Evidence map›Paper›PMID 27726047›Full record

ArticleClinical rheumatology2017

Elevated serum levels of soluble CD146 in patients with systemic sclerosis.

Tomoko Ito, Naoto Tamura, Sayuri Okuda, Kurisu Tada, Masakazu Matsushita, Ken Yamaji, Kazunori Kato, Yoshinari Takasaki

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Transcriptional landscape of CD4+ T cells in Systemic Sclerosis.bioRxiv : the preprint server for biology · 2026
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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

8 authors at 2 institutions in 1 country.

Tomoko ItoDepartment of Internal Medicine and Rheumatology, Juntendo University, Faculty of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo, 113-8421, Japan.
Naoto TamuraDepartment of Internal Medicine and Rheumatology, Juntendo University, Faculty of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo, 113-8421, Japan. tnaoto@juntendo.ac.jp.
Sayuri OkudaDepartment of Biomedical Engineering, Faculty of Science and Engineering, Toyo University, 2100, Kujirai, Kawagoe, Saitama, Japan.
Kurisu TadaDepartment of Internal Medicine and Rheumatology, Juntendo University, Faculty of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo, 113-8421, Japan.
Masakazu MatsushitaDepartment of Internal Medicine and Rheumatology, Juntendo University, Faculty of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo, 113-8421, Japan.
Ken YamajiDepartment of Internal Medicine and Rheumatology, Juntendo University, Faculty of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo, 113-8421, Japan.
Kazunori KatoDepartment of Biomedical Engineering, Faculty of Science and Engineering, Toyo University, 2100, Kujirai, Kawagoe, Saitama, Japan.
Yoshinari TakasakiDepartment of Internal Medicine and Rheumatology, Juntendo University, Faculty of Medicine, 2-1-1 Hongo, Bunkyo, Tokyo, 113-8421, Japan.
Juntendo University · JPToyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD146, a transmembrane glycoprotein member of the immunoglobulin superfamily, acts as an adhesion molecule that helps maintain the cell monolayer. Human endothelial cells expressing CD146 are involved in angiogenesis and inflammation. Recently, we developed a sandwich ELISA for detecting soluble CD146 (sCD146) in human serum specimens. The aim of this study is to determine serum levels of sCD146 in patients with systemic sclerosis (SSc) and to examine the relationship between sCD146 levels and clinical manifestations. We quantified serum sCD146 levels in 47 serum samples from patients fulfilling criteria for SSc, 23 serum samples from patients fulfilling criteria for rheumatoid arthritis (RA), and 25 healthy controls. We also investigated the relationship between sCD146 levels and various clinical characteristics with SSc patients. Levels of sCD146 were significantly higher in the 47 patients with SSc than in the 25 healthy controls and 23 patients with RA (12.50 vs. 6.91 vs. 9.95 ng/ml; p < 0.001). Serum sCD146 levels in SSc patients with pulmonary arterial hypertension (PAH) were lower than in SSc patients without PAH (10.12 vs.13.17 ng/ml; p < 0.01). The serum levels of sCD146 were elevated in patients with SSc. However, decreased sCD146 levels were observed in SSc patients with PAH. Further studies are necessary to elucidate the sources and the mechanisms.

Indexed as

Gene Expression RegulationAgedArthritis, RheumatoidCase-Control StudiesCD146 AntigenEnzyme-Linked Immunosorbent AssayFemaleHumansHypertension, PulmonaryMaleMiddle AgedScleroderma, SystemicT-Lymphocyte SubsetsCD146 AntigenPulmonary arterial hypertensionSoluble CD146Systemic sclerosis

Identifiers

PMID27726047
OpenAlexW2530510895

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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.