Evidence map›Paper›PMID 30723246›Full record

ArticleScientific reports2019

Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations.

Koji Habe, Hideo Wada, Ayaka Higashiyama, Tomoko Akeda, Kenshiro Tsuda, Ryoko Mori, Masato Kakeda, Keiichi Yamanaka, Hitoshi Mizutani

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

9 authors at 1 institution in 1 country.

Koji HabeDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan. habe-k@clin.medic.mie-u.ac.jp.
Hideo WadaDepartment of Molecular and Laboratory Medicine, Mie University Graduate School of Medicine, Mie, Tsu, Japan.
Ayaka HigashiyamaDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan.
Tomoko AkedaDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan.
Kenshiro TsudaDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan.
Ryoko MoriDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan.
Masato KakedaDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan.
Keiichi YamanakaDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan.ORCID 0000-0003-3055-5202
Hitoshi MizutaniDepartment of Dermatology, Mie University Graduate School of Medicine, Mie, Tsu, Japan.
Mie University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To explore the influence of dermatomyositis (DM)-specific cutaneous manifestations (scm) on systemic coagulation and fibrinolysis, we retrospectively studied plasma D-dimer levels with/without venous thromboembolism (VTE), malignancy, infection or other connective tissue diseases (CTDs) and scm. One hundred fifty patients with DM were retrospectively investigated using medical records regarding scm, VTE, malignancy, infection, other CTDs, laboratory data and systemic corticosteroid therapy. All DM patients were categorized as follows: group 1, without scm, VTE, infection, malignancy or other accompanying CTDs; group 2, with scm only; and group 3, with VTE, infection, malignancy and other accompanying CTDs but without scm. The D-dimer plasma levels were significantly increased in group 3 compared with healthy subjects and those in groups 1 and 2 (p < 0.001). The D-dimer plasma level in group 2 was significantly increased compared with healthy subjects and those in group 1 (p < 0.001). Increased D-dimer plasma levels were detected in DM patients with scm without detectable VTE, malignancy, infection or accompanying CTDs. In addition to the known risk factors for increased plasma D-dimer levels in DM patients, including VTE, malignancy, infection and other accompanying autoimmune diseases, the presence of cutaneous manifestations should be considered as a new clinical risk factor.

Indexed as

AgedAged, 80 and overAutoimmune DiseasesDermatomyositisFemaleFibrin Fibrinogen Degradation ProductsFibrinolysisFollow-Up StudiesHumansInfectionsMaleMiddle AgedNeoplasmsRetrospective StudiesRisk FactorsSkinFibrin Fibrinogen Degradation Productsfibrin fragment D

Identifiers

PMID30723246
PMCPMC6363793
OpenAlexW2911376467

What OpenQuestion holds

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LicenceCC BY
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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.