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Published on: August 25, 2020
Birth weight is not causally associated with adult asthma: results from instrumental variable analyses
Ping Zeng1, Xinghao Yu2, Xiang Zhou3,4
1Department of Epidemiology and Biostatistics, Xuzhou Medical University, Xuzhou, Jiangsu, 221004, China. zpstat@xzhmu.edu.cn.
Insights
Lower birth weight does not causally influence adult asthma risk. This study found no evidence that the association observed in childhood persists into adulthood, suggesting previous findings may be due to confounding factors.
Area of Science:
- Genetics
- Epidemiology
- Respiratory Medicine
Background:
- Lower birth weight is linked to childhood asthma.
- The persistence of this association into adulthood is not well understood.
Purpose of the Study:
- To investigate the causal relationship between birth weight and adult asthma risk.
- To determine if the fetal origins of disease hypothesis applies to adult asthma.
Main Methods:
- Mendelian randomization analysis utilizing genetic risk scores.
- Inverse-variance weighted method and iMAP for causal effect estimation.
- Sensitivity analyses including MR-PRESSO and MR-Egger regression.
Main Results:
- No significant causal effect of birth weight on adult asthma risk was detected (GRS: 1.00, IVW: 1.02).
- No nonlinear relationships or gender differences were observed.
- Sensitivity analyses confirmed the robustness of the findings, with no evidence of outliers or horizontal pleiotropy.
Conclusions:
- The study provides no evidence supporting a causal link between lower birth weight and adult asthma.
- The impact of birth weight on asthma does not appear to persist into adulthood.
- Previous associations may be influenced by unmeasured confounding factors.
Abstract:
The association between lower birth weight and childhood asthma is well established. However, it remains unclear whether the influence of lower birth weight on asthma can persist into adulthood. We conducted a Mendelian randomization analysis to assess the causal relationship of birth weight (~140,000 individuals) on the risk of adult asthma (~62,000 individuals). We estimated the causal effect of birth weight to be 1.00 (95% CI 0.98~1.03, p = 0.737) using the genetic risk score method. We did not observe nonlinear relationship or gender difference for the estimated causal effect. With the inverse-variance weighted method, the causal effect of birth weight on adult asthma was estimated to be 1.02 (95% CI 0.84~1.24, p = 0.813). Additionally, the iMAP method provides no additional genome-wide evidence supporting the causal effects of birth weight on adult asthma. Our results were robust against various sensitivity analyses, and MR-PRESSO and MR-Egger regression showed that no instrument outliers and no horizontal pleiotropy were likely to bias the results. Overall, our study provides no evidence for the fetal origins of diseases hypothesis for adult asthma, implying that the impact of birth weight on asthma in years of children and adolescents does not persist into adult and previous findings may be biased by confounders.
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