A proof of concept study of tolcapone for pathological gambling: Relationships with COMT genotype and brain activation
A proof of concept study of tolcapone for pathological gambling: Relationships with COMT genotype and brain activation
Pathological gambling (PG) is a disabling disorder experienced by 1-3% of adults, and empirically validated treatments are lacking. Perturbations of prefrontal-dependent cognitive functions are implicated in the pathophysiology of PG. The enzyme catechol-O-methyl-transferase (COMT) is responsible for degradation of dopamine in the cortices and thereby is known to regulate such cognitive functions and their neural substrates. The objective of this study was to determine whether tolcapone, a COMT inhibitor, improves symptoms of PG and to explore whether such effects are dependent on COMT val-158-met polymorphism status and relate to concomitant changes in fronto-parietal activation. Twenty-four indviduals with PG were enrolled in an 8-week trial of oral tolcapone (100. mg/day titrated to 100. mg thrice/day) and 12 undertook pre- and post-treatment fMRI to examine brain activation during an executive planning task in a pre-defined fronto-parietal network. At baseline, patients with PG showed fronto-parietal under-activation versus controls during executive planning. Treatment was associated with statistically significant reductions on PG-Yale Brown Obsessive Compulsive Scale (PG-YBOCS), the extent of which correlated significantly with augmentation of planning-related fronto-parietal activation. Symptom improvement was also significantly more pronounced in subjects with the val/val COMT polymorphism. Tolcapone improved PG symptoms, and the extent of symptomatic improvement was significantly related to augmentation of fronto-parietal activation (fMRI probe) and COMT status. Objective genetic and fMRI markers hold promise in the search for targeting treatment and elucidating brain mechanisms associated with optimal clinical outcomes.
Cognition, COMT, Dopamine, Gambling, Planning, Tolcapone
1587-1596
Grant, Jon E.
07372bd5-8a0d-42b4-b41b-e376c652acf3
Odlaug, Brian L.
f021d299-d250-44a2-bb17-6f7e16bfa0f6
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f
Hampshire, Adam
08af1acb-f59f-4f42-a1ca-99fd2fb66da2
Schreiber, Liana R.N.
5d659814-23de-4dec-b9d4-5341ad99738b
Kim, Suck Won
7906e44a-fb69-403c-b7ff-c37a1c2cf7e3
November 2013
Grant, Jon E.
07372bd5-8a0d-42b4-b41b-e376c652acf3
Odlaug, Brian L.
f021d299-d250-44a2-bb17-6f7e16bfa0f6
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f
Hampshire, Adam
08af1acb-f59f-4f42-a1ca-99fd2fb66da2
Schreiber, Liana R.N.
5d659814-23de-4dec-b9d4-5341ad99738b
Kim, Suck Won
7906e44a-fb69-403c-b7ff-c37a1c2cf7e3
Grant, Jon E., Odlaug, Brian L., Chamberlain, Samuel R., Hampshire, Adam, Schreiber, Liana R.N. and Kim, Suck Won
(2013)
A proof of concept study of tolcapone for pathological gambling: Relationships with COMT genotype and brain activation.
European Neuropsychopharmacology, 23 (11), .
(doi:10.1016/j.euroneuro.2013.07.008).
Abstract
Pathological gambling (PG) is a disabling disorder experienced by 1-3% of adults, and empirically validated treatments are lacking. Perturbations of prefrontal-dependent cognitive functions are implicated in the pathophysiology of PG. The enzyme catechol-O-methyl-transferase (COMT) is responsible for degradation of dopamine in the cortices and thereby is known to regulate such cognitive functions and their neural substrates. The objective of this study was to determine whether tolcapone, a COMT inhibitor, improves symptoms of PG and to explore whether such effects are dependent on COMT val-158-met polymorphism status and relate to concomitant changes in fronto-parietal activation. Twenty-four indviduals with PG were enrolled in an 8-week trial of oral tolcapone (100. mg/day titrated to 100. mg thrice/day) and 12 undertook pre- and post-treatment fMRI to examine brain activation during an executive planning task in a pre-defined fronto-parietal network. At baseline, patients with PG showed fronto-parietal under-activation versus controls during executive planning. Treatment was associated with statistically significant reductions on PG-Yale Brown Obsessive Compulsive Scale (PG-YBOCS), the extent of which correlated significantly with augmentation of planning-related fronto-parietal activation. Symptom improvement was also significantly more pronounced in subjects with the val/val COMT polymorphism. Tolcapone improved PG symptoms, and the extent of symptomatic improvement was significantly related to augmentation of fronto-parietal activation (fMRI probe) and COMT status. Objective genetic and fMRI markers hold promise in the search for targeting treatment and elucidating brain mechanisms associated with optimal clinical outcomes.
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Published date: November 2013
Keywords:
Cognition, COMT, Dopamine, Gambling, Planning, Tolcapone
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Local EPrints ID: 492995
URI: http://eprints.soton.ac.uk/id/eprint/492995
ISSN: 0924-977X
PURE UUID: f1213ddb-d602-46b1-b119-e3d7eeea017c
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Date deposited: 21 Aug 2024 17:12
Last modified: 30 Aug 2024 02:00
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Contributors
Author:
Jon E. Grant
Author:
Brian L. Odlaug
Author:
Samuel R. Chamberlain
Author:
Adam Hampshire
Author:
Liana R.N. Schreiber
Author:
Suck Won Kim
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