Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
39191867
TITLE
Markers of positive affect and brain state synchrony discriminate melancholic from non-melancholic depression using naturalistic stimuli.
ABSTRACT
Melancholia has been proposed as a qualitatively distinct depressive subtype associated with a characteristic symptom profile (psychomotor retardation, profound anhedonia) and a better response to biological therapies. Existing work has suggested that individuals with melancholia are blunted in their display of positive emotions and differ in their neural response to emotionally evocative stimuli. Here, we unify these brain and behavioural findings amongst a carefully phenotyped group of seventy depressed participants, drawn from an established Australian database (the Australian Genetics of Depression Study) and further enriched for melancholia (high ratings of psychomotor retardation and anhedonia). Melancholic (n = 30) or non-melancholic status (n = 40) was defined using a semi-structured interview (the Sydney Melancholia Prototype Index). Complex facial expressions were captured whilst participants watched a movie clip of a comedian and classified using a machine learning algorithm. Subsequently, the dynamics of sequential changes in brain activity were modelled during the viewing of an emotionally evocative movie in the MRI scanner. We found a quantitative reduction in positive facial expressivity amongst participants with melancholia, combined with differences in the synchronous expression of brain states during positive epochs of the movie. In non-melancholic depression, the display of positive affect was inversely related to the activity of cerebellar regions implicated in the processing of affect. However, this relationship was reduced in those with a melancholic phenotype. Our multimodal findings show differences in evaluative and motoric domains between melancholic and non-melancholic depression through engagement in ecologically valid tasks that evoke positive emotion. These findings provide new markers to stratify depression and an opportunity to support the development of targeted interventions.
© 2024. The Author(s).
DATE PUBLISHED
2024 Aug 27
HISTORY
PUBSTATUS PUBSTATUSDATE
received 2024/01/11
accepted 2024/08/14
revised 2024/08/11
medline 2024/08/28 02:56
pubmed 2024/08/28 02:56
entrez 2024/08/27 23:25
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Mosley PE Mosley Philip E PE Faculty of Medicine, School of Biomedical Sciences, University of Queensland, St Lucia, QLD, Australia. philip.mosley@qimrberghofer.edu.au.
van der Meer JN van der Meer Johan N JN School of Information Systems, Queensland University of Technology, Kelvin Grove, QLD, Australia.
Hamilton LHW Hamilton Lachlan H W LHW QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Fripp J Fripp Jurgen J Australian eHealth Research Centre, CSIRO Health and Biosecurity, Herston, QLD, Australia.
Parker S Parker Stephen S Metro North Mental Health, Royal Brisbane & Women's Hospital, Herston, QLD, Australia.
Jeganathan J Jeganathan Jayson J School of Medicine and Public Health, College of Medicine, Health and Wellbeing, University of Newcastle, Newcastle, NSW, Australia.
Breakspear M Breakspear Michael M School of Medicine and Public Health, College of Medicine, Health and Wellbeing, University of Newcastle, Newcastle, NSW, Australia.
Parker R Parker Richard R QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Holland R Holland Rebecca R QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Mitchell BL Mitchell Brittany L BL Faculty of Medicine, School of Biomedical Sciences, University of Queensland, St Lucia, QLD, Australia.
Byrne E Byrne Enda E Child Health Research Centre, University of Queensland, South Brisbane, QLD, Australia.
Hickie IB Hickie Ian B IB Brain and Mind Centre, University of Sydney, Camperdown, NSW, Australia.
Medland SE Medland Sarah E SE School of Psychology and Counselling, Queensland University of Technology, Kelvin Grove, QLD, Australia.
Martin NG Martin Nicholas G NG QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Cocchi L Cocchi Luca L Faculty of Medicine, School of Biomedical Sciences, University of Queensland, St Lucia, QLD, Australia.
INVESTIGATORS
JOURNAL
VOLUME:
ISSUE:
TITLE: Molecular psychiatry
ISOABBREVIATION: Mol Psychiatry
YEAR: 2024
MONTH: Aug
DAY: 27
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Internet
ISSN: 1476-5578
ISSNTYPE: Electronic
MEDLINE JOURNAL
MEDLINETA: Mol Psychiatry
COUNTRY: England
ISSNLINKING: 1359-4184
NLMUNIQUEID: 9607835
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
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