Breath hydrogen levels, which reflect colonic fermentation of undigest
ed starches, are usually low in the fasted state. Easting levels of br
eath hydrogen are important for estimation of oro-cecal transit time a
nd diagnosis of lactase deficiency. In young women, however, fasting l
evels of breath hydrogen are high. To clarify the reason for this, we
studied the circadian pattern of breath hydrogen and the effect of alp
ha-D-galactosidase on fasting breath hydrogen in one study, and the ef
fect of sleep deprivation on fasting breath hydrogen in another study,
in 13 women students aged 21-23 years. In the first study, two breath
samples were collected, one in the evening and the other the next mor
ning. On another occasion, alpha-D-galactosidase was given before dinn
er and breath samples were collected the next morning. In the second s
tudy, the circadian rhythm of breath hydrogen was assessed for 3 days
and the subjects were deprived of sleep on the second night. Breath sa
mples were collected every 30 min, except during the second night when
samples were collected at 1-h intervals. Easting breath hydrogen was
24 +/- 3.9 ppm (mean +/- SE), which did not differ from the value for
the previous night. alpha-D-galactosidase significantly decreased fast
ing breath hydrogen levels, to 17 +/- 2.4 ppm (P < 0.05). There was a
clear circadian pattern of breath hydrogen, high in the morning and de
creasing to the nadir by 16:00. After dinner, the level increased agai
n and stayed high during the night. Sleep deprivation did not affect f
asting levels of breath hydrogen. High fasting breath hydrogen levels
in young women followed a circadian pattern and this may have been due
. in part, to an high intake of dietary fiber on the previous day.