TY - JOUR
T1 - [13C]-galactose breath test
T2 - Correlation with liver fibrosis in chronic hepatitis C
AU - Mion, F.
AU - Rousseau, M.
AU - Scoazec, J. Y.
AU - Berger, F.
AU - Minaire, Y.
PY - 1999/1/1
Y1 - 1999/1/1
N2 - Background. The galactose elimination capacity test is a quantitative liver function test that has been shown to be a potential surrogate marker for death in advanced chronic liver diseases. However, this test lacks sensitivity in early liver disease. The goal of this study was to evaluate a [13C]-galactose breath test (GET) in a population of patients with chronic hepatitis C. Design. The GET was performed in 10 control subjects and 50 patients with chronic hepatitis C; the results were compared with the METAVIR pathological scoring of liver biopsy specimens and with standard biochemical liver function tests. Results. In 10 patients, oral vs. intravenous administration of galactose yielded similar results for the GET (3.01% ± 0.12% dose h-1 for oral galactose vs. 2.98 ± 0.21 for intravenous). The GET was then performed orally in the remaining 40 patients and 10 control subjects. A significant difference was observed between control subjects and patients (4.51% ± 0.18% vs. 2.97% ± 0.14% dose h-1, P < 0.0001). A significant difference for GET results was observed between each fibrosis stage, but not with regard to the activity score. Conclusions. The GET results are dependent on the severity of liver fibrosis in chronic hepatitis C. Further studies are needed to evaluate the usefulness of the GET for the follow-up up of chronic hepatitis C.
AB - Background. The galactose elimination capacity test is a quantitative liver function test that has been shown to be a potential surrogate marker for death in advanced chronic liver diseases. However, this test lacks sensitivity in early liver disease. The goal of this study was to evaluate a [13C]-galactose breath test (GET) in a population of patients with chronic hepatitis C. Design. The GET was performed in 10 control subjects and 50 patients with chronic hepatitis C; the results were compared with the METAVIR pathological scoring of liver biopsy specimens and with standard biochemical liver function tests. Results. In 10 patients, oral vs. intravenous administration of galactose yielded similar results for the GET (3.01% ± 0.12% dose h-1 for oral galactose vs. 2.98 ± 0.21 for intravenous). The GET was then performed orally in the remaining 40 patients and 10 control subjects. A significant difference was observed between control subjects and patients (4.51% ± 0.18% vs. 2.97% ± 0.14% dose h-1, P < 0.0001). A significant difference for GET results was observed between each fibrosis stage, but not with regard to the activity score. Conclusions. The GET results are dependent on the severity of liver fibrosis in chronic hepatitis C. Further studies are needed to evaluate the usefulness of the GET for the follow-up up of chronic hepatitis C.
KW - Human
KW - Liver function test
KW - Stable isotopes
UR - http://www.scopus.com/inward/record.url?scp=0032588192&partnerID=8YFLogxK
U2 - 10.1046/j.1365-2362.1999.00512.x
DO - 10.1046/j.1365-2362.1999.00512.x
M3 - Article
C2 - 10411669
AN - SCOPUS:0032588192
SN - 0014-2972
VL - 29
SP - 624
EP - 629
JO - European Journal of Clinical Investigation
JF - European Journal of Clinical Investigation
IS - 7
ER -