Evidence map›Paper›PMID 38226605›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2024

Circulating biomarker analyses in a longitudinal cohort of patients with IPF.

Christina Ebert, Alice M Walsh, Larisa Sereda, Carole L Wilson, Peter H Schafer, Aryeh Fischer, Lei Zhao, Francisco Ramirez-Valle, David Gordon, Lynn M Schnapp

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. 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

10 authors at 2 institutions in 1 country.

Christina EbertBristol Myers Squibb, Princeton, New Jersey, United States.
Alice M WalshBristol Myers Squibb, Princeton, New Jersey, United States.
Larisa SeredaBristol Myers Squibb, Princeton, New Jersey, United States.
Carole L WilsonDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin, United States.ORCID 0000-0001-6692-0430
Peter H SchaferBristol Myers Squibb, Princeton, New Jersey, United States.
Aryeh FischerBristol Myers Squibb, Princeton, New Jersey, United States.
Lei ZhaoBristol Myers Squibb, Princeton, New Jersey, United States.
Francisco Ramirez-ValleBristol Myers Squibb, Princeton, New Jersey, United States.
David GordonBristol Myers Squibb, Princeton, New Jersey, United States.
Lynn M SchnappDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin, United States.ORCID 0000-0002-9189-7567
Bristol-Myers Squibb (United States) · USUniversity of Wisconsin–Madison · US

Funding

Role of pericytes in scleroderma skin and lung fibrosisR01HL133751 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI FEGHALI-BOSTWICK, CAROL A., SCHNAPP, LYNN M · 2017 to 2020
$2.0M
Scleroderma Twin Study and analysis of Estrogen in patients with dcSScK24AR060297 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FEGHALI-BOSTWICK, CAROL A. · 2013 to 2025
$1.4M
NHLBI NIH HHS R01 HL133751NIAMS NIH HHS K24 AR060297
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is an incurable interstitial lung disease characterized by fibrosis. Two FDA-approved drugs, pirfenidone and nintedanib, only modestly prolong survival. In this study, we asked whether levels of select circulating biomarkers in patients with IPF demonstrated changes in response to treatment over time and whether treatment with pirfenidone and nintedanib led to differential biomarker expression. Serial plasma samples from 48 patients with IPF on usual treatment and six healthy volunteers were analyzed to identify differentially expressed blood protein. Hypothesis-driven potential biomarker selection was based on recent literature, internal preclinical data, and the PROLIFIC Consortium (Schafer P.

Indexed as

Antigens, NeoplasmIdiopathic Pulmonary FibrosisKeratin-19BiomarkersFibrosisHumansLungantigen CYFRA21.1Antigens, NeoplasmBiomarkersKeratin-19biomarkersfibrosisidiopathic pulmonary fibrosisprediction

Identifiers

PMID38226605
PMCPMC11281789
OpenAlexW4390918573

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.