Abstract
The association between maternal occupational exposure during pregnancy and the subsequent development of asthma in their children has always been a matter of debate, and the results of cohort studies on this issue have been controversial. The current study is the first systematic review and meta-analysis aimed at evaluating the risk of developing subsequent asthma in children based on maternal occupational exposure during the gestation period. To retrieve eligible studies, an advanced literature search was performed up to August 10, 2023 from the following databases: PubMed, Scopus, and Google Scholars. The title and abstract of related articles were screened; hence, the full texts were reviewed. Data extraction was conducted; hence, the included articles were analyzed to assess the mention association. From a total of 10 cohort studies with a total record of 5372, it was found that there is no significant relationship between occupational exposure to asthmogenic during pregnancy and later asthma in children. The pooled odds ratio of asthmatic children in patients with maternal occupational exposure to asthmogenic during pregnancy was 1.03 (95% confidence interval, 0.97-1.09) I2= 13% p=0.62. It was concluded that there is no significant association between maternal occupational exposure and future asthma in children. However, future large-scale studies are required to support these results.
PRECIS: Investigating maternal occupational exposure during pregnancy and childhood asthma risk, our meta-analysis found no significant association, suggesting further research is needed for conclusive evidence.
Introduction
As stated by the World Health Organization, non-communicable diseases (NCD) claim the lives of 41 million individuals annually, accounting for 74% of global mortality(1). Asthma, a prevalent NCD, imposes a substantial burden of morbidity and mortality. It is projected to impact almost 262 million individuals in 2019, resulting in 455,000 fatalities worldwide. Furthermore, it is the primary chronic disease among children on a global scale(2). There are over 300 million people worldwide who are affected by asthma, and each day 1,000 people die because of asthma(3, 4). Moreover, young adults with asthma are 20 times more prone to develop chronic obstructive pulmonary disease(5).
The apparent epidemic of asthma and allergies recently seems to follow in the footsteps of economic development, the process of production, consumption, and urbanization(6). Numerous studies have shed light on the connection between being exposed to various domestic and industrial ambient pollutants and experiencing bronchial wheezing(7). Occupational exposures are responsible for 5-25% of all asthma cases among adult workers(8-10) by inducing the mechanism of immunoglobulin E (IgE)-mediated responses(11). Promisingly, this number can be prevented if occupational exposures are obviated(12).
Potential risk factors have been identified for predisposing children to para-occupational asthma via their parents, such as stress(13), secondhand tobacco smoking(14), asbestos, pesticides, organic solvents, and mold(15-18). Organic solvents are volatile lipophilic compounds that can cross the placenta(19) and lead to a shift in the balance between (Th1) and (Th2) in offspring’s umbilical cord blood(20). They appear to play a key role in the development of childhood asthma(21). Studies indicate that persistent maternal exposure to organic pollutants, including organochlorine pesticides and polychlorinated biphenyls (PCB), is linked to a higher likelihood of respiratory symptoms and asthma in infants(22).
Several studies have shown that certain parenting occupations are linked with a higher risk of respiratory conditions in children(23-25). In contrast, Christensen et al.(23) reported no notable link between maternal job exposure and childhood asthma. For the first time, this study represents a systematic review/meta-analysis focusing on assessing the likelihood of children developing asthma later due to maternal occupational exposure during pregnancy.
Materials and Methods
In this meta-analysis, our objective was to investigate the influence of maternal occupational exposure to cosmogenic agents during pregnancy on the subsequent occurrence of asthma in their offspring. Our methodology adheres to the Preferred Reporting Items for Systematic Reviews and Meta-analyses(26) guidelines. The research protocol for this review has been registered on the Open Science Framework.
Literature Search
To retrieve eligible studies,an advanced literature search was performed up to August 10, 2023 from the following databases:Pubmed,Scopus,and Google scholar. The search strategy included three main keywords. One subgroup encompassed terms associated with pregnancy, whereas the other two subgroups encompassed terms related to asthma and occupational exposures. The subgroups were linked together using the “AND” operator, with no limitations on date, publication type, or language. The search strategy was modified on the basis of the query format for each database. Our search strategy methodology is summarized in Table 1. To minimize the risk of missing relevant articles, we investigated the reference lists of relevant systematic reviews and included studies that were assessable in our analysis. The procedure was performed by two reviewers, with any discrepancies being resolved through discussion between the reviewers.
Criteria for Selecting Studies
To be eligible for inclusion in this meta-analysis, studies must adhere to the following criteria:
1. The studies involved pregnant women and their children, with a focus on maternal occupational exposure during pregnancy and its potential impact on childhood asthma.
2. Studies should have evaluated maternal occupational exposure to asthmogenic or related environmental agents at work during pregnancy
3. The primary outcome of this study was the development of asthma or wheezing in children, which was typically investigated at several follow-up points throughout childhood.
4. Definitions of asthma were provided based on the study design
Studies including pregnant women with preexisting pathologic conditions or those focused on outcomes unrelated to asthma were excluded. In addition, case reports, review articles, papers in languages other than English, and animal studies were excluded from the review.
Data Extraction and Study Quality Assessment
Two independent reviewers conducted an initial assessment of each study’s title and abstract to assess whether it met the inclusion criteria for this meta-analysis. Articules that did not meet our predetermined criteria were excluded. Subsequently, the full texts of the remaining studies were further evaluated, and those meeting the eligibility criteria were included in the data extraction process. Next, data extraction was conducted in four distinct categories, comprising the following information:
1. Study Details (i.e. authors, location, year of publication, and study type)
2. Patient-Specific Factors (i.e. eligibility criteria for women included in the study and gestational age)
3. Study Design (i.e. the number of participants, sampling method and duration, and the definition of asthma)
4. Outcomes (i.e. the asthma rate and concentrations of exposures).
The two reviewers mentioned earlier used critical appraisal checklists specifically created for cohort, case-control, and analytical cross-sectional studies, as outlined by the Joanna Briggs Institute. If there were any discrepancies, a third author was involved in the assessment.
Statistical Analysis
We performed data analysis using STATA 13.1 software developed by StataCorp LP in College Station, TX. The outcomes are displayed as combined odd ratios (ORs) with a 95% confidence interval (CI), illustrated in a forest plot. The presence of heterogeneity among the qualified studies was evaluated using the I2 statistic, and in cases of significant heterogeneity (I2 >50%), a random-effects model was employed. In addition, we investigated the potential for publication bias by visually examining funnel plot symmetry and conducting Egger’s regression analysis.
Result
Study Selection and Characteristics
The search yielded 5372 records. The screening of titles and abstracts resulted in 50 potentially eligible studies. After reviewing the final full texts, nine studies and 121.710 patients remained as our final result, in which maternal occupational exposure to asthmogenic was measured and met the inclusion criteria (Figure 1). The studies included in this analysis were published from 2006 to 2021 and were conducted in Denmark, the USA, Canada, and the United Kingdom. All studies were cohort studies with varying follow-up durations ranging from 12 to 84 months. The mean age of the patients ranged from 5 to 30 years. The follow-up duration of the cohort studies varied from 4 to 7 years. The details of these studies can be found in Table 2.
The analysis results suggest no statistically significant association between maternal occupational exposure to asthmogenic during pregnancy and the development of asthma in children.
Meta-analysis
The combined odds ratio for asthmatic children in patients with maternal occupational exposure to asthmogenic during pregnancy was 1.03 (95% CI, 0.97-1.09). The meta-analysis showed moderate statistical heterogeneity with an I2 of 13%. Figure 2 illustrates the forest plot of the meta-analysis. Sensitivity analyses did not yield significantly different results from the overall analysis.
Publication Bias
Examination of the funnel plot (Figure 3) did not reveal any indication of publication bias because the graph appeared relatively symmetrical. Furthermore, Egger’s regression test did not show evidence of publication bias (p=0.62).
Discussion
This meta-analysis of nine cohort studies explored the association between maternal occupational exposure to asthmogenic during pregnancy and the risk of asthma in children. These findings did not provide significant evidence of a connection between maternal occupational exposure to asthmogenic during pregnancy and the risk of asthma in children.
Jøhnk et al.(27) did not find a correlation between prenatal exposure to phthalates and asthma in children. This could be attributed to the lower maternal exposure levels. In addition, the older age of the mothers in the study and their non-smoking status could be contributing factors to the lower prevalence of asthma (7.4%) in these children.
Christensen et al.(28) found a positive borderline association between maternal occupational exposure to low molecular weight/irritant agents OR = 1.11, 95% CI = (1.01,1.23)] and heavy molecular weight allergens [OR = 1.12, 95% CI = (0.85,1.47)] and asthma in their children.
Christensen et al.(23) found no association between mothers’ occupational exposures during pregnancy and asthma in their 7-year-old children. Exposure to low molecular weight agents during the postnatal period [OR = 1.13, 95% CI = (0.99, 1.29)] or a combination of prenatal and postnatal exposure [OR = 1.34, 95% CI = (1.19, 1.51)] was linked to a higher prevalence of asthma in children(23).
Magnusson et al.(16) found little association between occupational exposure of mothers to organic solvents and asthma in children.
Allergens with high molecular weight can contribute to the development of asthma through immune mechanisms mediated by IgE. In contrast, allergens with low weight, in addition to the above mechanism, may exert a role in asthma development through immunological reactions without IgE or even non-immunological reactions(16). Sensitivity to allergens can occur in the uterus without the mother’s sensitivity(29).
Pape et al.(30) found a correlation between maternal exposure to allergens and reactive chemicals before and after pregnancy and the development of early-onset asthma in children. Interestingly, no such association was found in men, specifically in relation to their occupational exposures. One possible explanation for this difference could be the increased vulnerability of women’s reproductive cells compared with men’s.
Another study by Tjalvin et al.(31) demonstrated that Occupational exposure of mothers to indoor cleaning products before and during pregnancy was linked to a higher likelihood of asthma in children [OR = 1.56, 95% CI = (1.05-2.31)]. At the same time, exposure after birth was unrelated to asthma outcomes [OR =1.13, 95% CI = (0.71, 1.80)].
A strong link between occupational exposure to PCBs and childhood asthma was reported [OR = 3.24, 95% CI = (1.30, 8.09)] in the study by Parker-Lalomio et al.(32).
Tagiyeva et al.(24) research revealed that exposure to latex and biocides/fungicides in the workplace during pregnancy can increase the chances of childhood wheezing and asthma. The likelihood of childhood wheezing and asthma is further amplified when there are elevated levels of exposure to latex, biocide/fungicide, or a combination of both, with odds ratios of 1.26, 1.22, and 1.22 [95% CI = (1.07, 1.50), (1.02, 2.05), and (1.03, 1.43)], respectively.
Children’s asthma was confirmed in two ways: diagnosis by a doctor or by reporting children’s wheezing episodes by parents. Inaccurate recall of wheezing episodes and differences in access to medical care could bias the results. In addition, some studies did not have access to the family history of allergic diseases. In addition, due to the possibility of mothers suffering from allergic diseases avoiding certain specific occupations, it can lead to incorrect occurrence of negative results.
Conclusion
The current meta-analysis did not reveal any statistically significant association between maternal occupational exposure during pregnancy and the likelihood of asthma in children. Additional cohort and cross-sectional studies are necessary to determine the precise relationship between exposure and asthmogenic during pregnancy and asthma risk in children.
