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Childhood atopic disorders in relation to placental changes-A systematic review and meta-analysis
Zaki Bakoyan1, Yang Cao2,3, Stefan R Hansson4
1School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Insights
The placenta may influence a child's risk of developing atopic disorders. Placental changes like inflammation and size are linked to childhood asthma and other atopic conditions.
Area of Science:
- Reproductive Biology
- Pediatric Allergy
- Developmental Origins of Health and Disease
Background:
- Fetal programming suggests prenatal exposures can increase later-life disease risk, with the placenta as a potential mediator.
- Atopic disorders, such as asthma and eczema, are significant childhood health concerns with complex etiologies.
Purpose of the Study:
- To systematically review and critically evaluate human placental changes associated with childhood atopic disorder risk.
- To synthesize evidence on the placenta's role in mediating fetal programming for atopic diseases.
Main Methods:
- Systematic review and meta-analysis following PRISMA guidelines.
- Searched MEDLINE and EMBASE databases for English-language studies.
- Assessed risk of bias using the ROBINS-I tool.
Main Results:
- Nineteen studies (n=12,997) were included, all with serious risk of bias.
- Histological chorioamnionitis in preterm infants correlated with asthma (OR=3.25).
- Large placentas (≥750g) in term infants were linked to increased asthma medication prescriptions.
Conclusions:
- Evidence suggests the placenta mediates increased risk for childhood atopic disorders.
- Further research is crucial to validate findings, control confounders, and elucidate mechanisms.
Abstract:
Fetal programming may arise from prenatal exposure and increase the risk of diseases later in life, potentially mediated by the placenta. The objective of this systematic review was to summarize and critically evaluate publications describing associations between human placental changes and risk of atopic disorders during childhood. The review adhered to the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines. The inclusion criteria were original research articles or case reports written in English describing a human placental change in relation to disease occurring in offspring during childhood. The MEDLINE and EMBASE databases were searched for eligible studies. Risk of bias (RoB) was assessed using the ROBINS-I tool. The results were pooled both in a narrative way and by a meta-analysis. Nineteen studies were included (n = 12,997 participants). All studies had an overall serious RoB, and publication bias could not be completely ruled out. However, five studies showed that histological chorioamnionitis in preterm-born children was associated with asthma-related problems (pooled odds ratio = 3.25 (95% confidence interval = 2.22-4.75)). In term-born children, a large placenta (≥750 g) increased the risk of being prescribed anti-asthma medications during the first year of life. Placental histone acetylation, DNA methylation, and gene expression differences were found to be associated with different atopic disorders in term-born children. There is some evidence supporting the idea that the placenta can mediate an increased risk of atopic disorders in children. However, further studies are needed to validate the findings, properly control for confounders, and examine potential mechanisms.
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