Abstract
The relationship between methanogenic flora and hydrogen (H2) production is considered to be a possible confounding factor in the interpretation of hydrogen breath tests (H2BT). Therefore, the present study was conducted prospectively and included 154 IBS patients (fulfilling Rome II criteria) and 286 age-and-sex-matched apparently healthy controls. Each subject underwent H2BT after overnight fasting using 25 g lactose. Methane and H2 were measured using an SC Microlyser from Quintron, USA, at baseline and every 30 min for a total of 4 h. Subjects with fasting methane concentration <10 ppm were labeled as low methane producers (LMP) and >10 ppm as predominant methane producers (PMP). A rise >20 ppm over base line in hydrogen concentration was taken as +ve hydrogen breath test. IBS and control groups included 66.78% and 67.53% males, respectively. Mean age in the two groups were 48.52 ± 30.54 years (range 15–68 years) and 45.67 ± 30.54 years (range 15–78 years), respectively. Hydrogen breath test was +ve in 77/154 (50%) IBS patients and in 142/286 (49.65%) in controls (P > 0.05). It was also observed that the hydrogen breath test was −ve due to PMP in 5/77 (6.49%) of IBS patients and in 29/154 (20.14%) in controls. PMP affected lactose hydrogen breath tests in 6.49–20.14% subjects. This effect is more apparent in apparently healthy subjects as compared to patients with IBS.
Similar content being viewed by others
References
Levitt MD, Furne JK, Kuskowski M, Ruddy J. Stability of human methanogenic flora over 35 years and a review of insights obtained from breath methane measurements. Clin Gastroenterol Hepatol. 2006;4(2):123–129. doi:10.1016/j.cgh.2005.11.006.
Myo-Khin, Bolin TD, Khin-Mar-Oo, Tin-Oo, Kyaw-Hla S, Thein-Myint T. Ineffectiveness of breath methane excretion as a diagnostic test for lactose malabsorption. J Pediatr Gastroenterol Nutr. 1999;28(5):474–479. doi:10.1097/00005176-199905000-00006.
Rosado JL, Solomons NW. Sensitivity and specificity of the hydrogen breath-analysis test for detecting malabsorption of physiological doses of lactose. Clin Chem. 1983;29(3):545–548.
McKay LF, Eastwood MA, Brydon WG. Methane excretion in man—a study of breath, flatus, and faeces. Gut. 1985;26(1):69–74. doi:10.1136/gut.26.1.69.
Peled Y, Weinberg D, Hallak A, Gilat T. Factors affecting methane production in humans. Gastrointestinal diseases and alterations of colonic flora. Dig Dis Sci. 1987;32(3):267–271. doi:10.1007/BF01297052.
Montes RG, Saavedra JM, Perman JA. Relationship between methane production and breath hydrogen excretion in lactose-malabsorbing individuals. Dig Dis Sci. 1993;38(3):445–448. doi:10.1007/BF01316497.
Corazza GR, Benati G, Strocchi A, Malservisi S, Gasbarrini G. The possible role of breath methane measurement in detecting carbohydrate malabsorption. J Lab Clin Med. 1994;124(5):695–700.
Cloarec D, Gouilloud S, Bornet F, Bruley Des Varannes S, Bizais Y, Galmiche JP. Lactase deficiency and lactose intolerance-related symptoms in adult healthy subjects from western France. Gastroenterol Clin Biol. 1991;15(8–9):588–593.
Vernia P, Camillo MD, Marinaro V, Caprilli R. Effect of predominant methanogenic flora on the outcome of lactose breath test in irritable bowel syndrome patients. Eur J Clin Nutr. 2003;57(9):1116–1119. doi:10.1038/sj.ejcn.1601651.
Kajs TM, Fitzgerald JA, Buckner RY, et al. Influence of a methanogenic flora on the breath H2 and symptom response to ingestion of sorbitol or oat fiber. Am J Gastroenterol. 1997;92(1):89–94.
Strocchi A, Levitt MD. Factors affecting hydrogen production and consumption by human fecal flora. The critical roles of hydrogen tension and methanogenesis. J Clin Invest. 1992;89(4):1304–1311. doi:10.1172/JCI115716.
Bond JH, Levitt MD. Use of breath hydrogen (H2) in the study of carbohydrate absorption. Am J Dig Dis. 1977;22(4):379–382. doi:10.1007/BF01072197.
Bond JH Jr, Engel RR, Levitt MD. Factors influencing pulmonary methane excretion in man. An indirect method of studying the in situ metabolism of the methane-producing colonic bacteria. J Exp Med. 1971;133(3):572–588. doi:10.1084/jem.133.3.572.
Weaver GA, Krause JA, Miller TL, Wolin MJ. Incidence of methanogenic bacteria in a sigmoidoscopy population: an association of methanogenic bacteria and diverticulosis. Gut. 1986;27(6):698–704. doi:10.1136/gut.27.6.698.
Miller TL, Weaver GA, Wolin MJ. Methanogens and anaerobes in a colon segment isolated from the normal fecal stream. Appl Environ Microbiol. 1984;48(2):449–450.
Pochart P, Lémann F, Flourié B, Pellier P, Goderel I, Rambaud JC. Pyxigraphic sampling to enumerate methanogens and anaerobes in the right colon of healthy humans. Gastroenterology. 1993;105(5):1281–1285.
Strocchi A, Ellis CJ, Furne JK, Levitt MD. Study of constancy of hydrogen-consuming flora of human colon. Dig Dis Sci. 1994;39(3):494–497. doi:10.1007/BF02088333.
Acknowledgments
The financial assistance by the ICMR to carry out this work is fully acknowledged.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Rana, S.V., Sinha, S.K., Sharma, S. et al. Effect of Predominant Methanogenic Flora on Outcome of Lactose Hydrogen Breath Test in Controls and Irritable Bowel Syndrome Patients of North India. Dig Dis Sci 54, 1550–1554 (2009). https://doi.org/10.1007/s10620-008-0532-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10620-008-0532-3