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The association between ambient temperature and preterm birth in Shenzhen, China: a distributed lag non-linear time series analysis
- Zhijiang Liang†1,
- Yan Lin†2,
- Yuanzhu Ma†1,
- Lei Zhang3,
- Xue Zhang4,
- Li Li5,
- Shaoqiang Zhang6,
- Yuli Cheng7,
- Xiaomei Zhou8,
- Hualiang Lin9,
- Huazhang Miao1 and
- Qingguo Zhao1Email author
© The Author(s). 2016
Received: 12 January 2016
Accepted: 24 July 2016
Published: 8 August 2016
A few studies have examined the association between ambient temperature and preterm birth (PTB), and the results have been inconsistent. This study explored the association between ambient temperature and PTB in Shenzhen, China.
Data of daily singleton PTB, air pollution and meteorological variables from 2005 to 2011 were collected in Shenzhen. A distributed lag non-linear model (DLNM) was used to investigate the association of the low and high temperatures (1st, 5th, 95th, and 99th percentiles) with PTB.
The median temperature was 24.5 °C and the 1st, 5th, 95th, and 99th percentiles of daily mean temperatures were 9, 12.5, 29.9 and 30.7 °C, respectively. The prevalence of singleton PTB was 5.61 % in Shenzhen. The association between temperature and PTB was not linear. There was an immediate positive association of low temperature (1st and 5th percentiles) and a negative association of high temperature (95th and 99th percentiles) with PTB. The effect of low temperature 9 °C (1st) on PTB on the current day was stronger than that of 12.5 °C (5th), with a relative risk (RR) of 1.54 (95 % CI: 1.36–1.75) and 1.49 (95 % CI: 1.35–1.63), respectively. The cumulative RR (up to 30 days) of 9 and 12.5 °C was 1.72 (95 % CI: 1.28–2.33) and 1.96 (95 % CI: 1.60–2.39), respectively. The cumulative effects (up to 30 days) of high temperature (95th and 99th percentiles) on PTB were 0.69 (95 % CI: 0.60–0.80) and 0.62 (95 % CI: 0.52–0.74), respectively. The cumulative effect (up to 30 days) of low temperatures on vaginal delivery PTB was lower than that of the cesarean section PTB with an RR of 1.58 (95 % CI: 1.12–2.22) and 1.93 (95 % CI: 1.21–3.08), respectively.
This study suggests that low temperature might be a risk factor, while high temperature might be a protective factor of PTB in Shenzhen.
Preterm birth (PTB), defined as any live birth before 37 completed weeks of gestation, is an important public health problem . It was estimated that there were 15 million PTB worldwide in 2010 . Globally, PTB is the leading cause of newborn deaths and the second largest direct cause of death only after pneumonia among children under five years, and over one million babies die annually from PTB-related complications .
The etiology of PTB remains unclear. Villar et al. proposed a PTB phenotype classification that incorporates five components-maternal conditions, fetal conditions, placental conditions, signs of parturition initiation, and the pathway to delivery . The present findings suggest that the causes of PTB are a complex mix of genetic, behavioral, socio-economic and environment factors. Race [5, 6], maternal chronic infections and hypertension , maternal smoking [8, 9], maternal age [10–13], and air pollution [14, 15] all were identified as potential risk factors.
With the emerging interest in climate change and its health impacts, some researchers focused their studies on the association between the extreme high temperature and PTB. Although having been studied in some countries, the findings remained inconclusive. For instance, studies in the US [16, 17], Israel , Greece , Spain [20, 21], Australia [22, 23], Italy , and Sweden  reported a significant association between high temperature and PTB, but another US study  and some studies in England  and Germany  did not find any significant association between high temperature and PTB. The discrepancies may be due to the significant heterogeneities in the study design, population characteristics, and the data analysis of these studies.
The mechanism by which high temperature triggered PTB is unclear. There are several possible mechanisms. First, insufficient fluids in the mother due to high temperature can decrease the blood flow available to the fetus and induce uterine contractions . Second, pregnant women may experience difficulty with thermoregulation and become dehydrated during the heat exposure, which may possibly result in a decrease in uterine blood flow and trigger labor . Third, maternal heat stress may also trigger a release of hormones such as cortisol, which may in turn induce labor . To our knowledge, few studies about the potential association between temperature and PTB have been carried out in China.
In the current study, we used a distributed lag non-linear time series analysis to explore the association between the ambient temperature and PTB in Shenzhen, China. The aim of this study is to increase the awareness of policy makers and clinicians regarding the role of temperature exposure on PTB in Shenzhen.
Daily data of preterm birth from January 1st, 2005 to December 31st, 2011 were collected from the birth registry database, which covered all midwifery clinics and hospitals in Shenzhen. Shenzhen maternal and children health information system has been constructed since 2000. One component of the system is birth certificate and all midwifery clinics and hospitals are using this system to report birth certificate through the network. The variables collected in birth registry database included date of birth, date of mother’s last menstrual period (LMP), birth weight, infant sex, maternal age, delivery mode, etc. Gestational age was computed as the number of weeks between the date of the last menstrual period (LMP) and the date of birth.
Daily meteorological data were obtained from the Shenzhen Meteorological Bureau websites. The variables included daily mean temperature (°C), relative humidity (RH, %), and atmospheric pressure (BP, hpa).
Daily 24-hour average air pollution data were collected from the Environmental Monitoring Center located in the center of Shenzhen. Air pollution data included particulate matter with an aerodynamic diameter less than or equal to 10 um (PM10, in ug/m3), sulfur dioxide (SO2, in ug/m3) and nitrogen dioxide (NO2, in ug/m3).
Twin pregnancy and multiple pregnancies were excluded from this study. There were a total of 1,040,638 singleton live births from January 1st, 2005 to December 31st, 2011 in Shenzhen. The births with eligible gestational age (20–44 weeks)  accounted for 99.85 % of the whole data. The births whose mother’s LMP date was missing or implausible (<20 or >44 weeks) accounted for 0.15 % and were excluded from the analysis. Eligible live births with gestational age fewer than 37 weeks were considered preterm.
This study was approved by the medical ethics committee of Guangdong Women and Children Hospital. Data used in this study were anonymous and no individual identifiable information was available for the analysis.
where Yt denotes the observed daily preterm count on day t, α is the intercept, cb means the “cross-basis” function, ns(·) indicates a natural cubic splines for non-linear variables, Zt represents the daily number of pregnancies at risk for preterm birth on day t (pregnancies between 20 and 36 weeks of gestation), β is the regression coefficient.
In addition, we conducted sensitivity analysis: use of alternative degrees of freedom (4, 6 df/year) for temporal adjustment and change the degrees of freedom (4–7 df) for meteorological variables to evaluate the robustness of results.
Although an important advantage of the time-series design is the inherently controlling for the non-time-varying risk factors, even unknown or unrecorded . In fact, the health effect of temperature is influenced by a variety of comprehensive factors including spatial distributions, exposure level, air pollution levels, and socio-demographic backgrounds. In the study of the association between the ambient temperature and PTB, the modification factors should be considered. The information on delivery mode, infant’s gender and maternal age are available in our database. By analyzing the potential modification effect of those variables on the association between temperature and PTB, it can help to identify the susceptible groups and estimate the degree of influence in different population and introduce more targeted public health interventions.
In order to completely capture the association of overall temperature on PTB and adjust for potential harvesting effect , we assumed a longer lag days, up to 30 days, between the exposure and preterm. We used the median of daily mean temperature of 24.5 °C as the reference temperature to report the relative risk (RR, with 95 % confidence intervals (CIs) of temperature (1st, 5th, 95th, and 99th percentiles of temperature) on PTB along specific lag days. This enabled us to obtain relative risk through the whole range of temperatures on different lag days. We also estimated the cumulative effects of low and high temperatures on preterm birth during lag periods (lag 0–30 days, where lag 0–30 represents the temperature on the day of preterm birth and the previous 30 days).
All statistical tests were two-sided and values of P < 0.05 were considered statistically significant. The DLNM package  in R software Version 3.0.2 (R Development Core Team, 2013) was utilized to fit all the models.
Summary statistics of singleton PTBs, daily weather conditions and air pollutants in Shenzhen
Atmospheric pressure (hpa)
Maternal age 15 ~ 19 group PTBs
Maternal age 20 ~ 34 group PTBs
Maternal age 35 ~ 49 group PTBs
Vaginal delivery PTBs
Cesarean section PTBs
PTBs rate from 2005 to 2011 in Shenzhen
Year of births
Maternal age 15 ~ 19 group
Maternal age 20 ~ 34 group
Maternal age 35 ~ 49 group
Other (including missing or implausible)
Sex of fetus
Maternal age categories relative risk (RR) and 95 % confidence intervals (CI) for total PTBs for temperature (1, 5, 95 and 99 % percentiles) at Different lag days with reference at 24.5 °C
RR(95 % CI)
Maternal age 15 ~ 19 group PTBs
Maternal age 20 ~ 34 group PTBs
Maternal age 35 ~ 49 group PTBs
Sex-specific and Delivery models relative risk (RR) and 95 % confidence intervals (CI) for total PTBs for temperature (1, 5, 95 and 99 % percentiles) at different lag days with reference at 24.5 °C
RR(95 % CI)
Vaginal delivery PTBs
Cesarean section PTBs
Table 3 described the relative risk of temperatures for preterm delivery at specific lag days (0, 5, 10, 15, 20, 25, and 30 days), and the temperatures (9.0, 12.5, 29.9, and 30.7 °C), which corresponded to the 1st, 5th, 95th, and 99th percentiles of the temperature distribution. It was found that for all of the singleton PTB, 9.0 °C and 12.5 °C were associated with an increased occurrence of PTBs, with 9 °C, RR = 1.54 (95 % CI: 1.36–1.75) exerted a stronger adverse effect than 12.5 °C, RR = 1.49 (95 % CI: 1.35–1.63) at lag 0. A positive association was also found with lag of 5, 25 to 30 days at 9 °C while the lag of 5, 15 to 25 days at 12.5 °C. The cumulative effect on PTB in 9 °C is lower than that in 12.5 °C, with RR = 1.72 (95 % CI: 1.28–2.33) and RR = 1.96 (95 %CI: 1.60–2.39), respectively. A negative association was found with lag of 10 to 30 days at 29.9 and 30.7 °C. The cumulative effects of high temperature (95th and 99th percentiles) on PTB are RR = 0.69 (95 % CI: 0.60–0.80) and RR = 0.62 (95 %CI: 0.52–0.74), respectively.
Table 3 also showed maternal age categories relative risk of the entire singleton preterm for temperatures (1st, 5th, 95th, and 99th percentiles) with reference at 24.5 °C at different days. The younger age (15 ~ 19 years) groups were only sensitive to low temperature (1st and 5th percentiles). In contrast, high temperature was negatively correlated with PTBs in the age (20 to 34 years) and (35 ~ 49 years) groups. The effects of 12.5 °C in the age groups of 15–19, 20–34, 35–49 years were RR = 1.62 (95 % CI: 1.06–2.49), RR = 1.54 (95 % CI: 1.39–1.71) and RR = 1.49 (95 % CI: 1.16–1.91) on the current day, respectively. The cumulative effects (30 days) of 12.5 °C in the age groups of 15 ~ 19, 20 ~ 34, 35 ~ 49 years were RR = 2.74 (95 % CI: 1.15–6.52), RR = 2.02 (95 % CI: 1.63–2.51) and RR = 2.27 (95 % CI: 1.36–3.79), respectively.
The protective effect of high temperature (95th and 99th percentiles) on the (20 ~ 34 years) groups was more endurable compared with the (35 ~ 49 years) groups. The cumulative effect at 30.7 °C was RR = 0.64 (95 % CI: 0.53–0.78) and RR = 0.57 (95 % CI: 0.36–0.92), respectively.
Table 4 presented relative risk of the singleton PTB for temperatures (1st, 5th, 95th, and 99th percentiles) by sex-specific and delivery mode categories at different days with reference at 24.5 °C. It showed that the association of the 1st percentile temperature (9.0 °C) in males was similar to that in females, RR = 1.58 (95 % CI: 1.35–1.84), RR = 1.49 (95 % CI: 1.25–1.77) on the current day, respectively.
A positive association on lag 0, lag 5, lag 25 and lag 30 at 9.0 °C was found in male preterm with the current day has the largest effect, RR = 1.58 (95 % CI: 1.35–1.84) while for female preterm, 9.0 °C was only correlated with PTBs increase on lag 0, with RR = 1.49 (95 % CI: 1.25–1.77). The positive association at 29.9 and 30.7 °C on female preterm was more endurable compared to the male preterm. For example, the RR for 29.9 °C was 0.97 (95 % CI: 0.95–1.00) on lag 30 in female preterm. Differences were found when stratifying the analysis by delivery mode, positive association of 1st and 5th percentiles of temperature on PTBs of cesarean section groups were more obvious than that of vaginal delivery groups. The effect on lag 0 with the RR = 1.78 (95 % CI: 1.46–2.17) in cesarean section preterm and RR = 1.36 (95 % CI: 1.18–1.57) in vaginal delivery preterm at 9.0 °C. The cumulative effects (up to 30 days) of 9 °C in cesarean section and vaginal delivery PTBs are RR = 1.93 (95 % CI: 1.21–308) and RR = 1.58 (95 % CI: 1.12–2.22), respectively A positive association on lag 5, 25 and lag 30 at 9.0 °C was also found in caesarian section preterm.
Along with the increasing temperatures associated with climate change, interests have been increasing to examine the association between high temperature and human health, including preterm birth, such as researches reported by Liajinian , Porter , Yackerson , Basu , Dadvand , Strand , and Vicedo-Cabrera . The previous studies  supported the association between the high temperature and the PTB. However, our study identified that in Shenzhen, high temperatures (95th and 99th percentiles) appears to be a protective factor on the PTB.
The protective effect of high temperature observed in this study was contrasting to a few previous studies. The potential biological mechanism remained largely unknown. Shenzhen is a subtropical and coastal city, even during the summer season, the high temperature is not as high as that in other cities. The average temperature was 23.14 °C, and the 95th percentile of daily mean temperature was 29.9 °C in Shenzhen during the study period. For example, in the studies in California, the average temperature was 31.5 °C and the 95th percentile temperature was 37.1 °C . Dadvand’s study in Spain had a temperature range of 27.9 ~ 38.8 °C, and the 95th percentile of temperature was 30.4 °C . Shenzhen is a developed city with highest social-economic status, most people living in this city have access to air conditioner, so the exposure to higher temperature in summer was minimal, especially for the pregnant women.
A few studies have examined the association between the low temperatures and the PTB in developed countries. For example, studies in London and Rome did not find significant association between low temperatures and PTB [24, 27], while the Sweden study found that cold temperature was associated with an increased risk of PTB , which is consistent with our study. In our study, the low temperatures (1st and 5th percentiles) were significantly associated with increased risk of the PTB, and the strongest association was observed for lag 0 at 9 °C (5th percentile), which means much greater magnitude of cold temperature effect at lag 0, compared to cold temperature effects at greater lags. Shenzhen is located in low latitudes. According to prior studies, although the populations in low latitude have fewer opportunities to exposure to low temperatures, they have a low adaptation to low ambient temperature . Compared with populations in high latitudes, they are more sensitive to the low temperatures [42, 43]. The humid and cold weather in Shenzhen has more harmful effects on physiology compared with the dry and cold weather in other high latitude areas (London is in 51.5° north latitude, and Rome is in 42° north latitude). Shenzhen is in southeast of China, the residents do not routinely use heat radiators in winter, so they are exposed to a colder temperatures indoors in winter .
Only two previous studies [17, 22] considered whether the temperature was related to the sex of a preterm infant, and these studies did not report a significant association. Our findings are consistent with the two studies. Our study showed the association between the low temperature and the male PTB is similar to that of the female PTB while the protective effect of the high temperature in avoiding female PTB is more endurable.
We found a significant association of the low temperature with the risk of PTB in younger age (15 ~ 19 years) groups, indicating they were more susceptible to PTB. For the younger mothers, they may be in poor nutrition, poor physical status or have limited self-protection awareness and insufficient health service which may trigger PTB [45, 46]. These early findings suggested that the health information about reducing exposure to cold temperatures should be emphasized in younger women. With this regard, more researches in other populations using different study design should be undertaken to determine the strength of the association and provide stronger evidence for this focused effort.
Recently, there was a report about the ambient temperature and the risk of preterm birth in Guangzhou, China. It showed that the cold temperature was associated with an increased risk of PTB . Our finding was in accordance with this study. However, the high temperature might be a protective factor of the PTB in Shenzhen while it is a risk factor in Guangzhou. This result might be explained by the fact that the high temperature in Shenzhen is lower than that of Guangzhou, the 99th percentile is 30.7 and 31.9 °C respectively. And urban heat island effect in Guangzhou is more severe than that of Shenzhen . Our study further classified singleton PTBs cohort according to different genders and maternal ages and analyzed the association of temperature on PTBs in those subgroups, which helps identify the susceptible groups and estimate the degree of influence in different subgroups. For the newborns in our study, the cesarean section presented 38.12 %, and cesarean section PTBs presented 43.32 % of all the PTBs. Our study also divided PTBs into the vaginal delivery and cesarean section cohort, which can be more comprehensive to grasp the influence of the temperature for all the PTBs. However, there is a limitation that the data were not available on whether preterm labour was spontaneous or induced.
This is a large-scale and population-based epidemiologic study of the association between the temperature and the PTB in China. Much of the prior evidence for the PTB from the environment exposures were based on air pollution [32, 33, 49, 50], and studies reported statistically significant association between the seasonal patterns and preterm birth [38, 51–54]. In this study, the variables of the air pollution and the seasonality of birth were controlled and hopefully negated any potential confounding by them. On the other hand, a few limitations should be considered when interpreting findings from our study. First, in data collection, we used environmental monitoring data to represent the individual exposure level to weather conditions, which might not accurately reflect the real individual exposure. This exposure misclassification may be more important for the high temperatures than the low temperatures, due to the widespread use of air conditioners, but the limited use of heating devices may explain the significant associations between the high temperatures and the PTB identified by other studies. Second, we had to rely on the data provided on the birth certificates, and we did not have the information on several characteristics such as the socio-demographic and maternal health condition, thus we could not account for these variables in our analyses.
In Shenzhen, the low temperatures appeared to be the risk factor for the PTB, and the high temperatures might be a protective factor of the PTB. Differences in results of the delivery mode reflect differences in population susceptibility.
AIC, Akaike’s information criterion; BP, barometric pressure; CI, confidence interval; df, the degrees of freedom; DLNM, distributed lag non-linear model; DOW, day of the week; DOY, day of the year; PH, public holiday; PM10, particulate matter with aerodynamic diameter ≤10 μm; PTB, preterm birth; RH, relative humidity; RR/RR(s), relative risk(s)
We want to thank Yan Lin, Lei Zhang, Xue Zhang, Li Li, Shaoqiang Zhang, Yuli Cheng and Xiaomei Zhou for providing research data. The interpretations contained here do not represent the views of these agencies. And Shannon Rutherford, Luwen Zhang and Hualiang Lin help us improving the style of writing English.
Ministry of Environmental Protection Fund (21111011101EHH(2011)-208) (PI: Qingguo Zhao) “The method of environmental and reproductive health survey” gave us basic support in the design of the study. Yan Lin, Lei Zhang, Xue Zhang, Li Li, Shaoqiang Zhang, Yuli Cheng and Xiaomei Zhou provided research data. Shannon Rutherford, Luwen Zhang and Hualiang Lin help us improving the style of writing English.
Availability of data and supporting material
Data were collected as mandatory work, and can be available throuth contact with the corresponding author.
QGZ and ZJL were involved in the development of the study’s protocol design, data collection, data quality monitoring, data analysis and preparation of the manuscript. ZJL and YZM were involved in analysis and editing draft manuscripts. ZJL were involved mainly in data analysis and its data quality management. All authors contributed to the revision of the final manuscript. All authors read and approved the final manuscript.
Personal Statement of Qingguo Zhao: My research fields include: (1) Pioneered in air pollution and women’s and children’s health epidemiological studies in China, with a focus on the impact of air pollution and meteorological factors on reproductive health and pregnancy outcomes using birth certificates data. These efforts have resulted in a number of well-cited peer-reviewed articles, in both English and Chinese. (2) Extensive experience in leading large-scale multicenter data collection and epidemiological studies, for example the molecular epidemiological study of Thalassemia throughout the 21 metropolitan cities in Guangdong, and the study of reproductive health status and needs of unmarried floating population.(3) Led the construction of the Guangdong province women and children hospitals communication network system, which facilitate efficient sharing of information and data resources within system, and cost-effective quality control. (4) Extensive research participation in pregnant women and children’ health.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was approved by the medical ethics committee of Guangdong Women and Children Hospital. Data used in this study were anonymous and no individual identifiable information was available for the analysis.
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- World Health Organization. WHO: recommended definitions, terminology and format for statistical tables related to the perinatal period and use of a new certificate for cause of perinatal deaths. Modifications recommended by FIGO as amended October 14, 1976. Acta Obstet Gynecol Scand. 1977;56(3):247-53.Google Scholar
- Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller AB, Narwal R, et al. National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications. Lancet. 2012;379(9832):2162–72. doi:10.1016/S0140-6736(12)60820-4.View ArticleGoogle Scholar
- Liu L, Oza S, Hogan D, Perin J, Rudan I, Lawn JE, et al. Global, regional, and national causes of child mortality in 2000-13, with projections to inform post-2015 priorities: an updated systematic analysis. Lancet. 2014. doi:10.1016/S0140-6736(14)61698-6.
- Villar J, Papageorghiou AT, Knight HE, Gravett MG, Iams J, Waller SA, et al. The preterm birth syndrome: a prototype phenotypic classification. Am J Obstet Gynecol. 2012;206(2):119–23. doi:10.1016/j.ajog.2011.10.866.View ArticleGoogle Scholar
- El-Sayed AM, Galea S. Explaining the low risk of preterm birth among arab americans in the United States: an analysis of 617451 births. Pediatrics. 2009;123(3):e438–45. doi:10.1542/peds.2008-1634.View ArticleGoogle Scholar
- Ananth CV, Misra DP, Demissie K, Smulian JC. Rates of preterm delivery among Black women and White women in the United States over two decades: an age-period-cohort analysis. Am J Epidemiol. 2001;154(7):657–65.View ArticleGoogle Scholar
- Mattison DR, Wilson S, Coussens C, Gilbert D. The role of environmental hazards in premature birth: workshop summary: National Academies Press; 2003.Google Scholar
- Rasmussen S, Irgens LM. The effects of smoking and hypertensive disorders on fetal growth. BMC Pregnancy Childbirth. 2006;6:16. doi:10.1186/1471-2393-6-16.View ArticleGoogle Scholar
- Andres RL, Day MC. Perinatal complications associated with maternal tobacco use. Semin Neonatol. 2000;5(3):231–41. doi:10.1053/siny.2000.0025.View ArticleGoogle Scholar
- Cleary-Goldman J, Malone FD, Vidaver J, Ball RH, Nyberg DA, Comstock CH, et al. Impact of maternal age on obstetric outcome. Obstet Gynecol. 2005;105(5 Pt 1):983–90. doi:10.1097/01.AOG.0000158118.75532.51.View ArticleGoogle Scholar
- Conde-Agudelo A, Belizan JM, Lammers C. Maternal-perinatal morbidity and mortality associated with adolescent pregnancy in Latin America: cross-sectional study. Am J Obstet Gynecol. 2005;192(2):342–9. doi:10.1016/j.ajog.2004.10.593.View ArticleGoogle Scholar
- Lisonkova S, Janssen PA, Sheps SB, Lee SK, Dahlgren L. The effect of maternal age on adverse birth outcomes: does parity matter? J Obstet Gynaecol Can. 2010;32(6):541–8.View ArticleGoogle Scholar
- Machado CJ. Impact of maternal age on birth outcomes: a population-based study of primiparous Brazilian women in the city of Sao Paulo. J Biosoc Sci. 2006;38(4):523–35. doi:10.1017/S0021932005026660.View ArticleGoogle Scholar
- Shah PS, Balkhair T. Air pollution and birth outcomes: a systematic review. Environ Int. 2011;37(2):498–516. doi:10.1016/j.envint.2010.10.009.View ArticleGoogle Scholar
- Stieb DM, Chen L, Eshoul M, Judek S. Ambient air pollution, birth weight and preterm birth: a systematic review and meta-analysis. Environ Res. 2012;117:100–11. doi:10.1016/j.envres.2012.05.007.View ArticleGoogle Scholar
- Lajinian S, Hudson S, Applewhite L, Feldman J, Minkoff HL. An association between the heat-humidity index and preterm labor and delivery: a preliminary analysis. Am J Public Health. 1997;87(7):1205–7.View ArticleGoogle Scholar
- Basu R, Malig B, Ostro B. High ambient temperature and the risk of preterm delivery. Am J Epidemiol. 2010;172(10):1108–17. doi:10.1093/aje/kwq170.View ArticleGoogle Scholar
- Yackerson N, Piura B, Sheiner E. The influence of meteorological factors on the emergence of preterm delivery and preterm premature rupture of membrane. J Perinatol. 2008;28(10):707–11. doi:10.1038/jp.2008.69.View ArticleGoogle Scholar
- Flouris AD, Spiropoulos Y, Sakellariou GJ, Koutedakis Y. Effect of seasonal programming on fetal development and longevity: links with environmental temperature. Am J Hum Biol. 2009;21(2):214–6. doi:10.1002/ajhb.20818.View ArticleGoogle Scholar
- Dadvand P, Basagana X, Sartini C, Figueras F, Vrijheid M, de Nazelle A, et al. Climate extremes and the length of gestation. Environ Health Perspect. 2011;119(10):1449–53. doi:10.1289/ehp.1003241.View ArticleGoogle Scholar
- Vicedo-Cabrera AM, Iniguez C, Barona C, Ballester F. Exposure to elevated temperatures and risk of preterm birth in Valencia, Spain. Environ Res. 2014;134:210–7. doi:10.1016/j.envres.2014.07.021.View ArticleGoogle Scholar
- Strand LB, Barnett AG, Tong S. Maternal exposure to ambient temperature and the risks of preterm birth and stillbirth in Brisbane, Australia. Am J Epidemiol. 2012;175(2):99–107. doi:10.1093/aje/kwr404.View ArticleGoogle Scholar
- Wang J, Williams G, Guo Y, Pan X, Tong S. Maternal exposure to heatwave and preterm birth in Brisbane, Australia. BJOG. 2013;120(13):1631–41. doi:10.1111/1471-0528.12397.View ArticleGoogle Scholar
- Schifano P, Lallo A, Asta F, De Sario M, Davoli M, Michelozzi P. Effect of ambient temperature and air pollutants on the risk of preterm birth, Rome 2001-2010. Environ Int. 2013;61:77–87. doi:10.1016/j.envint.2013.09.005.View ArticleGoogle Scholar
- Bruckner TA, Modin B, Vagero D. Cold ambient temperature in utero and birth outcomes in Uppsala, Sweden, 1915-1929. Ann Epidemiol. 2014;24(2):116–21. doi:10.1016/j.annepidem.2013.11.005.View ArticleGoogle Scholar
- Porter KR, Thomas SD, Whitman S. The relation of gestation length to short-term heat stress. Am J Public Health. 1999;89(7):1090–2.View ArticleGoogle Scholar
- Lee SJ, Hajat S, Steer PJ, Filippi V. A time-series analysis of any short-term effects of meteorological and air pollution factors on preterm births in London, UK. Environ Res. 2008;106(2):185–94. doi:10.1016/j.envres.2007.10.003.View ArticleGoogle Scholar
- Wolf J, Armstrong B. The association of season and temperature with adverse pregnancy outcome in two German states, a time-series analysis. PLoS One. 2012;7(7):e40228. doi:10.1371/journal.pone.0040228.View ArticleGoogle Scholar
- Stan CM, Boulvain M, Pfister R, Hirsbrunner-Almagbaly P. Hydration for treatment of preterm labour. Cochrane Database Syst Rev. 2013;11:CD003096. doi:10.1002/14651858.CD003096.pub2.Google Scholar
- Darrow LA, Klein M, Flanders WD, Waller LA, Correa A, Marcus M, et al. Ambient air pollution and preterm birth: a time-series analysis. Epidemiology. 2009;20(5):689–98. doi:10.1097/EDE.0b013e3181a7128f.View ArticleGoogle Scholar
- Carolan-Olah M, Frankowska D. High environmental temperature and preterm birth: a review of the evidence. Midwifery. 2014;30(1):50–9. doi:10.1016/j.midw.2013.01.011.View ArticleGoogle Scholar
- Sagiv SK, Mendola P, Loomis D, Herring AH, Neas LM, Savitz DA, et al. A time-series analysis of air pollution and preterm birth in Pennsylvania, 1997-2001. Environ Health Perspect. 2005;113(5):602–6.View ArticleGoogle Scholar
- Zhao Q, Liang Z, Tao S, Zhu J, Du Y. Effects of air pollution on neonatal prematurity in Guangzhou of China: a time-series study. Environ Health. 2011;10:2. doi:10.1186/1476-069X-10-2.View ArticleGoogle Scholar
- Gasparrini A, Armstrong B. Time series analysis on the health effects of temperature: advancements and limitations. Environ Res. 2010;110(6):633–8. doi:10.1016/j.envres.2010.06.005.View ArticleGoogle Scholar
- Gasparrini A, Armstrong B, Kenward MG. Distributed lag non-linear models. Stat Med. 2010;29(21):2224–34. doi:10.1002/sim.3940.View ArticleGoogle Scholar
- Akaike H. Data analysis by statistical models. No To Hattatsu. 1992;24(2):127–33.Google Scholar
- Darrow LA, Strickland MJ, Klein M, Waller LA, Flanders WD, Correa A, et al. Seasonality of birth and implications for temporal studies of preterm birth. Epidemiology. 2009;20(5):699–706. doi:10.1097/EDE.0b013e3181a66e96.View ArticleGoogle Scholar
- Strand LB, Barnett AG, Tong S. The influence of season and ambient temperature on birth outcomes: a review of the epidemiological literature. Environ Res. 2011;111(3):451–62. doi:10.1016/j.envres.2011.01.023.View ArticleGoogle Scholar
- Kinney PL, Schwartz J, Pascal M, Petkova E, Tertre AL, Medina S, et al. Winter season mortality: Will climate warming bring benefits? Environ Res Lett. 2015;10(6):064016. doi:10.1088/1748-9326/10/6/064016.View ArticleGoogle Scholar
- Guo Y, Barnett AG, Yu W, Pan X, Ye X, Huang C, et al. A large change in temperature between neighbouring days increases the risk of mortality. PLoS One. 2011;6(2):e16511. doi:10.1371/journal.pone.0016511.View ArticleGoogle Scholar
- Huang Z, Lin H, Liu Y, Zhou M, Liu T, Xiao J, et al. Individual-level and community-level effect modifiers of the temperature-mortality relationship in 66 Chinese communities. BMJ Open. 2015;5(9):e009172. doi:10.1136/bmjopen-2015-009172.View ArticleGoogle Scholar
- Wu W, Xiao Y, Li G, Zeng W, Lin H, Rutherford S, et al. Temperature-mortality relationship in four subtropical Chinese cities: a time-series study using a distributed lag non-linear model. Sci Total Environ. 2013;449:355–62. doi:10.1016/j.scitotenv.2013.01.090.View ArticleGoogle Scholar
- Curriero FC, Heiner KS, Samet JM, Zeger SL, Strug L, Patz JA. Temperature and mortality in 11 cities of the eastern United States. Am J Epidemiol. 2002;155(1):80–7.View ArticleGoogle Scholar
- Xie H, Yao Z, Zhang Y, Xu Y, Xu X, Liu T, et al. Short-term effects of the 2008 cold spell on mortality in three subtropical cities in Guangdong Province, China. Environ Health Perspect. 2013;121(2):210–6. doi:10.1289/ehp.1104541.Google Scholar
- Khoury MJ, Stewart W, Weinstein A, Panny S, Lindsay P, Eisenberg M. Residential mobility during pregnancy: implications for environmental teratogenesis. J Clin Epidemiol. 1988;41(1):15–20.View ArticleGoogle Scholar
- Holditch-Davis D, Schwartz T, Black B, Scher M. Correlates of mother-premature infant interactions. Res Nurs Health. 2007;30(3):333–46. doi:10.1002/nur.20190.View ArticleGoogle Scholar
- He JR, Liu Y, Xia XY, Ma WJ, Lin HL, Kan HD, et al. Ambient temperature and the risk of preterm birth in Guangzhou, China (2001-2011). Environ Health Perspect. 2015. doi:10.1289/ehp.1509778.
- Zhou D, Zhao S, Zhang L, Sun G, Liu Y. The footprint of urban heat island effect in China. Sci Rep. 2015;5:11160. doi:10.1038/srep11160.View ArticleGoogle Scholar
- Brauer M, Lencar C, Tamburic L, Koehoorn M, Demers P, Karr C. A cohort study of traffic-related air pollution impacts on birth outcomes. Environ Health Perspect. 2008;116(5):680–6. doi:10.1289/ehp.10952.View ArticleGoogle Scholar
- Ritz B, Wilhelm M, Hoggatt KJ, Ghosh JK. Ambient air pollution and preterm birth in the environment and pregnancy outcomes study at the University of California, Los Angeles. Am J Epidemiol. 2007;166(9):1045–52. doi:10.1093/aje/kwm181.View ArticleGoogle Scholar
- Cooperstock M, Wolfe RA. Seasonality of preterm birth in the Collaborative Perinatal Project: demographic factors. Am J Epidemiol. 1986;124(2):234–41.View ArticleGoogle Scholar
- Keller CA, Nugent RP. Seasonal patterns in perinatal mortality and preterm delivery. Am J Epidemiol. 1983;118(5):689–98.View ArticleGoogle Scholar
- Rayco-Solon P, Fulford AJ, Prentice AM. Differential effects of seasonality on preterm birth and intrauterine growth restriction in rural Africans. Am J Clin Nutr. 2005;81(1):134–9.Google Scholar
- Lee SJ, Steer PJ, Filippi V. Seasonal patterns and preterm birth: a systematic review of the literature and an analysis in a London-based cohort. BJOG. 2006;113(11):1280–8.View ArticleGoogle Scholar