Childhood asthma and type 1 diabetes mellitus: A meta‐analysis and bidirectional Mendelian randomization study

Background Worldwide incidence and prevalence of both asthma and type 1 diabetes mellitus (T1DM) in children have been increasing in past decades. Association between the two diseases has been found in some but not in other studies. Objective We conducted a meta‐analysis to verify such an associatio...

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Veröffentlicht in:Pediatric allergy and immunology 2022-09, Vol.33 (9), p.e13858-n/a
Hauptverfasser: Xie, Junyang, Chen, Gui, Liang, Tianhao, Li, Ang, Liu, Weixing, Wang, Yiyan, Wang, Xiaofen, Kuang, Xiaoxuan, Han, DeMin, Liao, Wenjing, Song, Lijuan, Zhang, Xiaowen
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Sprache:eng
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Zusammenfassung:Background Worldwide incidence and prevalence of both asthma and type 1 diabetes mellitus (T1DM) in children have been increasing in past decades. Association between the two diseases has been found in some but not in other studies. Objective We conducted a meta‐analysis to verify such an association, and bidirectional Mendelian randomization analysis to examine the potential cause‐effect relationships. Methods Three databases (PubMed, Embase, and Web of Science) were searched from their inception to February 1, 2021. Pooled hazard ratios (HR) or odds ratios (OR), and 95% confidence intervals, were calculated. Associations between single‐nucleotide polymorphisms with childhood asthma and T1DM were selected based on genome‐wide association studies. The outcome datasets were obtained from FinnGen study. We used the inverse‐variance‐weighted (IVW), weighted median and MR‐Egger methods to estimate causal effects. To assess robustness and horizontal pleiotropy, MR‐Egger regression and MR pleiotropy residual sum and outlier test were conducted. Results In meta‐analysis, childhood asthma was associated with an increased risk of T1DM (HR = 1.30, 95% CI 1.05–1.61, P = .014), whereas T1DM was not associated with the risk of asthma (HR = 0.98, 95% CI 0.64–1.51, P = .941; OR = 0.84, 95% CI 0.65–1.08, P = .168). MR analysis indicated increased genetic risk of T1DM in children with asthma (OR = 1.308; 95% CI 1.030–1.661; P = .028). Analysis using the IVW method indicated no association between T1DM and genetic risk of asthma (OR = 1.027, 95%CI 0.970–1.089, P = .358). Conclusion Both meta‐analysis and MR study suggested that childhood asthma was a risk factor for T1DM. No epidemiological or genetic evidence was found for an association of T1DM with asthma incidence. Further studies could be carried out to leverage this newfound insight into better clinical and experimental research in asthma and T1DM.
ISSN:0905-6157
1399-3038
DOI:10.1111/pai.13858