Irritable bowel syndrome and probiotics: from rationale to clinical use

被引:27
作者
Verdu, EF [1 ]
Collins, SM [1 ]
机构
[1] McMaster Univ, Intestinal Dis Res Programme, Hamilton, ON, Canada
关键词
functional bowel disorders; gut dysfunction; irritable bowel syndrome; probiotics;
D O I
10.1097/01.mog.0000182861.11669.4d
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review Few therapies are of proven efficacy in irritable bowel syndrome. Thus, there is great interest in the development of a natural therapy that can be both safe and effective. An understanding that probiotics are heterogeneous, with multiple targets and mechanisms of action, is fundamental to the development of clinical trials. Recent findings A bidirectional model for the pathogenesis of irritable bowel syndrome is proposed in which gut-driven and brain-driven mechanisms contribute to the genesis of gut dysfunction and symptoms. In-vitro and animal studies have generated most of the mechanistic rationale for the use of probiotics in functional bowel disorders. A MEDLINE search of publications from 1989 to date revealed only eight placebo-controlled clinical trials on the subject of probiotics and irritable bowel syndrome. All these studies suffer from methodologic problems. By contrast, numerous reviews have been published in the past 2 years on this subject. Summary Animal research will continue to identify novel targets and elucidate the mechanisms of action of probiotics, thus providing a rational basis for their use in irritable bowel syndrome. The notion of treating irritable bowel syndrome with probiotics is particularly attractive to patients and generates great interest, although clinical evidence is not yet sufficient to enable clear guidelines to be designed. Large, well-designed, controlled clinical trials using specific probiotics are warranted.
引用
收藏
页码:697 / 701
页数:5
相关论文
共 40 条
[1]  
BALSARI A, 1982, MICROBIOLOGICA, V5, P185
[2]   Activated mast cells in proximity to colonic nerves correlate with abdominal pain in irritable bowel syndrome [J].
Barbara, G ;
Stanghellini, V ;
De Giorgio, R ;
Cremon, C ;
Cottrell, GS ;
Santini, D ;
Pasquinelli, G ;
Morselli-Labate, AM ;
Grady, EF ;
Bunnett, NW ;
Collins, SM ;
Corinalidesi, R .
GASTROENTEROLOGY, 2004, 126 (03) :693-702
[3]   IRRITABLE BOWEL SYNDROME - RELATIONSHIP OF DISORDERS IN THE TRANSIT OF A SINGLE SOLID MEAL TO SYMPTOM PATTERNS [J].
CANN, PA ;
READ, NW ;
BROWN, C ;
HOBSON, N ;
HOLDSWORTH, CD .
GUT, 1983, 24 (05) :405-411
[4]   Activation of the mucosal immune system in irritable bowel syndrome [J].
Chadwick, VS ;
Chen, WX ;
Shu, DR ;
Paulus, B ;
Bethwaite, P ;
Tie, A ;
Wilson, I .
GASTROENTEROLOGY, 2002, 122 (07) :1778-1783
[5]  
Gade J, 1989, Scand J Prim Health Care, V7, P23, DOI 10.3109/02813438909103666
[6]   Interleukin 10 genotypes in irritable bowel syndrome: evidence for an inflammatory component? [J].
Gonsalkorale, WM ;
Perrey, C ;
Pravica, V ;
Whorwell, PJ ;
Hutchinson, IV .
GUT, 2003, 52 (01) :91-93
[7]   Increased rectal mucosal expression of interleukin 1β in recently acquired post-infectious irritable bowel syndrome [J].
Gwee, KA ;
Collins, SM ;
Read, NW ;
Rajnakova, A ;
Deng, Y ;
Graham, JC ;
McKendrick, MW ;
Moochhala, SM .
GUT, 2003, 52 (04) :523-526
[8]   Efficacy of probiotic use in acute diarrhea in children - A meta-analysis [J].
Huang, JS ;
Bousvaros, A ;
Lee, JW ;
Diaz, A ;
Davidson, EJ .
DIGESTIVE DISEASES AND SCIENCES, 2002, 47 (11) :2625-2634
[9]  
Isolauri E, 2002, GUT, V50, P54, DOI 10.1136/gut.50.suppl_3.iii54
[10]   Influence of synbiotic containing Lactobacillus acidophilus La5, Bifidobacterium lactis Bb 12, Streptococcus thermophilus, Lactobacillus bulgaricus and oligofructose on gut barrier function and sepsis in critically ill patients:: A randomised controlled trial [J].
Jain, PK ;
McNaught, CE ;
Anderson, ADG ;
MacFie, J ;
Mitchell, CJ .
CLINICAL NUTRITION, 2004, 23 (04) :467-475