating night shifts (n = 1,424) <3 y (n = 1,254) 3‐5 y (n = 946) ≥6 y (n = 420) Ever worked rotating night shifts (n = 2,620)
Mean (SD) % a Mean (SD) % Mean (SD) % Mean (SD) % Mean (SD) %
Maternal age at deliveryb 33.1 (3.5)33.2 (3.6)33.4 (3.5)35.0 (3.2)33.6 (3.5)
BMI before pregnancy22.7 (3.9)22.7 (3.8)23.0 (3.9)23.3 (4.2)22.9 (3.9)
AHEIc 42.6 (10.4)43.5 (9.9)43.7 (10.2)44.3 (10.2)43.7 (10.0)
Physical activity, METs/wkd 18.9 (21.4)23.2 (31.4)22.4 (28.7)22.6 (31.1)22.8 (30.4)
Smoking history before pregnancyb
Never75.374.073.163.271.9
Past18.219.620.226.320.9
Current6.56.46.710.57.2
Husband holds graduate degree31.936.537.131.135.9
Mom's chronotype
Definite morning type31.936.034.437.435.6
Intermediate type56.955.055.652.154.8
Definite evening type11.29.010.010.59.6
Parity before first included pregnancy
Nulliparity20.321.822.020.521.6
One previous pregnancy32.429.030.030.729.7
Two previous pregnancies24.025.826.025.225.8
Three previous pregnancies23.323.422.023.622.9
Number of pregnancies (n) 1,6831,5071,1324913,130
Gestational diabetes4.95.95.16.55.7
Preeclampsia2.32.43.32.72.8
Gestational hypertension4.13.75.05.34.4
Cesarean delivery21.621.623.727.123.2
Gestational age ≥ 42 weeks4.74.84.34.94.7
Maternal change in BMI from before to after current pregnancy1.0 (1.7)1.0 (1.6)1.1 (1.7)1.0 (1.8)1.1 (1.7)
Offspring sex
Male46.045.048.249.346.8
Female54.055.051.850.753.2
Offspring age at GUTS2 baseline, 200411.8 (1.2)11.6 (1.2)11.6 (1.2)11.6 (1.3)11.6 (1.2)
Offspring Tanner stagee 2.8 (1.3)2.6 (1.3)2.6 (1.3)2.7 (1.3)2.6 (1.3)
Offspring sedentary behavior, h/wke 4.0 (2.8)3.9 (2.7)3.9 (2.5)4.1 (2.4)3.9 (2.6)

METs, metabolic equivalent hours.

Percentages are of nonmissing values.

Recorded on the most recent questionnaire prior to conception of first included offspring.

Recorded in 1991.

One MET is proportional to the amount of energy spent sitting quietly for 1 hour.

At GUTS2 baseline (2004).

Maternal and offspring characteristics by rotating night shift work history before pregnancy for 4,044 mothers of a total of 4,813 children born between 1989 and 1995 enrolled in GUTS2 METs, metabolic equivalent hours. Percentages are of nonmissing values. Recorded on the most recent questionnaire prior to conception of first included offspring. Recorded in 1991. One MET is proportional to the amount of energy spent sitting quietly for 1 hour. At GUTS2 baseline (2004). Overall, when we evaluated the associations between night shift work history before pregnancy with different weight outcomes across childhood and adolescence, we observed few differences in offspring weight when comparing women with and without night shift work history (Table 4). Because differences between basic and multivariable models were small, we describe results of fully adjusted models only (i.e., MV model 1 including the most important confounding variables).
Table 4

Maternal and offspring characteristics by categories of average number of night shifts per month during pregnancy for 545 mothers and 545 children born between 1993 and 1995 enrolled in GUTS2 with whom they were pregnant during reported night work

Average number of night shifts per month during pregnancy
None ( n  = 435) <3 nights/month ( n  = 44) 3‐9 nights/month ( n  = 21) ≥10 nights/month ( n  = 45) Any number nights/month ( n  = 110)
Mean (SD) % a Mean (SD) % Mean (SD) % Mean (SD) % Mean (SD) %
Maternal age at deliveryb 34.9 (3.4)33.8 (2.5)34.4 (2.8)34.0 (3.1)34.0 (2.8)
BMI before pregnancy23.9 (4.5)23.1 (3.6)22.8 (3.4)24.1 (4.1)23.5 (3.8)
AHEIc 42.7 (9.9)44.4 (11.6)40.3 (8.9)38.4 (9.4)41.0 (10.5)
Physical activity, METs/wkd 23.2 (34.0)23.9 (27.2)13.3 (13.1)17.7 (19.6)19.3 (22.2)
Smoking before pregnancyb
Never76.072.776.271.172.7
Past18.725.014.322.221.8
Current5.32.39.56.75.5
Husband holding graduate degree29.422.733.324.425.5
Mom's chronotype
Definite morning type29.643.610.020.527.6
Intermediate type60.641.070.051.351.0
Definite evening type9.815.420.028.221.4
Parity
Nulliparity6.05.4015.48.5
One previous pregnancy28.329.733.328.229.8
Two previous pregnancies32.737.933.323.130.8
Three previous pregnancies33.027.033.333.330.9
History of rotating night shift work
None34.76.814.335.620.0
<3 y36.640.933.324.432.7
3‐5 y21.631.838.124.430.0
≥6 y7.120.514.315.617.3
Number of pregnancies (n) 435442145110
Gestational diabetes6.42.34.84.43.6
Preeclampsia0.90.00.02.20.9
Gestational hypertension3.02.30.06.73.6
Cesarean delivery22.318.214.320.018.2
Gestational age ≥42 weeks5.89.10.02.24.6
Maternal change in BMI from before to after current pregnancy0.8 (1.7)0.6 (1.9)0.8 (1.7)1.2 (2.0)0.9 (1.9)
Offspring gender
Male45.352.347.642.247.3
Female54.747.752.457.852.7
Offspring age at GUTS2 baseline, 200410.0 (0.6)9.9 (0.6)10.0 (0.6)10.0 (0.6)10.0 (0.6)
Offspring Tanner stagee 1.5 (0.7)1.6 (0.8)1.5 (0.8)1.5 (0.8)1.5 (0.8)
Offspring sedentary behavior (h/wk)e 3.5 (2.3)3.1 (1.5)3.9 (2.5)4.1 (2.4)3.7 (2.1)

Percentages are of nonmissing values.

Recorded on the most recent questionnaire prior to conception of first included offspring.

Recorded in 1991.

One MET is proportional to amount of energy spent sitting quietly for 1 hour.

At GUTS2 baseline (2004).

METs, metabolic equivalent hours.

Maternal and offspring characteristics by categories of average number of night shifts per month during pregnancy for 545 mothers and 545 children born between 1993 and 1995 enrolled in GUTS2 with whom they were pregnant during reported night work Percentages are of nonmissing values. Recorded on the most recent questionnaire prior to conception of first included offspring. Recorded in 1991. One MET is proportional to amount of energy spent sitting quietly for 1 hour. At GUTS2 baseline (2004). METs, metabolic equivalent hours. There were no associations of history of shift work with birth weight or somatotype at age 5 (Table 4). We did find a significantly higher risk of the offspring having overweight or obesity at any time during follow‐up between 2004 and 2013 for mothers with any history of night shift work before pregnancy (MV RRany 1.11; 95% CI: 1.02‐1.21) when compared with mothers who never worked any night shifts (Table 4). The association was slightly more pronounced for the risk of persistently having overweight or obesity (MV RRany 1.25; 95% CI: 1.00‐1.56). However, there was no evidence of a dose‐response association with increasing number of years of night shift work history (overweight/obesity MV RRextreme 1.07; 95% CI: 0.92‐1.23; P trend = 0.14; persistently overweight/obesity MV RRextreme 1.04; 95% CI: 0.71‐1.52; P trend = 0.17). Longer duration of night shift work was not associated with changes in BMI with age (P trend > 0.34) but was associated with greater differences in mean BMI (P trend < 0.01) at baseline age (Table 4). Because maternal diet was first assessed in 1991, we conducted a sensitivity analysis including only children who were born after 1991, and the results remained largely unchanged. In addition to adjustment for maternal BMI, we examined whether associations were different in children born to mothers with normal weight versus mothers with overweight or obesity. Formal tests for interactions revealed no significant effect modification (P interaction for all outcomes > 0.43). When examining whether associations were different in children born to mothers with reportedly different chronotypes (evening versus morning chronotypes), tests for interaction were not significant (all P interaction > 0.44).

Maternal night shift work exposure during pregnancy

Mothers included in the analyses exploring associations between night shift work during pregnancy and weight outcomes in their offspring were, on average, 34.7 (SD = 3.3) years old when they gave birth to the children considered in this analysis, while these children were, on average, 10.0 (SD = 0.6) years old at enrollment in GUTS2 (Table 1). Of the 545 women total, 110 women (20.2%) had worked night shifts during their pregnancy; they worked a mean of 6.0 (SD = 4.8) night shifts per month (range from 0.5 to 16 night shifts per month). Mothers reporting a higher number of night shifts were more likely to be either current or past smokers and more likely to describe themselves as definite evening chronotypes compared with women who did not work night shifts during pregnancy. They also exercised less and adhered to a less healthy diet than mothers with no night shift work during pregnancy. Because estimates comparing results from basic and multivariable‐adjusted models were similar, we report results from the fully adjusted models (MV model 1) only. We found no associations of night shift work during pregnancy with offspring birth weight, offspring somatotype at age 5, or RR of having overweight or obesity (Table 2); we were unable to examine the risk for persistently having overweight and/or obesity because of small numbers. We observed no differences in the change in BMI at baseline age or over time across exposure groups. When investigating potential effect modification by maternal BMI before pregnancy and mother's chronotype using collapsed exposure categories (no night shifts, 1‐5 nights per month and ≥6 nights per month), we did not find evidence for effect modification by maternal BMI (P interaction for all outcomes > 0.13) or mother's chronotype (all P interaction > 0.28).

Discussion

In this study conducted among NHS II participants and their children enrolled in GUTS2, we found little evidence to support the hypothesis that a history of night shift work before pregnancy or a higher frequency of night shift work during pregnancy increases the risk of adverse weight outcomes in offspring during childhood and adolescence. Although we observed a modest association between a history of night shift work before pregnancy and the offspring's risk of having overweight or obesity, there was no dose‐response association with longer duration of night shift work before pregnancy, and other weight outcomes were not related to the mother's shift work history before or during pregnancy. Animal studies have suggested that perturbations at critical windows of development can cause lifelong alterations in adiposity (29). Particularly, studies in rats have demonstrated that disruptions of the maternal photoperiod (i.e., exposing pregnant rats to chronic phase shifts, thereby mimicking shift work) negatively influence several metabolic parameters in the subsequent adult offspring, such as increased adiposity, hyperleptinemia, hyperinsulinemia, and reduced glucose tolerance and insulin sensitivity (12, 13, 30). A recent study modeling the impact of circadian disruption through mice with knockout clock genes did not find any of these associations. However, the authors suggested that previous findings might be explained by mediation through other pathways activated by circadian disruption that may not have been activated in the knockout gene experiment (14). Previous meta‐analyses have consistently suggested no association between shift work exposure during pregnancy and preterm birth (11, 31, 32) or low birth weight (31, 32), which is in line with our findings. We also did not observe any associations between shift work during pregnancy and birth weight even after adjusting for maternal history of prepregnancy night shift work. There are virtually no data regarding the potential long‐term impacts of night shift work on weight outcomes after birth on children born to night shift workers. In our study, we observed no association between night shift work before or during pregnancy and offspring childhood somatotype. While a recent study showed associations between nighttime feeding postpartum and risk for overweight in early childhood (33), our study is the first to examine the relationship between circadian disruption before and during pregnancy and offspring early life weight outcomes. We did find a modestly increased risk for overweight or obesity among offspring born to mothers who worked night shifts at any time before pregnancy, but the risk did not increase with longer duration of shift work. Night work during pregnancy did not further alter this association. To the best of our knowledge, there is no intergenerational study thus far relating preconception shift work exposure and shift work during pregnancy to offspring outcomes during childhood and adolescence. Strengths of the current study include the longitudinal follow‐up of mothers and children and detailed information on multiple potential confounders, including shift work information during pregnancy. However, our study also has several limitations. We had only limited information on paternal factors. Nevertheless, in all our multivariable models, we adjusted for husband's education, a proxy for socioeconomic status and important confounding variable possibly affecting both maternal shift work exposure and offspring weight outcomes. Most mothers gave birth to their respective child included in our study relatively late, i.e., in their early to mid‐30s. Therefore, our results might not be generalizable to women giving birth at a younger age. Furthermore, power was limited for some secondary analyses, including for mothers who continued to work night shifts throughout their pregnancies and in analyses differentiating having overweight or obesity. Other limitations include the retrospective assessment of body size at age 5 and the self‐reported nature of maternal and offspring weight measures. Previous validation studies within the Harvard cohorts (34, 35, 36, 37, 38) have shown reasonable accuracy of self‐reported maternal physical characteristics. Studies comparing measured versus self‐reported weight and height in US adolescents (39, 40, 41) have concluded that, on average, self‐reports are a useful proxy. Self‐reported history of rotating night shift work may have been misclassified, though likely randomly, biasing our results only toward the null. Furthermore, this exposure has previously been linked to several chronic disease outcomes (42).

Conclusion

Though women's night shift work before pregnancy was associated with a modestly increased risk of having overweight or obesity in their offspring through adolescence and young adulthood, there was no overall evidence that the duration of night shift work before pregnancy or night shift work during pregnancy was associated with offspring adiposity in this study. Further studies are needed with larger sample sizes and more detailed information on shift work exposure and outcomes into adulthood as well as more specific markers of metabolic alterations during adulthood.
  43 in total

1.  Reproducibility and validity of maternal recall of pregnancy-related events.

Authors:  C A Tomeo; J W Rich-Edwards; K B Michels; C S Berkey; D J Hunter; A L Frazier; W C Willett; S L Buka
Journal:  Epidemiology       Date:  1999-11       Impact factor: 4.822

2.  Easy SAS calculations for risk or prevalence ratios and differences.

Authors:  Donna Spiegelman; Ellen Hertzmark
Journal:  Am J Epidemiol       Date:  2005-06-29       Impact factor: 4.897

3.  The validity of self-reported weight change among adolescents and young adults.

Authors:  Alison E Field; Parul Aneja; Bernard Rosner
Journal:  Obesity (Silver Spring)       Date:  2007-09       Impact factor: 5.002

4.  Validation of a self-administered instrument to assess stage of adolescent development.

Authors:  N M Morris; J R Udry
Journal:  J Youth Adolesc       Date:  1980-06

5.  Childhood obesity: update on predisposing factors and prevention strategies.

Authors:  Miriam B Vos; Jean Welsh
Journal:  Curr Gastroenterol Rep       Date:  2010-08

Review 6.  Shift work and diabetes--a systematic review.

Authors:  Anders Knutsson; Anders Kempe
Journal:  Chronobiol Int       Date:  2014-10-07       Impact factor: 2.877

7.  Reproducibility and validity of a semiquantitative food frequency questionnaire.

Authors:  W C Willett; L Sampson; M J Stampfer; B Rosner; C Bain; J Witschi; C H Hennekens; F E Speizer
Journal:  Am J Epidemiol       Date:  1985-07       Impact factor: 4.897

8.  Remote recall of childhood height, weight, and body build by elderly subjects.

Authors:  A Must; W C Willett; W H Dietz
Journal:  Am J Epidemiol       Date:  1993-07-01       Impact factor: 4.897

Review 9.  Miscarriage and occupational activity: a systematic review and meta-analysis regarding shift work, working hours, lifting, standing, and physical workload.

Authors:  Jens Peter Bonde; Kristian Tore Jørgensen; Matteo Bonzini; Keith T Palmer
Journal:  Scand J Work Environ Health       Date:  2012-12-12       Impact factor: 5.024

10.  Night Shift Work Before and During Pregnancy and Offspring Weight Outcomes Through Adolescence.

Authors:  Susanne Strohmaier; Elizabeth E Devore; Celine Vetter; Stacey Missmer; A Heather Eliassen; Bernard Rosner; Janet Rich-Edwards; Alison E Field; Eva S Schernhammer
Journal:  Obesity (Silver Spring)       Date:  2018-09       Impact factor: 5.002

View more
  6 in total

1.  Simulated shift work disrupts maternal circadian rhythms and metabolism, and increases gestation length in sheep.

Authors:  Kathryn L Gatford; David J Kennaway; Hong Liu; David O Kleemann; Timothy R Kuchel; Tamara J Varcoe
Journal:  J Physiol       Date:  2019-02-10       Impact factor: 5.182

2.  Melatonin profiles during the third trimester of pregnancy and health status in the offspring among day and night workers: A case series.

Authors:  P A Nehme; F G Amaral; B Middleton; A Lowden; E Marqueze; I França-Junior; J L F Antunes; J Cipolla-Neto; D J Skene; C R C Moreno
Journal:  Neurobiol Sleep Circadian Rhythms       Date:  2019-04-13

3.  Maternal Chronodisruption Throughout Pregnancy Impairs Glucose Homeostasis and Adipose Tissue Physiology in the Male Rat Offspring.

Authors:  Diego Halabi; Hans G Richter; Natalia Mendez; Thilo Kähne; Carlos Spichiger; Esteban Salazar; Fabiola Torres; Karina Vergara; Maria Seron-Ferre; Claudia Torres-Farfan
Journal:  Front Endocrinol (Lausanne)       Date:  2021-08-16       Impact factor: 5.555

4.  Association between maternal shift work during pregnancy child overweight and metabolic outcomes in early childhood.

Authors:  Che-Wei Liao; Chih-Fu Wei; Mei-Huei Chen; Wu-Shiun Hsieh; Ching-Chun Lin; Pau-Chung Chen
Journal:  Front Public Health       Date:  2022-09-30

5.  Night Shift Work Before and During Pregnancy and Offspring Weight Outcomes Through Adolescence.

Authors:  Susanne Strohmaier; Elizabeth E Devore; Celine Vetter; Stacey Missmer; A Heather Eliassen; Bernard Rosner; Janet Rich-Edwards; Alison E Field; Eva S Schernhammer
Journal:  Obesity (Silver Spring)       Date:  2018-09       Impact factor: 5.002

6.  Night shift work surrounding pregnancy and offspring risk of atopic disease.

Authors:  Samantha Rada; Susanne Strohmaier; Aaron M Drucker; A Heather Eliassen; Eva S Schernhammer
Journal:  PLoS One       Date:  2020-04-16       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.