Evidence map›Paper›PMID 25582454›Full record

ArticleBMJ open2015

Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation.

Maki Tateyama, Kazuo Fujihara, Tatsuro Misu, Akira Arai, Tomohiro Kaneta, Masashi Aoki

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in BMJ open, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 66 citations in OpenAlex.

  1. ExtraosseousDiagnostics (Basel, Switzerland) · 2026
    Article
  2. Review
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  6. [Diagnostics (Basel, Switzerland) · 2023
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  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. MRI and muscle imaging for idiopathic inflammatory myopathies.Brain pathology (Zurich, Switzerland) · 2021
    Review
  16. Article
  17. Article
  18. European journal of hybrid imaging · 2020
    Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Maki TateyamaDepartment of Neurology, Tohoku University School of Medicine, Sendai, Japan Department of Neurology, Iwate National Hospital, Iwate, Japan.
Kazuo FujiharaDepartment of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Tatsuro MisuDepartment of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Akira AraiDepartment of Diagnostic Radiology, Tohoku University School of Medicine, Sendai, Japan.
Tomohiro KanetaDepartment of Diagnostic Radiology, Tohoku University School of Medicine, Sendai, Japan.
Masashi AokiDepartment of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Tohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectives[(18)F] Fluorodeoxyglucose positron emission tomography (FDG PET), a standard tool for evaluating malignancies, can also detect inflammatory lesions. However, its usefulness in evaluating muscle lesions in polymyositis and dermatomyositis syndromes (PM/DM) has not been established.

methods33 patients with PM/DM who had undergone FDG PET were retrospectively analysed. FDG uptake was visually evaluated (visually identified FDG uptake, vFDG) in 16 regions of the body using mediastinum blood vessels as a positivity criterion. We also calculated the maximum standardised uptake value (SUVmax) in all four limbs of the patients with PM/DM as well as in 22 patients with amyotrophic lateral sclerosis (ALS) with similar disabilities. In 24 patients with PM/DM, MRI and FDG PET findings were compared.

resultsvFDG was observed in multiple muscle lesions with varying distributions in two-thirds of the patients with PM/DM, with most lesions being symmetrical. The number of vFDG-positive regions strongly correlated with the mean SUVmax in all four limbs (p<0.0001). Histological grades of biopsied muscles correlated with both the mean SUVmax and number of vFDG-positive regions. Serum creatine kinase levels were higher in patients with more than two vFDG-positive regions than in those with two or less regions (p<0.05). While the inflamed muscles showed diffused, patchy or marginal signal abnormalities on MRI, FDG uptake was most prominent inside the muscles. Compared with ALS, the mean SUVmax was significantly higher in the patients with PM/DM (p<0.0001) and showed a striking correlation in the bilateral muscles, reflecting symmetrical muscle involvement in PM/DM.

conclusionsThe visual assessment of FDG uptake as well as calculation of SUV enabled us to comprehensively evaluate skeletal muscle. This method can improve clinical practices and provide insights into pathomechanisms of PM/DM.

Indexed as

Fluorodeoxyglucose F18RadiopharmaceuticalsAdultAgedAged, 80 and overAmyotrophic Lateral SclerosisCreatine KinaseDermatomyositisFemaleHumansInflammationMaleMiddle AgedMuscle, SkeletalPolymyositisPositron-Emission TomographyCreatine KinaseFluorodeoxyglucose F18RadiopharmaceuticalsHISTOPATHOLOGYIMMUNOLOGY

Identifiers

PMID25582454
PMCPMC4298089
OpenAlexW2114048463

What OpenQuestion holds

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LicenceCC BY-NC
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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.