Evidence map›Paper›PMID 32476947›Full record

ArticleSarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG2019

Cathepsin S, a new serum biomarker of sarcoidosis discovered by transcriptome analysis of alveolar macrophages.

Hiroyuki Tanaka, Etsuro Yamaguchi, Nobuhiro Asai, Toyoharu Yokoi, Masaki Nishimura, Haruhisa Nakao, Masashi Yoneda, Yoshinori Ohtsuka, Satoshi Konno, Noritaka Yamada

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In one paragraph

Article in Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Overview of multi-omics approaches for pulmonary sarcoidosis.EC pulmonology and respiratory medicine · 2025
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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

10 authors at 2 institutions in 1 country.

Hiroyuki TanakaDivision of Respiratory Medicine and Allergology, Department of Internal Medicine, School of Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Etsuro YamaguchiDivision of Respiratory Medicine and Allergology, Department of Internal Medicine, School of Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Nobuhiro AsaiDepartment of Infection Control and Prevention, School of Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Toyoharu YokoiDepartment of Pathology, Nagoya Ekisaikai Hospital, Nagoya, Aichi, Japan.
Masaki NishimuraDivision of Respiratory Medicine and Allergology, Department of Internal Medicine, School of Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Haruhisa NakaoDivision of Hepatology and Pancreatology, Department of Internal Medicine, School of Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Masashi YonedaDivision of Hepatology and Pancreatology, Department of Internal Medicine, School of Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Yoshinori OhtsukaDepartment of Medicine, Hokkaido Chuo Rosai Hospita, Iwamizawa, Japan.
Satoshi KonnoFirst Department of Medicine, Hokkaido University School of Medicine, Sapporo, Japan.
Noritaka YamadaDepartment of Respiratory Medicine, National Hospital Organization, Higashinagoya Hospital, Nagoya, Aichi, Japan.
Hokkaido University · JPNagoya Ekisaikai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDevelopment of reliable new biomarkers remains crucial to improve diagnosis and assessing disease activity in sarcoidosis. The objective of this study was to seek such markers from the gene expression signature of alveolar macrophages by transcriptome analysis.

methodsPooled RNA extracted from alveolar macrophages from patients with active sarcoidosis and control patients was subjected to transcriptome analysis using microarrays. Expressed gene intensity in sarcoidosis relative to that in control was calculated. We measured serum cathepsin S (CTSS) concentrations in 89 healthy volunteers, 107 patients with sarcoidosis, 26 with interstitial pneumonia, 150 with pneumoconiosis, and 76 with pulmonary mycobacteriosis by the enzyme-linked immunosorbent assay.

resultsAmong 12 genes with ratios higher than that of a housekeeping gene, we selected CTSS for scrutinizing protein expression in serum because of the feasibility of the protein assay. CTSS concentrations were significantly increased in sarcoidosis compared with not only controls but also all the other lung diseases. Receiver operating characteristics curve for sarcoidosis and parenchymal lung diseases revealed an area under the curve of 0.800 (95% confidence interval, 0.751-0.850; p=1.4 x 10

conclusionsCTSS has the potential to be a useful biomarker in sarcoidosis.

Indexed as

Gene Expression ProfilingTranscriptomeAdultAgedAged, 80 and overBiomarkersCase-Control StudiesCathepsinsFemaleHumansLungMacrophages, AlveolarMaleMiddle AgedPredictive Value of TestsSarcoidosis, PulmonaryBiomarkerscathepsin SCathepsinsbiomarkerscathepsinsmacrophagessarcoidosistranscriptome

Identifiers

PMID32476947
PMCPMC7247107
OpenAlexW3030148277

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.