Christopher J H Pirrung, Garima Singh, Jeremy Hogeveen, Davin Quinn, James F Cavanagh
{"title":"重度抑郁症患者腹内侧额叶皮层激活不足:奖励积极性的 MEG 研究。","authors":"Christopher J H Pirrung, Garima Singh, Jeremy Hogeveen, Davin Quinn, James F Cavanagh","doi":"10.1016/j.bpsc.2024.11.002","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The Reward Positivity (RewP) is a sensitive and specific electrophysiological marker of reward receipt. These characteristics make it a compelling candidate marker of dysfunctional reward processing in Major Depressive Disorder (MDD). We previously proposed that the RewP is a temporal nexus for multiple dimensions of reward value, and that a diminished RewP in depression might only reflect a deficit in some of these features. Specifically, we predicted a diminished ventromedial contribution in depression in the context of maintained reward learning.</p><p><strong>Methods: </strong>We collected magnetoencephalographic (MEG) recordings of reward receipt in 43 individuals with MDD (35 female) and 38 healthy controls (21 female). MEG allows effective source estimation due to the absence of volume conduction that compromises electroencephalographic recordings.</p><p><strong>Results: </strong>The MEG RewP analogue was generated by a broad set of cortical areas, yet only right ventromedial and right ventral temporal areas were diminished in MDD. These areas correlated with a principal component of anhedonia derived from multiple questionnaires. Compellingly, BA25 was the frontal region with the largest representation in both of these effects.</p><p><strong>Conclusions: </strong>These findings not only advance our understanding underlying the computation of the RewP, but they also dovetail with convergent findings from other types of functional source imaging in depression, as well as from deep brain stimulation treatments. Together, these discoveries suggest that the RewP may be a valuable marker for objective assessment of reward affect and its disruption in anhedonia.</p>","PeriodicalId":93900,"journal":{"name":"Biological psychiatry. Cognitive neuroscience and neuroimaging","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hypoactivation of ventromedial frontal cortex in major depressive disorder: an MEG study of the Reward Positivity.\",\"authors\":\"Christopher J H Pirrung, Garima Singh, Jeremy Hogeveen, Davin Quinn, James F Cavanagh\",\"doi\":\"10.1016/j.bpsc.2024.11.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The Reward Positivity (RewP) is a sensitive and specific electrophysiological marker of reward receipt. These characteristics make it a compelling candidate marker of dysfunctional reward processing in Major Depressive Disorder (MDD). We previously proposed that the RewP is a temporal nexus for multiple dimensions of reward value, and that a diminished RewP in depression might only reflect a deficit in some of these features. Specifically, we predicted a diminished ventromedial contribution in depression in the context of maintained reward learning.</p><p><strong>Methods: </strong>We collected magnetoencephalographic (MEG) recordings of reward receipt in 43 individuals with MDD (35 female) and 38 healthy controls (21 female). MEG allows effective source estimation due to the absence of volume conduction that compromises electroencephalographic recordings.</p><p><strong>Results: </strong>The MEG RewP analogue was generated by a broad set of cortical areas, yet only right ventromedial and right ventral temporal areas were diminished in MDD. These areas correlated with a principal component of anhedonia derived from multiple questionnaires. Compellingly, BA25 was the frontal region with the largest representation in both of these effects.</p><p><strong>Conclusions: </strong>These findings not only advance our understanding underlying the computation of the RewP, but they also dovetail with convergent findings from other types of functional source imaging in depression, as well as from deep brain stimulation treatments. Together, these discoveries suggest that the RewP may be a valuable marker for objective assessment of reward affect and its disruption in anhedonia.</p>\",\"PeriodicalId\":93900,\"journal\":{\"name\":\"Biological psychiatry. 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Hypoactivation of ventromedial frontal cortex in major depressive disorder: an MEG study of the Reward Positivity.
Background: The Reward Positivity (RewP) is a sensitive and specific electrophysiological marker of reward receipt. These characteristics make it a compelling candidate marker of dysfunctional reward processing in Major Depressive Disorder (MDD). We previously proposed that the RewP is a temporal nexus for multiple dimensions of reward value, and that a diminished RewP in depression might only reflect a deficit in some of these features. Specifically, we predicted a diminished ventromedial contribution in depression in the context of maintained reward learning.
Methods: We collected magnetoencephalographic (MEG) recordings of reward receipt in 43 individuals with MDD (35 female) and 38 healthy controls (21 female). MEG allows effective source estimation due to the absence of volume conduction that compromises electroencephalographic recordings.
Results: The MEG RewP analogue was generated by a broad set of cortical areas, yet only right ventromedial and right ventral temporal areas were diminished in MDD. These areas correlated with a principal component of anhedonia derived from multiple questionnaires. Compellingly, BA25 was the frontal region with the largest representation in both of these effects.
Conclusions: These findings not only advance our understanding underlying the computation of the RewP, but they also dovetail with convergent findings from other types of functional source imaging in depression, as well as from deep brain stimulation treatments. Together, these discoveries suggest that the RewP may be a valuable marker for objective assessment of reward affect and its disruption in anhedonia.