Evidence map›Paper›PMID 32599095›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2020

The acute respiratory distress syndrome biomarker pipeline: crippling gaps between discovery and clinical utility.

Christian Bime, Sara M Camp, Nancy Casanova, Radu C Oita, Juliet Ndukum, Heather Lynn, Joe G N Garcia

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07774338 (Early Admission Serum Soluble Receptor for Advanced Glycation End Products), which is not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.9field-weighted citation impact, top 7% 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.

NCT07774338 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Early Admission Serum Soluble Receptor for Advanced Glycation End Products (sRAGE), Club Cell Protein-16 (CC16), and Syndecan-1 as Independent Predictors of Acute Respiratory Distress Syndrome and In-Hospital Mortality Following Severe Isolated Chest Trauma: A Prospective Cohort Study.

TypeobservationalSponsorAssiut UniversityRan2026 to 2028Enrolled85ConditionsAcute Respiratory Distress Syndrome, Chest TraumaArmsNo intervention - observational study
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Observational
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Proteomics techniques in protein biomarker discovery.Quantitative biology (Beijing, China) · 2024
    Review
  13. Advances in Biomarkers for Diagnosis and Treatment of ARDS.Diagnostics (Basel, Switzerland) · 2023
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Observational
  19. Discovery Proteomics for COVID-19: Where We Are Now.Journal of proteome research · 2021
    Review
  20. Observational
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

7 authors at 1 institution in 1 country.

Christian BimeCollege of Medicine, University of Arizona Health Sciences, Tucson, Arizona. Electronic address: cbime@deptofmed.arizona.edu.
Sara M CampCollege of Medicine, University of Arizona Health Sciences, Tucson, Arizona.
Nancy CasanovaCollege of Medicine, University of Arizona Health Sciences, Tucson, Arizona.
Radu C OitaCollege of Medicine, University of Arizona Health Sciences, Tucson, Arizona.
Juliet NdukumCollege of Medicine, University of Arizona Health Sciences, Tucson, Arizona.
Heather LynnCollege of Medicine, University of Arizona Health Sciences, Tucson, Arizona.
Joe G N GarciaCollege of Medicine, University of Arizona Health Sciences, Tucson, Arizona.
University of Arizona · US

Funding

Structure-Function Analysis of nmMLCK in EC Barrier ResponsesP01HL126609 · NHLBI · UNIVERSITY OF FLORIDA · PI Joe G. N. Garcia · 2016 to 2026
$24.4M
Protein Chemistry & Biophysics CoreP01HL134610 · NHLBI · UNIVERSITY OF ARIZONA · PI BLACK, STEPHEN M · 2018 to 2022
$11.6M
A Randomized Phase 2A Clinical Trial Pioneering the Utility of an eNAMPT-Reducing Therapy in ARDS/VILI: the PUERTA TrialR44HL145930 · NHLBI · AQUALUNG THERAPEUTICS CORP. · PI GARCIA, JOE G. N. · 2023 to 2024
$2.5M
Novel Therapeutic Antibody Targeting of Extracellular NAMPT in Ventilator-Induced Lung Injury (VILI)R42HL145930 · NHLBI · AQUALUNG THERAPEUTICS CORP. · PI GARCIA, JOE G. N. · 2019 to 2021
$1.7M
SELPLG as a candidate gene in Acute Respiratory Distress SyndromeK08HL141623 · NHLBI · UNIVERSITY OF ARIZONA · PI BIME, CHRISTIAN · 2018 to 2022
$863k
The CRIT-ICU Biomarker Panel for Stratification of Mortality Risk in ARDS PatientsR41HL147769 · NHLBI · AQUALUNG THERAPEUTICS CORP. · PI GARCIA, JOE G. N. · 2019 to 2019
$225k
NHLBI NIH HHS K08 HL141623NHLBI NIH HHS P01 HL126609NHLBI NIH HHS P01 HL134610NHLBI NIH HHS R41 HL147769NHLBI NIH HHS R42 HL145930NHLBI NIH HHS R44 HL145930
6 · The paper itself

Abstract

Recent innovations in translational research have ushered an exponential increase in the discovery of novel biomarkers, thereby elevating the hope for deeper insights into "personalized" medicine approaches to disease phenotyping and care. However, a critical gap exists between the fast pace of biomarker discovery and the successful translation to clinical use. This gap underscores the fundamental biomarker conundrum across various acute and chronic disorders: how does a biomarker address a specific unmet need? Additionally, the gap highlights the need to shift the paradigm from a focus on biomarker discovery to greater translational impact and the need for a more streamlined drug approval process. The unmet need for biomarkers in acute respiratory distress syndrome (ARDS) is for reliable and validated biomarkers that minimize heterogeneity and allow for stratification of subject selection for enrollment in clinical trials of tailored therapies. This unmet need is particularly highlighted by the ongoing SARS-CoV-2/COVID-19 pandemic. The unprecedented numbers of COVID-19-induced ARDS cases has strained health care systems across the world and exposed the need for biomarkers that would accelerate drug development and the successful phenotyping of COVID-19-infected patients at risk for development of ARDS and ARDS mortality. Accordingly, this review discusses the current state of ARDS biomarkers in the context of the drug development pipeline and highlight gaps between biomarker discovery and clinical implementation while proposing potential paths forward. We discuss potential ARDS biomarkers by category and by context of use, highlighting progress in the development continuum. We conclude by discussing challenges to successful translation of biomarker candidates to clinical impact and proposing possible novel strategies.

Indexed as

BetacoronavirusBiomarkersCoronavirus InfectionsCOVID-19HumansPandemicsPneumonia, ViralRespiratory Distress SyndromeSARS-CoV-2Translational Research, BiomedicalBiomarkers

Identifiers

PMID32599095
PMCPMC7319618
OpenAlexW3037691424

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.