Evidence map›Paper›PMID 35679511›Full record

ArticleAmerican journal of respiratory cell and molecular biology2022

New Insights into Clinical and Mechanistic Heterogeneity of the Acute Respiratory Distress Syndrome: Summary of the Aspen Lung Conference 2021.

Thomas R Martin, Rachel L Zemans, Lorraine B Ware, Eric P Schmidt, David W H Riches, Lisa Bastarache, Carolyn S Calfee, Tushar J Desai, Susanne Herold, Catherine L Hough and 6 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Lung endothelial cytopathic tau is sufficient to impair long-term potentiation during infection.American journal of respiratory cell and molecular biology · 2026
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Unraveling the Complexities of Mesenchymal Stromal Cell-based Therapies: One Size Doesn't Fit All.American journal of respiratory and critical care medicine · 2024
    Article
  13. cUMP elicits interendothelial gap formation duringAmerican journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Gamma secretase activating protein promotes end-organ dysfunction after bacterial pneumonia.American journal of physiology. Lung cellular and molecular physiology · 2023
    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

16 authors at 15 institutions in 2 countries.

Thomas R MartinDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington.ORCID 0000-0002-8193-909X
Rachel L ZemansDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine and Program in Cellular and Molecular Biology, University of Michigan School of Medicine, Ann Arbor, Michigan.ORCID 0000-0003-3537-9869
Lorraine B WareDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine and.ORCID 0000-0002-9429-4702
Eric P SchmidtDivision of Pulmonary Sciences and Critical Care, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado.ORCID 0000-0002-7360-0504
David W H RichesDivision of Pulmonary Sciences and Critical Care, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado.ORCID 0000-0002-9587-3335
Lisa BastaracheDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.ORCID 0000-0003-3020-447X
Carolyn S CalfeeDivision of Pulmonary, Critical Care, Allergy, and Sleep Medicine, Department of Medicine.ORCID 0000-0001-9208-6865
Tushar J DesaiDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Stem Cell Institute, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-8794-5319
Susanne HeroldDepartment of Internal Medicine VI and Cardio-Pulmonary Institute (CPI), Universities of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany.ORCID 0000-0001-6343-0911
Catherine L HoughDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0001-6425-0867
Mark R LooneyDepartment of Laboratory Medicine, and.ORCID 0000-0003-0241-9190
Michael A MatthayDepartments of Medicine and Anesthesia, Cardiovascular Research Institute, University of California San Francisco, San Francisco, California.ORCID 0000-0003-3039-8155
Nuala MeyerDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-4597-5584
Samir M ParikhCenter for Vascular Biology Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-1038-981X
Troy StevensDepartment of Physiology and Cell Biology, College of Medicine, Center for Lung Biology, University of South Alabama, Mobile, Alabama; and.ORCID 0000-0001-9689-929X
B Taylor ThompsonDivision of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Boston, Massachusetts.ORCID 0000-0001-6391-0448
Advanced ENT and Allergy · USBeth Israel Deaconess Medical Center · USMassachusetts General Hospital · USOregon Health & Science University · USStanford University · USUnited States University · USUniversities of Giessen and Marburg Lung Center · DEUniversity of California, San Francisco · USUniversity of Colorado Denver · USUniversity of Michigan · USUniversity of Pennsylvania · USUniversity of South Alabama · USUniversity of Washington · USVanderbilt University · USVanderbilt University Medical Center · US

Funding

CCC for NHLBI Prevention and Early Treatment of Acute Lung Injury PETAL NetworkU01HL123009 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI FOULKES, ANDREA S, THOMPSON, BOYD TAYLOR · 2014 to 2021
$67.2M
T-type Calcium Channels and von Willebrand Factor ReleaseP01HL066299 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI TOWNSLEY, MARY I · 2001 to 2022
$34.6M
Precision Medicine in the Acute Respiratory Distress SyndromeR35HL140026 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CALFEE, CAROLYN · 2018 to 2024
$6.8M
Tie2-driven vascular control in critical illnessR35HL139424 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI PARIKH, SAMIR M · 2018 to 2024
$6.4M
From GWAS to PheWAS: Scanning the EMR Phenome for Gene-disease AssociationsR01LM010685 · NLM · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BASTARACHE, LISA · 2011 to 2022
$6.3M
Nosocomial pneumonias impair cognitive functionR01HL140182 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI Mike Lin · 2018 to 2026
$4.9M
Immunobiology of the normal and injured lungR35HL161241 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARK ROBERTS LOONEY · 2022 to 2026
$4.2M
NOVEL PARACRINE MECHANISMS FOR CELL-BASED THERAPY OF INJURED LUNGSR01HL134828 · NHLBI · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI JI, HONG-LONG · 2017 to 2025
$3.4M
Immunomodulation by splenic megakaryocytes and platelets in sepsisR01AI165919 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2022 to 2025
$3.2M
Mechanisms and pathogenicity of SARS-CoV-2-induced neutrophil extracellular trapsR01AI160167 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2021 to 2025
$3.1M
Effect of randomization to neuromuscular blockade on physical functional impairment and recovery in ARDSR01HL132232 · NHLBI · UNIVERSITY OF WASHINGTON · PI HOUGH, CATHERINE LEE, IWASHYNA, THEODORE J · 2016 to 2019
$2.9M
The GOLD Study: Goal of Open Lung Ventilation in DonorsR01HL126176 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WARE, LORRAINE B · 2015 to 2020
$2.8M
BLRD VA I01 BX003471NHLBI NIH HHS 1R01 HL140595NHLBI NIH HHS 1UO1HL123009NHLBI NIH HHS 5R01HL14254902NHLBI NIH HHS HL103836NHLBI NIH HHS HL126176NHLBI NIH HHS HL126456NHLBI NIH HHS HL131608NHLBI NIH HHS HL134828NHLBI NIH HHS HL135849NHLBI NIH HHS HL137006NHLBI NIH HHS HL137915NHLBI NIH HHS HL140026NHLBI NIH HHS HL140182NHLBI NIH HHS HL143896NHLBI NIH HHS HL147920NHLBI NIH HHS HL148069NHLBI NIH HHS HL155804NHLBI NIH HHS HL66299NHLBI NIH HHS K24 HL103836NHLBI NIH HHS K24 HL141526NHLBI NIH HHS K24HL141526NHLBI NIH HHS K24 HL155804NHLBI NIH HHS P01 HL066299NHLBI NIH HHS R01 HL126176NHLBI NIH HHS R01 HL131608NHLBI NIH HHS R01 HL132232NHLBI NIH HHS R01 HL134828NHLBI NIH HHS R01 HL135849NHLBI NIH HHS R01 HL137006NHLBI NIH HHS R01 HL137915NHLBI NIH HHS R01 HL140182NHLBI NIH HHS R01 HL140595NHLBI NIH HHS R01 HL143896NHLBI NIH HHS R01 HL147920NHLBI NIH HHS R01 HL148069NHLBI NIH HHS R01 HL158906NHLBI NIH HHS R13 HL152479NHLBI NIH HHS R35 HL139424NHLBI NIH HHS R35 HL140026NHLBI NIH HHS R35 HL161241NHLBI NIH HHS R41 HL126456NHLBI NIH HHS R42 HL126456NHLBI NIH HHS RO1HL132232NHLBI NIH HHS U01 HL123009NIAID NIH HHS R01 AI160167NIAID NIH HHS R01 AI165919NIA NIH HHS R01 AG049493NIGMS NIH HHS GM12509NIGMS NIH HHS R01 GM125095NLM NIH HHS R01 LM010685
6 · The paper itself

Abstract

Clinical and molecular heterogeneity are common features of human disease. Understanding the basis for heterogeneity has led to major advances in therapy for many cancers and pulmonary diseases such as cystic fibrosis and asthma. Although heterogeneity of risk factors, disease severity, and outcomes in survivors are common features of the acute respiratory distress syndrome (ARDS), many challenges exist in understanding the clinical and molecular basis for disease heterogeneity and using heterogeneity to tailor therapy for individual patients. This report summarizes the proceedings of the 2021 Aspen Lung Conference, which was organized to review key issues related to understanding clinical and molecular heterogeneity in ARDS. The goals were to review new information about ARDS phenotypes, to explore multicellular and multisystem mechanisms responsible for heterogeneity, and to review how best to account for clinical and molecular heterogeneity in clinical trial design and assessment of outcomes. The report concludes with recommendations for future research to understand the clinical and basic mechanisms underlying heterogeneity in ARDS to advance the development of new treatments for this life-threatening critical illness.

Indexed as

Respiratory Distress SyndromeHumansLungRisk FactorsSeverity of Illness IndexThoraxARDSbiological mechanismsclinical trialscritical care

Identifiers

PMID35679511
PMCPMC9447141
OpenAlexW4281667251

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.