Literature DB >> 11164759

Cognitive impairment in depression is not associated with neuropathologic evidence of increased vascular or Alzheimer-type pathology.

J O'Brien1, A Thomas, C Ballard, A Brown, N Ferrier, E Jaros, R Perry.   

Abstract

BACKGROUND: Cognitive impairment is common in depression, but underlying mechanisms remain unknown. We examined whether increases in Alzheimer-type or vascular pathology are associated with cognitive impairments in elderly depressed subjects.
METHODS: Eleven subjects who had died during a well-documented episode of DSM-IV major depression were included. Neuropathologic assessments, blind to group membership, included standardized assessment of neuritic plaques, neurofibrillary tangles, and Lewy Bodies in frontal, temporal, parietal, and occipital cortices. Braak staging of Alzheimer pathology was also performed. Cerebral microvascular disease was scored according to a previously validated scale, and a score for cerebral and systemic atheroma of large and medium sized arteries was obtained.
RESULTS: No subject had Lewy bodies. Plaque and tangle counts for all subjects were well within published norms for age-matched control subjects. There were no significant differences in plaque or tangle counts between subjects who were cognitively impaired (n = 5) and those who were nonimpaired (n = 6) during their depressive illness. Similarly, neither total microvascular pathology nor deep frontal microvascular pathology differed between the two groups.
CONCLUSIONS: Our results indicate that the liability for some patients to develop cognitive impairment during a depressive episode is not related to an increase in Alzheimer-type or vascular neuropathologic change. This indicates that other mechanisms must underlie both the cognitive impairment associated with depression and the observation that depression is a risk factor for dementia.

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Year:  2001        PMID: 11164759     DOI: 10.1016/s0006-3223(00)00944-6

Source DB:  PubMed          Journal:  Biol Psychiatry        ISSN: 0006-3223            Impact factor:   13.382


  9 in total

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Review 2.  The effects of chronic glucocorticoid exposure on dendritic length, synapse numbers and glial volume in animal models: implications for hippocampal volume reductions in depression.

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3.  Organic bases of late-life depression: a critical update.

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Review 4.  What causes the hippocampal volume decrease in depression? Are neurogenesis, glial changes and apoptosis implicated?

Authors:  Boldizsár Czéh; Paul J Lucassen
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5.  APOE-epsilon4, depressive symptoms, and cognitive decline in Chinese older adults: Singapore Longitudinal Aging Studies.

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6.  Rates of depression in individuals with pathologic but not clinical Alzheimer disease are lower than those in individuals without the disease: findings from the Baltimore Longitudinal Study on Aging (BLSA).

Authors:  Melissa D Morgan; Michelle M Mielke; Richard O'Brien; Juan C Troncoso; Alan B Zonderman; Constantine G Lyketsos
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7.  Depression and anxiety symptoms are associated with cerebral FDDNP-PET binding in middle-aged and older nondemented adults.

Authors:  Helen Lavretsky; Prabha Siddarth; Vladimir Kepe; Linda M Ercoli; Karen J Miller; Alison C Burggren; Susan Y Bookheimer; Sung-Cheng Huang; Jorge R Barrio; Gary W Small
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8.  Vascular depression consensus report - a critical update.

Authors:  Howard J Aizenstein; Andrius Baskys; Maura Boldrini; Meryl A Butters; Breno S Diniz; Manoj Kumar Jaiswal; Kurt A Jellinger; Lev S Kruglov; Ivan A Meshandin; Milija D Mijajlovic; Guenter Niklewski; Sarah Pospos; Keerthy Raju; Kneginja Richter; David C Steffens; Warren D Taylor; Oren Tene
Journal:  BMC Med       Date:  2016-11-03       Impact factor: 8.775

Review 9.  Mechanisms and treatment of late-life depression.

Authors:  George S Alexopoulos
Journal:  Transl Psychiatry       Date:  2019-08-05       Impact factor: 6.222

  9 in total

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