Literature DB >> 7550858

Clinical significance of the trimethadione tolerance test in chronic hepatitis: a useful indicator of hepatic drug metabolizing capacity.

M Abei1, E Tanaka, N Tanaka, Y Matsuzaki, T Ikegami, A Ishikawa, T Osuga.   

Abstract

Trimethadione (TMO) was chosen as an indicator of quantitative hepatic microsomal function, and its pharmacokinetics were studied in 52 patients with chronic hepatitis. Findings in these patients were compared with those for 26 healthy subjects and 13 patients with renal failure. Patients with chronic hepatitis, but not those with renal failure, showed significant reduction in clearance (CL) and prolongation of half-life (t1/2), and the extent of abnormalities was found to reflect the severity of histologic changes in liver tissue. The serum dimethadione (DMO)/TMO ratio 4 h after the administration of TMO altered in parallel with the CL and t1/2 of TMO, and abnormalities in this simple ratio were also related to the histologic severity of changes in the liver tissue. A low DMO/TMO ratio (< 0.4) was associated with advanced histologic changes (chronic active hepatitis with bridging or chronic active hepatitis with cirrhosis), whereas a high DMO/TMO ratio (> 0.4) was associated with mild histologic changes (chronic persistent hepatitis or chronic active hepatitis) (sensitivity, 0.81; specificity, 0.86). These results indicate that the DMO/TMO ratio, which can be obtained from a single blood sampling, reflects the histologic severity of changes in tissue liver, and that the TMO tolerance test is a useful indicator of quantitative liver function.

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Year:  1995        PMID: 7550858     DOI: 10.1007/bf02347564

Source DB:  PubMed          Journal:  J Gastroenterol        ISSN: 0944-1174            Impact factor:   7.527


  33 in total

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Authors:  W J WADDELL; T C BUTLER
Journal:  Proc Soc Exp Biol Med       Date:  1957-12

2.  Influence of smoking on caffeine elimination in healthy volunteers and in patients with alcoholic liver cirrhosis.

Authors:  R Joeres; H Klinker; H Heusler; J Epping; W Zilly; E Richter
Journal:  Hepatology       Date:  1988 May-Jun       Impact factor: 17.425

3.  Time course of the demethylation of trimethadione.

Authors:  H H Frey; R Schulz
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1970

4.  Drugs as indicators of hepatic function.

Authors:  R A Branch
Journal:  Hepatology       Date:  1982 Jan-Feb       Impact factor: 17.425

5.  Trimethadione as a model drug for the evaluation of hepatic drug-metabolizing capacity in normal and D-galactosamine intoxicated rats.

Authors:  E Tanaka; H Kinoshita; T Yoshida; Y Kuroiwa
Journal:  Jpn J Pharmacol       Date:  1982-12

Review 6.  Plasma level monitoring of anticonvulsants.

Authors:  M J Eadie
Journal:  Clin Pharmacokinet       Date:  1976       Impact factor: 6.447

7.  Trimethadione tolerance tests for the assessment of feasible size of hepatic resection in patients with hepatocellular carcinoma.

Authors:  A Ishikawa; K Fukao; K Tsuji; A Osada; Y Yamamoto; M Ohtsuka; E Tanaka
Journal:  J Gastroenterol Hepatol       Date:  1993 Sep-Oct       Impact factor: 4.029

8.  Quantitative studies of the demethylation of trimethadione (tridione).

Authors:  T C BUTLER
Journal:  J Pharmacol Exp Ther       Date:  1953-05       Impact factor: 4.030

9.  Effects of allyl alcohol and bromobenzene on trimethadione metabolism in the rat.

Authors:  E Tanaka; T Nakamura; S Misawa; T Yoshida; Y Kuroiwa
Journal:  Res Commun Chem Pathol Pharmacol       Date:  1984-07

10.  Trimethadione tolerance test for evaluation of functional reserve of the liver in patients with liver cirrhosis and esophageal varices.

Authors:  E Tanaka; A Ishikawa; A Ono; T Okamura; S Kobayashi; H Yasuhara; S Misawa
Journal:  J Pharmacobiodyn       Date:  1986-03
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