Exploring genetic association of insomnia with allergic disease and asthma: a bidirectional Mendelian randomization study.
Exploring genetic association of insomnia with allergic disease and asthma: a bidirectional Mendelian randomization study.
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探索失眠与过敏性疾病和哮喘的遗传关联:双向孟德尔随机研究
DOI:
10.1186/s12931-022-02009-6
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发表时间:
2022-04-07
影响因子:
5.8
通讯作者:
Li S
中科院分区:
文献类型:
--
作者:
Li R;Chen Y;Zhao A;Huang L;Long Z;Kang W;Yin Y;Tong S;Guo Y;Li S
Insomnia is highly prevalent among patients with allergic disease and asthma; however, few studies have investigated their causal relationship. We aim to explore the causal association between insomnia and allergic disease/asthma by performing bidirectional Mendelian randomization (MR) study. Instrumental variables were constructed using single nucleotide polymorphisms (SNPs). Summary statistics for insomnia, allergic disease, and asthma were obtained from four large-scale genome-wide association studies (GWAS) of European ancestry. The pleiotropy analysis was applied by using the MR-Egger intercept test and the MR pleiotropy residual sum and outlier (MR-PRESSO) test. MR analyses were conducted by using inverse variance weighted (IVW), weighted median, and MR-Egger method. Based on the multiplicative random effects IVW method, the MR analysis showed that genetically predicted insomnia was causally associated with an increased risk of allergic disease [odds ratio (OR) = 1.054, 95% confidence interval (CI) = 1.031–1.078, P = 3.817 × 10–06], asthma (OR = 1.043, 95% CI = 1.010–1.077, P = 9.811 × 10–03), moderate-severe asthma (OR = 1.168, 95% CI = 1.069–1.277, P = 6.234 × 10–04), and adult-onset asthma (OR = 1.086, 95% CI = 1.037–1.138, P = 4.922 × 10–04). In bidirectional analyses, we did not find evidence supporting the reverse causality relations. Our MR study suggested that genetically predicted insomnia was the risk factor for allergic disease and asthma. Improving sleep quality could be one of the cornerstones in the prevention of allergic disease and asthma. The online version contains supplementary material available at 10.1186/s12931-022-02009-6.
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影响因子:
7.7
作者:
Bowden J;Del Greco M F;Minelli C;Davey Smith G;Sheehan NA;Thompson JR
通讯作者:
Thompson JR
影响因子:
4.6
作者:
Kim DJ;Ha TW;Jung HU;Baek EJ;Lee WJ;Kim HK;Kang JO;Won S;Lim JE;Oh B
通讯作者:
Oh B
影响因子:
2.1
作者:
Bowden J;Davey Smith G;Haycock PC;Burgess S
通讯作者:
Burgess S
DOI:
10.1097/ede.0000000000000559
发表时间:
2017-01
期刊:
Epidemiology (Cambridge, Mass.)
影响因子:
--
作者:
Burgess S;Bowden J;Fall T;Ingelsson E;Thompson SG
通讯作者:
Thompson SG
影响因子:
14.2
作者:
Chang, Yung-Sen;Chiang, Bor-Luen
通讯作者:
Chiang, Bor-Luen