Literature DB >> 21860825

How to interpret hydrogen breath tests.

Uday C Ghoshal1.   

Abstract

Hydrogen breath tests using various substrates like glucose, lactulose, lactose and fructose are being used more and more to diagnose small intestinal bacterial overgrowth (SIBO) and lactose or fructose malabsorption. Though quantitative culture of jejunal aspirate is considered as gold standard for the diagnosis of SIBO, hydrogen breath tests, in spite of their low sensitivity, are popular for their non-invasiveness. Glucose hydrogen breath test is more acceptable for the diagnosis of SIBO as conventionally accepted double-peak criterion on lactulose hydrogen breath test is very insensitive and recently described early-peak criterion is often false positive. Hydrogen breath test is useful to diagnose various types of sugar malabsorption. Technique and interpretation of different hydrogen breath tests are outlined in this review.

Entities:  

Keywords:  Breath tests; Hydrogen; Intestine, small; Irritable bowel syndrome

Year:  2011        PMID: 21860825      PMCID: PMC3155069          DOI: 10.5056/jnm.2011.17.3.312

Source DB:  PubMed          Journal:  J Neurogastroenterol Motil        ISSN: 2093-0879            Impact factor:   4.924


Introduction

Recently, hydrogen breath test (HBT) has become popular in clinical practice as it is useful for diagnosing small intestinal bacterial overgrowth (SIBO) and carbohydrate intolerance such as lactose and fructose malabsorption (Table).1 Though quantitative culture of jejunal aspirate is considered as gold standard for the diagnosis of SIBO, HBT is popular as it is non-invasive.1,2 In spite of the simplicity of performance, there is lack of uniformity regarding the interpretation of various HBTs. Therefore, technique and interpretation of commonly used HBTs are reviewed here.
Table

Various Hydrogen Breath Tests Used in Clinical Practice and Their Clinical Utility

Principle of Hydrogen Breath Tests

In these tests, hydrogen exhaled in the breath is estimated using a gas chromatograph. Bacteria, especially anaerobic, colonizing the large bowel in health and small bowel in diseased conditions produce hydrogen by fermentation of unabsorbed carbohydrates. Though small amount of hydrogen is produced from limited amounts of unabsorbed carbohydrate reaching the colon, large amounts of hydrogen may be produced if there is malaborption of carbohydrate in the small intestine allowing larger amount to reach the colon or if there is excess of bacteria in the small bowel. The hydrogen produced by the bacteria is absorbed through the wall of the small or large intestine or both. The hydrogen-containing blood travels to the lungs where the hydrogen is released and exhaled in the breath where it can be measured. About 15%-30% people have gut flora that contain Methanobrevibacter smithii, which converts 4 atoms of hydrogen into 1 molecule of methane.3 These subjects may not exhale much hydrogen in the breath in spite of having SIBO or carbohydrate malabsorption as excess hydrogen produced in them is converted into methane. Figure 1 summarizes the principle of HBTs.
Figure 1

A schematic diagram that shows principle of hydrogen breath test. SIBO, small intestinal bacterial overgrowth; ppm, parts per million.

Patient Preparation

The subjects are asked to avoid slowly absorbed carbohydrates (like bread and potato) and fiber the previous night as these would cause delayed excretion of hydrogen in breath.2 Cigarette smoking and exercise are avoided 2 hours before and during the test, as hyperventilation can cause changes in breath hydrogen content.2 Pro-motility, anti-motility drugs, antibiotics and other drugs that can cause SIBO including proton pump inhibitors should be discontinued before performing breath tests.

Procedure of the Breath Test

Breath test is performed after overnight fast. Before the test, subjects are asked to brush their teeth and rinse mouth with antiseptic mouth wash and tap water, to eliminate an early hydrogen peak due to action of oral bacteria on test sugars.2 End-expiratory breath samples are collected either in bag or syringes. At the start of the test, fasting breath hydrogen is estimated 3 to 4 times and the average of these values is taken as the basal breath hydrogen. Subsequently, the subject ingests a fixed amount of the test sugar (10 g lactulose, 100 g glucose, 50 g lactose or 25 g fructose). All samples of breath are analyzed for hydrogen and methane every 15 minutes for 2 to 4 hours. These values are written on a diary. Special computer softwares are also available to record values of the breath tests. Development of symptoms following ingestion of the substrate is also noted.4 Lactose tolerance test, which involves estimation of blood sugar in fasting state and 30-minutes after ingestion of lactose, is usually combined with lactose HBT.5

Interpretation of Breath Tests

Figure 2 shows some typical HBT graphs. HBTs are interpreted as follows.
Figure 2

Some typical hydrogen breath test graphs are shown. It shows glucose hydrogen breath test negative for small intestinal bacterial overgrowth (SIBO) (A), glucose hydrogen breath test positive for SIBO (B), lactose hydrogen breath and tolerance test negative for lactose malabsorption (C) and lactose hydrogen breath and tolerance test positive for lactose malabsorption (D). It shows a graph negative for fructose malabsorption (E) and a graph positive for fructose malabsorption (F). ppm, parts per million; FBS, fasting blood sugar; PPBS, post-prandial blood sugar.

High Basal Breath Hydrogen

If average basal values of breath hydrogen is more than 16 parts per million (ppm), it is generally considered as a high value.6 The substrate may not be administered if basal breath hydrogen is high and the test would be abandoned. In such situation, the test is repeated with proper preparation again. Some investigators considered high basal breath hydrogen to be suggestive of SIBO7 though evidences available are contradictory.6

Diagnosis of Small Intestinal Bacterial Overgrowth on Glucose and Lactulose Hydrogen Breath Test

SIBO is diagnosed on glucose HBT if there is a rise in breath hydrogen by 12 ppm above the basal. The sensitivity and specificity of this criterion to diagnose SIBO are 40% and 80%, respectively.2 Conventionally, double peak in lactulose HBT (one due to SIBO and the other from colon) is considered as diagnostic of SIBO. Sensitivity and specificity of lactulose HBT to diagnose SIBO using this conventional criterion are 31% and 86%, respectively when considering the quantitative culture of jejunal aspirate (bacterial colony count ≥ 105 CFU/mL) as gold standard.2

Glucose or Lactulose Hydrogen Breath Test to Diagnose Small Intestinal Bacterial Overgrowth?

A double-peak criteria on lactulose HBT as mentioned above is only 31% sensitive to diagnose SIBO.2 Pimentel et al8 suggested that a rise in breath hydrogen 20 ppm above basal levels within 90 minutes after ingestion of lactulose should be considered as diagnostic of SIBO. This criterion has not been validated. Moreover, it presumes that mouth-to-cecum transit time is always greater than 90 minutes, so that a peak in breath hydrogen within 90 minutes after lactulose ingestion must be due to bacterial fermentation in the small bowel. However, this assumption is not correct. Mouth-to-cecum transit time in Asian populations is often shorter than 90 minutes. For example, in our study, median mouth-to-cecum transit time in 12 healthy Indian subjects was 65 minutes (range 40 to 110 minutes).9 In a study of 45 healthy Taiwanese, mean mouth-to-cecum transit time was 85 minutes (standard deviation 37).10 Therefore, a large proportion of these healthy subjects would have been diagnosed as having SIBO if Pimentel's criterion had been employed. Hence, lactulose HBT should not be used to diagnose SIBO. Even the double-peak criterion to diagnose SIBO on lactulose HBT has lower sensitivity than glucose HBT (31% vs 40%).2 Therefore, glucose HBT should be used for diagnosing SIBO.

Limitations of Hydrogen Breath Test to Diagnose Small Intestinal Bacterial Overgrowth

There are several limitations of HBT for the diagnosis of SIBO. (1) HBT with lactulose may be able to diagnose only one-third of patients with SIBO.2 Since glucose is absorbed completely in the upper small intestine, it may not be able to diagnose SIBO of the distal small intestine (ileum).11 A major problem is that there is no "gold standard" for the diagnosis of SIBO since culture of the bacteria has its own limitations, as only 30% of gut bacteria are culturable.11 However, in our study we have found GHBT to be highly specific for diagnosis of SIBO.2 Hence, it is important to realize that GHBT can underestimate but is unlikely to overestimate SIBO. (2) There may be similarities in the pattern of gas production with SIBO and rapid intestinal transit, thus making distinctions difficult. (3) Some normal individuals may have slow transit through the small intestine leading to prolonged testing, up to 5 hours and many individuals may not like to undergo such a time consuming procedure. (4) A proportion of individuals have bacteria that do not produce hydrogen but produce other gases such as methane and hydrogen sulphide; therefore, their SIBO, if present, may not be detected with the HBT.3 Estimation of methane may be useful in such situation. There is no commercially available machine currently that measures hydrogen sulphide. (5) Some individuals may produce a combination of hydrogen and methane. There is much less experience with methane as compared with hydrogen for the diagnosis of SIBO. However, the production of methane is more complex than the production of hydrogen. Therefore, it is not clear if the pattern of methane production after ingestion of sugars can be interpreted in the same way as hydrogen production. Furthermore, all the equipments available in the market for HBTs do not have facilities for estimation of methane. As mentioned above, the equipments that have facilities for estimation of methane as well as hydrogen are superior for HBT. Methane is a marker of constipation.12 (6) A positive HBT may not always mean that a patient's symptoms are caused by SIBO. The only way to establish whether the symptoms are caused by SIBO is to treat and eradicate the bacteria. If the symptoms disappear, it is likely that SIBO rather than the underlying disease is responsible for the symptoms.

Lactulose Hydrogen Breath Test to Estimate Oro-Cecal Transit Time

The time interval between ingestion of lactulose and rise in breath hydrogen 20 ppm above basal is a measure of oro-cecal transit time. It is important to note that value of breath hydrogen to diagnose an abnormality is generally higher if fermentation of the substrate occurs in the colon rather than small intestine. For this reason, the cut-off value of hydrogen to estimate oro-cecal transit time, lactose and fructose malabsorption is 20 ppm above basal; in contrast, the cut-off value of hydrogen to diagnose bacterial overgrowth in the small intestine is 12 ppm above basal. Recently, in a study in which lactulose HBT was compared with radio-nuclide scintigraphic method for estimation of oro-cecal transit time, the former was shown to have reasonable accuracy for this purpose.13

Lactose Hydrogen Breath test for Diagnosis of Lactose Malabsorption

Rise in hydrogen by 20 ppm above basal after lactose ingestion is considered as positive lactose HBT. Failure of blood sugar to rise by 20 mg/dL at 30 minutes after ingestion of lactose is considered as positive lactose tolerance test, which is indicative of lactose malabsorption.4,5 There are some issues in the current protocol for lactose HBT. Some data suggest that lactose tolerance test may be as good as or more sensitive than lactose HBT. Lactose dose of 50 g, as suggested in the current protocol, may be too high and non-physiological. This may lead to overestimation of frequency of lactose malabsorption which may not always be clinically important in areas of the world where frequency of the condition is too high.4

Interpretation of Fructose Hydrogen Breath Test

Rise in hydrogen by 20 ppm above basal after fructose ingestion is considered as positive fructose HBT.14

Clinical Importance of Breath Gas Profile

Some data suggest that basal breath hydrogen both in fasting state and following ingestion of a substrate is higher among patients with irritable bowel syndrome, particularly in those with diarrhea-predominant disease than controls.15 In contrast, people with constipation may have high methane.3 Therefore, hydrogen may be a biomarker for diarrhea and methane of constipation.6,12,15 Reduction of methane by rifaximin may improve constipation.12 Hydrogen may also contribute to development of abdominal bloating.

Conclusion

HBTs are easy to perform and are non-invasive. These may be useful to understand abnormal pathophysiology such as SIBO and carbohydrate malabsorption contributing to symptoms in patients presenting with irritable bowel syndrome. It is suggested that uniform criteria should be developed and used for diagnosis of various disorders by HBTs.
  15 in total

1.  Frequency of lactose malabsorption among healthy southern and northern Indian populations by genetic analysis and lactose hydrogen breath and tolerance tests.

Authors:  Janaki Babu; Sunil Kumar; P Babu; Jaishri H Prasad; Uday C Ghoshal
Journal:  Am J Clin Nutr       Date:  2009-11-04       Impact factor: 7.045

Review 2.  Review article: fructose malabsorption and the bigger picture.

Authors:  P R Gibson; E Newnham; J S Barrett; S J Shepherd; J G Muir
Journal:  Aliment Pharmacol Ther       Date:  2007-01-08       Impact factor: 8.171

3.  Utility of hydrogen breath tests in diagnosis of small intestinal bacterial overgrowth in malabsorption syndrome and its relationship with oro-cecal transit time.

Authors:  Uday C Ghoshal; Ujjala Ghoshal; Kshaunish Das; Asha Misra
Journal:  Indian J Gastroenterol       Date:  2006 Jan-Feb

4.  Combined oro-caecal scintigraphy and lactulose hydrogen breath testing demonstrate that breath testing detects oro-caecal transit, not small intestinal bacterial overgrowth in patients with IBS.

Authors:  Derek Yu; Frank Cheeseman; Stephen Vanner
Journal:  Gut       Date:  2010-11-26       Impact factor: 23.059

5.  Frequency of small intestinal bacterial overgrowth in patients with irritable bowel syndrome and chronic non-specific diarrhea.

Authors:  Uday C Ghoshal; Sunil Kumar; Mansi Mehrotra; Cp Lakshmi; Asha Misra
Journal:  J Neurogastroenterol Motil       Date:  2010-01-31       Impact factor: 4.924

6.  Characteristics of small bowel motility in patients with irritable bowel syndrome and normal humans: an Oriental study.

Authors:  C L Lu; C Y Chen; F Y Chang; S D Lee
Journal:  Clin Sci (Lond)       Date:  1998-08       Impact factor: 6.124

7.  Lactose intolerance in patients with irritable bowel syndrome from northern India: a case-control study.

Authors:  Dinesh Gupta; Uday C Ghoshal; Amita Misra; Asha Misra; Gourdas Choudhuri; Kartar Singh
Journal:  J Gastroenterol Hepatol       Date:  2007-06-07       Impact factor: 4.029

8.  Hydrogen breath testing in adults: what is it and why is it performed?

Authors:  Deborah A Lindberg
Journal:  Gastroenterol Nurs       Date:  2009 Jan-Feb       Impact factor: 0.978

9.  Small-intestinal bacterial overgrowth in cirrhosis is related to the severity of liver disease.

Authors:  C Pande; A Kumar; S K Sarin
Journal:  Aliment Pharmacol Ther       Date:  2009-03-06       Impact factor: 8.171

10.  Slow transit constipation associated with excess methane production and its improvement following rifaximin therapy: a case report.

Authors:  Uday C Ghoshal; Deepakshi Srivastava; Abhai Verma; Asha Misra
Journal:  J Neurogastroenterol Motil       Date:  2011-04-27       Impact factor: 4.924

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Authors:  Mohammad-Ayman A Safi; Asif A Jiman-Fatani; Omar I Saadah
Journal:  Turk J Gastroenterol       Date:  2020-11       Impact factor: 1.852

2.  A randomized double-blind placebo-controlled trial showing rifaximin to improve constipation by reducing methane production and accelerating colon transit: A pilot study.

Authors:  Uday C Ghoshal; Deepakshi Srivastava; Asha Misra
Journal:  Indian J Gastroenterol       Date:  2018-11-08

3.  Fructose malabsorption is not uncommon among patients with irritable bowel syndrome in India: a case-control study.

Authors:  Atul Sharma; Deepakshi Srivastava; Abhai Verma; Asha Misra; Uday C Ghoshal
Journal:  Indian J Gastroenterol       Date:  2014-07-29

4.  The role of small intestinal bacterial overgrowth in cystic fibrosis: a randomized case-controlled clinical trial with rifaximin.

Authors:  Manuele Furnari; Alessandra De Alessandri; Federico Cresta; Maria Haupt; Marta Bassi; Angela Calvi; Riccardo Haupt; Giorgia Bodini; Iftikhar Ahmed; Francesca Bagnasco; Edoardo Giovanni Giannini; Rosaria Casciaro
Journal:  J Gastroenterol       Date:  2018-09-19       Impact factor: 7.527

5.  SIBO in gastroparesis: sci-fi or science fact?

Authors:  John O Clarke
Journal:  Dig Dis Sci       Date:  2014-01-17       Impact factor: 3.199

6.  Poor reproducibility of breath hydrogen testing: Implications for its application in functional bowel disorders.

Authors:  Chu K Yao; Caroline J Tuck; Jacqueline S Barrett; Kim Ek Canale; Hamish L Philpott; Peter R Gibson
Journal:  United European Gastroenterol J       Date:  2016-07-07       Impact factor: 4.623

7.  Use of an over-the-scope clipping device for closure of a jejuno-sigmoid fistula: a case report with long-term follow-up.

Authors:  Yuichi Sagara; Satoshi Shinozaki; Tomonori Yano; Hirotsugu Sakamoto; Yoshikazu Hayashi; Alan Kawarai Lefor; Hironori Yamamoto
Journal:  Clin J Gastroenterol       Date:  2016-09-23

Review 8.  Update on diagnostic value of breath test in gastrointestinal and liver diseases.

Authors:  Imran Siddiqui; Sibtain Ahmed; Shahab Abid
Journal:  World J Gastrointest Pathophysiol       Date:  2016-08-15

9.  Serum diamine oxidase activity in patients with histamine intolerance.

Authors:  G Manzotti; D Breda; M Di Gioacchino; S E Burastero
Journal:  Int J Immunopathol Pharmacol       Date:  2015-11-16       Impact factor: 3.219

10.  Gastrointestinal complications of diabetes mellitus.

Authors:  Babu Krishnan; Shithu Babu; Jessica Walker; Adrian B Walker; Joseph M Pappachan
Journal:  World J Diabetes       Date:  2013-06-15
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