Effect of Bifidobacterium bifidum G9-1 on the Intestinal Environment and Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)-like Symptoms in Patients with Quiescent Crohn's Disease: A Prospective Pilot Study
Diarrhea-predominant irritable bowel syndrome (IBS-D)-like symptoms are distressing for patients with quiescent Crohn's disease (qCD) and worsen their quality of life. In the present study, we assessed the effect of the probiotic G9-1 (BBG9-1) on the intestinal environment and clinical features...
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Published in | Journal of clinical medicine Vol. 12; no. 10; p. 3368 |
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Main Authors | , , , , , , , , , , |
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Abstract | Diarrhea-predominant irritable bowel syndrome (IBS-D)-like symptoms are distressing for patients with quiescent Crohn's disease (qCD) and worsen their quality of life. In the present study, we assessed the effect of the probiotic
G9-1 (BBG9-1) on the intestinal environment and clinical features in patients with qCD. Eleven patients with qCD, who met the Rome III diagnostic criteria for IBS-D, received BBG9-1 (24 mg) orally three times daily for 4 weeks. Indices of the intestinal environment (fecal calprotectin level and gut microbiome) and clinical features (CD/IBS-related symptoms, quality of life and stool irregularities) were evaluated before and after treatment. Treatment with BBG9-1 tended to reduce the IBS severity index in the studied patients (
= 0.07). Among gastrointestinal symptoms, abdominal pain and dyspepsia tended to be improved by the BBG9-1 treatment (
= 0.07 and
= 0.07, respectively), and IBD-related QOL showed a significant improvement (
= 0.007). With regard to mental status, the patient anxiety score was significantly lower at the endpoint of BBG9-1 treatment than at the baseline (
= 0.03). Although BBG9-1 treatment did not affect the fecal calprotectin level, it suppressed the serum MCP-1 level significantly and increased the abundance of intestinal
in the study patients. The probiotic BBG9-1 is able to improve IBD-related QOL with a reduction of anxiety score in patients with quiescent CD and IBS-D-like symptoms. |
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AbstractList | Diarrhea-predominant irritable bowel syndrome (IBS-D)-like symptoms are distressing for patients with quiescent Crohn’s disease (qCD) and worsen their quality of life. In the present study, we assessed the effect of the probiotic Bifidobacterium bifidum G9-1 (BBG9-1) on the intestinal environment and clinical features in patients with qCD. Eleven patients with qCD, who met the Rome III diagnostic criteria for IBS-D, received BBG9-1 (24 mg) orally three times daily for 4 weeks. Indices of the intestinal environment (fecal calprotectin level and gut microbiome) and clinical features (CD/IBS-related symptoms, quality of life and stool irregularities) were evaluated before and after treatment. Treatment with BBG9-1 tended to reduce the IBS severity index in the studied patients (p = 0.07). Among gastrointestinal symptoms, abdominal pain and dyspepsia tended to be improved by the BBG9-1 treatment (p = 0.07 and p = 0.07, respectively), and IBD-related QOL showed a significant improvement (p = 0.007). With regard to mental status, the patient anxiety score was significantly lower at the endpoint of BBG9-1 treatment than at the baseline (p = 0.03). Although BBG9-1 treatment did not affect the fecal calprotectin level, it suppressed the serum MCP-1 level significantly and increased the abundance of intestinal Bacteroides in the study patients. The probiotic BBG9-1 is able to improve IBD-related QOL with a reduction of anxiety score in patients with quiescent CD and IBS-D-like symptoms. Diarrhea-predominant irritable bowel syndrome (IBS-D)-like symptoms are distressing for patients with quiescent Crohn’s disease (qCD) and worsen their quality of life. In the present study, we assessed the effect of the probiotic Bifidobacterium bifidum G9-1 (BBG9-1) on the intestinal environment and clinical features in patients with qCD. Eleven patients with qCD, who met the Rome III diagnostic criteria for IBS-D, received BBG9-1 (24 mg) orally three times daily for 4 weeks. Indices of the intestinal environment (fecal calprotectin level and gut microbiome) and clinical features (CD/IBS-related symptoms, quality of life and stool irregularities) were evaluated before and after treatment. Treatment with BBG9-1 tended to reduce the IBS severity index in the studied patients ( p = 0.07). Among gastrointestinal symptoms, abdominal pain and dyspepsia tended to be improved by the BBG9-1 treatment ( p = 0.07 and p = 0.07, respectively), and IBD-related QOL showed a significant improvement ( p = 0.007). With regard to mental status, the patient anxiety score was significantly lower at the endpoint of BBG9-1 treatment than at the baseline ( p = 0.03). Although BBG9-1 treatment did not affect the fecal calprotectin level, it suppressed the serum MCP-1 level significantly and increased the abundance of intestinal Bacteroides in the study patients. The probiotic BBG9-1 is able to improve IBD-related QOL with a reduction of anxiety score in patients with quiescent CD and IBS-D-like symptoms. Diarrhea-predominant irritable bowel syndrome (IBS-D)-like symptoms are distressing for patients with quiescent Crohn's disease (qCD) and worsen their quality of life. In the present study, we assessed the effect of the probiotic G9-1 (BBG9-1) on the intestinal environment and clinical features in patients with qCD. Eleven patients with qCD, who met the Rome III diagnostic criteria for IBS-D, received BBG9-1 (24 mg) orally three times daily for 4 weeks. Indices of the intestinal environment (fecal calprotectin level and gut microbiome) and clinical features (CD/IBS-related symptoms, quality of life and stool irregularities) were evaluated before and after treatment. Treatment with BBG9-1 tended to reduce the IBS severity index in the studied patients ( = 0.07). Among gastrointestinal symptoms, abdominal pain and dyspepsia tended to be improved by the BBG9-1 treatment ( = 0.07 and = 0.07, respectively), and IBD-related QOL showed a significant improvement ( = 0.007). With regard to mental status, the patient anxiety score was significantly lower at the endpoint of BBG9-1 treatment than at the baseline ( = 0.03). Although BBG9-1 treatment did not affect the fecal calprotectin level, it suppressed the serum MCP-1 level significantly and increased the abundance of intestinal in the study patients. The probiotic BBG9-1 is able to improve IBD-related QOL with a reduction of anxiety score in patients with quiescent CD and IBS-D-like symptoms. |
Author | Miwa, Hiroto Nakai, Keisuke Kitayama, Yoshitaka Shinzaki, Shinichiro Eda, Hirotsugu Oshima, Tadayuki Fukui, Hirokazu Tomita, Toshihiko Okugawa, Takuya Mieno, Masatoshi Nakanishi, Takashi |
AuthorAffiliation | Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan; tomita@hyo-med.ac.jp (T.T.); okugawat@hyo-med.ac.jp (T.O.); ta-nakanishi@hyo-med.ac.jp (T.N.); ma-mieno@hyo-med.ac.jp (M.M.); k-nakai@hyo-med.ac.jp (K.N.); eda@hyo-med.ac.jp (H.E.); yoshitaka591027@hyo-med.ac.jp (Y.K.); t-oshima@hyo-med.ac.jp (T.O.); sh-shinzaki@hyo-med.ac.jp (S.S.) |
AuthorAffiliation_xml | – name: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan; tomita@hyo-med.ac.jp (T.T.); okugawat@hyo-med.ac.jp (T.O.); ta-nakanishi@hyo-med.ac.jp (T.N.); ma-mieno@hyo-med.ac.jp (M.M.); k-nakai@hyo-med.ac.jp (K.N.); eda@hyo-med.ac.jp (H.E.); yoshitaka591027@hyo-med.ac.jp (Y.K.); t-oshima@hyo-med.ac.jp (T.O.); sh-shinzaki@hyo-med.ac.jp (S.S.) |
Author_xml | – sequence: 1 givenname: Toshihiko orcidid: 0000-0003-1283-9009 surname: Tomita fullname: Tomita, Toshihiko organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 2 givenname: Hirokazu surname: Fukui fullname: Fukui, Hirokazu organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 3 givenname: Takuya orcidid: 0009-0000-6293-566X surname: Okugawa fullname: Okugawa, Takuya organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 4 givenname: Takashi surname: Nakanishi fullname: Nakanishi, Takashi organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 5 givenname: Masatoshi surname: Mieno fullname: Mieno, Masatoshi organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 6 givenname: Keisuke surname: Nakai fullname: Nakai, Keisuke organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 7 givenname: Hirotsugu surname: Eda fullname: Eda, Hirotsugu organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 8 givenname: Yoshitaka surname: Kitayama fullname: Kitayama, Yoshitaka organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 9 givenname: Tadayuki orcidid: 0000-0001-6949-932X surname: Oshima fullname: Oshima, Tadayuki organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 10 givenname: Shinichiro orcidid: 0000-0002-7051-618X surname: Shinzaki fullname: Shinzaki, Shinichiro organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan – sequence: 11 givenname: Hiroto orcidid: 0000-0001-9844-642X surname: Miwa fullname: Miwa, Hiroto organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan |
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Keywords | anxiety gut microbiome inflammation irritable bowel syndrome Crohn’s disease probiotics |
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Title | Effect of Bifidobacterium bifidum G9-1 on the Intestinal Environment and Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)-like Symptoms in Patients with Quiescent Crohn's Disease: A Prospective Pilot Study |
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