Volume 64, Issue 3 pp. 866-875
Vasculitis

The role of 18F-fluorodeoxyglucose–positron emission tomography in the assessment of disease activity in patients with Takayasu arteritis

Kwang-Hoon Lee

Kwang-Hoon Lee

Yonsei University College of Medicine, Seoul, South Korea

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Arthur Cho

Arthur Cho

Severance Hospital and Yonsei University College of Medicine, Seoul, South Korea

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Yun-Jung Choi

Yun-Jung Choi

Severance Hospital and Yonsei University College of Medicine, Seoul, South Korea

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Sang-Won Lee

Sang-Won Lee

Yonsei University College of Medicine, Seoul, South Korea

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You-Jung Ha

You-Jung Ha

Yonsei University College of Medicine, Seoul, South Korea

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Se-Jin Jung

Se-Jin Jung

Yonsei University College of Medicine, Seoul, South Korea

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Min-Chan Park

Min-Chan Park

Yonsei University College of Medicine, Seoul, South Korea

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Jong-Doo Lee

Jong-Doo Lee

Severance Hospital and Yonsei University College of Medicine, Seoul, South Korea

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Soo-Kon Lee

Soo-Kon Lee

Yonsei University College of Medicine, Seoul, South Korea

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Yong-Beom Park

Corresponding Author

Yong-Beom Park

Yonsei University College of Medicine, Seoul, South Korea

Department of Internal Medicine, Yonsei University College of Medicine, 250 Sungsanno, Seodaemoon-gu, Seoul 120-752, South KoreaSearch for more papers by this author
First published: 11 October 2011
Citations: 86

Abstract

Objective

The assessment of disease activity in Takayasu arteritis (TA) is difficult in clinical situations because clinical symptoms and laboratory parameters do not always reflect the actual inflammation of the arterial wall. We undertook this study to comprehensively investigate the role of 18F-fluorodeoxyglucose–positron emission tomography (FDG-PET) in the assessment of disease activity in patients with TA.

Methods

We performed a retrospective chart review of 53 FDG-PET scans in 38 patients with TA. We measured 18F-fluorodeoxyglucose (18F-FDG) accumulation in the vascular wall of the large vessel using semiquantitative (visual grade) and quantitative (standard uptake value intensity) analyses. Clinical disease activity was evaluated based on the National Institutes of Health criteria for active TA, and erythrocyte sedimentation rates (ESRs) and C-reactive protein (CRP) levels were measured.

Results

At baseline, active vascular 18F-FDG uptake (visual grade ≥2) was observed in 18 of 24 patients with active disease and in 5 of 14 patients with inactive disease. There was a significant association between clinical disease activity and disease activity judged by FDG-PET (P = 0.008). Visual grade, standard uptake value intensity, and the number of vascular lesions with active 18F-FDG uptake were significantly higher in patients with active disease and correlated well with the ESR and CRP levels. In 15 followup FDG-PET scans, the changes in visual grade, areas of active vascular 18F-FDG uptake, and standard uptake value intensity reflected changes in clinical disease activity.

Conclusion

18F-FDG uptake was associated with clinical disease activity and markers of inflammation, and FDG-PET reflected changes in clinical disease activity in patients with TA. FDG-PET may be a useful tool for aiding in the assessment of disease activity in patients with TA.

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