Probiotic treatment of collagenous colitis: A randomized, double‐blind, placebo‐controlled trial with lactobacillus acidophilus and bifidobacterium animalis subsp. lactis
Background: Probiotic treatment may be effective in diseases involving gut microflora and intestinal inflammation. In collagenous colitis (CC), a potential pathogenic role of the gut microflora has been proposed. The effect of probiotic treatment in CC is unknown. Our aim was to investigate the clin...
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Veröffentlicht in: | Inflammatory bowel diseases 2006-05, Vol.12 (5), p.395-401 |
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creator | Wildt, Signe Munck, Lars K. Vinter‐Jensen, Lars Hanse, Birgit Fischer Nordgaard‐Lassen, Inge Christensen, Steen Avnstroem, Soeren Rasmussen, Sten Noerby Rumessen, Jüri J. |
description | Background: Probiotic treatment may be effective in diseases involving gut microflora and intestinal inflammation. In collagenous colitis (CC), a potential pathogenic role of the gut microflora has been proposed. The effect of probiotic treatment in CC is unknown. Our aim was to investigate the clinical effect of treatment with Lactobacillus acidophilus LA‐5 and Bifidobacterium animalis subsp. lactis BB‐12 (AB‐Cap‐10) in patients with CC. Materials and Methods: Patients with CC and diarrhea were in a double‐blind placebo‐controlled study randomized (2:1) to AB‐Cap‐10 or placebo for 12 weeks. The primary end point was reduction in bowel frequency per week of ≥50%. Secondary end points were changes in bowel frequencies, stool consistency, stool weight, histopathology, and abdominal bloating and pain. Results: Twenty‐nine patients were randomized: 21 to probiotics and 8 to placebo. Reduction in bowel frequency per week of ≥50% occurred in 6 of 21 (29%) and in 1 of 8 (13%) patients receiving probiotic and placebo, respectively (P = 0.635). No differences between treatments were observed regarding the secondary end points. Post hoc analysis showed a median reduction in bowel frequency per week from 32 (range 18–84) to 23 (range 11–56; P < 0.005), a reduction in number of days with liquid stools per week from 6 days (range 0–7 days) to 1 day (range 0–7 days; P < 0.005), and an increase in number of days with solid stools per week (P < 0.05) in the AB‐Cap‐10 group. Conclusions: AB‐Cap‐10 had no significant effect on the chosen end points. Post hoc analysis demonstrated amelioration of clinical symptoms in the AB‐Cap‐10 group, indicating that probiotic treatment may potentially influence the disease course of CC. |
doi_str_mv | 10.1097/01.MIB.0000218763.99334.49 |
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In collagenous colitis (CC), a potential pathogenic role of the gut microflora has been proposed. The effect of probiotic treatment in CC is unknown. Our aim was to investigate the clinical effect of treatment with Lactobacillus acidophilus LA‐5 and Bifidobacterium animalis subsp. lactis BB‐12 (AB‐Cap‐10) in patients with CC. Materials and Methods: Patients with CC and diarrhea were in a double‐blind placebo‐controlled study randomized (2:1) to AB‐Cap‐10 or placebo for 12 weeks. The primary end point was reduction in bowel frequency per week of ≥50%. Secondary end points were changes in bowel frequencies, stool consistency, stool weight, histopathology, and abdominal bloating and pain. Results: Twenty‐nine patients were randomized: 21 to probiotics and 8 to placebo. Reduction in bowel frequency per week of ≥50% occurred in 6 of 21 (29%) and in 1 of 8 (13%) patients receiving probiotic and placebo, respectively (P = 0.635). No differences between treatments were observed regarding the secondary end points. Post hoc analysis showed a median reduction in bowel frequency per week from 32 (range 18–84) to 23 (range 11–56; P < 0.005), a reduction in number of days with liquid stools per week from 6 days (range 0–7 days) to 1 day (range 0–7 days; P < 0.005), and an increase in number of days with solid stools per week (P < 0.05) in the AB‐Cap‐10 group. Conclusions: AB‐Cap‐10 had no significant effect on the chosen end points. Post hoc analysis demonstrated amelioration of clinical symptoms in the AB‐Cap‐10 group, indicating that probiotic treatment may potentially influence the disease course of CC.</description><identifier>ISSN: 1078-0998</identifier><identifier>EISSN: 1536-4844</identifier><identifier>DOI: 10.1097/01.MIB.0000218763.99334.49</identifier><identifier>PMID: 16670529</identifier><language>eng</language><publisher>Philadelphia: Lippincott Williams & Wilkins, Inc</publisher><subject>Adult ; Aged ; Bifidobacterium - physiology ; Bifidobacterium animalis ; Clinical trials ; Colitis ; Colitis, Collagenous - pathology ; Colitis, Collagenous - therapy ; Collagen ; collagenous colitis ; Diarrhea ; Digestive tract ; Double-Blind Method ; Drug Tolerance ; Feces ; Female ; Follow-Up Studies ; Humans ; Inflammatory bowel diseases ; Intestine ; lactic acid bacteria ; Lactobacillus acidophilus ; Lactobacillus acidophilus - physiology ; Male ; Microflora ; Middle Aged ; Pain ; Placebos ; probiotics ; Probiotics - adverse effects ; Probiotics - therapeutic use ; Treatment Outcome</subject><ispartof>Inflammatory bowel diseases, 2006-05, Vol.12 (5), p.395-401</ispartof><rights>Copyright © 2006 Crohn's & Colitis Foundation of America, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4639-c94e6d0a4ccb3bcd18110da386290c384160b32f2307c493f90cfa3fd443e87c3</citedby><cites>FETCH-LOGICAL-c4639-c94e6d0a4ccb3bcd18110da386290c384160b32f2307c493f90cfa3fd443e87c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1097%2F01.MIB.0000218763.99334.49$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1097%2F01.MIB.0000218763.99334.49$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27931,27932,45581,45582</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16670529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wildt, Signe</creatorcontrib><creatorcontrib>Munck, Lars K.</creatorcontrib><creatorcontrib>Vinter‐Jensen, Lars</creatorcontrib><creatorcontrib>Hanse, Birgit Fischer</creatorcontrib><creatorcontrib>Nordgaard‐Lassen, Inge</creatorcontrib><creatorcontrib>Christensen, Steen</creatorcontrib><creatorcontrib>Avnstroem, Soeren</creatorcontrib><creatorcontrib>Rasmussen, Sten Noerby</creatorcontrib><creatorcontrib>Rumessen, Jüri J.</creatorcontrib><title>Probiotic treatment of collagenous colitis: A randomized, double‐blind, placebo‐controlled trial with lactobacillus acidophilus and bifidobacterium animalis subsp. lactis</title><title>Inflammatory bowel diseases</title><addtitle>Inflamm Bowel Dis</addtitle><description>Background: Probiotic treatment may be effective in diseases involving gut microflora and intestinal inflammation. In collagenous colitis (CC), a potential pathogenic role of the gut microflora has been proposed. The effect of probiotic treatment in CC is unknown. Our aim was to investigate the clinical effect of treatment with Lactobacillus acidophilus LA‐5 and Bifidobacterium animalis subsp. lactis BB‐12 (AB‐Cap‐10) in patients with CC. Materials and Methods: Patients with CC and diarrhea were in a double‐blind placebo‐controlled study randomized (2:1) to AB‐Cap‐10 or placebo for 12 weeks. The primary end point was reduction in bowel frequency per week of ≥50%. Secondary end points were changes in bowel frequencies, stool consistency, stool weight, histopathology, and abdominal bloating and pain. Results: Twenty‐nine patients were randomized: 21 to probiotics and 8 to placebo. Reduction in bowel frequency per week of ≥50% occurred in 6 of 21 (29%) and in 1 of 8 (13%) patients receiving probiotic and placebo, respectively (P = 0.635). No differences between treatments were observed regarding the secondary end points. Post hoc analysis showed a median reduction in bowel frequency per week from 32 (range 18–84) to 23 (range 11–56; P < 0.005), a reduction in number of days with liquid stools per week from 6 days (range 0–7 days) to 1 day (range 0–7 days; P < 0.005), and an increase in number of days with solid stools per week (P < 0.05) in the AB‐Cap‐10 group. Conclusions: AB‐Cap‐10 had no significant effect on the chosen end points. Post hoc analysis demonstrated amelioration of clinical symptoms in the AB‐Cap‐10 group, indicating that probiotic treatment may potentially influence the disease course of CC.</description><subject>Adult</subject><subject>Aged</subject><subject>Bifidobacterium - physiology</subject><subject>Bifidobacterium animalis</subject><subject>Clinical trials</subject><subject>Colitis</subject><subject>Colitis, Collagenous - pathology</subject><subject>Colitis, Collagenous - therapy</subject><subject>Collagen</subject><subject>collagenous colitis</subject><subject>Diarrhea</subject><subject>Digestive tract</subject><subject>Double-Blind Method</subject><subject>Drug Tolerance</subject><subject>Feces</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Inflammatory bowel diseases</subject><subject>Intestine</subject><subject>lactic acid bacteria</subject><subject>Lactobacillus acidophilus</subject><subject>Lactobacillus acidophilus - physiology</subject><subject>Male</subject><subject>Microflora</subject><subject>Middle Aged</subject><subject>Pain</subject><subject>Placebos</subject><subject>probiotics</subject><subject>Probiotics - adverse effects</subject><subject>Probiotics - therapeutic use</subject><subject>Treatment Outcome</subject><issn>1078-0998</issn><issn>1536-4844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUUtuFDEQtRCIhIErIIsF2TCN3fa429klIcBIQbCAteVfEyN3u7HdisKKI3ASDsVJqMyMlB0S9qLKr1492_UQekFJQ4nsXhPafNieNwRWS_tOsEZKxnjD5QN0TDdMrHnP-UPISdeviZT9EXpSyjegw5aP0REVoiObVh6j359yMiHVYHHNXtfRTxWnAdsUo_7qp7SUuzzUUE7xGc56cmkMP7x7hV1aTPR_fv4yMUxwnqO23iQAbJpqBgHvQDToiG9CvcZQrsloG2IEUYguzddhl08OmzAAAOXqc1hGwMKoYyi4LKbMza47lKfo0aBj8c8OcYW-vL38fPF-ffXx3fbi7GptuWBybSX3whHNrTXMWEd7SonTrBetJJb1nApiWDu0jHSWSzYAOmg2OM6Z7zvLVuhkrzvn9H3xpaoxFOthJpOHkShJWpg4bXtgvvwnU3SSCSo4EE_3RJtTKdkPas7wxXyrKFF3vipCFfiq7n1VO18VPHCFnh9uWczo3X3rwUggXO4JNyH62_-QVtvzN6zrCW3Jhkj2FxjVuII</recordid><startdate>200605</startdate><enddate>200605</enddate><creator>Wildt, Signe</creator><creator>Munck, Lars K.</creator><creator>Vinter‐Jensen, Lars</creator><creator>Hanse, Birgit Fischer</creator><creator>Nordgaard‐Lassen, Inge</creator><creator>Christensen, Steen</creator><creator>Avnstroem, Soeren</creator><creator>Rasmussen, Sten Noerby</creator><creator>Rumessen, Jüri J.</creator><general>Lippincott Williams & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>200605</creationdate><title>Probiotic treatment of collagenous colitis: A randomized, double‐blind, placebo‐controlled trial with lactobacillus acidophilus and bifidobacterium animalis subsp. lactis</title><author>Wildt, Signe ; Munck, Lars K. ; Vinter‐Jensen, Lars ; Hanse, Birgit Fischer ; Nordgaard‐Lassen, Inge ; Christensen, Steen ; Avnstroem, Soeren ; Rasmussen, Sten Noerby ; Rumessen, Jüri J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4639-c94e6d0a4ccb3bcd18110da386290c384160b32f2307c493f90cfa3fd443e87c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Bifidobacterium - physiology</topic><topic>Bifidobacterium animalis</topic><topic>Clinical trials</topic><topic>Colitis</topic><topic>Colitis, Collagenous - pathology</topic><topic>Colitis, Collagenous - therapy</topic><topic>Collagen</topic><topic>collagenous colitis</topic><topic>Diarrhea</topic><topic>Digestive tract</topic><topic>Double-Blind Method</topic><topic>Drug Tolerance</topic><topic>Feces</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Inflammatory bowel diseases</topic><topic>Intestine</topic><topic>lactic acid bacteria</topic><topic>Lactobacillus acidophilus</topic><topic>Lactobacillus acidophilus - physiology</topic><topic>Male</topic><topic>Microflora</topic><topic>Middle Aged</topic><topic>Pain</topic><topic>Placebos</topic><topic>probiotics</topic><topic>Probiotics - adverse effects</topic><topic>Probiotics - therapeutic use</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wildt, Signe</creatorcontrib><creatorcontrib>Munck, Lars K.</creatorcontrib><creatorcontrib>Vinter‐Jensen, Lars</creatorcontrib><creatorcontrib>Hanse, Birgit Fischer</creatorcontrib><creatorcontrib>Nordgaard‐Lassen, Inge</creatorcontrib><creatorcontrib>Christensen, Steen</creatorcontrib><creatorcontrib>Avnstroem, Soeren</creatorcontrib><creatorcontrib>Rasmussen, Sten Noerby</creatorcontrib><creatorcontrib>Rumessen, Jüri J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Inflammatory bowel diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wildt, Signe</au><au>Munck, Lars K.</au><au>Vinter‐Jensen, Lars</au><au>Hanse, Birgit Fischer</au><au>Nordgaard‐Lassen, Inge</au><au>Christensen, Steen</au><au>Avnstroem, Soeren</au><au>Rasmussen, Sten Noerby</au><au>Rumessen, Jüri J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Probiotic treatment of collagenous colitis: A randomized, double‐blind, placebo‐controlled trial with lactobacillus acidophilus and bifidobacterium animalis subsp. lactis</atitle><jtitle>Inflammatory bowel diseases</jtitle><addtitle>Inflamm Bowel Dis</addtitle><date>2006-05</date><risdate>2006</risdate><volume>12</volume><issue>5</issue><spage>395</spage><epage>401</epage><pages>395-401</pages><issn>1078-0998</issn><eissn>1536-4844</eissn><abstract>Background: Probiotic treatment may be effective in diseases involving gut microflora and intestinal inflammation. In collagenous colitis (CC), a potential pathogenic role of the gut microflora has been proposed. The effect of probiotic treatment in CC is unknown. Our aim was to investigate the clinical effect of treatment with Lactobacillus acidophilus LA‐5 and Bifidobacterium animalis subsp. lactis BB‐12 (AB‐Cap‐10) in patients with CC. Materials and Methods: Patients with CC and diarrhea were in a double‐blind placebo‐controlled study randomized (2:1) to AB‐Cap‐10 or placebo for 12 weeks. The primary end point was reduction in bowel frequency per week of ≥50%. Secondary end points were changes in bowel frequencies, stool consistency, stool weight, histopathology, and abdominal bloating and pain. Results: Twenty‐nine patients were randomized: 21 to probiotics and 8 to placebo. Reduction in bowel frequency per week of ≥50% occurred in 6 of 21 (29%) and in 1 of 8 (13%) patients receiving probiotic and placebo, respectively (P = 0.635). No differences between treatments were observed regarding the secondary end points. Post hoc analysis showed a median reduction in bowel frequency per week from 32 (range 18–84) to 23 (range 11–56; P < 0.005), a reduction in number of days with liquid stools per week from 6 days (range 0–7 days) to 1 day (range 0–7 days; P < 0.005), and an increase in number of days with solid stools per week (P < 0.05) in the AB‐Cap‐10 group. Conclusions: AB‐Cap‐10 had no significant effect on the chosen end points. Post hoc analysis demonstrated amelioration of clinical symptoms in the AB‐Cap‐10 group, indicating that probiotic treatment may potentially influence the disease course of CC.</abstract><cop>Philadelphia</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>16670529</pmid><doi>10.1097/01.MIB.0000218763.99334.49</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Access via Wiley Online Library; Oxford University Press Journals All Titles (1996-Current) |
subjects | Adult Aged Bifidobacterium - physiology Bifidobacterium animalis Clinical trials Colitis Colitis, Collagenous - pathology Colitis, Collagenous - therapy Collagen collagenous colitis Diarrhea Digestive tract Double-Blind Method Drug Tolerance Feces Female Follow-Up Studies Humans Inflammatory bowel diseases Intestine lactic acid bacteria Lactobacillus acidophilus Lactobacillus acidophilus - physiology Male Microflora Middle Aged Pain Placebos probiotics Probiotics - adverse effects Probiotics - therapeutic use Treatment Outcome |
title | Probiotic treatment of collagenous colitis: A randomized, double‐blind, placebo‐controlled trial with lactobacillus acidophilus and bifidobacterium animalis subsp. lactis |
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