Evidence map›Paper›PMID 35743491›Full record

ArticleJournal of clinical medicine2022

Impaired Antibody Response Is Associated with Histone-Release, Organ Dysfunction and Mortality in Critically Ill COVID-19 Patients.

Rickard Lagedal, Oskar Eriksson, Anna Sörman, Joram B Huckriede, Bjarne Kristensen, Stephanie Franzén, Anders Larsson, Anders Bergqvist, Kjell Alving, Anders Forslund and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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

18 authors at 4 institutions in 4 countries.

Rickard LagedalDepartment of Surgical Sciences, Anaesthesia and Intensive Care, Uppsala University, 752 36 Uppsala, Sweden.
Oskar ErikssonDepartment of Immunology, Genetics and Pathology, Uppsala University, 752 36 Uppsala, Sweden.
Anna SörmanDepartment of Immunology, Genetics and Pathology, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0002-1037-1601
Joram B HuckriedeDepartment of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, 6211 LK Maastricht, The Netherlands.
Bjarne KristensenThermo Fisher Scientific, 3450 Allerod, Denmark.
Stephanie FranzénDepartment of Surgical Sciences, Anaesthesia and Intensive Care, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0002-5003-2508
Anders LarssonDepartment of Medical Sciences, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0003-3161-0402
Anders BergqvistDepartment of Medical Sciences, Section of Clinical Microbiology, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0002-5789-8777
Kjell AlvingDepartment of Women's and Children's Health, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0003-0784-0443
Anders ForslundDepartment of Women's and Children's Health, Uppsala University, 752 36 Uppsala, Sweden.
Barbro PerssonDepartment of Immunology, Genetics and Pathology, Uppsala University, 752 36 Uppsala, Sweden.
Kristina N EkdahlDepartment of Immunology, Genetics and Pathology, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0001-7888-1571
Pablo Garcia de FrutosDepartment of Cell Death and Proliferation, IIBB-CSIC, IDIBAPS and CIBERCV, 08036 Barcelona, Spain.ORCID 0000-0003-1547-1190
Bo NilssonDepartment of Immunology, Genetics and Pathology, Uppsala University, 752 36 Uppsala, Sweden.
Gerry A F NicolaesDepartment of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, 6211 LK Maastricht, The Netherlands.
Miklos LipcseyDepartment of Surgical Sciences, Anaesthesia and Intensive Care, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0002-1976-4129
Michael HultströmDepartment of Surgical Sciences, Anaesthesia and Intensive Care, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0003-4675-1099
Robert FrithiofDepartment of Surgical Sciences, Anaesthesia and Intensive Care, Uppsala University, 752 36 Uppsala, Sweden.ORCID 0000-0003-2278-7951
Uppsala University · SEMaastricht University · NLCentro de Investigación en Red en Enfermedades Cardiovasculares · ESThermo Fisher Scientific (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposethe pathophysiologic mechanisms explaining differences in clinical outcomes following COVID-19 are not completely described. This study aims to investigate antibody responses in critically ill patients with COVID-19 in relation to inflammation, organ failure and 30-day survival.

methodsAll patients with PCR-verified COVID-19 and gave consent, and who were admitted to a tertiary Intensive care unit (ICU) in Sweden during March-September 2020 were included. Demography, repeated blood samples and measures of organ function were collected. Analyses of anti-SARS-CoV-2 antibodies (IgM, IgA and IgG) in plasma were performed and correlated to patient outcome and biomarkers of inflammation and organ failure.

resultsA total of 115 patients (median age 62 years, 77% male) were included prospectively. All patients developed severe respiratory dysfunction, and 59% were treated with invasive ventilation. Thirty-day mortality was 22.6% for all included patients. Patients negative for any anti-SARS-CoV-2 antibody in plasma during ICU admission had higher 30-day mortality compared to patients positive for antibodies. Patients positive for IgM had more ICU-, ventilator-, renal replacement therapy- and vasoactive medication-free days. IgA antibody concentrations correlated negatively with both SAPS3 and maximal SOFA-score and IgM-levels correlated negatively with SAPS3. Patients with antibody levels below the detection limit had higher plasma levels of extracellular histones on day 1 and elevated levels of kidney and cardiac biomarkers, but showed no signs of increased inflammation, complement activation or cytokine release. After adjusting for age, positive IgM and IgG antibodies were still associated with increased 30-day survival, with odds ratio (OR) 7.1 (1.5-34.4) and 4.2 (1.1-15.7), respectively.

conclusionIn patients with severe COVID-19 requiring intensive care, a poor antibody response is associated with organ failure, systemic histone release and increased 30-day mortality.

Indexed as

antibody responseCOVID-19critical carehistonesNETSARS-CoV-2

Identifiers

PMID35743491
PMCPMC9225468
OpenAlexW4282916917

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.