Evidence map›Paper›PMID 31178484›Full record

ArticleInternal medicine (Tokyo, Japan)2019

An Anti-PM/Scl-75 Antibody-positive Japanese Woman Who Developed Inflammatory Myopathy.

Yuki Nakamura, Rei Miyanaga, Hirohiko Shizukawa, Shun Shimohama

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Yuki NakamuraDepartment of Neurology, Sapporo Kosei General Hospital, Japan.
Rei MiyanagaDepartment of Neurology, Sapporo Kosei General Hospital, Japan.
Hirohiko ShizukawaDepartment of Neurology, Sapporo Kosei General Hospital, Japan.
Shun ShimohamaDepartment of Neurology, Sapporo Medical University School of Medicine, Japan.
Sapporo Kosei General Hospital · JPSapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 69-year-old Japanese woman presented with mild muscle weakness of the neck and symmetrical proximal parts of the upper and lower limbs. Laboratory tests, needle electromyography, and a muscle biopsy revealed inflammatory myopathy with an apparent clinical classification of polymyositis and positive findings for anti-PM/Scl-75 antibody. This antibody is rare among Japanese populations, and most Japanese patients with the antibody are not classified with the inflammatory myopathy seen in polymyositis. The muscle biopsy also showed marked necrotic and regenerative fibers. We need to collectively investigate patients with the potential to develop this disease, and to identify any unique characteristics for Asian populations, including Japanese.

Indexed as

AgedAsian PeopleAutoantibodiesBiopsyElectromyographyExosome Multienzyme Ribonuclease ComplexFemaleHumansJapanMagnetic Resonance ImagingMuscle WeaknessMyositisPolymyositisRNA-Binding ProteinsAutoantibodiesEXOSC9 protein, humanExosome Multienzyme Ribonuclease ComplexRNA-Binding Proteinsanti-PM/Scl antibodyinflammatory myopathyJapanesemuscle biopsyneurology

Identifiers

PMID31178484
PMCPMC6794191
OpenAlexW2973210169

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.