» Articles » PMID: 2921843

Correlation of Caffeine Elimination and Child's Classification in Liver Cirrhosis

Overview
Journal Klin Wochenschr
Specialty General Medicine
Date 1989 Jan 4
PMID 2921843
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Apparent pharmacokinetic parameters of caffeine elimination from the circulation were determined in 27 patients with histologically confirmed liver cirrhosis, 8 patients with miscellaneous liver disease, and 8 patients with other than liver disease. The usefullness of this quantitative test to assess the severity of liver cirrhosis was compared to the Child-Turcotte or Child-Pugh classification score as well as to the galactose elimination capacity of these patients. Using reversed-phase high pressure liquid chromatography caffeine, paraxanthine, theophylline, and theobromine were analysed in blood plasma collected before and after an oral dose of caffeine. Compared to apparent caffeine pharmacokinetics in patients with normal livers or miscellaneous liver disease, cirrhosis was characterized by a statistically significant reduction in apparent caffeine clearance and prolongation in half-life. The reduced apparent plasma disappearance rate of caffeine in cirrhotics was related to the retarded formation of paraxanthine which was the main metabolite of caffeine in blood plasma both in the absence or presence of liver disease. The apparent caffeine clearance in cirrhosis decreased with increasing Child-Turcotte classification score: Child's class A patients differed significantly from Child's class B or Child's class C patients, whereas the difference between Child's class B and C patients did not reach statistical significance (Wilcoxon's rank test). In addition there was a strong correlation between the Child-Pugh classification score and apparent caffeine clearance (P less than 0.001). However, no correlation existed between Child's classification and galactose elimination capacity. Our data emphasize the value of the Child-Turcotte or Child-Pugh classification in assessing the severity of liver cirrhosis in a simpler and less time-consuming way than using quantitative liver function tests.

Citing Articles

Identification of Gut Microbial Lysine and Histidine Degradation and CYP-Dependent Metabolites as Biomarkers of Fatty Liver Disease.

Driuchina A, Hintikka J, Lehtonen M, Keski-Rahkonen P, OConnell T, Juvonen R mBio. 2023; 14(1):e0266322.

PMID: 36715540 PMC: 9973343. DOI: 10.1128/mbio.02663-22.


Pharmacokinetics of Caffeine: A Systematic Analysis of Reported Data for Application in Metabolic Phenotyping and Liver Function Testing.

Grzegorzewski J, Bartsch F, Koller A, Konig M Front Pharmacol. 2022; 12:752826.

PMID: 35280254 PMC: 8914174. DOI: 10.3389/fphar.2021.752826.


The role of salivary caffeine clearance in the diagnosis of chronic liver disease.

Tripathi A, Tiwari B, Patil R, Khanna V, Singh V J Oral Biol Craniofac Res. 2015; 5(1):28-33.

PMID: 25853045 PMC: 4382505. DOI: 10.1016/j.jobcr.2014.12.003.


Use of methylxanthine therapies for the treatment and prevention of apnea of prematurity.

Schoen K, Yu T, Stockmann C, Spigarelli M, Sherwin C Paediatr Drugs. 2014; 16(2):169-77.

PMID: 24399614 PMC: 5609880. DOI: 10.1007/s40272-013-0063-z.


Reliability of total overnight salivary caffeine assessment (TOSCA) for liver function evaluation in compensated cirrhotic patients.

Tarantino G, Conca P, Capone D, Gentile A, Polichetti G, Basile V Eur J Clin Pharmacol. 2006; 62(8):605-12.

PMID: 16841221 DOI: 10.1007/s00228-006-0146-7.


References
1.
Wang T, Kleber G, Stellaard F, Paumgartner G . Caffeine elimination: a test of liver function. Klin Wochenschr. 1985; 63(21):1124-8. DOI: 10.1007/BF02291094. View

2.
Villeneuve J, Infante-Rivard C, Ampelas M, Pomier-Layrargues G, Huet P, Marleau D . Prognostic value of the aminopyrine breath test in cirrhotic patients. Hepatology. 1986; 6(5):928-31. DOI: 10.1002/hep.1840060520. View

3.
BIRCHER J . Assessment of prognosis in advanced liver disease: to score or to measure, that's the question. Hepatology. 1986; 6(5):1036-7. DOI: 10.1002/hep.1840060536. View

4.
Kotake A, Schoeller D, Lambert G, Baker A, Schaffer D, JOSEPHS H . The caffeine CO2 breath test: dose response and route of N-demethylation in smokers and nonsmokers. Clin Pharmacol Ther. 1982; 32(2):261-9. DOI: 10.1038/clpt.1982.157. View

5.
Wahllander A, Renner E, Preisig R . Fasting plasma caffeine concentration. A guide to the severity of chronic liver disease. Scand J Gastroenterol. 1985; 20(9):1133-41. DOI: 10.3109/00365528509088884. View