医学
孟德尔随机化
哮喘
优势比
荟萃分析
危险系数
内科学
置信区间
单核苷酸多态性
出版偏见
全基因组关联研究
1型糖尿病
糖尿病
遗传学
内分泌学
基因型
遗传变异
基因
生物
作者
Junyang Xie,Gui Chen,Tianhao Liang,Ang Li,Weixing Liu,Sheng Wang,Xiaofen Wang,Xiaoxuan Kuang,DeMin Han,Wenjing Liao,Lijuan Song,Xiaowen Zhang
摘要
Abstract 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.
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