Evidence map›Paper›PMID 30416782›Full record

ArticleJournal of thoracic disease2018

Serum decorin is a potential prognostic biomarker in patients with acute exacerbation of idiopathic pulmonary fibrosis.

Takefumi Nikaido, Yoshinori Tanino, Xintao Wang, Yuki Sato, Ryuichi Togawa, Masami Kikuchi, Kenichi Misa, Kazue Saito, Naoko Fukuhara, Takaya Kawamata and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of thoracic disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Roles of extracellular matrix in lung diseases.Fukushima journal of medical science · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Targeting Asporin in Lung Fibrosis: A New Approach to an Old Concept.American journal of respiratory cell and molecular biology · 2022
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Acute Exacerbation of Idiopathic Pulmonary Fibrosis.Medicina (Kaunas, Lithuania) · 2019
    Review
  18. Review
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

24 authors at 1 institution in 1 country.

Takefumi NikaidoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yoshinori TaninoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Xintao WangDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yuki SatoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Ryuichi TogawaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Masami KikuchiDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kenichi MisaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kazue SaitoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Naoko FukuharaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Takaya KawamataDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Mami RikimaruDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Takashi UmedaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Julia MorimotoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Tatsuhiko KoizumiDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yasuhito SuzukiDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kenichiro HiraiDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Manabu UematsuDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hiroyuki MinemuraDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Atsuro FukuharaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Suguru SatoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Junpei SaitoDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hiroshi YokouchiDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kenya KanazawaDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yoko ShibataDepartment of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.
Fukushima Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDecorin is a small leucine-rich repeat proteoglycan that plays a critical role in collagen fibrillogenesis, and regulates inflammation, wound healing and angiogenesis. In idiopathic pulmonary fibrosis (IPF), decorin is expressed in fibrotic lesions; furthermore, intratracheal gene transfer of decorin has been demonstrated to inhibit bleomycin-induced pulmonary fibrosis. Although these results suggest the critical role of decorin in pulmonary fibrosis, the role of decorin in the acute exacerbation of idiopathic interstitial pneumonia (AE-IIP) has not been clarified in detail. Thus, the goal of this study was to determine the role of decorin in AE-IIP.

methodsWe retrospectively analyzed AE-IIP patients who had been admitted to our hospital. First, serum decorin levels were compared among patients with AE-IIP, patients with stable idiopathic interstitial pneumonia (SD-IIP), and healthy subjects. Next, the relationship between serum decorin levels and clinical parameters was analyzed in AE-IIP patients. Finally, the association between serum decorin levels and prognosis was evaluated in AE-IIP patients. IIP was divided into IPF and non-IPF, according to the published guidelines.

resultsThe serum decorin levels of AE-IIP patients were significantly lower than those of both healthy subjects and SD-IIP patients. Serum decorin levels were not related with the clinical parameters and prognosis, when all IIP patients were analyzed. In IPF patients, serum decorin levels had a significant correlation with oxygenation, and IPF patients with low serum decorin levels had a significantly higher survival rate than those with high serum decorin levels.

conclusionsSerum decorin levels are a potential prognostic biomarker in AE-IPF.

Indexed as

acute exacerbation (AE)biomarkerDecorinidiopathic pulmonary fibrosis (IPF)prognosis

Identifiers

PMID30416782
PMCPMC6196213
OpenAlexW2891956556

What OpenQuestion holds

Textmetadata
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Registered trials

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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.