Neural Correlates of Procedural Variants in Cognitive-Behavioral Therapy: A Randomized, Controlled Multicenter fMRI Study
Background: Cognitive behavioral therapy (CBT) is an effective treatment for panic disorder with agoraphobia (PD/AG). It is unknown, how variants of CBT differentially modulate brain networks involved in PD/AG. This study was aimed to evaluate the effects of therapist-guided (T+) versus self-guided...
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creator | Straube, Benjamin Lueken, Ulrike Jansen, Andreas Konrad, Carsten Gloster, Andrew T. Gerlach, Alexander L. Ströhle, Andreas Wittmann, André Pfleiderer, Bettina Gauggel, Siegfried Wittchen, Ulrich Arolt, Volker Kircher, Tilo |
description | Background: Cognitive behavioral therapy (CBT) is an effective treatment for panic disorder with agoraphobia (PD/AG). It is unknown, how variants of CBT differentially modulate brain networks involved in PD/AG. This study was aimed to evaluate the effects of therapist-guided (T+) versus self-guided (T-) exposure on the neural correlates of fear conditioning in PD/AG. Method: In a randomized, controlled multicenter clinical trial in medication-free patients with PD/AG who were treated with 12 sessions of manualized CBT, functional magnetic resonance imaging (fMRI) was used during fear conditioning before (t1) and after CBT (t2). Quality-controlled fMRI data from 42 patients and 42 healthy subjects (HS) were obtained. Patients were randomized to two variants of CBT (T+, n = 22, and T-, n = 20). Results: The interaction of diagnosis (PD/AG, HS), treatment group (T+, T-), time point (t1, t2) and stimulus type (conditioned stimulus: yes, no) revealed activation in the left hippocampus and the occipitotemporal cortex. The T+ group demonstrated increased activation of the hippocampus at t2 (t2 > t1), which was positively correlated with treatment outcome, and a decreased connectivity between the left inferior frontal gyrus and the left hippocampus across time (t1 > t2). Conclusion: After T+ exposure, contingency-encoding processes related to the posterior hippocampus are augmented and more decoupled from processes of the left inferior frontal gyrus, previously shown to be dysfunctionally activated in PD/AG. Linking single procedural variants to neural substrates offers the potential to inform about the optimization of targeted psychotherapeutic interventions. |
doi_str_mv | 10.1159/000359955 |
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It is unknown, how variants of CBT differentially modulate brain networks involved in PD/AG. This study was aimed to evaluate the effects of therapist-guided (T+) versus self-guided (T-) exposure on the neural correlates of fear conditioning in PD/AG. Method: In a randomized, controlled multicenter clinical trial in medication-free patients with PD/AG who were treated with 12 sessions of manualized CBT, functional magnetic resonance imaging (fMRI) was used during fear conditioning before (t1) and after CBT (t2). Quality-controlled fMRI data from 42 patients and 42 healthy subjects (HS) were obtained. Patients were randomized to two variants of CBT (T+, n = 22, and T-, n = 20). Results: The interaction of diagnosis (PD/AG, HS), treatment group (T+, T-), time point (t1, t2) and stimulus type (conditioned stimulus: yes, no) revealed activation in the left hippocampus and the occipitotemporal cortex. The T+ group demonstrated increased activation of the hippocampus at t2 (t2 > t1), which was positively correlated with treatment outcome, and a decreased connectivity between the left inferior frontal gyrus and the left hippocampus across time (t1 > t2). Conclusion: After T+ exposure, contingency-encoding processes related to the posterior hippocampus are augmented and more decoupled from processes of the left inferior frontal gyrus, previously shown to be dysfunctionally activated in PD/AG. Linking single procedural variants to neural substrates offers the potential to inform about the optimization of targeted psychotherapeutic interventions.</description><identifier>ISSN: 0033-3190</identifier><identifier>EISSN: 1423-0348</identifier><identifier>DOI: 10.1159/000359955</identifier><identifier>PMID: 24970601</identifier><identifier>CODEN: PSPSBF</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Adult ; Adult and adolescent clinical studies ; Agoraphobia - physiopathology ; Agoraphobia - therapy ; Anxiety disorders. Neuroses ; Behavior therapy. Cognitive therapy ; Biological and medical sciences ; Cerebral Cortex - physiopathology ; Cognitive Therapy - methods ; Conditioning (Psychology) - physiology ; Fear - physiology ; Female ; Hippocampus - physiopathology ; Humans ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Middle Aged ; Panic disorder ; Panic Disorder - physiopathology ; Panic Disorder - therapy ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Regular Article ; Treatment Outcome ; Treatments</subject><ispartof>Psychotherapy and psychosomatics, 2014-01, Vol.83 (4), p.222-233</ispartof><rights>2014 S. Karger AG</rights><rights>2014 S. Karger AG, Basel</rights><rights>2015 INIST-CNRS</rights><rights>2014 S. Karger AG, Basel.</rights><rights>Copyright (c) 2014 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-3191133cb68bc4b0dbca615092b9e6ff4553059896f38653af4c0f317670e98a3</citedby><cites>FETCH-LOGICAL-c454t-3191133cb68bc4b0dbca615092b9e6ff4553059896f38653af4c0f317670e98a3</cites><orcidid>0000-0002-3751-0878</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/48515905$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/48515905$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,2423,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28577619$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24970601$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Straube, Benjamin</creatorcontrib><creatorcontrib>Lueken, Ulrike</creatorcontrib><creatorcontrib>Jansen, Andreas</creatorcontrib><creatorcontrib>Konrad, Carsten</creatorcontrib><creatorcontrib>Gloster, Andrew T.</creatorcontrib><creatorcontrib>Gerlach, Alexander L.</creatorcontrib><creatorcontrib>Ströhle, Andreas</creatorcontrib><creatorcontrib>Wittmann, André</creatorcontrib><creatorcontrib>Pfleiderer, Bettina</creatorcontrib><creatorcontrib>Gauggel, Siegfried</creatorcontrib><creatorcontrib>Wittchen, Ulrich</creatorcontrib><creatorcontrib>Arolt, Volker</creatorcontrib><creatorcontrib>Kircher, Tilo</creatorcontrib><title>Neural Correlates of Procedural Variants in Cognitive-Behavioral Therapy: A Randomized, Controlled Multicenter fMRI Study</title><title>Psychotherapy and psychosomatics</title><addtitle>Psychother Psychosom</addtitle><description>Background: Cognitive behavioral therapy (CBT) is an effective treatment for panic disorder with agoraphobia (PD/AG). It is unknown, how variants of CBT differentially modulate brain networks involved in PD/AG. This study was aimed to evaluate the effects of therapist-guided (T+) versus self-guided (T-) exposure on the neural correlates of fear conditioning in PD/AG. Method: In a randomized, controlled multicenter clinical trial in medication-free patients with PD/AG who were treated with 12 sessions of manualized CBT, functional magnetic resonance imaging (fMRI) was used during fear conditioning before (t1) and after CBT (t2). Quality-controlled fMRI data from 42 patients and 42 healthy subjects (HS) were obtained. Patients were randomized to two variants of CBT (T+, n = 22, and T-, n = 20). Results: The interaction of diagnosis (PD/AG, HS), treatment group (T+, T-), time point (t1, t2) and stimulus type (conditioned stimulus: yes, no) revealed activation in the left hippocampus and the occipitotemporal cortex. The T+ group demonstrated increased activation of the hippocampus at t2 (t2 > t1), which was positively correlated with treatment outcome, and a decreased connectivity between the left inferior frontal gyrus and the left hippocampus across time (t1 > t2). Conclusion: After T+ exposure, contingency-encoding processes related to the posterior hippocampus are augmented and more decoupled from processes of the left inferior frontal gyrus, previously shown to be dysfunctionally activated in PD/AG. Linking single procedural variants to neural substrates offers the potential to inform about the optimization of targeted psychotherapeutic interventions.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Agoraphobia - physiopathology</subject><subject>Agoraphobia - therapy</subject><subject>Anxiety disorders. Neuroses</subject><subject>Behavior therapy. Cognitive therapy</subject><subject>Biological and medical sciences</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Cognitive Therapy - methods</subject><subject>Conditioning (Psychology) - physiology</subject><subject>Fear - physiology</subject><subject>Female</subject><subject>Hippocampus - physiopathology</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Panic disorder</subject><subject>Panic Disorder - physiopathology</subject><subject>Panic Disorder - therapy</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. 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It is unknown, how variants of CBT differentially modulate brain networks involved in PD/AG. This study was aimed to evaluate the effects of therapist-guided (T+) versus self-guided (T-) exposure on the neural correlates of fear conditioning in PD/AG. Method: In a randomized, controlled multicenter clinical trial in medication-free patients with PD/AG who were treated with 12 sessions of manualized CBT, functional magnetic resonance imaging (fMRI) was used during fear conditioning before (t1) and after CBT (t2). Quality-controlled fMRI data from 42 patients and 42 healthy subjects (HS) were obtained. Patients were randomized to two variants of CBT (T+, n = 22, and T-, n = 20). Results: The interaction of diagnosis (PD/AG, HS), treatment group (T+, T-), time point (t1, t2) and stimulus type (conditioned stimulus: yes, no) revealed activation in the left hippocampus and the occipitotemporal cortex. The T+ group demonstrated increased activation of the hippocampus at t2 (t2 > t1), which was positively correlated with treatment outcome, and a decreased connectivity between the left inferior frontal gyrus and the left hippocampus across time (t1 > t2). Conclusion: After T+ exposure, contingency-encoding processes related to the posterior hippocampus are augmented and more decoupled from processes of the left inferior frontal gyrus, previously shown to be dysfunctionally activated in PD/AG. Linking single procedural variants to neural substrates offers the potential to inform about the optimization of targeted psychotherapeutic interventions.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>24970601</pmid><doi>10.1159/000359955</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-3751-0878</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Adult and adolescent clinical studies Agoraphobia - physiopathology Agoraphobia - therapy Anxiety disorders. Neuroses Behavior therapy. Cognitive therapy Biological and medical sciences Cerebral Cortex - physiopathology Cognitive Therapy - methods Conditioning (Psychology) - physiology Fear - physiology Female Hippocampus - physiopathology Humans Magnetic Resonance Imaging Male Medical sciences Middle Aged Panic disorder Panic Disorder - physiopathology Panic Disorder - therapy Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Regular Article Treatment Outcome Treatments |
title | Neural Correlates of Procedural Variants in Cognitive-Behavioral Therapy: A Randomized, Controlled Multicenter fMRI Study |
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