Evidence map›Paper›PMID 26451097›Full record

ArticleInternational journal of chronic obstructive pulmonary disease2015

Proteoglycan 4 is a diagnostic biomarker for COPD.

Kang-Yun Lee, Hsiao-Chi Chuang, Tzu-Tao Chen, Wen-Te Liu, Chien-Ling Su, Po-Hao Feng, Ling-Ling Chiang, Mauo-Ying Bien, Shu-Chuan Ho

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in International journal of chronic obstructive pulmonary disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02764658 (Studies in Pulmonary Inflammation and the Effectiveness of Pulmonary Recovery in COPD Patients:the Mechanism of Proteoglycan 4), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% 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.

NCT02764658 naunknown statusnot on this mapstarted 2016, after this paper: background citation

Studies in Pulmonary Inflammation and the Effectiveness of Pulmonary Recovery in COPD Patients:the Mechanism of Proteoglycan 4

TypeinterventionalSponsorTaipei Medical UniversityRan2016 to 2019Enrolled90ConditionsCOPDArmsPulmonary recovery on the AECOPD, Routine care on the AECOPD, Routine care on the stable COPD
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 22 citations in OpenAlex.

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  11. Neonatal hyperoxia depletes pulmonary vein cardiomyocytes in adult mice via mitochondrial oxidation.American journal of physiology. Lung cellular and molecular physiology · 2018
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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

9 authors at 2 institutions in 1 country.

Kang-Yun LeeDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan ; Department of Internal Medicine, School of Medicine, Taipei Medical University, Taipei, Taiwan.
Hsiao-Chi ChuangDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan ; School of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Tzu-Tao ChenDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Wen-Te LiuDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan ; School of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Chien-Ling SuDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan ; School of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Po-Hao FengDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan ; Department of Internal Medicine, School of Medicine, Taipei Medical University, Taipei, Taiwan.
Ling-Ling ChiangDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan ; School of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Mauo-Ying BienSchool of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan ; Division of Pulmonary Medicine, Department of Internal Medicine, Taipei Medical University Hospital, Taipei Medical University, Taipei, Taiwan.
Shu-Chuan HoSchool of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Taipei Medical University · TWTaipei Medical University-Shuang Ho Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe measurement of C-reactive protein (CRP) to confirm the stability of COPD has been reported. However, CRP is a systemic inflammatory biomarker that is related to many other diseases.

objectiveThe objective of this study is to discover a diagnostic biomarker for COPD.

methodsSixty-one subjects with COPD and 15 healthy controls (10 healthy non-smokers and 5 smokers) were recruited for a 1-year follow-up study. Data regarding the 1-year acute exacerbation frequency and changes in lung function were collected. CRP and the identified biomarkers were assessed in the validation COPD cohort patients and healthy subjects. Receiver operating characteristic values of CRP and the identified biomarkers were determined. A validation COPD cohort was used to reexamine the identified biomarker. Correlation of the biomarker with 1-year lung function decline was determined.

resultsProteoglycan 4 (PRG4) was identified as a biomarker in COPD. The serum concentrations of PRG4 in COPD Global initiative for chronic Obstructive Lung Disease (GOLD) stages 1+2 and 3+4 were 10.29 ng/mL and 13.20 ng/mL, respectively; 4.99 ng/mL for healthy controls (P<0.05); and 4.49 ng/mL for healthy smokers (P<0.05). PRG4 was more sensitive and specific than CRP for confirming COPD severity and acute exacerbation frequency. There was no correlation between CRP and PRG4 levels, and PRG4 was negatively correlated with the 1-year change in predicted forced vital capacity percent (R (2)=0.91, P=0.013).

conclusionPRG4 may be a biomarker for identification of severity in COPD. It was related to the 1-year forced vital capacity decline in COPD patients.

Indexed as

AdultAgedAged, 80 and overBiomarkersCase-Control StudiesC-Reactive ProteinFemaleFollow-Up StudiesForced Expiratory VolumeHumansLungMaleMiddle AgedProteoglycan 4ProteoglycansPulmonary Disease, Chronic ObstructiveBiomarkersC-Reactive ProteinPRG4 protein, humanProteoglycan 4ProteoglycansC-reactive proteinexacerbationinflammationlung function decline

Identifiers

PMID26451097
PMCPMC4583110
OpenAlexW1730310984

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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.