A. Hesse et al., Intestinal hyperabsorption of oxalate in calcium oxalate stone formers: Application of a new test with [C-13(2)]oxalate, J AM S NEPH, 10, 1999, pp. S329-S333
In up to one-third of patients with calcium oxalate stones, a hyperoxaluria
can be detected. Hyperoxaluria can result from increased endogenous produc
tion, from excessive oxalate content of the food, or from intestinal hypera
bsorption. For a causal therapy, it is important to discriminate between me
tabolic and hyperabsorptive hyperoxaluria. Our new C-13-oxalate test allows
this differentiation. Under standardized conditions, 50 mg of disodium sal
t of [C-13(2)]oxalic acid was applied. From the amount of labeled oxalate e
xcreted in urine as measured by a gas chromatographic-mass spectrometric as
say, the intestinal absorption was calculated. Seventy patients with recurr
ent calcium oxalate urolithiasis who had no signs of inflammatory bowel dis
ease were tested. Their mean intestinal oxalate absorption was 9.2 +/- 5.1%
. This was significantly higher than the mean absorption of 50 healthy volu
nteers (6.7 +/- 3.9%). There was no difference in oxalate absorption betwee
n male (n = 25) and female volunteers. Oxalate absorption correlated with t
he oxalate excretion in the 24-h urine (volunteers: r = 0.46, P < 0.01; pat
ients: r = 0.62, P < 0.001). Oxalate hyperabsorption was defined as an abso
rption exceeding 10%. According to this definition, 34% of the patients had
oxalate hyperabsorption; 20% of the volunteers showed a hyperabsorption, t
oo. The C-13-oxalate absorption test allows reliable determination of intes
tinal oxalate absorption. Because of the use of a stable isotope, this test
may be repeated as often as required. It will allow the control of therape
utic regimens and also help to unravel genetic influences in stone formatio
n.