Gut and Liver is an international journal of gastroenterology, focusing on the gastrointestinal tract, liver, biliary tree, pancreas, motility, and neurogastroenterology. Gut atnd Liver delivers up-to-date, authoritative papers on both clinical and research-based topics in gastroenterology. The Journal publishes original articles, case reports, brief communications, letters to the editor and invited review articles in the field of gastroenterology. The Journal is operated by internationally renowned editorial boards and designed to provide a global opportunity to promote academic developments in the field of gastroenterology and hepatology. +MORE
Yong Chan Lee |
Professor of Medicine Director, Gastrointestinal Research Laboratory Veterans Affairs Medical Center, Univ. California San Francisco San Francisco, USA |
Jong Pil Im | Seoul National University College of Medicine, Seoul, Korea |
Robert S. Bresalier | University of Texas M. D. Anderson Cancer Center, Houston, USA |
Steven H. Itzkowitz | Mount Sinai Medical Center, NY, USA |
All papers submitted to Gut and Liver are reviewed by the editorial team before being sent out for an external peer review to rule out papers that have low priority, insufficient originality, scientific flaws, or the absence of a message of importance to the readers of the Journal. A decision about these papers will usually be made within two or three weeks.
The remaining articles are usually sent to two reviewers. It would be very helpful if you could suggest a selection of reviewers and include their contact details. We may not always use the reviewers you recommend, but suggesting reviewers will make our reviewer database much richer; in the end, everyone will benefit. We reserve the right to return manuscripts in which no reviewers are suggested.
The final responsibility for the decision to accept or reject lies with the editors. In many cases, papers may be rejected despite favorable reviews because of editorial policy or a lack of space. The editor retains the right to determine publication priorities, the style of the paper, and to request, if necessary, that the material submitted be shortened for publication.
Uday C. Ghoshal, Ratnakar Shukla, Ujjala Ghoshal
Correspondence to: Uday C. Ghoshal, Department of Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, India Tel: +91-522-249-4405, Fax: +91-522-266-8017, E-mail: udayghoshal@gmail.com
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Gut Liver 2017;11(2):196-208. https://doi.org/10.5009/gnl16126
Published online March 15, 2017, Published date March 15, 2017
Copyright © Gut and Liver.
The pathogenesis of irritable bowel syndrome (IBS), once thought to be largely psychogenic in origin, is now understood to be multifactorial. One of the reasons for this paradigm shift is the realization that gut dysbiosis, including small intestinal bacterial overgrowth (SIBO), causes IBS symptoms. Between 4% and 78% of patients with IBS and 1% and 40% of controls have SIBO; such wide variations in prevalence might result from population differences, IBS diagnostic criteria, and, most importantly, methods to diagnose SIBO. Although quantitative jejunal aspirate culture is considered the gold standard for the diagnosis of SIBO, noninvasive hydrogen breath tests have been popular. Although the glucose hydrogen breath test is highly specific, its sensitivity is low; in contrast, the early-peak criteria in the lactulose hydrogen breath test are highly nonspecific. Female gender, older age, diarrhea-predominant IBS, bloating and flatulence, proton pump inhibitor and narcotic intake, and low hemoglobin are associated with SIBO among IBS patients. Several therapeutic trials targeting gut microbes using antibiotics and probiotics have further demonstrated that not all symptoms in patients with IBS originate in the brain but rather in the gut, providing support for the micro-organic basis of IBS. A recent proof-of-concept study showing the high frequency of symptom improvement in patients with IBS with SIBO further supports this hypothesis.
Keywords: Bacterial overgrowth, Dysbiosis, Breath tests, Gastrointestinal microbiota, Probiotics, Rifaximin
Gut and Liver 2017; 11(2): 196-208
Published online March 15, 2017 https://doi.org/10.5009/gnl16126
Copyright © Gut and Liver.
Uday C. Ghoshal, Ratnakar Shukla, Ujjala Ghoshal
Department of Gastroenterology and Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India
Correspondence to:Uday C. Ghoshal, Department of Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, India Tel: +91-522-249-4405, Fax: +91-522-266-8017, E-mail: udayghoshal@gmail.com
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
The pathogenesis of irritable bowel syndrome (IBS), once thought to be largely psychogenic in origin, is now understood to be multifactorial. One of the reasons for this paradigm shift is the realization that gut dysbiosis, including small intestinal bacterial overgrowth (SIBO), causes IBS symptoms. Between 4% and 78% of patients with IBS and 1% and 40% of controls have SIBO; such wide variations in prevalence might result from population differences, IBS diagnostic criteria, and, most importantly, methods to diagnose SIBO. Although quantitative jejunal aspirate culture is considered the gold standard for the diagnosis of SIBO, noninvasive hydrogen breath tests have been popular. Although the glucose hydrogen breath test is highly specific, its sensitivity is low; in contrast, the early-peak criteria in the lactulose hydrogen breath test are highly nonspecific. Female gender, older age, diarrhea-predominant IBS, bloating and flatulence, proton pump inhibitor and narcotic intake, and low hemoglobin are associated with SIBO among IBS patients. Several therapeutic trials targeting gut microbes using antibiotics and probiotics have further demonstrated that not all symptoms in patients with IBS originate in the brain but rather in the gut, providing support for the micro-organic basis of IBS. A recent proof-of-concept study showing the high frequency of symptom improvement in patients with IBS with SIBO further supports this hypothesis.
Keywords: Bacterial overgrowth, Dysbiosis, Breath tests, Gastrointestinal microbiota, Probiotics, Rifaximin
Table 1 Prevalence of Small Intestinal Bacterial Overgrowth among Patients with Irritable Bowel Syndrome
Study no. | Prevalence of SIBO in cases | Prevalence of SIBO in controls | Methane producers in cases | Methane producers in controls | Country | Year | Reference |
---|---|---|---|---|---|---|---|
Culture of jejunal aspirate (≥105 CFU/mL colonic-type bacteria) | |||||||
1 | 7/162 (4) | 1/26 (4) | ND | ND | Sweden | 2007 | Posserud |
2 | 4/12 (33) | 0/9 | ND | ND | The Netherlands | 2008 | Kerckhoffs |
3 | 15/80 (18) | 0/10 | 2/15 (13) | ND | India | 2014 | Ghoshal |
4 | 42/112 (37) | ND | ND | ND | Greece | 2012 | Pyleris |
Culture of jejunal aspirate (≥103 CFU/mL colonic-type bacteria) | |||||||
5 | 62/139 (44.6) | ND | ND | ND | United States | 2015 | Erdogan |
Lactulose hydrogen breath test | |||||||
6 | 157/202 (78) | ND | ND | ND | United States | 2000 | Pimentel |
7 | 64/98 (65) | ND | ND | ND | Italy | 2005 | Nucera |
8 | 39/390 (10) | ND | ND | ND | Canada | 2005 | Walters and Vanner55 |
9 | 35/89 (39) | 1/13 (8) | ND | ND | China | 2014 | Zhao |
10 | 25/40 (63) | ND | ND | ND | Canada | 2011 | Yu |
11 | 34/76 (45) | 16/40 (40) | 19/76 (25) | 10/40 (25) | Korea | 2010 | Park |
12 | 28/43 (65) | 4/56 (7) | 4/43 (9) | 0 | Italy | 2009 | Scarpellini |
13 | 55/127 (43) | ND | ND | ND | Italy | 2008 | Carrara |
14 | 89/258 (34.5) | ND | ND | ND | United States | 2009 | Mann and Limoges-Gonzales60 |
15 | 60/175 (34.3) | 45/150 (30) | ND | ND | India | 2008 | Rana |
16 | 22/119 (18.4) | ND | ND | ND | Pakistan | 2011 | Yakoob |
Glucose hydrogen breath test | |||||||
17 | 25/225 (11.1) | 1/100 (1) | ND | ND | India | 2012 | Rana |
18 | 93/204 (46) | ND | 27/204 (13) | ND | United States | 2007 | Majewski and McCallum63 |
19 | 105/331 (32) | 7/105 (7) | ND | ND | Rome | 2014 | Moraru |
20 | 14/59 (24) | 1/37 (2.7) | 5/59 (9) | 9/37 (24) | India | 2011 | Sachdeva |
21 | 11/129 (8.5) | 1/51 (2) | ND | ND | India | 2010 | Ghoshal |
22 | 44/96 (45.8) | ND | ND | ND | Italy | 2006 | Cuoco and Salvangnini65 |
23 | 20/65 (31) | 4/102 (4) | ND | ND | Italy | 2005 | Lupascu |
24 | 8/72 (11.1) | ND | ND | ND | Rome | 2013 | Moraru |
25 | 49/200 (24.5) | 3/50 (6) | ND | ND | Italy | 2010 | Lombardo |
26 | 38/139 (27.3) | ND | ND | ND | United States | 2015 | Erdogan |
27 | 11/175 (6.2) | 1/150 (0.66) | ND | ND | India | 2012 | Rana |
28 | 40/107 (37.3) | 14/107 (13) | ND | ND | Iran | 2015 | Abbasi |
Data are presented as number (%).
SIBO, small intestinal bacterial overgrowth; CFU, colony forming unit; ND, not done.
Table 2 Clinical Trials of Antibiotics among Patients with Small Intestinal Bacterial Overgrowth and Irritable Bowel Syndrome
Study no. | Antibiotics (dosage) | Duration, day | Study subject | Clinical outcome | Reference |
---|---|---|---|---|---|
1 | Rifaximin (1,600 mg/day) vs rifaximin (1,200 mg/day) | 7 | 80 Patients with SIBO | Rate of normalization of GHBT was greater with higher dose of rifaximin than lower dose (80% vs 58%, p<0.05). | Scarpellini |
2 | Rifaximin (group 1, 600; group 2, 800; group 3, 1,200 mg/day) | 7 | 90 Patients with SIBO and 30 patients in each group | Rate of normalization of GHBT was higher in group 3 than group 1 and 2 (60% vs 17%, p<0.001; 60% vs 27%, p<0.01). | Lauritano |
3 | Neomycin (n=55) or placebo (n=56) | 7 | 111 Patients with IBS | Neomycin reduced the symptoms of IBS more often than placebo (35% vs 11%, p<0.05) and normalized lactulose hydrogen breath test result. | Pimentel |
4 | Ciprofloxacin (500 mg, twice daily) | 10 | 7 Patients with SIBO | Ciprofloxacin decreased viable bacterial counts in five patients (71%), while four (57%) still fulfilled criteria for SIBO. Three patients (43%) reported at least 25% improvement in IBS symptoms. | Posserud |
5 | Norfloxacin (800 mg/day) or placebo | 10 | 80 IBS patients | Norfloxacin significantly reduced the symptom scores among patients with SIBO than without but not with placebo at 1 month. Symptoms resolved to turn Rome III negative more often in SIBO patients receiving norfloxacin than placebo at 1 month (7/8, 87.5 vs 0/7, p=0.004). | Ghoshal |
SIBO, small intestinal bacterial overgrowth; GHBT, glucose hydrogen breath test; IBS, irritable bowel syndrome.