Abstract
Objective
Over 12% of women in the United States have reduced fertility and/or fecundity. Environmental factors, such as temperature, and socioeconomic factors have been implicated in reducing female fecundity. The purpose of this study is to investigate the effect of environmental factors coupled with socioeconomic factors on birth rate at the country-level. We use birth rate as a proxy for female fecundity. This will enable us to identify the most important factors affecting female fecundity.
Methods
Using country-specific data from 182 countries, we constructed a regression model of the effects of environmental and socioeconomic factors on birth rate at the country-level. Our model assesses the role of temperature, Gross Domestic Product (GDP) per capita, fine air particulate matter (PM 2.5), and prevalence of male and female Body Mass Index (BMI) > = 25 (age-standardized) on birth rate per country. Because many of these factors are inter-dependent, we include all possible two-way interaction terms to assess the role of individual factors and interactions between multiple factors in the model.
Results
In the full regression model, we found that GDP per capita along with 5 interaction terms were significant after adjusting for multiple testing. Female BMI was only nominally significant. GDP per capita was independently associated with birth rate (adjusted p-value <0.001). Prevalence of BMI > = 25 age-standardized in males and females were also significant when interacting with air pollution or GDP on female fecundity (birth rate). Temperature did not affect birth rate either independently or as an interaction unless BMI was removed from the model.
Conclusion
A country’s economic wealth was the most significant factor in predicting birth rate in a statistical model that includes environmental and socioeconomic variables. This is important for future studies investigating environmental factors involved in increasing or decreasing female fecundity.
Introduction
Over 12% of women in the United States have reduced fertility and/or fecundity [1]. Maternal birth season plays an important role in fertility in women [2–4]. Other fertility-related processes have been linked to birth season including the time of menarche [5] and menopause [6] in women. The main hypothesized biological mechanism underlying this relationship was that oocytes’ exposure to high temperatures at birth resulted in increased oocyte loss early in life [2, 7–9]. This reduction in oocyte volume thereby reduces a woman’s fertility when she goes to bear children later in life. This hypothesis was supported by the results from studies conducted in Austria [3], New Zealand [10] and NYC [2]. However, results from Vietnam [11] and Romania [12] appeared to find the opposite result, namely females born in high heat environments had increased fertility. This reveals an incomplete understanding regarding the relationship between seasonal temperature variation and female fertility/fecundity later in life.
Other factors are known to affect female fecundity and birth rate. High socioeconomic status (SES), which is related to income, is inversely correlated with fertility and birth rate [13, 14]. High-income countries provide their citizens with increased access to birth control methods and other forms of contraception[15]. Thereby affecting the birth rate. In addition fine air particulates (PM 2.5) or air pollution has been shown to affect the fertility rate [16] with a sperm related effect also reported [17]. On a global scale, air pollution is linked to poor countries (i.e., lower GDP) as poor countries often have more factories. This explains why countries with higher GDP often have improved environmental factors [18]. Finally, both male [19] and female [20] Body Mass Index (BMI) have been linked to birth rate and fertility outcomes through separate mechanisms. Furthermore, studies have stressed the importance of female waist-to-hip ratio in fertility with waist-to-hip ratio being more informative then BMI [21].
The purpose of this study is to investigate the relationship between environmental factors and socioeconomic factors on female fecundity as measured using birth rate. We aim to measure this at the country-level to simultaneously assess the effects of multiple socioeconomic and environmental factors from around the world on female fecundity (i.e., birth rate). We will also include interactions between the various inter-dependent factors to reveal the strongest global determinants in female fecundity.
Materials and methods
Integrating data from global datasets on birth rate and socioeconomic and environmental factors
We assembled a country-specific dataset on birth rate and other socioeconomic and environmental factors using data integrated from publically available data sources. For female fecundity, we used country-specific birth rate per 1,000 population as a proxy. To obtain birth rate data, we used data collected and maintained by the Central Intelligence Agency (CIA) [22]. For environmental factors, we obtained average annual temperature per country as measured in Celsius. This was obtained from the Climatic Research Unit [23]. We also obtained fine particulate matter (PM 2.5) from the World Health Organization (WHO). PM 2.5 data was obtained from the WHO’s Data Integration Model for Air Quality (DIMAQ). DIMAQ produces estimates of air pollution based on ground measurements and satellite retrievals of aerosol optical depth and chemical transport models [24]. The DIMAQ provides global annual exposures of PM 2.5 levels at high spatial resolution, which equates to approximately 11x11 kilometers at the equator. Data used in this paper is annual global estimates from 2014. For socioeconomic factors, we used the Gross Domestic Product (GDP) per Capita in 2016 from the WorldBank.org [25] to provide an overall assessment of a country’s wealth. We also included the prevalence of Body Mass Index (BMI) > = 25 (age-standardized) for males and females separately for each country. Each factor included in our analysis along with sources and agencies used to obtain the data are included in Table 1.
Table 1. Global data containing variables included in the fertility–temperature models.
Variable | Source/Agency Housing Data | Total Num. Countries Included in Dataset | Ref. |
---|---|---|---|
Female Fecundity: | |||
Birth rate per 1000 population | Central Intelligence Agency | 226 | [22] |
Environmental Factors: | |||
Average annual temperature in Celsius from 1961–1990 | Climatic Research Unit /Wikipedia | 191 | [23] |
Fine Particulate Matter (PM 2.5) | World Health Organization | 185 | [24] |
Socioeconomic Factors: | |||
Gross Domestic Product per Capita in 2016 | WorldBank.org | 264 | [25] |
Prevalence of Body Mass Index > = 25 (Age-Standardized) for Males and Females from 2014 | World Health Organization | 195 | [26] |
We included the total number of countries included in each dataset in Table 1 to illustrate the variance across datasets. Determining the number of independent countries in the world is complex. There are 193 countries that are recognized as such by the United Nations (UN) with 2 countries–Vatican City and Palestine–having ‘permanent observer’ status at the UN [27]. In addition, 2 states–Kosovo and Taiwan–are only recognized by subsets of UN members [27]. According to the CIA World Factbook, and as of 2018, there are 195 recognized independent countries [28]. We used these 195 countries as our definitive list of ‘countries’ with mappings available to the International Standards Organization (ISO) Alpha-3 standard country codes [28].
Clearly, some datasets contained many more country names (sometimes including non-independent states), especially the birth rate dataset and the Gross Domestic Product (GDP) dataset with 226 and 264 countries respectively. The GDP dataset also included assessments of regions that were given their own country codes, but were in fact groupings of other countries already included in the dataset. Therefore, we decided to integrate these datasets together, understanding that we would have at most only 185 countries captured in the integrated dataset because the air pollution dataset did not contain data from the all 195 independent countries. Whenever possible, we utilized the ISO Alpha-3 standard country codes to map across datasets. In some cases, this was not possible and we used the country names to map across datasets. However, different datasets used different nomenclatures for country-names. The birth rate and temperature datasets contained country names without corresponding ISO Alpha-3 codes. All records were manually reviewed to ensure that harmonization was accurate. Overall, our dataset contained information on six variables: birth rate, average air pollution, and average country temperature, GDP from 2016, BMI for males and BMI for females from 182 countries (S1 Dataset). This dataset captures 93.3% (182/195) of the independent states from around the world. Thirteen recognized independent countries by the CIA are missing from these analysis [28]. These thirteen countries are: Saint Kitts and Nevis, Liechtenstein, Monaco, Marshall Islands, Nauru, Palau, San Marino, South Sudan, Tonga, Tuvalu, Taiwan, Vatican City and Samoa. Our dataset of 182 countries is missing GDP information for 12 countries (Timor-Leste, Eritrea, North Korea, Djibouti, Papua New Guinea, Cuba, Syria, Iran, Libya, Venezuela, Andorra and Kuwait). and male and female BMI for 1 country (the Sudan).
Regression model for relationship between environmental and socioeconomic factors and birth rate
We constructed a linear regression model with birth rate as the outcome variable. This is linear regression and therefore, we are predicting the actual birth rate per 1,000 individuals in the population and we did not use a binned birth rate statistic. We included in this full model, known predictors of fecundity (birth rate), including environmental factors: temperature and air pollution, socio-economic: GDP per capita and lifestyle: prevalence of BMI> = 25 (age-standardized) for males and females per country. We also included in this model pairwise interaction terms due to the inherent interdependency of these variables. A total of 16 terms were included in the model, including the intercept term, 5 covariates, and 10 interaction terms. We report the raw p-values, and also the Bonferroni-adjusted p-values (adjusted for 16 tests).
Regression model for relationship between environmental and socioeconomic factors and birth rate without including body mass index
We also constructed a linear regression model excluding the two BMI factors. We again modeled birth rate as the outcome variable, and the following set of dependent variables: annual temperature, GDP, and fine air particulates (PM 2.5). In addition three pairwise interaction terms were included in the model (interaction of temperature and pollution; interaction of GDP and pollution and interaction of GDP and temperature). This model is the same as the one described in section 2.2 except that we removed the male and female BMI terms and their corresponding interaction terms.
Results
Global variance in birth rate and associated factors
We investigated the relationship between fecundity (birth rate) and two environmental factors–temperature and air pollution–and also socio-economic factors–GDP, male and female BMI. We found that the prevalence of males with BMI > = 25 (age-standardized) was inversely correlated with fecundity across all countries (Fig 1). Interestingly, female BMI exhibited a different pattern. In countries with lower fecundity (between 10–20 births per 1,000 population), the prevalence of females with BMI> = 25 (age-standardized) was positively correlated with fecundity. However, when a country’s fecundity passed a certain threshold (around 20) then the prevalence of females with BMI > = 25 (age-standardized) became inversely correlated (Fig 1). Importantly, poor countries (low GDP) had higher air pollution and were warmer overall (Fig 1). This is an important consideration for analyses that demonstrate the effect of temperature on fecundity and was part of our motivation to include all factors into our global analysis of factors affecting female fecundity.
The global variation in birth rate and its correlated factors can also be observed from the maps (Fig 2). Asia, South America and Africa have high temperatures and in general high fecundity (birth rate). However, these countries are also poorer (low GDP) and are exposed to higher air pollution levels (Fig 2). These countries also have lower prevalence of BMI > = 25 (age-standardized) for females and males. (Fig 2), which could be driven by the type of work they engage in (e.g., increased manual labor).
Many of the factors that are involved in fecundity are also correlated or anti-correlated with each other. Therefore, regression models that include interaction terms are important to capture this source of variation. Fig 1 illustrates the correlation among the six factors. Birth rate on its own was significantly correlated with each variable. Therefore each was included in the regression model described in section 3.2. Birth rate was negative correlated with GDP (R = -0.51, p<0.001), positively correlated with temperature (R = 0.53, p<0.001), slightly positively correlated with air pollution (R = 0.33, p<0.001) and negatively correlated with male and female BMI (R = -0.76 and R = -0.46, respectively). Interestingly, male BMI was more strongly correlated with birth rate then female BMI. However, this is likely due to the interaction between GDP, pollution and BMI among males (often low-income males work in more labor intensive occupations). Hence our regression model (described in section 3.2) includes additional interaction terms to determine the most important factors.
Regression model results for birth rate: Integrating data from across the globe
Our comprehensive model of environmental and socioeconomic factors and their role on female fecundity (birth rate) included average temperature per country from 1961–1990, GDP per capita, average air pollution (PM 2.5) and prevalence of BMI > = 25 (age-standardized) for males and females. We also included 10 pairwise interaction terms in the model. We report nominal p-values and also Bonferroni adjusted p-values (adjusting for 16 tests–one test for each factor included in the model). The model results are shown in Table 2.
Table 2. Regression model with BMI Included as confounder.
Variable Included in Model | Estimate | CI 2.5% | CI 97.5% | P-value | Adjusted P-value |
---|---|---|---|---|---|
Covariates | |||||
Average Temperature 1961–1990 (Celsius) | -0.11 | -0.81 | 0.60 | 0.77 | 1 |
GDP per Capita in 2016 USD | -8.02 X 10−4 | -0.0012 | -0.0005 | 1.18 X 10−5 | 1.88 X 10−4 |
Annual Estimated Average PM 2.5 in 2014 | -0.30 | -0.604 | 0.008 | 0.06 | 0.90 |
Prevalence Male BMI > = 25 (age-standardized) in 2014 | -0.33 | -0.71 | 0.042 | 0.08 | 1 |
Prevalence Female BMI > = 25 (age-standardized) in 2014 | -0.47 | -0.92 | -0.02 | 0.04 | 0.65 |
Interaction Terms (term 1 : term 2) |
|||||
Prevalence Male BMI > = 25 (age-standardized) in 2014: Prevalence Female BMI > = 25 (age-standardized) in 2014 | 6.51 X 10−3 | 2.26 X 10−3 | 0.01 | 0.003 | 0.046 |
Temperature in C: GDP per Capita in 2016 USD | 9.91 X 10−6 | -3.98 X 10−7 | 2.02 X 10−5 | 0.06 | 0.95 |
Temperature in C: Annual Estimated PM 2.5 in 2014 | 3.30 X 10−3 | -9.00 X 10−3 | 0.016 | 0.60 | 1 |
Temperature in C: Prevalence Male BMI > = 25 (age-standardized) in 2014 | -0.015 | -0.032 | 0.001 | 0.07 | 1 |
Temperature in C: Prevalence Female BMI > = 25 (age-standardized) in 2014 | 0.015 | -0.004 | 0.034 | 0.13 | 1 |
GDP per Capita in 2016 USD : Prevalence Female BMI > = 25 (age-standardized) in 2014 | -1.57 X 10−5 | -2.47 X 10−5 | -6.64 X 10−6 | 7.84 X 10−4 | 0.013 |
Annual Estimated PM 2.5 in 2014: Prevalence Female BMI > = 25 (age-standardized) in 2014 | 0.019 | 0.009 | 0.029 | 2.89 X 10−4 | 0.005 |
GDP per Capita in 2016 USD: Prevalence Male BMI > = 25 (age-standardized) in 2014 | 2.29 X 10−5 | 1.41 X 10−5 | 3.17 X 10−5 | 8.68 X 10−7 | 1.39 X 10−5 |
Annual Estimated PM 2.5 in 2014: Prevalence Male BMI > = 25 (age-standardized) in 2014 | -0.016 | -0.026 | -0.006 | 0.002 | 0.038 |
GDP per Capita in 2016 USD: Annual Estimated PM 2.5 in 2014 | -1.75 X 10−6 | -6.31 X 10−6 | 2.80 X 10−6 | 0.45 | 1 |
P-values are bold if they are significant (<0.05), and rows containing significant terms are shown in grey
Both female BMI and GDP per capita were nominally significant (p-value <0.05) in the model for birth rate. Although prevalence of female BMI > = 25 was not significant after adjusting for multiple testing (Table 2). After adjusting for multiple testing, GDP per capita was still significantly negatively correlated with birth rate (p<0.001). Five interaction terms were also significant.
Significant interaction terms included an interaction between male and female BMI > = 25 (age-standardized); GDP and BMI (male and female each a separate term); and air pollution and BMI. The air pollution (PM 2.5) term was not associated with birth rate in the full model (unadjusted p = 0.06, and adjusted p = 0.90), but only interactions between air pollution and BMI. Overall, prevalence of female BMI > = 25 (age-standardized) was nominally significant in determining birth rate independently and also via indirect mechanisms (i.e., GDP, air pollution, male BMI); whereas, prevalence of male BMI > = 25 (age-standardized) was not independently associated with birth rate. This indicates that the strong anti-correlation between prevalence of male BMI > = 25 (age-standardized) and female fecundity is through correlation with other variables (Fig 1).
Regression model predicting birth rate without body mass index
The model result for our linear regression model constructed without the two BMI terms is shown in Table 3. This model is the same as the one described in section 2.2 except that we removed the male and female BMI terms and their corresponding interaction terms. We used this second model to determine how the inclusion of BMI affects the environmental factors relationship with fecundity (birth rate). Temperature and the interaction term for temperature and GDP were significant. Importantly, GDP was not significant in this model, but only the interaction between GDP and temperature.
Table 3. Regression model results for factors that influence birth rate without including BMI.
Variable Included in Model | Estimate | CI 2.5% | CI 97.5% | P-value | Adjusted P-value |
---|---|---|---|---|---|
Covariates | |||||
Average Temperature 1961–1990 | 0.65 | 0.205 | 0.819 | 0.001 | 0.009 |
GDP per Capita in 2016 | 7.26 X 10−5 | -5.07 X 10−5 | 1.96 X 10−4 | 0.246 | 1 |
PM 2.5 | -0.038 | -0.307 | 0.232 | 0.781 | 1 |
Interaction Terms (term 1 : term 2) |
|||||
Temperature: GDP | -2.05 X 10−5 | -3.01 X 10−5 | -1.10 X 10−5 | 3.40 X 10−5 | 2.38 X 10−4 |
Temperature: PM 2.5 | 0.007 | -0.004 | 0.019 | 0.195 | 1 |
GDP: PM 2.5 | -1.50 X 10−6 | -5.13 X 10−6 | 2.14 X 10−6 | 0.417 | 1 |
P-values are bold if they are significant (<0.05), and rows containing significant terms are shown in grey
Without BMI in the model, temperature and the interaction of temperature and GDP were significantly associated with birth rate. Importantly temperature was positive associated with fecundity (estimate = 0.65, adjusted p-value = 0.009). The interaction between temperature and GDP was significant with adjusted p-value = 2.38 X 10−4 (Table 3). None of the air pollution terms in this model were significant.
Discussion
In this study, we constructed a country-level model of factors involved in fecundity (birth rate) using data from 182 countries across the world. A high-level global analysis was performed to look at factors correlated with birth rate on the global scale to identify the most important factors in female fecundity or birth rate. We modeled interactions between multiple factors because of the high-degree of interdependency among factors. Overall, we found that a country’s economic wealth (i.e., GDP per capita) was the most significant in predicting fecundity in a full model that includes male and female BMI (Table 2). Air pollution (PM 2.5) and BMI were also important contributory factors (as interaction terms) in predicting fecundity (birth rate). However, temperature did not affect birth rate either independently or as an interaction unless the BMI terms were removed from the model (i.e., prevalence of BMI > = 25 in males and females, age-standardized).
Many studies have pointed to the role of temperature on female fecundity. Some studies point to an in-direct mechanism, through impairment of the male’s fertility. Spermatogenesis in males is impaired when temperature increases resulting in impaired fertility [29]. This suggests that certain seasons of the year may result in increased fertility periods due to increases in sperm viability and quality [30]. Male sperm motility and/or concentration (but not quality) have been linked to seasonally dependent variables including vitamin D [31] and vitamin C (ascorbic acid) [32]. Many of these seasonally dependent variables (e.g., vitamin D) are also related to temperature variation in different regions of the world. However, the results of our model point to the role of income (GDP) on female fecundity and interactions between GDP and BMI, air pollution (PM 2.5) and GDP on female fecundity. Temperature was insignificant in the model with BMI (Table 2), but was significant in the model without BMI (Table 3). Studies in insects have shown that temperature and the size of the female were both important in determining fecundity indicating that temperature was not the only variable of importance [33]. Studies in humans have shown that body fat distribution was more important in fertility outcomes then age or obesity status [34] indicating the importance not only of BMI but also body fat distribution on fecundity.
Importantly, we include the results of the model without the inclusion of the male and female BMI parameters (i.e., prevalence of BMI> = 25, age-standardized) in Table 3. In the model without BMI, temperature was a significant factor even after adjusting for multiple testing (p = 0.009). Temperature is highly correlated with many other variables that are important in fecundity, which was the rationale for constructing this global model. In addition, the significant interaction terms point to the importance of capturing the inherent inter-dependency among a number of these variables (Fig 1). In addition, the significant interaction term may point to a third un-measured variable that is underlying both factors that could explain the fecundity effect.
Significant factors in the full model (Table 2) demonstrate the importance of other factors (e.g., BMI) and their interactions with environmental factors (BMI and air pollution) on female fertility and birth rate on a global scale. This is important because many of these factors correlate with temperature indicating that earlier work seeking to demonstrate a relationship between perinatal exposure of females to high temperatures decreases female fertility later in life may be capturing an environmental exposure that is coupled with temperature, but not temperature itself [2, 3, 10–12].
Importantly, our analysis focuses on birth rate, which is a measure of fecundity. We are not able to assess the number of pregnancies lost in various countries and how variance in pregnancy loss (i.e., spontaneous abortion or miscarriage) affects a country’s birth rate. Pregnancy loss is very difficult to capture in many countries due to lack of reporting. Even outcomes such as preterm birth and still birth (which are easier to capture then pregnancy loss) are still difficult to capture globally [35]. This is why we restricted our analyses to birthrate. Temperature has been implicated in pregnancy loss and conception rates in several studies among dairy cows [36–39]. We have found that temperature was only significantly related to a country’s birth rate if BMI was excluded (Table 3). However, in a full model that includes male and female BMI, the GDP of the country was the most significant variable along with interactions between air pollution, BMI and GDP (Table 2). Some of these findings could be related to our inability to assess the pregnancy loss rate across countries.
There are several limitations to this study. First, we perform a global analysis investigating each country equally. However, not all countries are the same size. We use statistics such as birth rate per 1,000 population and GDP per capita, which should help to address some of these issues. However, there are some fundamental differences between large and small countries that are not fully addressed by our methods. Therefore, this remains a limitation of our approach. We only investigated variables that have been reported to impact female fecundity and that had data available at the country-level for the majority of countries included in our study. Therefore, not every factor implicated in female fecundity was included in our model. The major factors (income, body mass, temperature and air pollution) were included.
Conclusions
In conclusion, we constructed a global model of female fecundity using data from 182 countries. Our model captured known environmental and socioeconomic factors that have been implicated in reducing or increasing female fecundity. We included at the country-level measures of average annual temperature, average air pollution, GDP per capita and prevalence of BMI > = 25 for males and females (age-standardized). We also included interaction terms to capture the inherent inter-dependency among many of these factors. We found that GDP per capita was independently associated with fecundity (birth rate). In addition, air pollution (PM 2.5), and BMI were important contributory factors as interaction terms. BMI was found in significant interactions with GDP and air pollution. Annual temperature was only significant in the model that did not include BMI pointing to other mechanisms underlying the temperature to fecundity relationship.
Ethics approval and consent to participate
This study only includes publically available data. No patient-level data was used only aggregate statistics therefore no consent was required to conduct this study.
Supporting information
Acknowledgments
This project was made possible by generous funding from the Perelman School of Medicine, University of Pennsylvania.
Data Availability
The integrated global dataset of 182 countries will be included as a supplemental data-file and made available on the author’s laboratory website (http://fertilityandhealthinformaticslab.org/).
Funding Statement
This project was made possible by generous funding from the Perelman School of Medicine, University of Pennsylvania. The funder had no role in the study design, data collection, data analysis, decision to publish or preparation of the final manuscript.
References
- 1.CDC. Is Infertility a Common Problem? Accessed in November 2017. 2017;<https://www.cdc.gov/reproductivehealth/infertility/index.htm>.
- 2.Boland MR, Shahn Z, Madigan D, Hripcsak G, Tatonetti NP. Birth month affects lifetime disease risk: a phenome-wide method. Journal of the American Medical Informatics Association. 2015;22:1042–53. 10.1093/jamia/ocv046 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Huber S, Fieder M, Wallner B, Moser G, Arnold W. Brief communication: birth month influences reproductive performance in contemporary women. Hum Reprod. 2004;19(5):1081–2. Epub 2004/05/04. 10.1093/humrep/deh247 . [DOI] [PubMed] [Google Scholar]
- 4.Hurtado AM, Hill KR. Seasonality in a Foraging Society: Variation in Diet, Work Effort, Fertility, and Sexual Division of Labor among the Hiwi of Venezuela. Journal of Anthropological Research. 1990;46(3):293–346. 10.1086/jar.46.3.3630428 [Google Scholar]
- 5.Gueresi P. Monthly distribution of menarche in three provinces of North Italy. Annals of Human Biology. 1997;24(2):157–68. 10.1080/03014469700004892 [DOI] [PubMed] [Google Scholar]
- 6.Cagnacci A, Pansini FS, Bacchi-Modena A, Giulini N, Mollica G, De Aloysio D, et al. Season of birth influences the timing of menopause. Human Reproduction. 2005;20(8):2190–3. 10.1093/humrep/dei040 [DOI] [PubMed] [Google Scholar]
- 7.Hansen PJ. Early embryonic loss due to heat stress. Bovine Reproduction. 2015:580–8. [Google Scholar]
- 8.Edwards JL, Hansen PJ. Differential responses of bovine oocytes and preimplantation embryos to heat shock. Molecular reproduction and development. 1997;46(2):138–45. 10.1002/(SICI)1098-2795(199702)46:2<138::AID-MRD4>3.0.CO;2-R [DOI] [PubMed] [Google Scholar]
- 9.Kemkes A. The impact of maternal birth month on reproductive performance: controlling for socio-demographic confounders. Journal of biosocial science. 2010;42(2):177–94. 10.1017/S002193200999054X [DOI] [PubMed] [Google Scholar]
- 10.Huber S, Didham R, Fieder M. Month of birth and offspring count of women: data from the Southern hemisphere. Hum Reprod. 2008;23(5):1187–92. Epub 2008/03/11. 10.1093/humrep/den079 ; PubMed Central PMCID: PMC2981771. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Huber S, Fieder M. Strong association between birth month and reproductive performance of Vietnamese women. American journal of human biology: the official journal of the Human Biology Council. 2009;21(1):25–35. Epub 2008/06/19. 10.1002/ajhb.20799 ; PubMed Central PMCID: PMC3072539. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Huber S, Fieder M. Perinatal winter conditions affect later reproductive performance in Romanian women: intra and intergenerational effects. American journal of human biology: the official journal of the Human Biology Council. 2011;23(4):546–52. Epub 2011/06/02. 10.1002/ajhb.21184 . [DOI] [PubMed] [Google Scholar]
- 13.Dribe M, Hacker JD, Scalone F. The impact of socio-economic status on net fertility during the historical fertility decline: A comparative analysis of Canada, Iceland, Sweden, Norway, and the USA. Population Studies. 2014;68(2):135–49. 10.1080/00324728.2014.889741 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Bollen KA, Glanville JL, Stecklov G. Socio-economic status, permanent income, and fertility: A latent-variable approach. Population studies. 2007;61(1):15–34. 10.1080/00324720601103866 [DOI] [PubMed] [Google Scholar]
- 15.Chandra-Mouli V, McCarraher DR, Phillips SJ, Williamson NE, Hainsworth G. Contraception for adolescents in low and middle income countries: needs, barriers, and access. Reproductive Health. 2014;11(1):1 10.1186/1742-4755-11-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Nieuwenhuijsen MJ, Basagaña X, Dadvand P, Martinez D, Cirach M, Beelen R, et al. Air pollution and human fertility rates. Environment International. 2014;70:9–14. 10.1016/j.envint.2014.05.005. [DOI] [PubMed] [Google Scholar]
- 17.Hammoud A, Carrell DT, Gibson M, Sanderson M, Parker-Jones K, Peterson CM. Decreased sperm motility is associated with air pollution in Salt Lake City. Fertility and Sterility. 2010;93(6):1875–9. 10.1016/j.fertnstert.2008.12.089. [DOI] [PubMed] [Google Scholar]
- 18.Grossman GM, Krueger AB. Economic Growth and the Environment*. The Quarterly Journal of Economics. 1995;110(2):353–77. 10.2307/2118443 [Google Scholar]
- 19.Kort HI, Massey JB, Elsner CW, Mitchell‐Leef D, Shapiro DB, Witt MA, et al. Impact of body mass index values on sperm quantity and quality. Journal of andrology. 2006;27(3):450–2. 10.2164/jandrol.05124 [DOI] [PubMed] [Google Scholar]
- 20.Clark AM, Thornley B, Tomlinson L, Galletley C, Norman RJ. Weight loss in obese infertile women results in improvement in reproductive outcome for all forms of fertility treatment. Human Reproduction. 1998;13(6):1502–5. 10.1093/humrep/13.6.1502 [DOI] [PubMed] [Google Scholar]
- 21.Wass P, Waldenström U, Rössner S, Hellberg D. An android body fat distribution in females impairs the pregnancy rate of in-vitro fertilization-embryo transfer. Human reproduction (Oxford, England). 1997;12(9):2057–60. [DOI] [PubMed] [Google Scholar]
- 22.CIA. Country Comparison: Birth Rate. 2017;<https://www.cia.gov/library/publications/the-world-factbook/rankorder/2054rank.html> (Accessed on August 18, 2017).
- 23.Wikipedia. List of countries by average yearly temperature. 2017;<https://en.wikipedia.org/wiki/List_of_countries_by_average_yearly_temperature> (Accessed on August 18, 2017).
- 24.WHO. Modelled Global Ambient Air Pollution Estimates. 2017;<http://www.who.int/phe/health_topics/outdoorair/databases/modelled-estimates/en/> (Accessed on August 22, 2017).
- 25.WorldBank.org. GDP per Capita All Countries and Economies. 2017;<http://data.worldbank.org/indicator/NY.GDP.PCAP.CD> (Accessed on August 18, 2017).
- 26.WHO. Global Health Observatory data repository Age Standardized Body Mass Index. 2017;<http://apps.who.int/gho/data/node.main.A897A?lang=en> (Accessed on August 22, 2017).
- 27.List of Countries of the World. 2018;<https://www.countries-ofthe-world.com/> (Accessed in June 2018).
- 28.Statoids. Country Codes. 2018;<http://www.statoids.com/wab.html> (Accessed on September 08, 2018).
- 29.Thonneau P, Bujan L, Multigner L, Mieusset R. Occupational heat exposure and male fertility: a review. Human Reproduction. 1998;13(8):2122–5. 10.1093/humrep/13.8.2122 [DOI] [PubMed] [Google Scholar]
- 30.Centola GM, Eberly S. Seasonal variations and age-related changes in human sperm count, motility, motion parameters, morphology, and white blood cell concentration. Fertility and Sterility. 1999;72(5):803–8. 10.1016/S0015-0282(99)00395-7. [DOI] [PubMed] [Google Scholar]
- 31.Blomberg Jensen M, Bjerrum PJ, Jessen TE, Nielsen JE, Joensen UN, Olesen IA, et al. Vitamin D is positively associated with sperm motility and increases intracellular calcium in human spermatozoa. Human reproduction. 2011;26(6):1307–17. 10.1093/humrep/der059 [DOI] [PubMed] [Google Scholar]
- 32.Ciereszko A, Dabrowski K. Sperm quality and ascorbic acid concentration in rainbow trout semen are affected by dietary vitamin C: an across-season study. Biology of Reproduction. 1995;52(5):982–8. [DOI] [PubMed] [Google Scholar]
- 33.Berger D, Walters R, Gotthard K. What limits insect fecundity? Body size‐and temperature‐dependent egg maturation and oviposition in a butterfly. Functional Ecology. 2008;22(3):523–9. [Google Scholar]
- 34.Zaadstra BM, Seidell JC, Van Noord P, te Velde ER, Habbema J, Vrieswijk B, et al. Fat and female fecundity: prospective study of effect of body fat distribution on conception rates. Bmj. 1993;306(6876):484–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Lawn JE, Gravett MG, Nunes TM, Rubens CE, Stanton C, Group tGR. Global report on preterm birth and stillbirth (1 of 7): definitions, description of the burden and opportunities to improve data. BMC Pregnancy and Childbirth. 2010;10(1):S1 10.1186/1471-2393-10-s1-s1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.López-Gatius F. Is fertility declining in dairy cattle?: a retrospective study in northeastern Spain. Theriogenology. 2003;60(1):89–99. [DOI] [PubMed] [Google Scholar]
- 37.Her E, Wolfenson D, Flamenbaum I, Folman Y, Kaim M, Berman A. Thermal, Productive, and Reproductive Responses of High Yielding Cows Exposed to Short-Term Cooling in Summer. Journal of Dairy Science. 1988;71(4):1085–92. 10.3168/jds.S0022-0302(88)79656-3 [DOI] [PubMed] [Google Scholar]
- 38.Salah MS, Mogawer HH. Reproductive performance of Friesian cows in Saudi Arabia. II. Resting and service interval, conception rate, and number of services per conception. Beitr Trop Landwirtsch Veterinarmed. 1990;28(1):85–91. . [PubMed] [Google Scholar]
- 39.Sartori R, Sartor-Bergfelt R, Mertens S, Guenther J, Parrish J, Wiltbank M. Fertilization and early embryonic development in heifers and lactating cows in summer and lactating and dry cows in winter. Journal of dairy science. 2002;85(11):2803–12. 10.3168/jds.S0022-0302(02)74367-1 [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The integrated global dataset of 182 countries will be included as a supplemental data-file and made available on the author’s laboratory website (http://fertilityandhealthinformaticslab.org/).