Relevance of orbitofrontal neurochemistry for the outcome of cognitive-behavioural therapy in patients with obsessive-compulsive disorder.

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Relevance of orbitofrontal neurochemistry for the outcome of cognitive-behavioural therapy in patients with obsessive-compulsive disorder. / Zurowski, Bartosz; Kordon, Andreas; Weber-Fahr, Wolfgang; Voderholzer, Ulrich; Kuelz, Anne Katrin; Freyer, Tobias; Wahl, Karina; Büchel, Christian; Hohagen, Fritz.

In: EUR ARCH PSY CLIN N, Vol. 262, No. 7, 7, 2012, p. 617-624.

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@article{7483943add274ca08b5a1829ba896def,
title = "Relevance of orbitofrontal neurochemistry for the outcome of cognitive-behavioural therapy in patients with obsessive-compulsive disorder.",
abstract = "Since the advent of non-invasive methods such as proton magnetic resonance spectroscopy ((1)H-MRS), obsessive-compulsive disorder (OCD) has been increasingly associated with an altered composition of neurometabolites and neurotransmitters in several brain areas. Particularly, Inositol has not only been implicated in OCD pathophysiology, but also shown effective in pilot studies in therapy-refractory OCD patients. However, the relevance of regional brain neurochemistry for therapy outcome has not yet been investigated. Whereas numerous neuroimaging findings support a dysfunction of the orbitofrontal cortex (OFC) in OCD, MR-spectroscopic investigations of this region are missing. (1)H-MRS and psychometric measurements were obtained from twenty unmedicated patients with OCD, subsequently enrolled in a 3-month structured inpatient cognitive-behavioural therapy programme, and from eleven matched control subjects. Multiple regression of symptom score changes (Y-BOCS) on (myo-)inositol concentrations in three areas (right orbitofrontal cortex (OFC), right striatum and anterior cingulate cortex) was performed. The concentration of (myo-)inositol in the OFC only predicted the outcome of subsequent CBT regarding Y-BOCS score reduction (Spearman's r(s) = .81, P < 0.003, corrected). The (myo-)inositol concentration did not differ between OCD patients and healthy controls and did not change during therapy. We provide preliminary evidence for a neurochemical marker that may prove informative about a patient's future benefit from behaviour therapy. Inositol, a metabolite involved in cellular signal transduction and a spectroscopic marker of glial activity, predicted the response to CBT selectively in the OFC, adding to the evidence for OFC involvement in OCD and highlighting neurobiological underpinnings of psychotherapy.",
keywords = "Adult, Humans, Male, Aged, Female, Middle Aged, Psychiatric Status Rating Scales, Adolescent, Young Adult, Statistics as Topic, Magnetic Resonance Spectroscopy, Cognitive Therapy/*methods, Creatine/metabolism, Aspartic Acid/analogs & derivatives/metabolism, *Obsessive-Compulsive Disorder/pathology/psychology/rehabilitation, Prefrontal Cortex/*metabolism, Adult, Humans, Male, Aged, Female, Middle Aged, Psychiatric Status Rating Scales, Adolescent, Young Adult, Statistics as Topic, Magnetic Resonance Spectroscopy, Cognitive Therapy/*methods, Creatine/metabolism, Aspartic Acid/analogs & derivatives/metabolism, *Obsessive-Compulsive Disorder/pathology/psychology/rehabilitation, Prefrontal Cortex/*metabolism",
author = "Bartosz Zurowski and Andreas Kordon and Wolfgang Weber-Fahr and Ulrich Voderholzer and Kuelz, {Anne Katrin} and Tobias Freyer and Karina Wahl and Christian B{\"u}chel and Fritz Hohagen",
year = "2012",
language = "English",
volume = "262",
pages = "617--624",
journal = "EUR ARCH PSY CLIN N",
issn = "0940-1334",
publisher = "D. Steinkopff-Verlag",
number = "7",

}

RIS

TY - JOUR

T1 - Relevance of orbitofrontal neurochemistry for the outcome of cognitive-behavioural therapy in patients with obsessive-compulsive disorder.

AU - Zurowski, Bartosz

AU - Kordon, Andreas

AU - Weber-Fahr, Wolfgang

AU - Voderholzer, Ulrich

AU - Kuelz, Anne Katrin

AU - Freyer, Tobias

AU - Wahl, Karina

AU - Büchel, Christian

AU - Hohagen, Fritz

PY - 2012

Y1 - 2012

N2 - Since the advent of non-invasive methods such as proton magnetic resonance spectroscopy ((1)H-MRS), obsessive-compulsive disorder (OCD) has been increasingly associated with an altered composition of neurometabolites and neurotransmitters in several brain areas. Particularly, Inositol has not only been implicated in OCD pathophysiology, but also shown effective in pilot studies in therapy-refractory OCD patients. However, the relevance of regional brain neurochemistry for therapy outcome has not yet been investigated. Whereas numerous neuroimaging findings support a dysfunction of the orbitofrontal cortex (OFC) in OCD, MR-spectroscopic investigations of this region are missing. (1)H-MRS and psychometric measurements were obtained from twenty unmedicated patients with OCD, subsequently enrolled in a 3-month structured inpatient cognitive-behavioural therapy programme, and from eleven matched control subjects. Multiple regression of symptom score changes (Y-BOCS) on (myo-)inositol concentrations in three areas (right orbitofrontal cortex (OFC), right striatum and anterior cingulate cortex) was performed. The concentration of (myo-)inositol in the OFC only predicted the outcome of subsequent CBT regarding Y-BOCS score reduction (Spearman's r(s) = .81, P < 0.003, corrected). The (myo-)inositol concentration did not differ between OCD patients and healthy controls and did not change during therapy. We provide preliminary evidence for a neurochemical marker that may prove informative about a patient's future benefit from behaviour therapy. Inositol, a metabolite involved in cellular signal transduction and a spectroscopic marker of glial activity, predicted the response to CBT selectively in the OFC, adding to the evidence for OFC involvement in OCD and highlighting neurobiological underpinnings of psychotherapy.

AB - Since the advent of non-invasive methods such as proton magnetic resonance spectroscopy ((1)H-MRS), obsessive-compulsive disorder (OCD) has been increasingly associated with an altered composition of neurometabolites and neurotransmitters in several brain areas. Particularly, Inositol has not only been implicated in OCD pathophysiology, but also shown effective in pilot studies in therapy-refractory OCD patients. However, the relevance of regional brain neurochemistry for therapy outcome has not yet been investigated. Whereas numerous neuroimaging findings support a dysfunction of the orbitofrontal cortex (OFC) in OCD, MR-spectroscopic investigations of this region are missing. (1)H-MRS and psychometric measurements were obtained from twenty unmedicated patients with OCD, subsequently enrolled in a 3-month structured inpatient cognitive-behavioural therapy programme, and from eleven matched control subjects. Multiple regression of symptom score changes (Y-BOCS) on (myo-)inositol concentrations in three areas (right orbitofrontal cortex (OFC), right striatum and anterior cingulate cortex) was performed. The concentration of (myo-)inositol in the OFC only predicted the outcome of subsequent CBT regarding Y-BOCS score reduction (Spearman's r(s) = .81, P < 0.003, corrected). The (myo-)inositol concentration did not differ between OCD patients and healthy controls and did not change during therapy. We provide preliminary evidence for a neurochemical marker that may prove informative about a patient's future benefit from behaviour therapy. Inositol, a metabolite involved in cellular signal transduction and a spectroscopic marker of glial activity, predicted the response to CBT selectively in the OFC, adding to the evidence for OFC involvement in OCD and highlighting neurobiological underpinnings of psychotherapy.

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Psychiatric Status Rating Scales

KW - Adolescent

KW - Young Adult

KW - Statistics as Topic

KW - Magnetic Resonance Spectroscopy

KW - Cognitive Therapy/methods

KW - Creatine/metabolism

KW - Aspartic Acid/analogs & derivatives/metabolism

KW - Obsessive-Compulsive Disorder/pathology/psychology/rehabilitation

KW - Prefrontal Cortex/metabolism

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Psychiatric Status Rating Scales

KW - Adolescent

KW - Young Adult

KW - Statistics as Topic

KW - Magnetic Resonance Spectroscopy

KW - Cognitive Therapy/methods

KW - Creatine/metabolism

KW - Aspartic Acid/analogs & derivatives/metabolism

KW - Obsessive-Compulsive Disorder/pathology/psychology/rehabilitation

KW - Prefrontal Cortex/metabolism

M3 - SCORING: Journal article

VL - 262

SP - 617

EP - 624

JO - EUR ARCH PSY CLIN N

JF - EUR ARCH PSY CLIN N

SN - 0940-1334

IS - 7

M1 - 7

ER -