Cargando…

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

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. METHO...

Descripción completa

Detalles Bibliográficos
Autores principales: Tateyama, Maki, Fujihara, Kazuo, Misu, Tatsuro, Arai, Akira, Kaneta, Tomohiro, Aoki, Masashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298089/
https://www.ncbi.nlm.nih.gov/pubmed/25582454
http://dx.doi.org/10.1136/bmjopen-2014-006763
_version_ 1782353221788893184
author Tateyama, Maki
Fujihara, Kazuo
Misu, Tatsuro
Arai, Akira
Kaneta, Tomohiro
Aoki, Masashi
author_facet Tateyama, Maki
Fujihara, Kazuo
Misu, Tatsuro
Arai, Akira
Kaneta, Tomohiro
Aoki, Masashi
author_sort Tateyama, Maki
collection PubMed
description 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. METHODS: 33 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. RESULTS: vFDG 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. CONCLUSIONS: The 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.
format Online
Article
Text
id pubmed-4298089
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-42980892015-01-23 Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation Tateyama, Maki Fujihara, Kazuo Misu, Tatsuro Arai, Akira Kaneta, Tomohiro Aoki, Masashi BMJ Open Neurology 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. METHODS: 33 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. RESULTS: vFDG 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. CONCLUSIONS: The 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. BMJ Publishing Group 2015-01-10 /pmc/articles/PMC4298089/ /pubmed/25582454 http://dx.doi.org/10.1136/bmjopen-2014-006763 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Neurology
Tateyama, Maki
Fujihara, Kazuo
Misu, Tatsuro
Arai, Akira
Kaneta, Tomohiro
Aoki, Masashi
Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation
title Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation
title_full Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation
title_fullStr Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation
title_full_unstemmed Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation
title_short Clinical values of FDG PET in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation
title_sort clinical values of fdg pet in polymyositis and dermatomyositis syndromes: imaging of skeletal muscle inflammation
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298089/
https://www.ncbi.nlm.nih.gov/pubmed/25582454
http://dx.doi.org/10.1136/bmjopen-2014-006763
work_keys_str_mv AT tateyamamaki clinicalvaluesoffdgpetinpolymyositisanddermatomyositissyndromesimagingofskeletalmuscleinflammation
AT fujiharakazuo clinicalvaluesoffdgpetinpolymyositisanddermatomyositissyndromesimagingofskeletalmuscleinflammation
AT misutatsuro clinicalvaluesoffdgpetinpolymyositisanddermatomyositissyndromesimagingofskeletalmuscleinflammation
AT araiakira clinicalvaluesoffdgpetinpolymyositisanddermatomyositissyndromesimagingofskeletalmuscleinflammation
AT kanetatomohiro clinicalvaluesoffdgpetinpolymyositisanddermatomyositissyndromesimagingofskeletalmuscleinflammation
AT aokimasashi clinicalvaluesoffdgpetinpolymyositisanddermatomyositissyndromesimagingofskeletalmuscleinflammation