Evidence map›Paper›PMID 28983101›Full record

ReviewNature reviews. Drug discovery2017

Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease.

Ana L Mora, Mauricio Rojas, Annie Pardo, Moises Selman

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 175 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

175 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Dysregulated iron metabolism in remodeling of aging asthmatic human airways.American journal of physiology. Cell physiology · 2026
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  9. Targeting the senescence‒autophagy axis via p16Signal transduction and targeted therapy · 2026
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115 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Ana L MoraDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, E1246 BST, 200 Lothrop Street, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.
Mauricio RojasDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, E1246 BST, 200 Lothrop Street, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.
Annie PardoFacultad de Ciencias, Universidad Nacional Autónoma de México, Avenida Universidad 3000; CP 04510, México City, Mexico.
Moises SelmanInstituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Tlalpan 4502; CP 14080, México City, Mexico.

Funding

Aging of Mesenchymal Stem Cells Missing Link in IPFR01HL123766 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROJAS, MAURICIO · 2015 to 2018
$1.9M
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is a fatal age-associated disease that is characterized by progressive and irreversible scarring of the lung. The pathogenesis of IPF is not completely understood and current therapies are limited to those that reduce the rate of functional decline in patients with mild-to-moderate disease. In this context, new therapeutic approaches that substantially improve the survival time and quality of life of these patients are urgently needed. Our incomplete understanding of the pathogenic mechanisms of IPF and the lack of appropriate experimental models that reproduce the key characteristics of the human disease are major challenges. As ageing is a major risk factor for IPF, age-related cell perturbations such as telomere attrition, senescence, epigenetic drift, stem cell exhaustion, loss of proteostasis and mitochondrial dysfunction are becoming targets of interest for IPF therapy. In this Review, we discuss current and emerging therapies for IPF, particularly those targeting age-related mechanisms, and discuss future therapeutic approaches.

Indexed as

AnimalsCellular SenescenceHumansIdiopathic Pulmonary FibrosisMolecular Targeted Therapy

Identifiers

PMID28983101

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.