Evidence map›Paper›PMID 34203210›Full record

ArticleJournal of clinical medicine2021

Soluble C-Type Lectin-Like Receptor 2 Is a Biomarker for Disseminated Intravascular Coagulation.

Akitaka Yamamoto, Hideo Wada, Yuhuko Ichkawa, Motoko Tanaka, Haruhiko Tashiro, Katsuya Shiraki, Hideto Shimpo, Yoshiki Yamashita, Takeshi Mastumoto, Motomu Shimaoka and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  6. Biomarkers of Hypercoagulability in COVID-19.Journal of clinical medicine · 2023
    Article
  7. Article
  8. Article
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  11. Super Formula for Soluble C-Type Lectin-Like Receptor 2 × D-Dimer in Patients With Acute Cerebral Infarction.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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 5 institutions in 1 country.

Akitaka YamamotoDepartment of Emergency and Critical Care Center, Mie Prefectural General Medical Center, Yokkaichi 510-0885, Japan.
Hideo WadaDepartment of Central Laboratory, Mie Prefectural General Medical Center, Yokkaichi 510-0885, Japan.ORCID 0000-0001-9021-8633
Yuhuko IchkawaDepartment of Central Laboratory, Mie Prefectural General Medical Center, Yokkaichi 510-0885, Japan.
Motoko TanakaDepartment of Central Laboratory, Mie Prefectural General Medical Center, Yokkaichi 510-0885, Japan.
Haruhiko TashiroDepartment of Emergency and Critical Care Center, Mie Prefectural General Medical Center, Yokkaichi 510-0885, Japan.
Katsuya ShirakiDepartment of Central Laboratory, Mie Prefectural General Medical Center, Yokkaichi 510-0885, Japan.
Hideto ShimpoMie Prefectural General Medical Center, Yokkaichi 510-0885, Japan.
Yoshiki YamashitaDepartment of Hematology and Oncology, Mie University Hospital, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Takeshi MastumotoDepartment of Blood Transfusion and Cell Therapy, Mie University Hospital, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Motomu ShimaokaDepartment of Molecular Pathobiology and Cell Adhesion Biology, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
Toshiaki IbaDepartment of Emergency and Disaster Medicine, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0002-0255-4088
Katsue Suzuki-InoueDepartment of Clinical and Laboratory Medicine, Yamanashi Medical University, Yamanashi 400-8510, Japan.
Mie Chuo Medical Center · JPMie University Hospital · JPJuntendo University · JPMie University · JPUniversity of Yamanashi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disseminated intravascular coagulation (DIC) is induced by excess activation coagulation, and activated platelets are also involved in pathogenesis. Therefore, plasma levels of soluble C-type lectin-like receptor 2 (sCLEC-2), a new marker for platelet activation, can be expected as a marker of DIC in critically ill patients. Plasma levels of sCLEC-2 and D-dimer were measured using the STACIA system. Plasma sCLEC-2 and D-dimer levels were significantly higher in patients with underlying diseases of DIC than in those with unidentified clinical syndrome (UCS). Plasma sCLEC-2 levels were significantly higher in the patients with DIC and Pre-DIC than in those without DIC or Pre-DIC. Similarly, plasma D-dimer levels were also significantly higher in patients with DIC and Pre-DIC than in those without DIC or Pre-DIC. The plasma sCLEC-2 levels in all patients and those with a DIC score ≤ 4 were significantly higher in non-survivors than survivors. The plasma D-dimer levels in all patients, those with a DIC score ≥ 5 and those with a DIC score ≤ 4, were significantly higher in non-survivors than in survivors. The plasma sCLEC-2 is expected as a marker for DIC/Pre-DIC as well as the prognostic marker in critically ill patients.

Indexed as

DICplatelet activationpoor outcomesCLEC-2

Identifiers

PMID34203210
PMCPMC8269023
OpenAlexW3174510575

What OpenQuestion holds

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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.