Evidence map›Paper›PMID 38567566›Full record

ArticleSarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG2024

Characteristics of chest high-resolution computed tomography in patients with anti-aminoacyl-tRNA synthetase antibody-positive interstitial lung disease.

Masato Mima, Seidai Sato, Takayoshi Shinya, Nobuhito Naito, Takatoshi Shoji, Saki Harada, Ryoko Suzue, Kojin Murakami, Kazuya Koyama, Yasuhiko Nishioka

Open access · greenAbstract read
In one paragraph

Article in Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Chest radiography in interstitial lung disease: Accuracy and radiological features from a systematic review and meta-analysis.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2025
    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

10 authors at 1 institution in 1 country.

Masato MimaDepartment of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences,Tokushima University.
Seidai SatoDepartment of Respiratory Medicine and Rheumatology,Graduate School of Biomedical Sciences,Tokushima University.
Takayoshi ShinyaDepartment of Radiology, Tokushima University Hospital, Tokushima, Japan.
Nobuhito NaitoDepartment of Respiratory Medicine and Rheumatology,Graduate School of Biomedical Sciences,Tokushima University.
Takatoshi ShojiDepartment of Respiratory Medicine and Rheumatology,Graduate School of Biomedical Sciences,Tokushima University.
Saki HaradaDepartment of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences,Tokushima University.
Ryoko SuzueDepartment of Respiratory Medicine and Rheumatology,Graduate School of Biomedical Sciences,Tokushima University.
Kojin MurakamiDepartment of Respiratory Medicine and Rheumatology,Graduate School of Biomedical Sciences,Tokushima University.
Kazuya KoyamaDepartment of Respiratory Medicine and Rheumatology,Graduate School of Biomedical Sciences,Tokushima University.
Yasuhiko NishiokaDepartment of Respiratory Medicine and Rheumatology,Graduate School of Biomedical Sciences,Tokushima University.
Tokushima University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimAnti-aminoacyl-tRNA synthetase (ARS) antibodies form a condition called Antisynthetase syndrome (ASSD). While interstitial lung disease (ILD) is a particularly frequent manifestation of ASSD and is closely associated with morbidity and mortality, few studies have been conducted on its characteristics on high-resolution computed tomography (HRCT). In this study, we clarified the HRCT findings in patients with anti-ARS antibody-positive ILD (ARS-ILD).  Methods: The HRCT findings at the time of the ILD diagnosis in 24 ARS-ILD patients were retrospectively evaluated by 2 pulmonologists and one radiologist. We also assessed the clinical symptoms, physical examination findings, and laboratory data including the type of anti-ARS antibodies. For a further analysis, the data of patients were divided into two groups: the polymyositis (PM)/dermatomyositis (DM) group and the non-PM/DM group.

resultsThe ratio of men to women was almost 1:1. The median age at the time of the diagnosis was 53 years old. Anti-glycyl (anti-EJ) and anti-histidyl (anti-Jo-1) antibodies were more common than others. An analysis of the HRCT patterns of 23 ARS-ILD patients showed that the most common pattern was the nonspecific interstitial pneumonia (NSIP) pattern. The second most common pattern was the usual interstitial pneumonia (UIP) pattern. Between the PM/DM and non-PM/DM groups, no clear trends were noted in the age, sex ratio, proportion of HRCT patterns, or type of anti-ARS antibodies.

conclusionsThis retrospective study demonstrated that ARS-ILD patients, regardless of myositis symptoms, most often showed the NSIP pattern on HRCT, as previously reported. However, unlike previous reports, the UIP pattern on HRCT was not rare.

Identifiers

PMID38567566
PMCPMC11008333
OpenAlexW4394763095

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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.