A double-blind, placebo-controlled trial of lamotrigine for pathological skin picking: treatment efficacy and neurocognitive predictors of response
A double-blind, placebo-controlled trial of lamotrigine for pathological skin picking: treatment efficacy and neurocognitive predictors of response
Although a relatively common behavior, treatment data for pathological skin picking (PSP) are limited. The current study sought to examine the efficacy and tolerability of lamotrigine in adults with PSP and to examine neurocognitive predictors of treatment response. Thirty-two subjects (29 female subjects [90.6%]; mean age, 32.8 ± 13.3 years) with PSP were treated in a 12-week randomized, double-blind, placebo-controlled trial of lamotrigine as monotherapy. Baseline cognitive assessment comprised the stop signal and intradimensional/extradimensional set shift tasks. Lamotrigine dosing ranged from 12.5 to 300 mg/d. The primary outcome measure was picking symptoms measured by the Yale-Brown Obsessive Compulsive scale Modified for Neurotic Excoriation. Subjects also were assessed with measures of psychosocial functioning. No significant overall differences were noted between lamotrigine and placebo on the primary or secondary end points. Seven subjects assigned to lamotrigine (43.8%) were considered responders (defined as ≤35% n the Yale-Brown Obsessive Compulsive scale Modified for Neurotic Excoriation) compared with 5 (31.3%) assigned to placebo. Those who ultimately responded to lamotrigine exhibited impaired cognitive flexibility (extradimensional shifting) at baseline compared with lamotrigine nonresponders. These findings suggest that, although safe and well tolerated, lamotrigine treatment may not be efficacious in patients with PSP as a whole, compared with placebo. However, these neurocognitive data suggest that lamotrigine may be valuable in a subset of patients who exhibit relatively impaired cognitive flexibility.
cognition, compulsion, glutamate, impulse control disorder, inhibition, neurotic excoriation, pharmacology, skin picking, treatment
396-403
Grant, Jon E.
07372bd5-8a0d-42b4-b41b-e376c652acf3
Odlaug, Brian L.
f021d299-d250-44a2-bb17-6f7e16bfa0f6
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f
Kim, Suck Won
7906e44a-fb69-403c-b7ff-c37a1c2cf7e3
August 2010
Grant, Jon E.
07372bd5-8a0d-42b4-b41b-e376c652acf3
Odlaug, Brian L.
f021d299-d250-44a2-bb17-6f7e16bfa0f6
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f
Kim, Suck Won
7906e44a-fb69-403c-b7ff-c37a1c2cf7e3
Grant, Jon E., Odlaug, Brian L., Chamberlain, Samuel R. and Kim, Suck Won
(2010)
A double-blind, placebo-controlled trial of lamotrigine for pathological skin picking: treatment efficacy and neurocognitive predictors of response.
Journal of Clinical Psychopharmacology, 30 (4), .
(doi:10.1097/JCP.0b013e3181e617a1).
Abstract
Although a relatively common behavior, treatment data for pathological skin picking (PSP) are limited. The current study sought to examine the efficacy and tolerability of lamotrigine in adults with PSP and to examine neurocognitive predictors of treatment response. Thirty-two subjects (29 female subjects [90.6%]; mean age, 32.8 ± 13.3 years) with PSP were treated in a 12-week randomized, double-blind, placebo-controlled trial of lamotrigine as monotherapy. Baseline cognitive assessment comprised the stop signal and intradimensional/extradimensional set shift tasks. Lamotrigine dosing ranged from 12.5 to 300 mg/d. The primary outcome measure was picking symptoms measured by the Yale-Brown Obsessive Compulsive scale Modified for Neurotic Excoriation. Subjects also were assessed with measures of psychosocial functioning. No significant overall differences were noted between lamotrigine and placebo on the primary or secondary end points. Seven subjects assigned to lamotrigine (43.8%) were considered responders (defined as ≤35% n the Yale-Brown Obsessive Compulsive scale Modified for Neurotic Excoriation) compared with 5 (31.3%) assigned to placebo. Those who ultimately responded to lamotrigine exhibited impaired cognitive flexibility (extradimensional shifting) at baseline compared with lamotrigine nonresponders. These findings suggest that, although safe and well tolerated, lamotrigine treatment may not be efficacious in patients with PSP as a whole, compared with placebo. However, these neurocognitive data suggest that lamotrigine may be valuable in a subset of patients who exhibit relatively impaired cognitive flexibility.
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Published date: August 2010
Keywords:
cognition, compulsion, glutamate, impulse control disorder, inhibition, neurotic excoriation, pharmacology, skin picking, treatment
Identifiers
Local EPrints ID: 492851
URI: http://eprints.soton.ac.uk/id/eprint/492851
ISSN: 0271-0749
PURE UUID: 1d39bcf9-635f-45f9-aeb2-7f2ea71818f2
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Date deposited: 15 Aug 2024 17:04
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:
Suck Won Kim
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