Evidence map›Paper›PMID 36691221›Full record

ArticleBMJ open2022

Cohort profile:

Erin Collins, Yannick Galipeau, Corey Arnold, Cameron Bosveld, Aliisa Heiskanen, Alexa Keeshan, Kiran Nakka, Khatereh Shir-Mohammadi, Frederic St-Denis-Bissonnette, Laura Tamblyn and 10 more

Abstract read
In one paragraph

Article in BMJ open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Observational
  2. Autoantibodies targeting angiotensin-converting enzyme 2 are prevalent and not induced by SARS-CoV-2 infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Erin CollinsSchool of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada ecoll098@uottawa.ca.ORCID 0000-0002-4209-1786
Yannick GalipeauDepartment of Biochemistry, Microbiology & Immunology, University of Ottawa, Ottawa, Ontario, Canada.
Corey ArnoldDepartment of Biochemistry, Microbiology & Immunology, University of Ottawa, Ottawa, Ontario, Canada.
Cameron BosveldChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Aliisa HeiskanenSchool of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Alexa KeeshanSchool of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Kiran NakkaDepartment of Biochemistry, Microbiology & Immunology, University of Ottawa, Ottawa, Ontario, Canada.
Khatereh Shir-MohammadiDepartment of Biochemistry, Microbiology & Immunology, University of Ottawa, Ottawa, Ontario, Canada.
Frederic St-Denis-BissonnetteChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.ORCID 0000-0003-3355-4950
Laura TamblynChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Agatha VranjkovicChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Leah C WoodChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Ronald BoothDepartment of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada.
C Arianne BuchanDivision of Infectious Diseases, Department of Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Angela M CrawleyDepartment of Biochemistry, Microbiology & Immunology, University of Ottawa, Ottawa, Ontario, Canada.ORCID 0000-0002-7453-7922
Julian LittleSchool of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.ORCID 0000-0001-5026-5531
Michaeline McGuintyDivision of Infectious Diseases, Department of Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Raphael SaginurDivision of Infectious Diseases, Department of Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Marc-André LangloisDepartment of Biochemistry, Microbiology & Immunology, University of Ottawa, Ottawa, Ontario, Canada.ORCID 0000-0003-4652-3029
Curtis L CooperClinical Epidemiology, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Funding

CIHR 175622CIHR 424425
6 · The paper itself

Abstract

purposeTo investigate the robustness and longevity of SARS-CoV-2 immune responses conferred by natural infection and vaccination among priority populations such as immunocompromised individuals and people with post-acute sequelae of COVID-19 in a prospective cohort study (Stop the Spread Ottawa-SSO) in adults living in the Ottawa region. In this paper, we describe the study design, ongoing data collection and baseline characteristics of participants.

participantsSince October 2020, participants who tested positive for COVID-19 (convalescents) or at high risk of exposure to the virus (under surveillance) have provided monthly blood and saliva samples over a 10-month period. As of 2 November 2021, 1026 adults had completed the baseline survey and 976 had attended baseline bloodwork. 300 participants will continue to provide bimonthly blood samples for 24 additional months (ie, total follow-up of 34 months). FINDINGS TO DATE: The median age of the baseline sample was 44 (IQR 23, range: 18-79) and just over two-thirds (n=688; 67.1%) were female. 255 participants (24.9%) had a history of COVID-19 infection confirmed by PCR and/or serology. Over 600 participants (60.0%) work in high-risk occupations (eg, healthcare, teaching and transportation). 108 participants (10.5%) reported immunocompromising conditions or treatments at baseline (eg, cancer, HIV, other immune deficiency, and/or use of immunosuppressants). FUTURE PLANS: SSO continues to yield rich research potential, given the collection of pre-vaccine baseline data and samples from the majority of participants, recruitment of diverse subgroups of interest, and a high level of participant retention and compliance with monthly sampling. The 24-month study extension will maximise opportunities to track SARS-CoV-2 immunity and vaccine efficacy, detect and characterise emerging variants, and compare subgroup humoral and cellular response robustness and persistence.

Indexed as

COVID-19AdultAntibodiesAntibodies, ViralAntibody FormationFemaleHumansImmunity, CellularMaleProspective StudiesSARS-CoV-2VaccinationAntibodiesAntibodies, ViralCOVID-19epidemiologyimmunologyinfectious diseasespublic healthvirology

Identifiers

PMID36691221
PMCPMC9461086

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.