Abstract
Summary
Both COA and AOA have a genetically causal effect on osteoporosis. COA and AOA were independently associated with incident osteoporosis, and the risk was greatly higher in AOA. Besides corticosteroids, the increased risk of osteoporosis among asthma patients should be attributed to genetic susceptibility and other asthma medications.
Purpose/Introduction
Childhood-onset asthma (COA) differs with adult-onset asthma (AOA) on genetic susceptibility, severity, and co-morbidities. Whether COA or AOA is independently associated with osteoporosis is unexplored. We aimed to determine the effects of COA and AOA on osteoporosis at genetic and individual level.
Methods
We used two-sample Mendelian randomization analysis to explore the causal effects of COA and AOA on osteoporosis. In the UK Biobank cohort, we included 478,289 osteoporosis-free participants at baseline (2006–2010). Participants were classified as non-asthma, COA, and AOA at recruitment. Multivariate Cox regression analysis was used to evaluate the effects of COA, AOA, and multiple asthma medications on incident osteoporosis risk.
Results
COA and AOA were causally related to osteoporosis, with odds ratio of 1.007 (95% confidence interval (CI), 1.0003–1.0132) and 1.012 (95% CI, 1.002–1.023), respectively. Multivariate Cox regression analysis suggested that COA (hazard ratio (HR), 1.46; 95% CI, 1.32–1.61) and AOA (HR, 1.70; 95% CI, 1.61–1.80) were independently associated with incident osteoporosis, and the risk was greatly higher in AOA (HR, 1.51; 95% CI, 1.34–1.70). In addition to corticosteroids, monotherapy with leukotriene modifiers (HR, 1.70; 95% CI, 1.20–2.42), long-acting beta agonists (HR, 1.49; 95% CI, 1.18–1.87), and short-acting beta agonists (HR, 1.72; 95% CI1.01–2.93) were independently associated with a higher risk of osteoporosis.
Conclusions
Both COA and AOA have a genetically causal effect on osteoporosis, and the risk of osteoporosis is greatly higher in AOA. Besides corticosteroids, the increased risk of osteoporosis among asthma patients should be attributed to genetic susceptibility and other asthma medications.
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Data availability
The underlying data are accessed from the UK Biobank Resource under the application ID 81888, and materials and methods will be made freely available through the UK Biobank as part of this project.
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Acknowledgements
We thank the participants in the UK Biobank for their participation in the research. The study was conducted using the UK Biobank Resource (Application ID: 81888).
Funding
The National Natural Science Foundation of China (No. 82072500, 82002354).
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Weizhong Ding, Yong Huang, Guanghui Li, Yimin Dong, Xiaochen Li, Minglong Wu, Kehan Song, and Feng Li declare that they have no conflict of interest.
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Ding, W., Huang, Y., Li, G. et al. Higher risk of osteoporosis in adult-onset asthma than childhood-onset asthma: from genetic and prospective evidence. Osteoporos Int 35, 659–668 (2024). https://doi.org/10.1007/s00198-023-07004-1
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DOI: https://doi.org/10.1007/s00198-023-07004-1