Interpretation of the breath hydrogen profile obtained after ingesting a solid meal containing unabsorbable carbohydrate

• Published in: Gut Vol. 26; no. 8; pp. 834 - 842
• Main Authors: Read, N W, Al-Janabi, M N, Bates, T E, Holgate, A M, Cann, P A, Kinsman, R I, McFarlane, A, Brown, C
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group Ltd and British Society of Gastroenterology 01-08-1985; BMJ; BMJ Publishing Group LTD
• Subjects: Absorption; Adult; Aged; Biological and medical sciences; Breath Tests; Colon - metabolism; Colonic Diseases, Functional - metabolism; Dietary Carbohydrates - metabolism; Female; Fermentation; Food; Functional investigation of the digestive system; Humans; Hydrogen - metabolism; Ileostomy; Investigative techniques, diagnostic techniques (general aspects); Lactulose - metabolism; Male; Medical sciences; Middle Aged; Mouth - metabolism; Human; Breath test; Absorption; Postprandial; Residue; Gut; Meal; Digestive diseases; Exploration; Intestinal disease; Carbohydrate; Solid
• ISSN: 0017-5749; 1468-3288; 1458-3288
• DOI: 10.1136/gut.26.8.834

The extent to which monitoring breath hydrogen excretion provides information concerning the entry of the residues of a solid test meal into the colon was investigated in 89 normal subjects, and 11 patients with the irritable bowel syndrome. The profile of breath hydrogen concentration showed an early peak, that occurred soon after ingesting the test meal in 89% subjects. This was followed by a later more prolonged rise in breath hydrogen concentration. The early peak occurred well before a radioactive marker, incorporated in the test meal, reached the caecum and the data suggest it was predominantly caused by the emptying of the remnants of the previous meal from the ileum into the colon. This hypothesis was supported by direct measurements of the rate of delivery of ileostomy effluent in 12 subjects with terminal ileostomies. Fermentation of carbohydrate in the mouth may, however, contribute to the initial peak, but this contribution may be avoided by collecting gas samples from the nares. The secondary rise in breath hydrogen excretion was closely correlated with the arrival of the radioactive marker in the caecum (r = 0.91), p less than 0.001), though the time, at which the secondary peak of breath hydrogen excretion occurred was poorly correlated with the time that all the radioactive test meal had entered the colon. When lactulose was infused directly into the colon, as little as 0.5 g produced a discernible hydrogen response, which occurred within two minutes of the infusion. Increasing the rate of colonic infusion of a 50 ml solution of 10% lactulose from 0.02 to 0.15 g/min in five subjects significantly increased the breath hydrogen concentration. At infusion rates below 0.075 g lactulose/minute, the peak breath hydrogen response preceded the end ot the infusion, while at higher rates of infusion, the peak hydrogen response occurred after the end of the infusion. Although these results confirmed that monitoring breath hydrogen concentration usefully signalled the time taken for a meal containing unabsorbed carbohydrate to reach the colon, it did not reliably indicate the time when all of the meal had entered the colon. Finally, the use of the maximum increase in breath hydrogen concentration as an index of the degree of carbohydrate malabsorption assumes uniform rates of entry into the colon.