Figures
Abstract
The sex of the conceived child is a significant concern for parents. To verify whether there women have pregnancy bias toward boys or girls, we investigated whether the history of continuous same-sex pregnancy was associated with the subsequent child’s sex. We prospectively analyzed data from the Japan Environment and Children’s Study, a birth cohort study. We included all cases of singleton live births (n = 98 412). Women with pregnancy due to infertility treatment were excluded (n = 6255); Similarly, women with a history of miscarriage, artificial abortion, stillbirth, and multiple pregnancies, and those with missing data on the sex of the previous child were excluded. Altogether, 62 718 women were included. For the first live birth, a male-biased sex ratio of 1.055 was observed. Further, no significant difference was found in the sex ratio of the conceived child between women with one boy and those with one girl previously. However, when there were more than two children previously, the subsequently conceived child’s male/female sex ratio was significantly higher among boy-only mothers than among girl-only mothers. The results indicated that several pregnant women are biased toward conceiving either boys or girls.
Citation: So S, Tawara F, Taniguchi Y, Kanayama N, the Japan Environment and Children’s Study (JECS) Group (2023) Pregnancy bias toward boys or girls: The Japan Environment and Children’s Study. PLoS ONE 18(6): e0287752. https://doi.org/10.1371/journal.pone.0287752
Editor: Bilal Sulaiman, University of Abuja Teaching Hospital, NIGERIA
Received: July 13, 2022; Accepted: June 13, 2023; Published: June 23, 2023
Copyright: © 2023 So et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript.
Funding: Shuhei So is affiliated with the funded laboratory of Tawara IVF Clinic. The funder provided support in the form of salaries for authors [S.S]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.
Competing interests: Shuhei So is affiliated with the funded laboratory of Tawara IVF Clinic. Fumiko Tawara, Yu Taniguchi, and Naohiro Kanayama declare that they have no conflict of interest. The funder provided support in the form of salaries for authors [S.S]. There are no patents, products in development or marketed products associated with this research to declare. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
Introduction
According to Fisher’s principle, the sex ratios of several organisms are balanced at 1:1 [1]. Moreover, the human male/female sex ratio is approximately 1:1 but reportedly has a slight male bias [1, 2]. Results from several studies have shown that the male bias in the secondary sex ratio (SSR) is due to the male bias in the primary sex ratio (PSR) at conception [1, 3, 4]. In contrast, Orzack et al. argued that the SSR becomes male-biased due to more pregnancy losses of girls than boys based on a meta-analysis of the sex ratios in chorionic villus sampling, amniocentesis, induced abortion, stillbirth, and live births [5]. Additionally, female-selective abortions lead to SSR imbalances in several countries [6]; thus, SSR contributes to both sex-biased pregnancy and loss.
To determine if there are women with pregnancy bias towards boys or girls, we investigated whether the history of continuous same-sex pregnancy was associated with the subsequent child’s sex.
Materials and methods
Study design
We analyzed data from the Japan Environmental Children’s Study (JECS), a birth cohort study undertaken to elucidate the influence of chemical exposure during the fetal period and early childhood on children’s health, with follow-up until the age of 13 years. This study’s protocol and baseline data are available elsewhere [7, 8]. The JECS is funded directly by Japan’s Ministry of the Environment and involves collaboration between the National Institute for Environmental Studies, the National Centre for Child Health and Development, and 15 Regional Centers. Pregnant women were recruited between January 2011 and March 2014. Eligibility criteria for participants (expectant mothers) were as follows: 1) residing in the study areas at the time of recruitment and enrolled with co-operating health care providers and local government offices issuing Maternal and Child Health Handbooks; 2) expected delivery date after 1 August 2011; and 3) capable of comprehending the Japanese language and completing the self-administered questionnaire.
Ethical approval
The JECS protocol was reviewed and approved by the Ministry of the Environment’s Institutional Review Board on Epidemiological Studies and the Ethics Committees of all participating institutions (No.100910001). The JECS was conducted in accordance with the principles of the Declaration of Helsinki and other internationally valid regulations and guidelines. Written informed consent was obtained from all the participants.
Personal information is managed strictly by limiting the number of people who can handle it. Biospecimens and questionnaires will be kept after removing any personally identifiable information. Since the research is conducted using only the reference number, the researcher will not be able to tell who the work belongs to.
Sample selection
This study was based on the ‘jecs-ta-20190930’ data set, which was released in October 2019. The data set included 104 062 records, and we included all cases of singleton live births (enrolled participants, n = 98 412). Further, cases with pregnancy due to infertility treatment were excluded because infertility treatments affect the sex ratio of children due to procedural intervention (enrolled participants, n = 92 139). In addition, women with a history of miscarriage, artificial abortion, and stillbirth, including those with a history of multiple pregnancies and missing data on the sex of the previous child, were.excludes. Finally, 62 718 women were included in the study (Fig 1).
Variables
Data transcribed from medical records at the time of study enrollment included information on maternal age, history of multiple pregnancies, miscarriage, artificial abortion and stillbirth, sex of siblings, use of in vitro fertilization, and embryo transfer (IVF-ET) for the present pregnancy. Data transcribed from medical records immediately after delivery included maternal and gestational age, single/multiple pregnancy status, infant sex, and pregnancy outcomes such as live/stillbirth and miscarriage/induced abortion.
Results
In this study, 62 718 women without a history of miscarriage, artificial abortion, and stillbirth were enrolled. For the first live birth, a male-biased sex ratio of 1.055 was observed (Table 1). Subsequently, no significant difference was found in the sex ratio of the conceived child between women with one boy previously and those with one girl previously (1.068 vs. 1.039, p = 0.290, Table 1). However, when there were more than two children previously, the subsequently conceived child’s male/female sex ratio was significantly higher among boy-only mothers than among girl-only mothers (1.112 vs. 0.972, p = 0.014, Table 1). As a subgroup analysis, the subsequently conceived child’s male/female sex ratios of mothers with two, three, and four boys children are higher than those of girl-only mothers in each case, although no significant difference is observed (1.100 vs 0.987 for two prior children, p = 0.058; 1.169 vs 0.824 for three prior children, p = 0.075; 1.750 vs 0.750 for four prior children, p = 0.167, Table 2).
Women with five children or more were excluded due to the small number of cases: women with five children, MMMMM (n = 2, one boy and one girl in the subsequent child), FFFFF (n = 3, two boys and one girl in the subsequent child). Women with six children, FFFFFF (n = 1, one boy in the subsequent child).
Discussion
Our study used a large Japanese database involving 62 718 early pregnant women without a history of miscarriage, artificial abortion, and stillbirth and found that women with more than two prior boys or girls were significantly more likely to have another boy or girl, respectively. Biggar et al. conducted an epidemiological study to explore the relationship between sex ratio and birth order using the Danish National Database, which records the sex and birth order of 1.4 million infants [6]. Although 51.2% of the first-birth children were boys, the probability of having another boy increased to 51.5%, 51.6%, 52.4%, and 54.2% for women who had previously conceived one, two, three, or four boys, respectively, suggesting the existence of families with child’s sex-biased toward boys. Although it was unclear whether such sex bias resulted from male-biased pregnancy or female-biased pregnancy loss, our findings suggest that the SSR bias toward either a boy or girl may be due to inherent sex bias upon subsequent pregnancy rather than sex bias due to pregnancy loss.
The sex ratio of a fertilized egg depends on the sex chromosomes carried by the spermatozoa. Most reports have shown no difference in the frequency of Y- and X-bearing spermatozoa [9–12]. Interestingly, Umehara et al. found that Toll-like receptors (TLR7/8) were expressed in the X-bearing spermatozoa in mice, and their active state showed decreased motility of the X-bearing spermatozoa [13]. This result suggested that males consuming an anti-viral compound, which is a ligand for TLR7/8, have decreased motility of X-bearing spermatozoa and may have increased XY embryo production. Males with a history of hepatitis B virus infection have been reported to have a high male/female sex ratio [14]. Differences were noted in motility, viability, electrophobicity, pH susceptibility, surface properties, and stress response between the X- and Y-bearing spermatozoa [4, 15]. These factors related to sperm activity will not only be affected by the testis and seminiferous tubules as male factors but also by the female vaginal environment. Thus, as an example, the sex bias of the activated sperm may be involved in the SSR.
This study has some limitations. First, since it was conducted using a Japanese database, almost all participants were Japanese, limiting the generalizability to other populations. Second, although some environmental factors might influence the sex ratio, we did not investigate the relationship between sex-biased pregnancies and these confounding factors, presuming that the environmental factors during the survey and the environment during the previous pregnancies differed. Third, it is unknown whether all children involved were born to the same father in all mothers’ pregnancies. Finally, we did not examine the relationship between sex bias upon subsequent pregnancy and paternal factors, including age and medical history.
In conclusion, mothers with a pregnancy history of consecutive boy or girl children were more likely to be biased toward boys or girls, respectively, for the sex of the subsequently conceived child. This epidemiological study will provide crucial insights into women who become pregnant with a bias for boys or girls. Further studies are required to clarify whether sex-biased pregnancy is influenced by PSR or conception and whether it is affected by paternal or maternal factors.
Acknowledgments
The findings and conclusions of this article are solely the responsibility of the authors and do not represent the official views of the above government. The authors are grateful to all study participants and Japan Environment and Children’s Study (JECS) members. Members of the JECS Group as of 2021: Michihiro Kamijima (principal investigator, Nagoya City University, Nagoya, Japan), Shin Yamazaki (National Institute for Environmental Studies, Tsukuba, Japan), Yukihiro Ohya (National Center for Child Health and Development, Tokyo, Japan), Reiko Kishi (Hokkaido University, Sapporo, Japan), Nobuo Yaegashi (Tohoku University, Sendai, Japan), Koichi Hashimoto (Fukushima Medical University, Fukushima, Japan), Chisato Mori (Chiba University, Chiba, Japan), Shuichi Ito (Yokohama City University, Yokohama, Japan), Zentaro Yamagata (University of Yamanashi, Chuo, Japan), Hidekuni Inadera (University of Toyama, Toyama, Japan), Takeo Nakayama (Kyoto University, Kyoto, Japan), Hiroyasu Iso (Osaka University, Suita, Japan), Masayuki Shima (Hyogo College of Medicine, Nishinomiya, Japan), Hiroshige Nakamura(Tottori University, Yonago, Japan), Narufumi Suganuma (Kochi University, Nankoku, Japan), Koichi Kusuhara (University of Occupational and Environmental Health, Kitakyushu, Japan), and Takahiko Katoh (Kumamoto University, Kumamoto, Japan).
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