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Systematic Mendelian randomization study of the effect of gut microbiome and plasma metabolome on severe COVID-19.
Yan, Han; Zhao, Si; Huang, Han-Xue; Xie, Pan; Cai, Xin-He; Qu, Yun-Dan; Zhang, Wei; Luo, Jian-Quan; Zhang, Longbo; Li, Xi.
Afiliação
  • Yan H; Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Zhao S; Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Huang HX; Institute of Clinical Pharmacology, Central South University, Changsha, Hunan, China.
  • Xie P; Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, Hunan, China.
  • Cai XH; Department of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Qu YD; Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Zhang W; Institute of Clinical Pharmacology, Central South University, Changsha, Hunan, China.
  • Luo JQ; Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, Hunan, China.
  • Zhang L; Department of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Li X; Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Front Immunol ; 14: 1211612, 2023.
Article em En | MEDLINE | ID: mdl-37662924
Background: COVID-19 could develop severe respiratory symptoms in certain infected patients, especially in the patients with immune disorders. Gut microbiome and plasma metabolome act important immunological modulators in the human body and could contribute to the immune responses impacting the progression of COVID-19. However, the causal relationship between specific intestinal bacteria, metabolites and severe COVID-19 remains not clear. Methods: Based on two-sample Mendelian randomization (MR) framework, the causal effects of 131 intestinal taxa and 452 plasma metabolites on severe COVID-19 were evaluated. Single nucleotide polymorphisms (SNPs) strongly associated with the abundance of intestinal taxa and the concentration of plasma metabolites had been utilized as the instrument variables to infer whether they were causal factors of severe COVID-19. In addition, mediation analysis was conducted to find the potential association between the taxon and metabolite, and further colocalization analysis had been performed to validate the causal relationships. Results: MR analysis identified 13 taxa and 53 metabolites, which were significantly associated with severe COVID-19 as causal factors. Mediation analysis revealed 11 mediated relationships. Myo-inositol, 2-stearoylglycerophosphocholine, and alpha-glutamyltyrosine, potentially contributed to the association of Howardella and Ruminiclostridium 6 with severe COVID-19, respectively. Butyrivibrio and Ruminococcus gnavus could mediate the association of myo-inositol and N-acetylalanine, respectively. In addition, Ruminococcus torques abundance was colocalized with severe COVID-19 (PP.H4 = 0.77) and the colon expression of permeability related protein RASIP1 (PP.H4 = 0.95). Conclusions: Our study highlights the potential causal relationships between gut microbiome, plasma metabolome and severe COVID-19, which potentially serve as clinical biomarkers for risk stratification and prognostication and benefit the mechanism mechanistic investigation of severe COVID-19.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbioma Gastrointestinal / COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbioma Gastrointestinal / COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China