TY - JOUR
T1 - Indigo naturalis is effective even in treatment-refractory patients with ulcerative colitis
T2 - a post hoc analysis from the INDIGO study
AU - For the INDIGO Study Group
AU - Naganuma, Makoto
AU - Sugimoto, Shinya
AU - Fukuda, Tomohiro
AU - Mitsuyama, Keiichi
AU - Kobayashi, Taku
AU - Yoshimura, Naoki
AU - Ohi, Hidehisa
AU - Tanaka, Shinji
AU - Andoh, Akira
AU - Ohmiya, Naoki
AU - Saigusa, Keiichiro
AU - Yamamoto, Takayuki
AU - Morohoshi, Yuichi
AU - Ichikawa, Hitoshi
AU - Matsuoka, Katsuyoshi
AU - Hisamatsu, Tadakazu
AU - Watanabe, Kenji
AU - Mizuno, Shinta
AU - Abe, Takayuki
AU - Suzuki, Yasuo
AU - Kanai, Takanori
AU - Naganuma, Makoto
AU - Nakazato, Yoshihiro
AU - Teratani, Toshiaki
AU - Ogata, Haruhiko
AU - Iwao, Yasushi
AU - Yamasaki, Hiroshi
AU - Toyonaga, Takahiko
AU - Nakano, Masaru
AU - Hibi, Toshifumi
AU - Sameshima, Yoichi
AU - Hayashi, Ryohei
AU - Ueno, Yoshitaka
AU - Bamba, Shigeki
AU - Watanabe, Mamoru
AU - Nakazawa, Atsushi
AU - Koike, Yuji
AU - Imai, Jin
AU - Shimoyama, Takahiro
AU - Takeuchi, Ken
AU - Nagasaka, Mitsuo
AU - Kitano, Atsuo
AU - Ashizuka, Shinya
AU - Inatsu, Haruhiko
AU - Onodera, Kei
AU - Nakase, Hiroshi
AU - Kitamura, Kazuya
AU - Ikeya, Kentaro
AU - Suda, Wataru
AU - Hirayama, Akiyoshi
N1 - Funding Information:
This study was funded by Keio Fukuzawa Memorial Fund. Acknowledgements
Funding Information:
This study was supported in part by grants from the Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research (to M. Naganuma). We would like to thank Editage (www.editage.jp) for English language editing. INDIGO study group: Members in the INDIGO Study Group are Makoto Naganuma, Shinya Sugimoto, Shinta Mizuno, Yoshihiro Nakazato, Tomohiro Fukuda, Toshiaki Teratani, Haruhiko Ogata, Yasushi Iwao, Takanori Kanai (Keio University School of Medicine), Hiroshi Yamasaki, Keiichi Mitsuyama (Kurume University School of Medicine), Taku Kobayashi, Takahiko Toyonaga, Masaru Nakano, Toshifumi Hibi (Kitasato Institute Hospital), Naoki Yoshimura (Yamate Medical Center), Yoichi Sameshima, Hidehisa Ohi (Imamura hospital), Ryohei Hayashi, Yoshitaka Ueno, Shinji Tanaka (Hiroshima University Hospital), Shigeki Bamba, Akira Andoh (Shiga University of Medical Science), Mamoru Watanabe (Tokyo Medical and Dental University), Keiichiro Saigusa, Atsushi Nakazawa (Tokyo Saiseikai Central Hospital), Yuichi Morohoshi, Yuji Koike (Yokohama Municipal Citizen?s Hospital), Jin Imai, Hitoshi Ichikawa (Tokai University Hachioji Hospital), Takahiro Shimoyama, Takayuki Yamamoto (Yokkaichi Hazu Medical Center), Katsuyoshi Matsuoka, Ken Takeuchi, Yasuo Suzuki (Toho University Sakura Medical Center), Mitsuo Nagasaka, Naoki Ohmiya (Fujita Health University School of Medicine), Atsuo Kitano (Wakakusa Daiichi Hospital), Shinya Ashizuka, Haruhiko Inatsu (University of Miyazaki), Kei Onodera, Hiroshi Nakase (Sapporo Medical University School of Medicine), Kazuya Kitamura (Kanazawa University Hospital), Kentaro Ikeya, Hiroyuki Hanai (Hamamatsu South Hospital), Chikako Watanabe, Ryota Hokari (National Defense Medical College), Fumihito Hirai (Fukuoka University Chikushi Hospital), Yuji Naito (Kyoto prefecture University), Namiko Hoshi (Kobe University), Fukunori Kinjo (Urazoe General Hospical), Yo Ishiguro (Hirosaki National Hospital), Makoto Sasaki (Aichi Medical University), Takayuki Matsumoto (Iwate Medical University), Kenji Watanabe (Hyogo College of Medicine), Tadakazu Hisamatsu (Kyorin University School of Medicine), Fumiya Sano, Rachel Roberts, Takayuki Abe (Keio University), Wataru Suda (The University of Tokyo) and Masahira Hattori (Waseda University), Shinji Fukuda, and Akiyoshi Hirayama (Institute for Advanced Biosciences, Keio University).
Funding Information:
This study was supported in part by grants from the Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research (to M. Naganuma). We would like to thank Editage ( www.editage.jp ) for English language editing.
Publisher Copyright:
© 2019, Japanese Society of Gastroenterology.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - Background: We recently reported the efficacy of indigo naturalis (IN) in patients with active ulcerative colitis (UC) in a randomized controlled trial (INDIGO study). However, few studies have been conducted to investigate whether IN is effective even in treatment-refractory cases, such as in those with steroid dependency and anti-TNF refractoriness. Methods: In the INDIGO study, 86 patients with active UC were randomly assigned to an IN group (0.5–2.0 g daily) or placebo group. The rate of clinical response (CR), mucosal healing (MH), and change in fecal calprotectin (FCP) levels was compared between refractory [patients with steroid-dependent disease, previous use of anti-TNF-α, and concomitant use of immunomodulators (IM)] and non-refractory patients. We also analyzed factors predicting CR and MH at week 8. Results: The rates of CR of IN group were significantly higher than placebo group, even in patients with steroid-dependent disease (p < 0.001), previous use of anti-TNF-α (p = 0.002), and concomitant use of IM (p = 0.013). The rates of MH in IN group were significantly higher than in placebo group in patients with steroid-dependent disease (p = 0.009). In the IN group, median FCP levels, at week 8, were significantly lower than baseline in patients with steroid-dependent disease and patients with the previous use of anti-TNF-α (p < 0.001, respectively). Multivariate analysis indicated that the previous use of anti-TNF-α was not a predictive factor for CR and MH at week 8. Conclusions: In a sub-analysis of data from a randomized placebo-controlled trial, we found that IN may be useful even in patients with steroid-dependent disease and patients with the previous use of anti-TNF-α.
AB - Background: We recently reported the efficacy of indigo naturalis (IN) in patients with active ulcerative colitis (UC) in a randomized controlled trial (INDIGO study). However, few studies have been conducted to investigate whether IN is effective even in treatment-refractory cases, such as in those with steroid dependency and anti-TNF refractoriness. Methods: In the INDIGO study, 86 patients with active UC were randomly assigned to an IN group (0.5–2.0 g daily) or placebo group. The rate of clinical response (CR), mucosal healing (MH), and change in fecal calprotectin (FCP) levels was compared between refractory [patients with steroid-dependent disease, previous use of anti-TNF-α, and concomitant use of immunomodulators (IM)] and non-refractory patients. We also analyzed factors predicting CR and MH at week 8. Results: The rates of CR of IN group were significantly higher than placebo group, even in patients with steroid-dependent disease (p < 0.001), previous use of anti-TNF-α (p = 0.002), and concomitant use of IM (p = 0.013). The rates of MH in IN group were significantly higher than in placebo group in patients with steroid-dependent disease (p = 0.009). In the IN group, median FCP levels, at week 8, were significantly lower than baseline in patients with steroid-dependent disease and patients with the previous use of anti-TNF-α (p < 0.001, respectively). Multivariate analysis indicated that the previous use of anti-TNF-α was not a predictive factor for CR and MH at week 8. Conclusions: In a sub-analysis of data from a randomized placebo-controlled trial, we found that IN may be useful even in patients with steroid-dependent disease and patients with the previous use of anti-TNF-α.
KW - Anti-TNFa treatment
KW - Indigo naturalis
KW - Steroid dependent
KW - Ulcerative colitis
UR - http://www.scopus.com/inward/record.url?scp=85073819029&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85073819029&partnerID=8YFLogxK
U2 - 10.1007/s00535-019-01625-2
DO - 10.1007/s00535-019-01625-2
M3 - Article
C2 - 31529220
AN - SCOPUS:85073819029
SN - 0944-1174
VL - 55
SP - 169
EP - 180
JO - Journal of gastroenterology
JF - Journal of gastroenterology
IS - 2
ER -