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Highly Bioavailable Curcumin Derivative Ameliorates Crohn’s Disease Symptoms: A Randomized, Double-Blind, Multicenter Study

Sugimoto, Ken, Ikeya, Kentaro, Bamba, Shigeki, Andoh, Akira, Yamasaki, Hiroshi, Mitsuyama, Keiichi, Nasuno, Masanao, Tanaka, Hiroki, Matsuura, Ai, Kato, Masaichi, Ishida, Natsuki, Tamura, Satoshi, Takano, Ryosuke, Tani, Shinya, Osawa, Satoshi, Nishihira, Jun, Hanai, Hiroyuki·2020·Journal of Crohn's and Colitis

Abstract

Background & Aims: The new curcumin derivative Theracurmin® has a 27–fold higher absorption rate than natural curcumin powder. Theracurmin® is an inhibitor of nuclear factor-κB, which mediates the expression of inflammatory cytokines. The effect of Theracurmin® on inflammatory bowel disease in humans has not been explored; therefore, we investigated the efficacy and safety of Theracurmin® in patients with Crohn’s disease. Methods: In this randomized, double-blinded study performed at 5 independent medical centers in Japan, Theracurmin® (360 mg/day, n = 20) or placebo (n = 10) was administered to patients with active mild-to-moderate Crohn’s disease for 12 weeks. The agent’s efficacy was assessed by evaluating clinical and endoscopic remission, healing of anal lesions, and blood levels of inflammatory markers. Results: In the Theracurmin® group, a significant reduction in clinical disease activity was observed in week 12 relative to that in week 0 (p = 0.005). On intention-to-treat analysis, clinical remission rates were 35%, 40%, and 40% at weeks 4, 8, and 12, respectively, which were significantly higher than those in the placebo group (all 0%; p = 0.033, p = 0.020, and p = 0.020, respectively). Furthermore, reduction in endoscopic Crohn’s disease severity (p = 0.032) was observed at week 12 in the Theracurmin® group. The endoscopic remission rates were 15% and 0% in the Theracurmin® and placebo groups, respectively. Significant healing of anal lesions (p = 0.017) was observed at week 8 in the Theracurmin® group. No serious adverse events were observed in either group throughout the study. Conclusions: Theracurmin® shows significant clinical and endoscopic efficacy together with a favorable safety profile in patients with active mild-to-moderate Crohn’s disease. Clinical trial UMIN registration ID: UMIN000015770.

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Citations

Cites

Research works printed but not linked: 28

  1. Baumgart, 2012, Crohn’s disease, Lancet, 380, 1590, 10.1016/S0140-6736(12)60026-9 · DOI
  2. Hanauer, 2002, Maintenance infliximab for Crohn’s disease: the ACCENT I randomised trial, Lancet, 359, 1541, 10.1016/S0140-6736(02)08512-4 · DOI
  3. Colombel, 2007, Adalimumab for maintenance of clinical response and remission in patients with Crohn’s disease: the CHARM trial, Gastroenterology, 132, 52, 10.1053/j.gastro.2006.11.041 · DOI
  4. Sandborn, 2012, Ustekinumab induction and maintenance therapy in refractory Crohn’s disease, N Engl J Med, 367, 1519, 10.1056/NEJMoa1203572 · DOI
  5. Govindarajan, 1980, Turmeric–chemistry, technology, and quality, Crit Rev Food Sci Nutr, 12, 199, 10.1080/10408398009527278 · DOI · Paper page
  6. Jobin, 1999, Curcumin blocks cytokine-mediated NF-kappa B activation and proinflammatory gene expression by inhibiting inhibitory factor I-kappa B kinase activity, J Immunol, 163, 3474, 10.4049/jimmunol.163.6.3474 · DOI
  7. Hanai, 2009, Curcumin has bright prospects for the treatment of inflammatory bowel disease, Curr Pharm Des, 15, 2087, 10.2174/138161209788489177 · DOI
  8. Sugimoto, 2002, Curcumin prevents and ameliorates trinitrobenzene sulfonic acid-induced colitis in mice, Gastroenterology, 123, 1912, 10.1053/gast.2002.37050 · DOI · Paper page
  9. Ali, 2012, Curcumin and inflammatory bowel disease: biological mechanisms and clinical implication, Digestion, 85, 249, 10.1159/000336720 · DOI
  10. Hanai, 2006, Curcumin maintenance therapy for ulcerative colitis: randomized, multicenter, double-blind, placebo-controlled trial, Clin Gastroenterol Hepatol, 4, 1502, 10.1016/j.cgh.2006.08.008 · DOI · Paper page
  11. Singla, 2014, Induction with NCB-02 (curcumin) enema for mild-to-moderate distal ulcerative colitis - a randomized, placebo-controlled, pilot study, J Crohns Colitis, 8, 208, 10.1016/j.crohns.2013.08.006 · DOI
  12. Lang, 2015, Curcumin in combination with mesalamine induces remission in patients with mild-to-moderate ulcerative colitis in a randomized controlled trial, Clin Gastroenterol Hepatol, 13, 1444, 10.1016/j.cgh.2015.02.019 · DOI · Paper page
  13. Sasaki, 2011, Innovative preparation of curcumin for improved oral bioavailability, Biol Pharm Bull, 34, 660, 10.1248/bpb.34.660 · DOI · Paper page
  14. Dei Cas, 2019, Dietary curcumin: correlation between bioavailability and health potential, Nutrients, 11, E2147, 10.3390/nu11092147 · DOI
  15. Ohno, 2017, Nanoparticle curcumin ameliorates experimental colitis via modulation of gut microbiota and induction of regulatory T cells, PLoS One, 12, e0185999, 10.1371/journal.pone.0185999 · DOI
  16. Lyakhovich, 2010, Systematic review: molecular chemoprevention of colorectal malignancy by mesalazine, Aliment Pharmacol Ther, 31, 202, 10.1111/j.1365-2036.2009.04195.x · DOI
  17. Zhang, 2016, Protective effect of curcumin on TNBS-induced intestinal inflammation is mediated through the JAK/STAT pathway, BMC Complement Altern Med, 16, 299, 10.1186/s12906-016-1273-z · DOI
  18. van Ede, 2008, Bioassay directed identification of natural aryl hydrocarbon-receptor agonists in marmalade, Anal Chim Acta, 617, 238, 10.1016/j.aca.2008.01.054 · DOI
  19. Sugimoto, 2008, IL-22 ameliorates intestinal inflammation in a mouse model of ulcerative colitis, J Clin Invest, 118, 534
  20. Lehmann, 2015, The role and utility of faecal markers in inflammatory bowel disease, Therap Adv Gastroenterol, 8, 23, 10.1177/1756283X14553384 · DOI
  21. Yang, 2007, Oral bioavailability of curcumin in rat and the herbal analysis from Curcuma longa by LC-MS/MS, J Chromatogr B Analyt Technol Biomed Life Sci, 853, 183, 10.1016/j.jchromb.2007.03.010 · DOI
  22. Kanai, 2012, Dose-escalation and pharmacokinetic study of nanoparticle curcumin, a potential anticancer agent with improved bioavailability, in healthy human volunteers, Cancer Chemother Pharmacol, 69, 65, 10.1007/s00280-011-1673-1 · DOI
  23. Kanai, 2013, A phase I study investigating the safety and pharmacokinetics of highly bioavailable curcumin (Theracurmin) in cancer patients, Cancer Chemother Pharmacol, 71, 1521, 10.1007/s00280-013-2151-8 · DOI
  24. Sunagawa, 2015, Colloidal submicron-particle curcumin exhibits high absorption efficiency-a double-blind, 3-way crossover study, J Nutr Sci Vitaminol (Tokyo), 61, 37, 10.3177/jnsv.61.37 · DOI
  25. Shin, 2017, Short-term effects of Theracurmin dose and exercise type on pain, walking ability, and muscle function in patients with knee osteoarthritis, J Exerc Rehabil, 13, 684, 10.12965/jer.1735064.532 · DOI
  26. Lacruz-Guzmán, 2013, Influence of polymorphisms and TNF and IL1β serum concentration on the infliximab response in Crohn’s disease and ulcerative colitis, Eur J Clin Pharmacol, 69, 431, 10.1007/s00228-012-1389-0 · DOI
  27. Gupta, 2013, Therapeutic roles of curcumin: lessons learned from clinical trials, AAPS J, 15, 195, 10.1208/s12248-012-9432-8 · DOI · Paper page
  28. Schneider, 2017, Comparison of remicade to curcumin for the treatment of Crohn’s disease: A systematic review, Complement Ther Med, 33, 32, 10.1016/j.ctim.2017.06.002 · DOI

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Metadata

Authors
Sugimoto, K., Ikeya, K., Bamba, S., Andoh, A., Yamasaki, H., Mitsuyama, K., Nasuno, M., Tanaka, H., Matsuura, A., Kato, M., Ishida, N., Tamura, S., Takano, R., Tani, S., Osawa, S., Nishihira, J., & Hanai, H.
Affiliations
  • The First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan
  • Centre for Gastroenterology & IBD Research, Hamamatsu South Hospital, Hamamatsu, Japan
  • Division of Clinical Nutrition, Shiga University of Medical Science, Otsu, Japan
  • Division of Gastroenterology, Shiga University of Medical Science, Otsu, Japan
  • Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan
  • Inflammatory Bowel Disease Centre, Kurume University School of Medicine, Kurume, Japan
  • IBD Centre, Sapporo Kosei General Hospital, Sapporo, Japan
  • Department of Endoscopic and Photodynamic Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan
  • Department of Medical Management and Informatics, Hokkaido Information University, Ebetsu, Japan
Venue
Journal of Crohn's and Colitis
Published
2020-05-15
Volume
14
Issue
12
Pages
1693-1701
ISSN
  • 1873-9946
  • 1876-4479
Cited by
63
References
1
Language
en

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