The urea breath test (UBT) is one of the most important non-invasive method
s for detecting Helicobacter pylori infection. The test exploits the hydrol
ysis of orally administered urea by the enzyme urease, which H pylori produ
ces in large quantities. Urea is hydrolysed to ammonia and carbon dioxide,
which diffuses into the blood and is excreted by the lungs. Isotopically la
belled CO2 can be detected in breath using various methods.
Labelling urea with C-13 is becoming increasingly popular because this non-
radioactive isotope is innocuous and can be safely used in children and wom
en of childbearing age. Breath samples can also be sent by post or courier
to remote analysis centres. The test is easy to perform and can be repeated
as often as required in the same patient. A meal must be given to increase
the contact time between the tracer and the H pylori urease inside the sto
mach. The test has been simplified to the point that two breath samples col
lected before and 30 minutes after the ingestion of urea in a liquid form s
uffice to provide reliable diagnostic information. The cost of producing C-
13-urea is high, but it may be possible to reduce the dosage further by adm
inistering it in capsule form.
An isotope ratio mass spectrometer (IRMS) is generally used to measure LSC
enrichment in breath samples, but this machine is expensive. In order to re
duce this cost, new and cheaper equipment based on non-dispersive, isotope
selective, infrared spectroscopy (NDIRS) and laser assisted ratio analysis
(LARA) have recently been developed. These are valid alternatives to IRMS a
lthough they cannot process the same large number of breath samples simulta
neously.
These promising advances will certainly promote the wider use of the C-13-U
BT, which is especially useful for epidemiological studies in children and
adults, for screening patients before endoscopy, and for assessing the effi
cacy of eradication regimens.