Volume 7, Issue 3 pp. 464-467
Original Article
Free Access

The aminopyrine breath test does not correlate with histologic disease severity in patients with cholestasis

Alfred L. Baker M.D.

Corresponding Author

Alfred L. Baker M.D.

Liver Study Unit and Section of Gastroenterology of the Department of Medicine, University of Chicago, Chicago, Illinois 60637

University of Chicago, Box 400, 5841 South Maryland Avenue, Chicago, Illinois 60637===Search for more papers by this author
Patricia S. Krager

Patricia S. Krager

Liver Study Unit and Section of Gastroenterology of the Department of Medicine, University of Chicago, Chicago, Illinois 60637

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Alvin N. Kotake

Alvin N. Kotake

Liver Study Unit and Section of Gastroenterology of the Department of Medicine, University of Chicago, Chicago, Illinois 60637

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Dale A. Schoeller

Dale A. Schoeller

Liver Study Unit and Section of Gastroenterology of the Department of Medicine, University of Chicago, Chicago, Illinois 60637

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First published: May/June 1987
Citations: 21

Abstract

To determine whether the aminopyrine breath test can be used to document the presence of cirrhosis in patients with cholestatic liver disease, 19 patients (13 primary biliary cirrhosis, 4 sclerosing cholangitis and 2 chronic extrahepatic bile duct obstruction) underwent clinical and biochemical evaluations, liver biopsies and an aminopyrine breath test. Results were compared with those in 10 patients with biopsy-proven chronic active hepatitis with bridging and/or cirrhosis and in 22 healthy subjects. The aminopyrine breath test results in the 10 cholestatic patients with cirrhosis were not significantly different from the results in precirrhotic cholestatic patients (mean ± S.D., 11.2 ± 5.0 vs. 11.6 ± 2.8 %dose per 2 hr, p < 0.05) or healthy subjects (11.5 ± 2.9 %dose per 2 hr). In contrast, the results in the patients with chronic hepatitis were markedly depressed (3.2 ± 1.9 %dose per 2 hr, p < 0.05). The aminopyrine breath test results did not correlate with results of conventional liver function tests in the cholestatic patients. These results demonstrate that the aminopyrine breath test is not clinically useful in identifying the presence of cirrhosis in patients with cholestatic liver disease, and provide further evidence that decreased microsomal enzyme function is a late feature of cholestatic liver disease.

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