Numerous studies suggest that sex steroids might play a role in sex disparity observed in allergic diseases in adults. However, whether sex hormones influence allergic diseases in children remains unclear. The aim of the present study was to examine the association of sex steroid hormones with allergic disease in Japanese children.
Methods
The present cross-sectional study included 145 6-year-old children participating in a pilot birth cohort study in the Japan Environment and Children’s Study. Data on allergic diseases were obtained from questionnaires, and serum levels of sex steroid hormones and allergen-specific IgE were measured. Logistic regression was performed to evaluate the association of sex hormones with allergic diseases.
Results
After adjusted sex, amount of body fat at 6 years, parental history of allergic disease, and exposure to tobacco smoke, serum dehydroepiandrosterone sulfate level was significantly associated with reduced odds of any allergic disease (adjusted odds ratio, 0.58; 95% confidence interval, 0.36–0.93; P = 0.024) and serum follicle-stimulating hormone level was significantly associated with increased odds of any allergic disease (adjusted odds ratio, 2.04; 95% confidence interval, 1.01–4.11, P = 0.046). Dehydroepiandrosterone sulfate level showed a significant association with number of allergic diseases.
Conclusions
The current study findings suggest that sex hormones may play an important role in the development of allergic diseases in prepubertal children.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
DHEA-S
Dehydroepiandrosterone sulfate
FSH
Follicle-stimulating hormone
JECS
Japan Environment and Children’s Study
Background
Several longitudinal studies have reported sex differences in allergic diseases [1‐5]. Before puberty, boys are more likely to be diagnosed with allergic disease and sensitization and are more likely to use medications for allergic diseases compared to girls [1, 2]. A shift in sex distribution of allergic disease prevalence is observed after puberty, and allergic diseases become more common and severe or more treatment-resistant in females than in males [3]. Specifically, numerous epidemiologic studies have reported sex-specific differences in asthma [1, 2]. The Prevention and Incidence of Asthma and Mite Allergy study reported that the cumulative incidence of parent-reported asthma was higher in boys than in girls (15.1% vs. 10.8%) at 8 years of age [3]. The TRacking Adolescents’ Individual Lives Survey study reported that the prevalence of asthma was similar between boys and girls (7.7% and 7.4%, respectively) at a mean age of 11.1 years and that the prevalence of asthma was significantly higher in females than in males (6.2% vs. 4.3%) at 16.3 years of age [4]. These studies indicate that sex differences in allergic diseases begin early in childhood, with a shift in prevalence occurring in puberty.
These sex disparities suggest that sex steroids might play a role in allergic diseases. A recent systematic review and meta-analysis of 57 studies on asthma, including 51 observational and 6 experimental studies, reported that more estrogenic state such as, menstruation, menopause onset, and hormonal replacement therapy, in females were associated with the increased risk of current and new-onset asthma [5]. Specific mechanism underlying the impact of sex hormones on allergic diseases in children is unclear.
Anzeige
The aim of the present study was to examine the association of sex steroid hormones with allergic diseases in Japanese children.
Methods
Study design and population
The present study included 6-year-old children participating in a pilot birth cohort study in the Japan Environment and Children’s Study (JECS) cohort, which collected data from the questionnaires and blood tests of children at multiple time points during the study [6]. A total of 453 pregnant women from the general population in Japan were recruited for the JECS Pilot Study between February 1, 2009 to March 31, 2010. The JECS Pilot Study included the following four research centers: Jichi Medical University (Tochigi Prefecture), University of Kyusyu (Fukuoka Prefecture), University of Occupational and Environmental Health (Fukuoka Prefecture), and University of Kumamoto (Kumamoto Prefecture). All pregnant women received informed consent, 436 of the 453 pregnant women participated in the JECS Pilot Study, and 440 children were born. As of 2022, the pediatric participants of the ongoing JECS Pilot Study were being continually followed for 12 years. The present study included only the participants who had not received any systemic steroids within 1 month before the blood tests (Fig. 1).
×
This cross-sectional study evaluated the relationship between sex hormone and allergic diseases at 6 years. The variables used for fitting model were extracted from the questionnaire and medical examination results mentioned above.
Ethics statement
The JECS Pilot Study was approved by the Institutional Review Board on Epidemiological Studies of the Ministry of the Environment and by the ethics committees of all participating institutions. The JECS Pilot Study was conducted in accordance with the Declaration of Helsinki and other national and international regulations and guidelines. The present study protocol was reviewed and approved by each regional research centers. Informed consent was obtained by all participants’ parents.
Anzeige
Outcomes variables: allergic disease and allergen-specific IgE titers
Allergic disease
Data on allergic diseases (no/yes) were obtained from the questionnaire administered to the caregivers at the time of medical evaluation of children at 6 years of age. Current asthma and Food allergy (FA) were defined as the presence of doctor diagnosed asthma or FA in the past 12 months, and rhinitis was defined as sneezing or runny/congested nose accompanied by itching in the absence of cold or flu in the past 12 months. Atopic dermatitis (AD) was defined based on the U.K. Working Party definition of AD in children, which was diagnosed by a doctor or medical stuff who took a course in a skin observational training session.
The definition of “any allergic disease” was the presence of at least one of the condition, such as current asthma, current rhinitis, AD, or food allergy. For the participants who answered all of the questions about whether they had any of the four allergic disorders, we have also defined the variable “number of allergic diseases” regrouped as 3 levels (0, 1 and ≥ 2).
Allergen-specific IgE titers
Allergen-specific IgE titers in serum samples of the participating children at 6 years of age were measured using the densely carboxylated protein microarray (AMERIC, Tokushima, Japan) and were reported as binding unit of IgE (BUe)/mL [7, 8]. Allergen-specific IgE titers were measured for 19 aeroallergen including house dust mite, Dermatophagoides farinae, [Der f 1], Dermatophagoides pteronyssinus, [Der p 1], dog dander, cat dander, the fungi Ascomycota, Alternaria alternata: [Alt a 1], Aspergillus fumigatus: [Asp f 1], and Cladosporium herbarum: [Cla h 8], Japanese cedar, Cryptomeria japonica: [Cry j 1], Japanese cypress, birch, alder, timothy grass, sweet vernal grass, orchard grass, and ragweed. The reported limit of aeroallergen-specific IgE was 0.01 BUe/mL for all aeroallergens tested in the current study [7, 9].
Exposure variables: measurement of sex steroid hormones in serum
In the present study, serum concentrations of total testosterone, estradiol, dehydroepiandrosterone sulfate (DHEA-S), luteinizing hormone (LH), and follicle-stimulating hormone (FSH) were measured in children at 6 years of age. Serum samples were analyzed by an independent clinical contract laboratory.
Other confounders
The body fat of the participating children at 6 years of age were measured by multi frequency segmental body composition analyzer (MC-780, TANITA, Japan), which calculates muscle mass, body water content, and body fat content at the JECS Pilot Study four research centers at the same day of blood tests. Sex, parental history of allergic disease, and exposure to tobacco smoking at 6 years of age were obtained from questionnaires.
Statistical analysis
The Mann–Whitney U test was used to compare continuous variables, and the χ2 test was used to compare categorical variables. Logistic regression analysis was used to evaluate the association of sex steroid hormones with allergic diseases. Covariates adjusted in the models included sex, amount of body fat at 6 years of age, parental history of allergic disease, and exposure to tobacco smoking at 6 years of age. We utilized ordinal logistic regression to build the models for analyzing the relationship between the “number of allergic diseases” and “sex steroid hormones” because the “number of allergic diseases” was an ordinal variable. We also assessed the association of sex steroid hormones with total IgE titers, and some allergens that showed sex differences in distribution. “Total IgE titers” was reclassified as low (< 110 BUe/mL) and high (≥ 110 BUe/mL) levels, and allergen-specific IgE titers were regrouped as low (< 0.01 BUe/mL) and high levels (≥ 0.01 BUe/mL) according to data distribution [10].
As a sensitivity analysis, we also employed the multiple imputations by chained equations (MICE) method to deal with the missing value. The pooled adjusted OR values were estimated using 50 imputed datasets.
The R statistical software version 4.2.3 (Institute for Statistics and Mathematics, Vienna, Austria; www.r-project.org) was used for all statistical analyses, and statistical significance was set at a P value of < 0.05.
Results
Basic characteristics
The present study included 145 eligible children among a total of 440 children who participated in the JECS Pilot Study (Fig. 1 and Table 1). The study cohort included 74 (51.0%) boys, and the median age was 6.1 (interquartile range [IQR], 6.0–6.1) years. In the entire cohort, 65 (44.8%) had a family history of allergic diseases, 53 (36.6%) children were exposed to secondhand smoke. In the entire cohort, 82 (56.6%) children, including 39 (52.7%) boys and 43 (60.0%) girls, had any allergic diseases (Table E1).
Table 1
Features of children in the study
Numbera
Sex, boy, n (%)
145
74 (51.0%)
Age, years, median (first quartile–third quartile)
145
6.1 (6.0–6.1)
Parental allergic history
145
65 (44.8%)
Exposure to tobacco smoking at 6 years of age, n (%)
145
46 (31.7%)
Body fat at 6 years of age, median (kg) (first quartile–third quartile)
139
2.8 (2.0–3.5)
Body fat in boys, median (kg) (first quartile–third quartile)
70
2.7 (2.0–3.6)
Body fat in girls, median (kg) (first quartile–third quartile)
69
2.8 (2.1–3.5)
aNumber of children without missing values
Sex hormones in serum by gender are presented in Fig. E1. Estradiol and FSH were significantly higher in girls compared to those in boys. The proportion of boy with LH above 0.1 was higher than that in girls. Sex hormones in serum by any allergic diseases are presented in Fig. E2. FSH showed a slight increase in the group of children with allergic diseases.
Figure E3 shows the total and aeroallergen-specific IgE levels. The levels of IgE specific for Dermatophagoides farina, Japanese cedar, Cry j 1, and Japanese cypress were significantly higher in boys than in girls.
Anzeige
Association between sex hormones in serum and allergic diseases
Table 2 shows the serum sex hormones levels by allergic disease and the ORs from logistic models. After adjusted sex, amount of body fat at 6 years, parental history of allergic disease, and exposure to tobacco smoke, the DHEA-S level was significantly associated with lower odds of any allergic disease (aOR, 0.58; 95%CI, 0.36–0.93; P = 0.024) and serum FSH level was significantly associated with higher odds of any allergic disease (aOR 2.04; 95%CI, 1.01–4.11; P = 0.046).
Table 2
Association between sex hormones in serum and allergic diseases with complete dataset
aThe exposure variable in the model was log-transformed
bAll models were adjusted for sex, body fat at age 6, parental history of allergy illness, and smoking exposure
DHEA-S level indicated a significant association with “number of allergic disorders” when the outcome variable was modified to “number of allergic diseases.” The possibility of developing allergy disorders (one or more vs. none) lowers by 44% for every unit increase in log DHEA-S level after adjusting confounders (Table 3).
Table 3
Association between sex hormones in serum and number of allergic diseases with the complete dataset
aThe number of allergic diseases was the model’s outcome event and ordinal logistic regression models were constructed. All models were adjusted for sex, body fat at age 6, parental history of allergy illness, and smoking exposure
bThe exposure variable in the model was log-transformed
Association between sex hormones in serum and aeroallergen-specific IgE levels
Table 4 represents the relationship between serum sex hormones and IgE levels. Elevated FSH were substantially associated with total IgE titers. High levels of DHEA-S (aOR 0.45, 95%CI: 0.24–0.82) and testosterone (aOR 0.34, 95%CI: 0.15–0.76) were associated with low levels of Japanese cedar IgE.
Table 4
Association of sex hormones in serum with total and allergen-specific IgE titers
aOutcome variable in the models was reclassified as a dichotomous variable (high level was outcome event), and logistic regression models were fitted. All models were adjusted for sex, body fat at age 6, parental history of allergy illness, and smoking exposure
bThe exposure variable in the model was log-transformed
Sensitive analysis
The pooled aORs from the multiple imputation approach (Table E2) matched those from the full dataset (Tables 2 and 3). High DHEA-S levels were associated with a decreased risk of allergy disorders after controlling for covariates (aOR: 0.62; 95%CI: 0.39–0.98 in the logistic regression model and 0.61 (0.40–0.92) in the ordinal logistic regression models).
Anzeige
Discussion
In the present study, which included 145 six-year-old Japanese children participating in the JECS Pilot Study, we found that higher serum DHEA-S level was significantly associated with decreased odds of any allergic disease Furthermore, DHEA-S level showed a significant association with number of allergic diseases. We discovered an association between high DHEA-S and testosterone levels and reduced IgE levels in Japanese cedar. To our knowledge, this is the first study to examine the relationship between Japanese children’s levels of sex-steroid hormones and allergic diseases.
In DHEA-S, there are several reports suggesting association with prevalence of the allergic disease. A cross-sectional study of children examining the association of sex steroid hormones with asthma, including 45 boys and 23 girls between the ages of 6 and 18 years reported that serum DHEA-S levels were negatively associated with asthma symptoms and were positively associated with forced expiratory volume in one second and forced vital capacity in boys. Conversely, serum estradiol levels were negatively associated with forced expiratory volume in one second and forced vital capacity in girls [11]. Another study found that serum levels of DHEA and testosterone were lower in male patients with AD compared to the reference group of males [12]. Lower serum levels of DHEA and DHEA-S irrespective of sex were also reported in patients with asthma or chronic spontaneous urticaria compared to the reference group [13]. The results of this study on serum DHEA-S levels agree with previous studies examining the association of sex steroid hormones with allergic diseases.
Sex hormone association with immune responses, such as IgE production and related allergic reactions, were reported in animal models. In mice, the levels of immunoglobulins, including IgM, IgG1, IgG2, and IgE, were higher in female than male. Moreover, estrogen inhibitor injection to the female mice have reduced the levels of allergen-specific IgG1, IgG2a, and IgE levels and attenuate clinical allergic disease symptoms [14]. Another report revealed that estrogen treatment in male mice has been shown to upregulate immunoglobulin levels and to induce antigen-specific antibody-producing cells [15, 16]. DHEA and testosterone are also known to have a significant relationship with allergic inflammation. In comparison to control male mice, eosinophil and lymphocyte infiltration caused by OVA, as well as the production of the IL-13 protein increased significantly in castrated male mice due to the reduction of testosterone. Additionally, when DHEA was injected into castrated male mice, the allergic airway inflammation of the mice was reduced in comparison to the control mice [17]. Furthermore, mice sensitized on house dust mite treated with DHEA had lower serum levels of eosinophils, IL-5, IL-4, and IFN-g but no change in serum IgE concentrations, compared to mice sensitized on house dust mite without DHEA treatment [17]. These reports indicate that estrogen may increase type 2 T helper cell (Th2)-mediated allergic inflammation and DHEA and testosterone may decrease the Th2-mediated allergic inflammation. Therefore, we think sex hormones, such as estrogen, testosterone, and DHEA-S, were important in regulating type 2 inflammation and many pathways are affected by ovarian hormone and/or testosterone signaling. Several studies in animal models have reported that allergen-induced, Th2-mediated allergic inflammation is promoted by estrogen signaling and attenuated by androgen signaling [18‐20]. Sex hormones could be involved in the regulation of the immune response, and this study adds evidence to this speculation. However, further confirmation is required by carrying out studies with a large sample size.
We also found that FSH was associated with higher odds of any allergic disease. Intriguingly, a study reported that the baseline FSH levels were higher in patients with premenstrual exacerbation of asthma than patients without exacerbation [21]. Although studies examining the association of FSH with allergic diseases are limited, it is possible that FSH might indirectly contribute to the increased prevalence of allergic diseases by upregulating the levels of hormones such as estrogen and progesterone, thereby enhancing Th2-mediated allergic inflammation.
Anzeige
Our study has several limitations. First, due to a relatively long time since the allergic sickness, parents may purposefully or inadvertently underreport allergic diseases in their children on the questionnaire. Second, the JECS cohort study measures sex hormone levels in participants aged 6 years or older, and the temporal relationships were not evaluated as data on older children were not yet available in the ongoing study. Third, the sample size might be small to evaluate the significant association between allergic diseases and sex. The ongoing JECS cohort will continue following the children included in the current study to examine the association between sex steroid hormones and allergic diseases.
Conclusions
Our findings suggest that sex hormones might play an important role in development of allergic diseases observed before puberty. Further studies are needed to elucidate the regulatory roles of sex hormones in allergy development, the mechanisms underlying inflammatory responses in allergic diseases, and the regulation of systematic inflammation for the development of hormonal therapeutic approaches in allergic diseases. The ongoing JECS cohort will continue following these children to examine changes in the association between sex steroid hormones and allergic diseases.
Acknowledgements
We would like to thank the children and their families participating in the Japan Environment and Children’s Study.
Declarations
Ethics approval and consent to participate
The JECS Pilot Study was approved by the Institutional Review Board on Epidemiological Studies of the Ministry of the Environment and by the ethics committees of all participating institutions. The JECS Pilot Study was conducted in accordance with the Declaration of Helsinki and other national and international regulations and guidelines. The present study protocol was reviewed and approved by each regional research centers. Informed consent was obtained by all participants’ caregivers.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Sex steroid hormones and allergic diseases in children: a pilot birth cohort study in the Japan Environment and Children’s Study cohort
verfasst von
Yumiko Miyaji Kiwako Yamamoto-Hanada Limin Yang Mayako Saito-Abe Miori Sato Hidetoshi Mezawa Minaho Nishizato Masayuki Ochiai Shouichi Ohga Masako Oda Hiroshi Mitsubuchi Masayuki Shimono Reiko Suga Nathan Mise Makiko Sekiyama Shoji F. Nakayama Yukihiro Ohya the Japan Environment and Children’s Study (JECS)
Erwachsene, die Medikamente gegen das Aufmerksamkeitsdefizit-Hyperaktivitätssyndrom einnehmen, laufen offenbar erhöhte Gefahr, an Herzschwäche zu erkranken oder einen Schlaganfall zu erleiden. Es scheint eine Dosis-Wirkungs-Beziehung zu bestehen.
Manifestiert sich ein Typ-1-Diabetes bei Kindern, ist das ein Notfall – ebenso wie eine diabetische Ketoazidose. Die Grundsäulen der Therapie bestehen aus Rehydratation, Insulin und Kaliumgabe. Insulin ist das Medikament der Wahl zur Behandlung der Ketoazidose.
Wie wichtig es ist, pädiatrische Patienten auf Bluthochdruck zu screenen, zeigt eine kanadische Studie: Hypertone Druckwerte in Kindheit und Jugend steigern das Risiko für spätere kardiovaskuläre Komplikationen.
Die große Mehrheit der vermeintlichen Penicillinallergien sind keine. Da das „Etikett“ Betalaktam-Allergie oft schon in der Kindheit erworben wird, kann ein frühzeitiges Delabeling lebenslange Vorteile bringen. Ein Team von Pädiaterinnen und Pädiatern aus Kanada stellt vor, wie sie dabei vorgehen.
Update Pädiatrie
Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.