Two patients with COMT inhibitor-induced hepatic dysfunction and UGT1A9 genetic polymorphism

E. Martignoni; M. Cosentino; M. Ferrari; G. Porta; E. Mattarucchi; F. Marino; S. Lecchini; G. Nappi

doi:10.1212/01.wnl.0000187066.81162.70

Two patients with COMT inhibitor-induced hepatic dysfunction and UGT1A9 genetic polymorphism

E. Martignoni, M. Cosentino, M. Ferrari, G. Porta, E. Mattarucchi, F. Marino, S. Lecchini, G. Nappi

Fondazione "Istituto Neurologico Casimiro Mondino"

Research output: Contribution to journal › Article › peer-review

Abstract

The authors report two cases of catechol-O-methyltransferase (COMT) inhibitor-induced asymptomatic hepatic dysfunction in women with Parkinson disease. The patients were genotyped for the UDP-glucuronosyltransferase (UGT) 1A9 gene (which encodes the main COMT inhibitor-metabolizing enzyme), and found to carry mutations leading to defective glucuronidation activity. This suggests that UGT1A9 poor metabolizer genotype(s) may be a predisposing factor for COMT inhibitor-induced hepatotoxicity.

Original language	English
Pages (from-to)	1820-1822
Number of pages	3
Journal	Neurology
Volume	65
Issue number	11
DOIs	https://doi.org/10.1212/01.wnl.0000187066.81162.70
Publication status	Published - Dec 2005

ASJC Scopus subject areas

Neuroscience(all)

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title = "Two patients with COMT inhibitor-induced hepatic dysfunction and UGT1A9 genetic polymorphism",

abstract = "The authors report two cases of catechol-O-methyltransferase (COMT) inhibitor-induced asymptomatic hepatic dysfunction in women with Parkinson disease. The patients were genotyped for the UDP-glucuronosyltransferase (UGT) 1A9 gene (which encodes the main COMT inhibitor-metabolizing enzyme), and found to carry mutations leading to defective glucuronidation activity. This suggests that UGT1A9 poor metabolizer genotype(s) may be a predisposing factor for COMT inhibitor-induced hepatotoxicity.",

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AU - Martignoni, E.

AU - Cosentino, M.

AU - Ferrari, M.

AU - Porta, G.

AU - Mattarucchi, E.

AU - Marino, F.

AU - Lecchini, S.

AU - Nappi, G.

PY - 2005/12

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N2 - The authors report two cases of catechol-O-methyltransferase (COMT) inhibitor-induced asymptomatic hepatic dysfunction in women with Parkinson disease. The patients were genotyped for the UDP-glucuronosyltransferase (UGT) 1A9 gene (which encodes the main COMT inhibitor-metabolizing enzyme), and found to carry mutations leading to defective glucuronidation activity. This suggests that UGT1A9 poor metabolizer genotype(s) may be a predisposing factor for COMT inhibitor-induced hepatotoxicity.

AB - The authors report two cases of catechol-O-methyltransferase (COMT) inhibitor-induced asymptomatic hepatic dysfunction in women with Parkinson disease. The patients were genotyped for the UDP-glucuronosyltransferase (UGT) 1A9 gene (which encodes the main COMT inhibitor-metabolizing enzyme), and found to carry mutations leading to defective glucuronidation activity. This suggests that UGT1A9 poor metabolizer genotype(s) may be a predisposing factor for COMT inhibitor-induced hepatotoxicity.

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Two patients with COMT inhibitor-induced hepatic dysfunction and UGT1A9 genetic polymorphism

Abstract

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