J Neurogastroenterol Motil 2011; 17(3): 312-317  https://doi.org/10.5056/jnm.2011.17.3.312
How to Interpret Hydrogen Breath Tests
Uday C Ghoshal*

Department of Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

Correspondence to: Uday C Ghoshal, MD, DNB, DM, FACG. Additional Professor, Department of Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow 226014, India. Tel: +91-962-8842456, Fax: +91-522-2668017 (or 2668078), udayghoshal@gmail.com
Received: June 7, 2011; Revised: June 19, 2011; Accepted: June 20, 2011; Published online: July 14, 2011.
© The Korean Society of Neurogastroenterology and Motility. All rights reserved.

cc This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: Breath tests, Hydrogen, Intestine, small, Irritable bowel syndrome
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.

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.

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.

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.

Figures
Fig. 1. A schematic diagram that shows principle of hydrogen breath test. SIBO, small intestinal bacterial overgrowth; ppm, parts per million.
Fig. 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.
Tables
Table. 1. Various Hydrogen Breath Tests Used in Clinical Practice and Their Clinical Utility


References
  1. Lindberg, DA. Hydrogen breath testing in adults: what is it and why is it performed?. Gastroenterol Nurs. 2009;32;19-24.
    Pubmed
  2. Ghoshal UC, Ghoshal U, Das K, Misra A. Utility of hydrogen breath tests in diagnosis of small intestinal bacterial overgrowth in malabsorption syndrome and its relationship with oro-cecal transit time. Indian J Gastroenterol. 2006;25;6-10.
    Pubmed
  3. 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;123-129.
    Pubmed
  4. Gupta D, Ghoshal UC, Misra A, Choudhuri G, Singh K. Lactose intolerance in patients with irritable bowel syndrome from northern India: a case-control study. J Gastroenterol Hepatol. 2007;22;2261-2265.
    Pubmed
  5. Babu J, Kumar S, Babu P, Prasad JH, Ghoshal UC. Frequency of lactose malabsorption among healthy southern and northern Indian populations by genetic analysis and lactose hydrogen breath and tolerance tests. Am J Clin Nutr. 2009;91;140-146.
    Pubmed
  6. Kumar S, Misra A, Ghoshal UC. Patients with irritable bowel syndrome exhale more hydrogen than healthy subjects in fasting state. J Neurogastroenterol Motil. 2010;16;299-305.
    Pubmed
  7. Pande C, Kumar A, Sarin SK. Small-intestinal bacterial overgrowth in cirrhosis is related to the severity of liver disease. Aliment Pharmacol Ther. 2009;29;1273-1281.
    Pubmed
  8. Pimentel M, Chow EJ, Lin HC. Eradication of small intestinal bacterial overgrowth reduces symptoms of irritable bowel syndrome. Am J Gastroenterol. 2000;95;3503-3506.
    Pubmed
  9. Ghoshal UC, Ghoshal U, Ayyagari A, et al. Tropical sprue is associated with contamination of small bowel with aerobic bacteria and reversible prolongation of orocecal transit time. J Gastroenterol Hepatol. 2003;18;540-547.
    Pubmed
  10. Lu CL, Chen CY, Chang FY, Lee SD. Characteristics of small bowel motility in patients with irritable bowel syndrome and normal humans: an Oriental study. Clin Sci (Lond). 1998;95;165-169.
    Pubmed
  11. Lin, HC. Small intestinal bacterial overgrowth: a framework for understanding irritable bowel syndrome. JAMA. 2004;292;852-858.
    Pubmed
  12. Ghoshal UC, Srivastava D, Verma A, Misra A. Slow transit constipation associated with excess methane production and its improvement following rifaximin therapy: a case report. J Neurogastroenterol Motil. 2011;17;185-188.
    Pubmed
  13. Yu D, Cheeseman F, Vanner S. 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. Gut. 2011;60;334-340.
    Pubmed
  14. Gibson PR, Newnman E, Barrett JS, Shepherd SJ, Muir JG. Review article: fructose malabsorption and the bigger picture. Aliment Pharmacol Ther. 2007;25;349-363.
    Pubmed
  15. Ghoshal UC, Kumar S, Mehrotra M, Lakshmi C, Misra A. Frequency of small intestinal bacterial overgrowth in patients with irritable bowel syndrome and chronic non-specific diarrhea. J Neurogastroenterol Motil. 2010;16;40-46.
    Pubmed


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