Neuropsychological Impairment in Major Depression: Its Nature, Origin and Clinical Significance
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Neuropsychological impairment is well established as a feature of major depressive disorder (MDD) but studies have shown a variable pattern of impairment. This paper seeks first to clarify this by examining methodological and clinical factors that give rise to variability in study findings. Second, it examines theories of the origin of these neuropsychological abnormalities. Third, it reviews evidence regarding the clinical significance of different patterns of deficit. A selective review was undertaken of the literature with a particular emphasis on methodological factors, the influence of clinical subtypes and prevalent theories of neuropsychological abnormality. Methodological issues and the heterogeneity of MDD account for considerable variability in results. Specific investigation of the subtypes of psychotic MDD, melancholic MDD and bipolar depression reduces this heterogeneity and results are more consistent in the elderly. Hypothalamic-pituitary-adrenal axis dysfunction is associated with neuropsychological dysfunction in MDD although evidence of direct causation is not definitive at present. Impairment of executive and psychomotor function is a consistent finding, particularly in the elderly, and may reflect frontostriatal-limbic dysfunction. There is growing evidence that this may have clinical significance. It is suggested that future research take very careful account of the exact phenotype of MDD. Classification based on neuropsychological profile may, in fact, b…
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Objective deficits in executive function, processing speed, attention, learning and memory occur during and after resolution of a major depressive episode.
“In addition to being a reason for frequent subjective complaints, objective deficits in measures of executive function, processing speed, attention, learning and memory during, and after resolution of an MDE have been reported (Porter et al., 2007; Hammar and Ardal, 2009; Baune et al., 2010).”
From A randomized, double-blind, placebo-controlled study of vortioxetine on cognitive function in depressed adults (2014) · cites this paper as Porter et al., 2007
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References 123 · Cited by 236
- Authors
- Porter, R. J., Bourke, C., & Gallagher, P.
- Affiliations
- Department of Psychological Medicine, Christchurch School of Medicine and Health Sciences, PO Box 4345, Christchurch, New Zealand
- Newcastle University (GB)
- Venue
- Australian & New Zealand Journal of Psychiatry
- Publisher
- SAGE Publications
- Published
- 2007-02
- Volume
- 41
- Issue
- 2
- Pages
- 115-128
- ISSN
- 0004-8674 (ISSN-L)
- 1440-1614
- OpenAlex
- W2089158781
- Cited by
- 236
- References
- 123
- Citations by year
- 2026: 9 · 2025: 6 · 2024: 4 · 2023: 6 · 2022: 10 · 2021: 14 · 2020: 17 · 2019: 13 · 2018: 15 · 2017: 9 · 2016: 15 · 2015: 15 · 2014: 16 · 2013: 18 · 2012: 19
- FWCI
- 1.33
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Australian & New Zealand Journal of Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
- Keywords
- major depressive disorder, neuropsychological deficits, executive dysfunction, psychomotor impairment, HPA axis dysregulation, endogenous depression, bipolar depression, psychotic depression, depression subtypes, geriatric depression, depression classification, cognitive deficits in depression
- MeSH terms
- Anxiety Disorders, Attention, Automatism, Circadian Rhythm, Cognition Disorders, Major Depressive Disorder, Female, Hippocampus, Humans, Hypothalamo-Hypophyseal System, Limbic System, Male, Neuropsychological Tests, Pituitary-Adrenal System, Psychotic Disorders, Severity of Illness Index, Sex Factors, Time Factors, Comorbidity
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