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Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome

INTRODUCTION: Arthritis is the most frequent manifestation of Blau syndrome, an autoinflammatory disorder caused by the genetic mutation of NOD2. However, detailed information on arthritis in Blau syndrome on which the therapeutic strategy should be based on is lacking. This multi-center study aimed...

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Autores principales: Ikeda, Kei, Kambe, Naotomo, Takei, Syuji, Nakano, Taiji, Inoue, Yuzaburo, Tomiita, Minako, Oyake, Natsuko, Satoh, Takashi, Yamatou, Tsuyoshi, Kubota, Tomohiro, Okafuji, Ikuo, Kanazawa, Nobuo, Nishikomori, Ryuta, Shimojo, Naoki, Matsue, Hiroyuki, Nakajima, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060485/
https://www.ncbi.nlm.nih.gov/pubmed/24713464
http://dx.doi.org/10.1186/ar4533
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author Ikeda, Kei
Kambe, Naotomo
Takei, Syuji
Nakano, Taiji
Inoue, Yuzaburo
Tomiita, Minako
Oyake, Natsuko
Satoh, Takashi
Yamatou, Tsuyoshi
Kubota, Tomohiro
Okafuji, Ikuo
Kanazawa, Nobuo
Nishikomori, Ryuta
Shimojo, Naoki
Matsue, Hiroyuki
Nakajima, Hiroshi
author_facet Ikeda, Kei
Kambe, Naotomo
Takei, Syuji
Nakano, Taiji
Inoue, Yuzaburo
Tomiita, Minako
Oyake, Natsuko
Satoh, Takashi
Yamatou, Tsuyoshi
Kubota, Tomohiro
Okafuji, Ikuo
Kanazawa, Nobuo
Nishikomori, Ryuta
Shimojo, Naoki
Matsue, Hiroyuki
Nakajima, Hiroshi
author_sort Ikeda, Kei
collection PubMed
description INTRODUCTION: Arthritis is the most frequent manifestation of Blau syndrome, an autoinflammatory disorder caused by the genetic mutation of NOD2. However, detailed information on arthritis in Blau syndrome on which the therapeutic strategy should be based on is lacking. This multi-center study aimed to accurately characterize the articular manifestation of Blau syndrome and also to demonstrate the utility of musculoskeletal ultrasound in Blau syndrome. METHODS: Patients who had been diagnosed with Blau syndrome by genetic analysis of NOD2 were recruited. A total of 102 synovial sites in 40 joints were assessed semiquantitatively by ultrasound for gray-scale synovitis and synovial power Doppler (PD) signal. RESULTS: In total, 10 patients whose age ranged from 10 months to 37 years enrolled in this study. Although only 4 joints (0.8%) were tender on physical examination, 81 joints (16.9%) were clinically swollen. Moreover, 240 (50.0%), and 124 (25.8%) joints showed gray-scale (GS) synovitis and synovial PD signal on ultrasound, respectively. Importantly, GS synovitis was present in 168 out of 399 non-swollen joints, in which 61 also exhibited synovial PD signal. Among 40 joint regions, the ankle, the wrist, and the proximal interphalangeal joints were the most frequently and severely affected joints. Comparisons between different synovial tissues demonstrated a significantly higher proportion of the joints with tenosynovitis as compared with that with intra-articular synovitis (41.5% versus 27.9%, P < 0.0001). In respect of age and treatment, synovial PD signals were minimal in the youngest patient and in the oldest two patients, and were relatively mild in patients receiving treatment with methotrexate plus TNF antagonists. In two patients who underwent the second ultrasound examination, total PD scores markedly decreased after initiating the treatment with a tumor necrosis factor (TNF) antagonist. CONCLUSIONS: The detailed information on synovial inflammation obtained by ultrasound confirms the dissociation between pain and inflammation and the frequently involved joint regions and synovial tissue in the arthritis of Blau syndrome. Our data also demonstrate that ultrasonography can be a potent tool in monitoring the activity of synovial inflammation and in investigating the pathophysiology of arthritis in this rare but archetypical autoinflammatory condition.
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spelling pubmed-40604852014-06-17 Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome Ikeda, Kei Kambe, Naotomo Takei, Syuji Nakano, Taiji Inoue, Yuzaburo Tomiita, Minako Oyake, Natsuko Satoh, Takashi Yamatou, Tsuyoshi Kubota, Tomohiro Okafuji, Ikuo Kanazawa, Nobuo Nishikomori, Ryuta Shimojo, Naoki Matsue, Hiroyuki Nakajima, Hiroshi Arthritis Res Ther Research Article INTRODUCTION: Arthritis is the most frequent manifestation of Blau syndrome, an autoinflammatory disorder caused by the genetic mutation of NOD2. However, detailed information on arthritis in Blau syndrome on which the therapeutic strategy should be based on is lacking. This multi-center study aimed to accurately characterize the articular manifestation of Blau syndrome and also to demonstrate the utility of musculoskeletal ultrasound in Blau syndrome. METHODS: Patients who had been diagnosed with Blau syndrome by genetic analysis of NOD2 were recruited. A total of 102 synovial sites in 40 joints were assessed semiquantitatively by ultrasound for gray-scale synovitis and synovial power Doppler (PD) signal. RESULTS: In total, 10 patients whose age ranged from 10 months to 37 years enrolled in this study. Although only 4 joints (0.8%) were tender on physical examination, 81 joints (16.9%) were clinically swollen. Moreover, 240 (50.0%), and 124 (25.8%) joints showed gray-scale (GS) synovitis and synovial PD signal on ultrasound, respectively. Importantly, GS synovitis was present in 168 out of 399 non-swollen joints, in which 61 also exhibited synovial PD signal. Among 40 joint regions, the ankle, the wrist, and the proximal interphalangeal joints were the most frequently and severely affected joints. Comparisons between different synovial tissues demonstrated a significantly higher proportion of the joints with tenosynovitis as compared with that with intra-articular synovitis (41.5% versus 27.9%, P < 0.0001). In respect of age and treatment, synovial PD signals were minimal in the youngest patient and in the oldest two patients, and were relatively mild in patients receiving treatment with methotrexate plus TNF antagonists. In two patients who underwent the second ultrasound examination, total PD scores markedly decreased after initiating the treatment with a tumor necrosis factor (TNF) antagonist. CONCLUSIONS: The detailed information on synovial inflammation obtained by ultrasound confirms the dissociation between pain and inflammation and the frequently involved joint regions and synovial tissue in the arthritis of Blau syndrome. Our data also demonstrate that ultrasonography can be a potent tool in monitoring the activity of synovial inflammation and in investigating the pathophysiology of arthritis in this rare but archetypical autoinflammatory condition. BioMed Central 2014 2014-04-08 /pmc/articles/PMC4060485/ /pubmed/24713464 http://dx.doi.org/10.1186/ar4533 Text en Copyright © 2014 Ikeda et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ikeda, Kei
Kambe, Naotomo
Takei, Syuji
Nakano, Taiji
Inoue, Yuzaburo
Tomiita, Minako
Oyake, Natsuko
Satoh, Takashi
Yamatou, Tsuyoshi
Kubota, Tomohiro
Okafuji, Ikuo
Kanazawa, Nobuo
Nishikomori, Ryuta
Shimojo, Naoki
Matsue, Hiroyuki
Nakajima, Hiroshi
Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome
title Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome
title_full Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome
title_fullStr Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome
title_full_unstemmed Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome
title_short Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome
title_sort ultrasonographic assessment reveals detailed distribution of synovial inflammation in blau syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060485/
https://www.ncbi.nlm.nih.gov/pubmed/24713464
http://dx.doi.org/10.1186/ar4533
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