TY - JOUR
T1 - Seven days triple therapy for eradication of Helicobacter pylori does not alter the disease activity of patients with inflammatory bowel disease
AU - Shinzaki, Shinichiro
AU - Fujii, Toshimitsu
AU - Bamba, Shigeki
AU - Ogawa, Maiko
AU - Kobayashi, Taku
AU - Oshita, Masahide
AU - Tanaka, Hiroki
AU - Ozeki, Keiji
AU - Takahashi, Sakuma
AU - Kitamoto, Hiroki
AU - Kani, Kazuhito
AU - Nanjo, Sohachi
AU - Sugaya, Takeshi
AU - Sakakibara, Yuko
AU - Inokuchi, Toshihiro
AU - Kakimoto, Kazuki
AU - Yamada, Akihiro
AU - Yasuhara, Hisae
AU - Yokoyama, Yoko
AU - Yoshino, Takuya
AU - Matsui, Akira
AU - Nakamura, Misaki
AU - Tomizawa, Taku
AU - Sakemi, Ryosuke
AU - Kamata, Noriko
AU - Hibi, Toshifumi
N1 - Funding Information:
The overall study meets the intent and requirements of the Declaration of Helsinki, Ethical Guidelines for Medical and Health Research Involving Human Subjects by the Ministry of Health, Labour, and Welfare-Japan and by the Japanese Ministry of Education, Culture, Sports, Science and Technology-Japan. The institutional ethics committees of each participating institution approved this study.
Funding Information:
SS received lecture fees from Mitsubishi-Tanabe Pharma, Kyorin Pharmaceutical, Abbvie, EA Pharma, Mochida Pharmaceutical, Zeria Pharmaceutical, Eisai, Mylan, advisory/ consultancy fees from Janssen, Kyorin Pharmaceutical, and research grant from Mitsubishi-Tanabe Pharma. TK received lecture fees from Mitsubishi-Tanabe Pharma, Eisai, Kyorin Pharmaceutical, Abbvie, Janssen, JIMRO, Ajinomoto Pharma, EA Pharma, Astellas, Mochida Pharmaceutical, Asahi Kasei Medical, Takeda Pharmaceutical, Gilead Sciences, Celltrion, Nippon Kayaku, Alfresa Pharma, Thermo Scientific, advisory/consultancy fees from Janssen, Pfizer, Kyorin Pharmaceutical, Mochida Pharmaceutical, Takeda Pharmaceutical, Eli Lilly, Ferring Pharmaceuticals, Nippon Kayaku, and research grants from EA Pharma, Thermo Scientific, and Alfresa Pharma. AY, TY, HT, and SR received lecture fees from EA Pharma. TF received research support from Eisai and lecture fees from EA Pharma. KO received research support from EA Pharma, Takeda and Daiichi Sankyo. KKak received research support from EA pharma. MN received research support from EA Pharma, Takeda, AstraZeneca and Daiichi Sankyo. TH received lecture fees from Mitsubishi-Ta-nabe Pharma, Kyorin Pharmaceutical, Abbvie, GK, Janssen, Mochida Pharmaceutical, JIMRO, Takeda Pharmaceutical, Gilead Sciences, Miyarisan Pharmaceutical, Kissei Pharmaceutical, Zeria Pharmaceutical, Ferring Pharmaceutical, Nippon Kayaku, advisory/consultancy fees from Mitsubishi-Ta-nabe Pharma, Takeda Pharmaceutical, EA Pharma, Janssen, Eli Lilly, and research grants from Abbvie, JIMRO, and Zeria Pharmaceutical. Other authors have no financial relationship to disclose. The manuscript was edited by SciTechEdit International, LLC (7012 East Mountain Brush Circle, Highlands Ranch, CO 80130, USA) without funding source.
Publisher Copyright:
© 2018. Korean Association for the Study of Intestinal Diseases.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Background/Aims: The influences of Helicobacter pylori eradication therapy on the disease course of inflammatory bowel disease (IBD) are still unclear. We therefore conducted a multicenter, retrospective cohort study to evaluate the safety of H. pylori eradication therapy for IBD patients. Methods: IBD patients with H. pylori eradication from 2005 to 2015 (eradication group) and control patients (non-eradication group; 2 paired IBD patients without H. pylori eradication matched with each eradicated patient) were included. IBD exacerbation (increased/additional IBD drug or IBD-associated hospitalization/surgery) and disease improvement based on the physicians' global assessment were investigated at baseline, and at 2 and 6 months after eradication or observation. Results: A total of 429 IBD (378 ulcerative colitis, 51 Crohn's disease) patients, comprising 144 patients in the eradication group and 285 patients in the non-eradication group, were enrolled at 25 institutions. IBD exacerbation was comparable between groups (eradication group: 8.3% at 2 months [odds ratio, 1.76; 95% confidence interval, 0.78-3.92; P=0.170], 11.8% at 6 months [odds ratio, 1.60; 95% confidence interval, 0.81-3.11; P=0.172]). Based on the physicians' global assessment at 2 months, none of the patients in the eradication group improved, whereas 3.2% of the patients in the non-eradication group improved (P=0.019). Multivariate analysis revealed that active disease at baseline, but not H. pylori eradication, was an independent factor for IBD exacerbation during 2 months' observation period. The overall eradication rate was 84.0%-comparable to previous reports in non-IBD patients. Conclusions: H. pylori eradication therapy does not alter the short-term disease activity of IBD.
AB - Background/Aims: The influences of Helicobacter pylori eradication therapy on the disease course of inflammatory bowel disease (IBD) are still unclear. We therefore conducted a multicenter, retrospective cohort study to evaluate the safety of H. pylori eradication therapy for IBD patients. Methods: IBD patients with H. pylori eradication from 2005 to 2015 (eradication group) and control patients (non-eradication group; 2 paired IBD patients without H. pylori eradication matched with each eradicated patient) were included. IBD exacerbation (increased/additional IBD drug or IBD-associated hospitalization/surgery) and disease improvement based on the physicians' global assessment were investigated at baseline, and at 2 and 6 months after eradication or observation. Results: A total of 429 IBD (378 ulcerative colitis, 51 Crohn's disease) patients, comprising 144 patients in the eradication group and 285 patients in the non-eradication group, were enrolled at 25 institutions. IBD exacerbation was comparable between groups (eradication group: 8.3% at 2 months [odds ratio, 1.76; 95% confidence interval, 0.78-3.92; P=0.170], 11.8% at 6 months [odds ratio, 1.60; 95% confidence interval, 0.81-3.11; P=0.172]). Based on the physicians' global assessment at 2 months, none of the patients in the eradication group improved, whereas 3.2% of the patients in the non-eradication group improved (P=0.019). Multivariate analysis revealed that active disease at baseline, but not H. pylori eradication, was an independent factor for IBD exacerbation during 2 months' observation period. The overall eradication rate was 84.0%-comparable to previous reports in non-IBD patients. Conclusions: H. pylori eradication therapy does not alter the short-term disease activity of IBD.
KW - Clarithromycin
KW - Helicobacter pylori eradication
KW - Metronidazole
KW - Proton pump inhibitor
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U2 - 10.5217/ir.2018.00044
DO - 10.5217/ir.2018.00044
M3 - Article
AN - SCOPUS:85056531455
SN - 1598-9100
VL - 16
SP - 609
EP - 618
JO - Intestinal Research
JF - Intestinal Research
IS - 4
ER -