Evidence map›Paper›PMID 29903047›Full record

ArticleRespiratory research2018

Bone marrow characterization in COPD: a multi-level network analysis.

Nuria Toledo-Pons, Guillaume Noell, Andreas Jahn, Amanda Iglesias, Maria Antonia Duran, Julio Iglesias, Angel Rios, Sergio Scrimini, Rosa Faner, Orlando Gigirey and 2 more

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Eosinophil-derived IL-13 promotes emphysema.The European respiratory journal · 2019
    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

12 authors at 2 institutions in 1 country.

Nuria Toledo-PonsCIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Guillaume NoellCIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Andreas JahnDepartment of Respiratory Medicine, Hospital Universitari Son Espases-IdISBa, Valldemossa 79, 07010, Palma de Mallorca, Spain.
Amanda IglesiasCIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Maria Antonia DuranDepartment of Hematology, Hospital Universitari Son Espases-IdISBa, Mallorca, Spain.
Julio IglesiasDepartment of Immunology, Hospital Universitari Son Espases-IdISBa, Mallorca, Spain.
Angel RiosDepartment of Respiratory Medicine, Hospital Universitari Son Espases-IdISBa, Valldemossa 79, 07010, Palma de Mallorca, Spain.
Sergio ScriminiDepartment of Respiratory Medicine, Hospital Universitari Son Espases-IdISBa, Valldemossa 79, 07010, Palma de Mallorca, Spain.
Rosa FanerCIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Orlando GigireyDepartment of Thoracic Surgery, Hospital Universitari Son Espases-IdISBa, Mallorca, Spain.
Alvar AgustíCIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Borja G CosíoCIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain. borja.cosio@ssib.es.ORCID 0000-0002-6388-8209
Health Research Institute of the Balearic Islands · ESInstituto de Salud Carlos III · ES

Funding

Instituto de Salud Carlos III PI08/0780Sociedad Española de Neumología y Cirugía Torácica 2008
6 · The paper itself

Abstract

backgroundBone marrow (BM) produces hematopoietic and progenitor cells that contribute to distant organ inflammation and repair. Chronic obstructive pulmonary disease (COPD) is characterized by defective lung repair. Yet, BM composition has not been previously characterized in COPD patients.

methodsIn this prospective and controlled study, BM was obtained by sternum fine-needle aspiration in 35 COPD patients and 25 healthy controls (10 smokers and 15 never-smokers). BM cell count and immunophenotype were determined by microscopy and flow cytometry, respectively. Circulating inflammatory (C-reactive protein, IL-6, IL-8) and repair markers (HGF, IGF, TGF-β, VEGF) were quantified by ELISA. Results were integrated by multi-level network correlation analysis.

resultsWe found that: (1) there were no major significant pair wise differences between COPD patients and controls in the BM structural characteristics; (2) multi-level network analysis including patients and controls identifies a relation between immunity, repair and lung function not previously described, that remains in the COPD network but is absent in controls; and (3) this novel network identifies eosinophils as a potential mediator relating immunity and repair, particularly in patients with emphysema.

conclusionsOverall, these results suggest that BM is activated in COPD with impaired repair capacity in patients with more emphysema and/or higher circulating eosinophils.

Indexed as

AgedAged, 80 and overBone MarrowBone Marrow CellsCohort StudiesFemaleHumansLungMaleMiddle AgedProspective StudiesProtein Interaction MapsPulmonary Disease, Chronic ObstructiveSmokingBone marrowCOPDEosinophilNetwork

Identifiers

PMID29903047
PMCPMC6003122
OpenAlexW2808319740

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.