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Renin-Angiotensin System Pathway Therapeutics Associated With Improved Outcomes in Males Hospitalized With COVID-19.
Rocheleau, Genevieve L Y; Lee, Terry; Mohammed, Yassene; Goodlett, David; Burns, Kevin; Cheng, Matthew P; Tran, Karen; Sweet, David; Marshall, John; Slutsky, Arthur S; Murthy, Srinivas; Singer, Joel; Patrick, David M; Du, Bin; Peng, Zhiyong; Lee, Todd C; Boyd, John H; Walley, Keith R; Lamontagne, Francois; Fowler, Robert; Winston, Brent W; Haljan, Greg; Vinh, Donald C; McGeer, Alison; Maslove, David; Patrigeon, Santiago Perez; Mann, Puneet; Donohoe, Kathryn; Hernandez, Geraldine; Russell, James A.
  • Rocheleau GLY; Centre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Lee T; Centre for Health Evaluation and Outcome Science (CHEOS), St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Mohammed Y; University of Victoria, Genome BC Proteomics Centre, Victoria, BC, Canada.
  • Goodlett D; Center for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, The Netherlands.
  • Burns K; University of Victoria, Genome BC Proteomics Centre, Victoria, BC, Canada.
  • Cheng MP; Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC, Canada.
  • Tran K; International Centre for Cancer Vaccine Science, University of Gdansk, Gdansk, Poland.
  • Sweet D; Division of Nephrology, Department of Medicine, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Marshall J; Divisions of Infectious Diseases & Medical Microbiology, McGill University Health Center, McGill's Interdisciplinary Initiative in Infection and Immunity, Montreal, QC, Canada.
  • Slutsky AS; Division of General Internal Medicine, Vancouver General Hospital and University of British Columbia, Vancouver, BC, Canada.
  • Murthy S; Division of Critical Care Medicine, Vancouver General Hospital, Vancouver, BC, Canada.
  • Singer J; Department of Surgery, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.
  • Patrick DM; Department of Surgery, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.
  • Du B; British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Peng Z; Centre for Health Evaluation and Outcome Science (CHEOS), St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Lee TC; British Columbia Centre for Disease Control (BCCDC), and School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.
  • Boyd JH; Medical ICU, Peking Union Medical College Hospital, Beijing, China.
  • Walley KR; Department of Critical Care Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
  • Lamontagne F; Divisions of Infectious Diseases & Medical Microbiology, McGill University Health Center, McGill's Interdisciplinary Initiative in Infection and Immunity, Montreal, QC, Canada.
  • Fowler R; Centre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Winston BW; Division of Critical Care Medicine, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Haljan G; Centre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Vinh DC; Division of Critical Care Medicine, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • McGeer A; University of Sherbrooke, Sherbrooke, QC, Canada.
  • Maslove D; Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
  • Patrigeon SP; Departments of Critical Care Medicine, Medicine and Biochemistry and Molecular Biology, University of Calgary, Calgary, AB, Canada.
  • Mann P; Department of Medicine, Surrey Memorial Hospital, Surrey, BC, Canada.
  • Donohoe K; Divisions of Infectious Diseases & Medical Microbiology, McGill University Health Center, McGill's Interdisciplinary Initiative in Infection and Immunity, Montreal, QC, Canada.
  • Hernandez G; Mt. Sinai Hospital and University of Toronto, Toronto, ON, Canada.
  • Russell JA; Department of Medicine, Kingston General Hospital and Queen's University, Kingston, ON, Canada.
Crit Care Med ; 50(9): 1306-1317, 2022 09 01.
Article in English | MEDLINE | ID: covidwho-1860941
ABSTRACT

OBJECTIVES:

To determine whether angiotensin receptor blockers (ARBs) or angiotensin-converting enzyme (ACE) inhibitors are associated with improved outcomes in hospitalized patients with COVID-19 according to sex and to report sex-related differences in renin-angiotensin system (RAS) components.

DESIGN:

Prospective observational cohort study comparing the effects of ARB or ACE inhibitors versus no ARBs or ACE inhibitors in males versus females. Severe acute respiratory syndrome coronavirus 2 downregulates ACE-2, potentially increasing angiotensin II (a pro-inflammatory vasoconstrictor). Sex-based differences in RAS dysregulation may explain sex-based differences in responses to ARBs because the ACE2 gene is on the X chromosome. We recorded baseline characteristics, comorbidities, prehospital ARBs or ACE inhibitor treatment, use of organ support and mortality, and measured RAS components at admission and days 2, 4, 7, and 14 in a subgroup ( n = 46), recorded d -dimer ( n = 967), comparing males with females.

SETTING:

ARBs CORONA I is a multicenter Canadian observational cohort of patients hospitalized with acute COVID-19. This analysis includes patients admitted to 10 large urban hospitals across the four most populated provinces. PATIENTS One-thousand six-hundred eighty-six patients with polymerase chain reaction-confirmed COVID-19 (February 2020 to March 2021) for acute COVID-19 illness were included.

INTERVENTIONS:

None. MEASUREMENTS AND MAIN

RESULTS:

Males on ARBs before admission had decreased use of ventilation (adjusted odds ratio [aOR] = 0.52; p = 0.007) and vasopressors (aOR = 0.55; p = 0.011) compared with males not on ARBs or ACE inhibitors. No significant effects were observed in females for these outcomes. The test for interaction was significant for use of ventilation ( p = 0.006) and vasopressors ( p = 0.044) indicating significantly different responses to ARBs according to sex. Males had significantly higher plasma ACE-1 at baseline and angiotensin II at day 7 and 14 than females.

CONCLUSIONS:

ARBs use was associated with less ventilation and vasopressors in males but not females. Sex-based differences in RAS dysregulation may contribute to sex-based differences in outcomes and responses to ARBs in COVID-19.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment / Hypertension Type of study: Cohort study / Observational study / Prognostic study Limits: Female / Humans / Male Country/Region as subject: North America Language: English Journal: Crit Care Med Year: 2022 Document Type: Article Affiliation country: CCM.0000000000005589

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment / Hypertension Type of study: Cohort study / Observational study / Prognostic study Limits: Female / Humans / Male Country/Region as subject: North America Language: English Journal: Crit Care Med Year: 2022 Document Type: Article Affiliation country: CCM.0000000000005589