Evidence map›Paper›PMID 32931480›Full record

Trial reportThe Journal of clinical investigation2021

The ABO histo-blood group, endothelial activation, and acute respiratory distress syndrome risk in critical illness.

John P Reilly, Nuala J Meyer, Michael Gs Shashaty, Brian J Anderson, Caroline Ittner, Thomas G Dunn, Brian Lim, Caitlin Forker, Michael P Bonk, Ethan Kotloff and 13 more

Open access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Association between Age and Mortality in Pediatric and Adult Acute Respiratory Distress Syndrome.American journal of respiratory and critical care medicine · 2024
    Article
  8. Adolescents and Young Adults: An Understudied, yet Likely Informative, Population in ARDS.American journal of respiratory and critical care medicine · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. ABO blood groups and nosocomial infection.Epidemiology and infection · 2023
    Article
  15. Article
  16. The ultimate tradeoff: how red cell adaptations to malaria alter the host response during critical illness.American journal of physiology. Lung cellular and molecular physiology · 2023
    Review
  17. Article
  18. Article
  19. Observational
  20. Patient variability in severity of COVID-19 disease. Main suspect: vascular endothelium.The journal of allergy and clinical immunology. In practice · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 8 institutions in 3 countries.

John P ReillyDivision of Pulmonary, Allergy, and Critical Care.
Nuala J MeyerDivision of Pulmonary, Allergy, and Critical Care.
Michael Gs ShashatyDivision of Pulmonary, Allergy, and Critical Care.
Brian J AndersonDivision of Pulmonary, Allergy, and Critical Care.
Caroline IttnerDivision of Pulmonary, Allergy, and Critical Care.
Thomas G DunnDivision of Pulmonary, Allergy, and Critical Care.
Brian LimDivision of Pulmonary, Allergy, and Critical Care.
Caitlin ForkerDivision of Pulmonary, Allergy, and Critical Care.
Michael P BonkDivision of Pulmonary, Allergy, and Critical Care.
Ethan KotloffDivision of Pulmonary, Allergy, and Critical Care.
Rui FengCenter for Clinical Epidemiology and Biostatics, and.
Edward CantuCenter for Translational Lung Biology.
Nilam S MangalmurtiDivision of Pulmonary, Allergy, and Critical Care.
Carolyn S CalfeeDepartment of Medicine and.
Michael A MatthayDepartment of Medicine and.
Carmen MikacenicDivision of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, Washington, USA.
Keith R WalleyCentre for Heart Lung Innovation, University of British Columbia, Vancouver, British Columbia, Canada.
James RussellCentre for Heart Lung Innovation, University of British Columbia, Vancouver, British Columbia, Canada.
David C ChristianiT.H. Chan School of Public Health, Harvard University, Boston, Massachusetts, USA.
Mark M WurfelDivision of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, Washington, USA.
Paul N LankenDivision of Pulmonary, Allergy, and Critical Care.
Muredach P ReillyIrving Institute for Clinical and Translational Research, Columbia University Irving Medical Center, New York, New York, USA.
Jason D ChristieDivision of Pulmonary, Allergy, and Critical Care.
Pulmonary and Allergy Associates · USUniversity of British Columbia · CAUniversity of California, San Francisco · USUniversity of Washington · USCenter for Clinical Research (United States) · USCenter for Translational Molecular Medicine · NLColumbia University Irving Medical Center · USHarvard University · US

Funding

Genetic risks for ALI in ARDSnet and the iSPAAR ConsortiumRC2HL101779 · NHLBI · UNIVERSITY OF WASHINGTON · PI WURFEL, MARK M · 2009 to 2010
$4.7M
Targeting Angiopoietin-2 in ARDSR01HL137006 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MEYER, NUALA JENNINGS · 2017 to 2021
$2.5M
Reconsidering the IL-1 axis in sepsis-associated ARDSR01HL137915 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MEYER, NUALA JENNINGS · 2017 to 2020
$2.1M
Mentored Patient Oriented Research in Lung TransplantationK24HL115354 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHRISTIE, JASON D · 2012 to 2021
$1.2M
Neurocognitive Impairment in Acute Respiratory Failure and Shock: Understanding the Role of Neuronal ExcitotoxicityK23HL140482 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI ANDERSON, BRIAN J. · 2018 to 2022
$959k
The Role of ABO Glycosyltransferases in the Acute Respiratory Distress SyndromeK23HL125723 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI REILLY, JOHN PATRICK · 2015 to 2019
$840k
Acute Adipose Inflammation as a Contributor to Acute Kidney Injury After TraumaK23DK097307 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI SHASHATY, MICHAEL G. S. · 2013 to 2016
$626k
Mentoring Patient-Oriented Research to Promote ARDS Precision MedicineK24HL155804 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MEYER, NUALA JENNINGS · 2021 to 2021
$124k
ABO Glycosyltransferases in Sepsis Associated Acute Respiratory Distress SyndromeF32HL122075 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI REILLY, JOHN PATRICK · 2014 to 2014
$65k
NHLBI NIH HHS F32 HL122075NHLBI NIH HHS K23 HL125723NHLBI NIH HHS K23 HL140482NHLBI NIH HHS K24 HL115354NHLBI NIH HHS K24 HL155804NHLBI NIH HHS R01 HL137006NHLBI NIH HHS R01 HL137915NHLBI NIH HHS RC2 HL101779NIDDK NIH HHS K23 DK097307
6 · The paper itself

Abstract

BACKGROUNDThe ABO histo-blood group is defined by carbohydrate modifications and is associated with risk for multiple diseases, including acute respiratory distress syndrome (ARDS). We hypothesized that genetically determined blood subtype A1 is associated with increased risk of ARDS and markers of microvascular dysfunction and coagulation.METHODSWe conducted analyses in 3 cohorts of critically ill trauma and sepsis patients (n = 3710) genotyped on genome-wide platforms to determine the association of the A1 blood type genotype with ARDS risk. We subsequently determined whether associations were present in FUT2-defined nonsecretors who lack ABO antigens on epithelium, but not endothelium. In a patient subgroup, we determined the associations of blood type with plasma levels of endothelial glycoproteins and disseminated intravascular coagulation (DIC). Lastly, we tested whether blood type A was associated with less donor lung injury recovery during human ex vivo lung perfusion (EVLP).RESULTSThe A1 genotype was associated with a higher risk of moderate to severe ARDS relative to type O in all 3 populations. In sepsis, this relationship was strongest in nonpulmonary infections. The association persisted in nonsecretors, suggesting a vascular mechanism. The A1 genotype was also associated with higher DIC risk as well as concentrations of thrombomodulin and von Willebrand factor, which in turn were associated with ARDS risk. Blood type A was also associated with less lung injury recovery during EVLP.CONCLUSIONWe identified a replicable association between ABO blood type A1 and risk of ARDS among the critically ill, possibly mediated through microvascular dysfunction and coagulation.FUNDINGNIH HL122075, HL125723, HL137006, HL137915, DK097307, HL115354, HL101779, and the University of Pennsylvania McCabe Fund Fellowship Award.

Indexed as

ABO Blood-Group SystemAdultAgedCritical IllnessEndothelium, VascularFemaleHumansMaleMiddle AgedRespiratory Distress SyndromeRisk FactorsSepsisWounds and InjuriesABO Blood-Group SystemCoagulationendothelial cellsEpidemiologyPulmonology

Identifiers

PMID32931480
PMCPMC7773362
OpenAlexW3087272604

What OpenQuestion holds

Textmetadata
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.