TY - JOUR
T1 - Leucine-rich alpha-2 glycoprotein is a potential biomarker to monitor disease activity in inflammatory bowel disease receiving adalimumab
T2 - PLANET study
AU - Shinzaki, Shinichiro
AU - Matsuoka, Katsuyoshi
AU - Tanaka, Hiroki
AU - Takeshima, Fuminao
AU - Kato, Shingo
AU - Torisu, Takehiro
AU - Ohta, Yuki
AU - Watanabe, Kenji
AU - Nakamura, Shiro
AU - Yoshimura, Naoki
AU - Kobayashi, Taku
AU - Shiotani, Akiko
AU - Hirai, Fumihito
AU - Hiraoka, Sakiko
AU - Watanabe, Mamoru
AU - Matsuura, Minoru
AU - Nishimoto, Shohei
AU - Mizuno, Shinta
AU - Iijima, Hideki
AU - Takehara, Tetsuo
AU - Naka, Tetsuji
AU - Kanai, Takanori
AU - Matsumoto, Takayuki
N1 - Funding Information:
This study was supported by Eisai Co., Ltd. (Tokyo, Japan). Eisai Co., Ltd. was not involved in the study design, data collection, or interpretation of data. Statistical analysis was performed by RPM Co. Ltd. (Tokyo, Japan).
Funding Information:
KM reports personal fees from EA Pharma Co., Ltd., Mitsubishi Tanabe Pharma, Takeda Pharmaceutical Co. Ltd., Janssen Pharmaceutical K.K., Abbvie Inc., Mochida Pharmaceutical Co., Ltd., Kissei Pharmaceutical Co., Ltd., Alfressa Pharma Corporation, JIMRO Co., Ltd.; research grant from Janssen Pharmaceutical K.K., outside the submitted work. HT reports personal fees from JIMRO Co., Ltd., AbbVie GK, EA Pharma Co., Ltd., Mochida Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., outside the submitted work. SK reports personal fees from Abbvie Inc., Mitsubishi Tanabe Pharma Corporation, Janssen Pharmaceutical K.K.; grants from Abbvie Inc., EA Pharma Co., Ltd., outside the submitted work. TTo reports grants from Mitsubishi Tanabe Pharma Corporation, Abbvie Inc., EA Pharma Co., Ltd., outside the submitted work. KW reports grants and personal fees from AbbVie Japan Co., Ltd., EA Pharma Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Takeda Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., Pfizer Japan Inc., Kissei Pharmaceutical Co., Ltd., outside the submitted work; endowed chair from AbbVie Japan Co., Ltd., EA Pharma Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Kyorin Pharmaceutical Co., Ltd., Zeria Pharmaceutical Co., Ltd., JIMRO Co Ltd., Mochida Pharmaceutical Co., Ltd., Asahi Kasei Medical Co., Ltd., Otsuka Pharma Factory Inc. SNa reports personal fees and endowed chair from Mitsubishi Tanabe Pharma Corporation, Abbvie Inc., EA Pharma Co., Ltd., Janssen Pharmaceutical K.K., Mochida Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co. Ltd., Kyorin Holdings Inc., JIMRO Co Ltd., Zeria Pharmaceutical Co., Ltd.; research grants from Mitsubishi Tanabe Pharma Corporation, Mochida Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co. Ltd., endowed chair from Otsuka Pharma Factory Inc., outside the submitted work. YN reports personal fees from Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, Mochida Pharmaceutical Co., Ltd., outside the submitted work. TKo reports personal fees from Alfresa Pharma, Mochida Pharmaceutical, Takeda Pharmaceutical, Mitsubishi Tanabe Pharma, Janssen, Abbvie GK, Pfizer; grants from Abbvie GK, EA Pharma, Otsuka Holdings, ZERIA, EA Pharma, Nippon Kayaku, JIMRO, outside the submitted work. AK reports personal fees from Takeda Pharmaceutical Co., Ltd., Astellas Pharma Inc., Daiichisankyo Co., Ltd.; research grants from Takeda Pharmaceutical Co., Ltd., Mochida Pharmaceutical Co., Ltd., AstraZeneca K. K., Daiichisankyo Co., Ltd., outside the submitted work. FH reports personal fees from Abbvie GK, EA Pharma Co., Ltd, Janssen Pharmaceutical K.K, Mochida Pharmaceutical Co., Ltd., Takdeda Pharmaceutical Co., Ltd and Mitsubishi Tanabe Pharma, outside the submitted work. SH reports personal fees from Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, outside the submitted work. WM reports personal fees from Mitsubishi Tanabe Pharma Corporation, Takeda Pharmaceutical Co., Ltd., Zeria Pharmaceutical Co., Ltd., Pfizer Japan Inc., Janssen Pharmaceutical K.K., Gilead Sciences, Inc., EA Pharma Co., Ltd.; research grants from Alfresa Pharma Corporation.; scholarship grants from Abbvie GK., Mitsubishi Tanabe Pharma Corporation, Takeda Pharmaceutical Co., Ltd., Zeria Pharmaceutical Co., Ltd., Astellas Pharma Inc., Taiho Pharmaceutical Co., Ltd., Nippon Kayaku Co., Ltd., Mochida Pharmaceutical Co., Ltd., Miyarisan Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., EA Pharma Co., Ltd., Kissei Pharmaceutical Co., Ltd., Alfresa Pharma Corporation., outside the submitted work. MM reports personal fees from Janssen Pharmaceutical K.K. and grants from Nippon Kayaku Co., Ltd., outside the submitted work. SNi is an employee of Eisai Co. Ltd. TTa reports personal fees from Abbvie GK, and grants from Abbvie GK, EA Pharma Co., Ltd, Eisai Co., Ltd., outside the submitted work. TN reports grants from Sekisui Medical Co., Ltd., outside the submitted work. TKa reports research grants from Miyarisan Pharmaceutical Co., Ltd., Ezaki Glico Co., Ltd.; scholarship grants from Abbvie GK, Mochida Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., Taiho Pharmaceutical Co., Ltd., Daiichisankyo Co., Ltd., Mitsubishi Tanabe Pharma, Takeda Pharmaceutical Company Ltd, JIMRO Co., Ltd., outside the submitted work. TM reports personal fees from Abbvie GK, EA Pharma Co., Ltd, Mitsubishi Tanabe Pharma, Takeda Pharmaceutical Co. Ltd.; grants from Mitsubishi Tanabe Pharma, Nippon Kayaku Co., Ltd., outside the submitted work. The other authors have no conflict of interest to disclose. Kochi University is a Patent holder for LRG.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/6
Y1 - 2021/6
N2 - Background: This multicenter prospective study (UMIN000019958) aimed to evaluate the usefulness of serum leucin-rich alpha-2 glycoprotein (LRG) levels in monitoring disease activity in inflammatory bowel disease (IBD). Methods: Patients with moderate-to-severe IBD initiated on adalimumab therapy were enrolled herein. Serum LRG, C-reactive protein (CRP), and fecal calprotectin (fCal) levels were measured at week 0, 12, 24, and 52. Colonoscopy was performed at week 0, 12, and 52 for ulcerative colitis (UC), and at week 0, 24, and 52 for Crohn’s disease (CD). Endoscopic activity was assessed using the Simple Endoscopic Score for Crohn’s Disease (SES-CD) for CD and the Mayo endoscopic subscore (MES) for UC. Results: A total of 81 patients was enrolled. Serum LRG levels decreased along with improvements in clinical and endoscopic outcomes upon adalimumab treatment (27.4 ± 12.6 μg/ml at week 0, 15.5 ± 7.7 μg/ml at week 12, 15.7 ± 9.6 μg/ml at week 24, and 14.5 ± 6.8 μg/ml at week 52), being correlated with endoscopic activity at each time point (SES-CD: r = 0.391 at week 0, r = 0.563 at week 24, r = 0.697 at week 52; MES: r = 0.534 at week 0, r = 0.429 at week 12, r = 0.335 at week 52). Endoscopic activity better correlated with LRG compared to CRP and fCal on pooled analysis at all time points (SES-CD: LRG: r = 0.636, CRP: r = 0.402, fCal: r = 0.435; MES: LRG: r = 0.568, CRP: 0.389, fCal: r = 0.426). Conclusions: Serum LRG is a useful biomarker of endoscopic activity both in CD and UC during the adalimumab treatment.
AB - Background: This multicenter prospective study (UMIN000019958) aimed to evaluate the usefulness of serum leucin-rich alpha-2 glycoprotein (LRG) levels in monitoring disease activity in inflammatory bowel disease (IBD). Methods: Patients with moderate-to-severe IBD initiated on adalimumab therapy were enrolled herein. Serum LRG, C-reactive protein (CRP), and fecal calprotectin (fCal) levels were measured at week 0, 12, 24, and 52. Colonoscopy was performed at week 0, 12, and 52 for ulcerative colitis (UC), and at week 0, 24, and 52 for Crohn’s disease (CD). Endoscopic activity was assessed using the Simple Endoscopic Score for Crohn’s Disease (SES-CD) for CD and the Mayo endoscopic subscore (MES) for UC. Results: A total of 81 patients was enrolled. Serum LRG levels decreased along with improvements in clinical and endoscopic outcomes upon adalimumab treatment (27.4 ± 12.6 μg/ml at week 0, 15.5 ± 7.7 μg/ml at week 12, 15.7 ± 9.6 μg/ml at week 24, and 14.5 ± 6.8 μg/ml at week 52), being correlated with endoscopic activity at each time point (SES-CD: r = 0.391 at week 0, r = 0.563 at week 24, r = 0.697 at week 52; MES: r = 0.534 at week 0, r = 0.429 at week 12, r = 0.335 at week 52). Endoscopic activity better correlated with LRG compared to CRP and fCal on pooled analysis at all time points (SES-CD: LRG: r = 0.636, CRP: r = 0.402, fCal: r = 0.435; MES: LRG: r = 0.568, CRP: 0.389, fCal: r = 0.426). Conclusions: Serum LRG is a useful biomarker of endoscopic activity both in CD and UC during the adalimumab treatment.
KW - Biomarker
KW - Crohn’s disease
KW - Leucine-rich alpha-2 glycoprotein
KW - Ulcerative colitis
UR - http://www.scopus.com/inward/record.url?scp=85105381402&partnerID=8YFLogxK
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U2 - 10.1007/s00535-021-01793-0
DO - 10.1007/s00535-021-01793-0
M3 - Article
C2 - 33942166
AN - SCOPUS:85105381402
SN - 0944-1174
VL - 56
SP - 560
EP - 569
JO - Journal of Gastroenterology
JF - Journal of Gastroenterology
IS - 6
ER -