Evidence map›Paper›PMID 35607951›Full record

Observational studyCritical care medicine2022

Renin-Angiotensin System Pathway Therapeutics Associated With Improved Outcomes in Males Hospitalized With COVID-19.

Genevieve L Y Rocheleau, Terry Lee, Yassene Mohammed, David Goodlett, Kevin Burns, Matthew P Cheng, Karen Tran, David Sweet, John Marshall, Arthur S Slutsky and 21 more

Open access · hybridAbstract readComparative StudyMulticenter StudyObservational Study
In one paragraph

Observational study in Critical care medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Effects of Losartan on Patients Hospitalized for Acute COVID-19: A Randomized Controlled Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Trial
  4. Article
  5. Observational
  6. Article
  7. Article
  8. Association between blood pressure and COVID-19 severity.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  9. Article
  10. COVID-19 and cardiovascular disease in patients with chronic kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. The authors reply.Critical care medicine · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 15 institutions in 5 countries.

Genevieve L Y RocheleauCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
Terry LeeCentre for Health Evaluation and Outcome Science (CHEOS), St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
Yassene MohammedUniversity of Victoria, Genome BC Proteomics Centre, Victoria, BC, Canada.
David GoodlettUniversity of Victoria, Genome BC Proteomics Centre, Victoria, BC, Canada.
Kevin BurnsDivision of Nephrology, Department of Medicine, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada.
Matthew P ChengDivisions of Infectious Diseases & Medical Microbiology, McGill University Health Center, McGill's Interdisciplinary Initiative in Infection and Immunity, Montreal, QC, Canada.
Karen TranDivision of General Internal Medicine, Vancouver General Hospital and University of British Columbia, Vancouver, BC, Canada.
David SweetDivision of Critical Care Medicine, Vancouver General Hospital, Vancouver, BC, Canada.
John MarshallDepartment of Surgery, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.
Arthur S SlutskyDepartment of Surgery, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.
Srinivas MurthyBritish Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Joel SingerCentre for Health Evaluation and Outcome Science (CHEOS), St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
David M PatrickBritish Columbia Centre for Disease Control (BCCDC), and School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.
Bin DuMedical ICU, Peking Union Medical College Hospital, Beijing, China.
Zhiyong PengDepartment of Critical Care Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Todd C LeeDivisions of Infectious Diseases & Medical Microbiology, McGill University Health Center, McGill's Interdisciplinary Initiative in Infection and Immunity, Montreal, QC, Canada.
John H BoydCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
Keith R WalleyCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
Francois LamontagneUniversity of Sherbrooke, Sherbrooke, QC, Canada.
Robert FowlerSunnybrook Health Sciences Centre, Toronto, ON, Canada.
Brent W WinstonDepartments of Critical Care Medicine, Medicine and Biochemistry and Molecular Biology, University of Calgary, Calgary, AB, Canada.
Greg HaljanDepartment of Medicine, Surrey Memorial Hospital, Surrey, BC, Canada.
Donald C VinhDivisions of Infectious Diseases & Medical Microbiology, McGill University Health Center, McGill's Interdisciplinary Initiative in Infection and Immunity, Montreal, QC, Canada.
Alison McGeerMt. Sinai Hospital and University of Toronto, Toronto, ON, Canada.
David MasloveDepartment of Medicine, Kingston General Hospital and Queen's University, Kingston, ON, Canada.
Santiago Perez PatrigeonDepartment of Medicine, Kingston General Hospital and Queen's University, Kingston, ON, Canada.
Puneet MannBlack Tusk Research Group Inc., Vancouver, BC, Canada.
Kathryn DonohoeBlack Tusk Research Group Inc., Vancouver, BC, Canada.
Geraldine HernandezBlack Tusk Research Group Inc., Vancouver, BC, Canada.
James A RussellCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.
for ARBs CORONA I Investigators
University of British Columbia · CAUniversity of Victoria · CAQueen's University · CASt. Paul's Hospital · CAApple (Israel) · ILLeiden University Medical Center · NLPeking Union Medical College Hospital · CNSt. Michael's Hospital · CASunnybrook Health Science Centre · CASurrey Memorial Hospital · CAUniversity of Calgary · CAUniversity of Gdańsk · PLUniversity of Toronto · CAVancouver General Hospital · CAWuhan University · CN

Funding

CIHR 439993CIHR 442999
6 · The paper itself

Abstract

objectivesTo 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.

designProspective 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.

settingARBs 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.

interventionsNone. MEASUREMENTS AND MAIN

resultsMales 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.

conclusionsARBs 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.

Indexed as

COVID-19 Drug TreatmentHypertensionAngiotensin-Converting Enzyme InhibitorsAngiotensin IIAngiotensin Receptor AntagonistsCanadaFemaleHumansMaleProspective StudiesRenin-Angiotensin SystemSex CharacteristicsAngiotensin-Converting Enzyme InhibitorsAngiotensin IIAngiotensin Receptor Antagonists

Identifiers

PMID35607951
PMCPMC9380153
OpenAlexW4281386954

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.