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Total lesion glycolysis as an IgG4-related disease activity marker.

Authors :
Nakatsuka, Yoshinari
Handa, Tomohiro
Nakamoto, Yuji
Nobashi, Tomomi
Yoshihuji, Hajime
Tanizawa, Kiminobu
Ikezoe, Kohei
Sokai, Akihiko
Kubo, Takeshi
Hirai, Toyohiro
Chin, Kazuo
Togashi, Kaori
Mimori, Tsuneyo
Mishima, Michiaki
Source :
Modern Rheumatology; Jul2015, Vol. 25 Issue 4, p579-584, 6p
Publication Year :
2015

Abstract

Objectives. 2-[18F]-fluoro-2-deoxy-D-glucose-positron emission tomography/computed tomography (FDG-PET/CT) was reported to be useful for monitoring immunoglobulin G4-related disease (IgG4-RD); however, a quantitative FDG-PET/CT analysis such as total lesion glycolysis (TLG) has not yet been conducted. This study aimed to investigate whether TLG would correlate with serum markers in IgG4-RD, and the utility of TLG for disease monitoring. Methods. This retrospective study included 17 patients (12 men; median age, 62 years) who were followed up at Kyoto University Hospital and underwent FDG-PET/CT from April 2009 to November 2013. TLG was calculated for the involved lesions. Correlations between serum markers [IgG4, soluble IL-2 receptor (sIL-2R), lactate dehydrogenase (LDH), and C-reactive protein (CRP)] and TLG concomitant with FDG-PET/CT scans were investigated. Serial changes in TLG were assessed in patients who underwent follow-up FDG-PET/CT ( n = 6). Results. The calculated median (IQL) TLG value was 154.8 (63.7-324.4). A significant correlation was found between the sIL-2R level and TLG ( P = 0.001, rs = 0.763). In contrast, no correlations were found between the IgG4, LDH, or CRP levels and TLG. Increased or decreased TLG corresponded with clinical disease improvement or worsening. Conclusions. TLG correlated significantly with the serum sIL-2R level and may be useful for disease monitoring in IgG4-RD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14397595
Volume :
25
Issue :
4
Database :
Complementary Index
Journal :
Modern Rheumatology
Publication Type :
Academic Journal
Accession number :
103364543
Full Text :
https://doi.org/10.3109/14397595.2014.990674