A systematic two-sample and bidirectional MR process highlights a unidirectional genetic causal effect of allergic diseases on COVID-19 infection/severity

被引:0
作者
Xiao-tong Chen
Shuai Zhi
Xin-yu Han
Jian-wei Jiang
Guang-ming Liu
Shi-tao Rao
机构
[1] Fujian Medical University,Department of Bioinformatics, Fujian Key Laboratory of Medical Bioinformatics, Institute of Precision Medicine, School of Medical Technology and Engineering
[2] Jimei University,Xiamen Key Laboratory of Marine Functional Food, College of Ocean Food and Biological Engineering, Fujian Provincial Engineering Technology Research Center of Marine Functional Food
[3] The Chinese University of Hong Kong,School of Biomedical Sciences
来源
Journal of Translational Medicine | / 22卷
关键词
Allergic diseases; Asthma; COVID-19 infection/severity; GWAS summary statistics; Mendelian randomization; Molecular mechanism; Immune-related cells; Hematological traits;
D O I
暂无
中图分类号
学科分类号
摘要
We performed a two-sample, bidirectional Mendelian randomization study for five types of allergic diseases with COVID-19 infection/severity (critically ill, hospitalized, and infection cases), and also further elucidated the potential underlying molecular mechanisms.Our MR analyses consistently suggest a unidirectional protective causal effect of asthma on COVID-19 infection/severity, but the reverse is not true.Food allergies such as shrimp allergy showed significant causal correlations with the risk of COVID-19 phenotypes.Allergic diseases may be causally correlated with COVID-19 infection/severity by inducing abnormal fluctuations of multiple immune-related cells and hematological traits in peripheral blood.The findings call for more attention to clinical monitoring of hematological traits and may be beneficial in developing effective therapeutic strategies for allergic patients following infection with COVID-19.
引用
收藏
相关论文
共 189 条
  • [31] Hasan SS(2022)Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis J Allergy Clin Immunol 149 745-1769
  • [32] Morais-Almeida M(2018)Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks Nat Genet 50 88-1184
  • [33] Barbosa MT(2009)Sequence variants in three loci influence monocyte counts and erythrocyte volume Am J Hum Genet 85 14357-834
  • [34] Sousa CS(2010)Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control Am J Hum Genet 86 1398-602
  • [35] Aguiar R(2017)Connecting genetic risk to disease end points through the human blood plasma proteome Nat Commun 8 559-776
  • [36] Bousquet J(2022)Genetic landscape of the ACE2 coronavirus receptor Circulation 145 1742-1769
  • [37] Song J(2007)PLINK: a tool set for whole-genome association and population-based linkage analyses Am J Hum Genet 81 1177-664
  • [38] Zeng M(2020)Statistical inference in two-sample summary-data Mendelian randomization using robust adjusted profile score Ann Statist 48 831-558
  • [39] Wang H(2017)Orienting the causal relationship between imprecisely measured traits using GWAS summary data PLoS Genet 13 2247-1913.e19
  • [40] Lighter J(2013)Efficient design for Mendelian randomization studies: subsample and 2-sample instrumental variable estimators Am J Epidemiol 178 581-646