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COVID-19: disease pathways and gene expression changes predict methylprednisolone can improve outcome in severe cases.
Draghici, Sorin; Nguyen, Tuan-Minh; Sonna, Larry A; Ziraldo, Cordelia; Vanciu, Radu; Fadel, Raef; Morrison, Austin; Kenney, Rachel M; Alangaden, George; Ramesh, Mayur; Mor, Gil.
Afiliação
  • Draghici S; Department of Computer Science and.
  • Nguyen TM; Department of Obstetrics and Gynecology, Wayne State University, Michigan 48202, USA.
  • Sonna LA; Advaita Bioinformatics, Ann Arbor, MI 48105, USA.
  • Ziraldo C; Department of Computer Science and.
  • Vanciu R; Bon Air Consulting, Bon Air, Vancouver, WA 98683, USA.
  • Fadel R; Department of Internal Medicine.
  • Morrison A; Department of Internal Medicine.
  • Kenney RM; Department of Internal Medicine.
  • Alangaden G; Department of Pharmacy.
  • Ramesh M; Department of Pharmacy.
  • Mor G; Division of Infectious Diseases, Henry Ford Health System, Detroit, MI 48202, USA.
Bioinformatics ; 37(17): 2691-2698, 2021 Sep 09.
Article em En | MEDLINE | ID: mdl-33693506
ABSTRACT
MOTIVATION COVID-19 has several distinct clinical phases a viral replication phase, an inflammatory phase and in some patients, a hyper-inflammatory phase. High mortality is associated with patients developing cytokine storm syndrome. Treatment of hyper-inflammation in these patients using existing approved therapies with proven safety profiles could address the immediate need to reduce mortality.

RESULTS:

We analyzed the changes in the gene expression, pathways and putative mechanisms induced by SARS-CoV2 in NHBE, and A549 cells, as well as COVID-19 lung versus their respective controls. We used these changes to identify FDA approved drugs that could be repurposed to help COVID-19 patients with severe symptoms related to hyper-inflammation. We identified methylprednisolone (MP) as a potential leading therapy. The results were then confirmed in five independent validation datasets including Vero E6 cells, lung and intestinal organoids, as well as additional patient lung sample versus their respective controls. Finally, the efficacy of MP was validated in an independent clinical study. Thirty-day all-cause mortality occurred at a significantly lower rate in the MP-treated group compared to control group (29.6% versus 16.6%, P = 0.027). Clinical results confirmed the in silico prediction that MP could improve outcomes in severe cases of COVID-19. A low number needed to treat (NNT = 5) suggests MP may be more efficacious than dexamethasone or hydrocortisone. AVAILABILITY AND IMPLEMENTATION iPathwayGuide is available at https//advaitabio.com/ipathwayguide/. SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article