Literature DB >> 22157280

Neural correlates associated with cognitive decline in late-life depression.

Lihong Wang1, Guy G Potter, R K Ranga Krishnan, Florin Dolcos, Gwenn S Smith, David C Steffens.   

Abstract

OBJECTIVES: Persistent cognitive impairment (PCI) after remission of depressive symptoms is a major adverse outcome of late-life depression (LLD). The purpose of this study was to examine neural substrates associated with PCI in LLD.
DESIGN: Longitudinal study.
SETTING: Outpatient depression treatment study at Duke University. PARTICIPANTS: Twenty-three patients with LLD completed a 2-year follow-up study, and were in a remitted or partially remitted state at Year 2.
METHODS: At first entry to the study (Year 0), all participants had a functional magnetic resonance imaging scan while performing an emotional oddball task. For the purpose of this report, the primary functional magnetic resonance imaging outcome was brain activation during target detection, which is a measure of executive function. The Consortium to Establish a Registry for Alzheimer's Disease neuropsychological battery was used to assess cognitive status yearly, and the Montgomery-Åsberg Depression Rating Scale was used to assess severity of depression at Year 0 and every 6 months thereafter for 2 years. We investigated changes in brain activation at Year 0 associated with PCI over 2 years.
RESULTS: Patients with PCI at the 2-year follow-up date had significantly decreased activation at Year 0 in the dorsal anterior cingulate cortex, hippocampus, inferior frontal cortex, and insula compared to non-PCI patients.
CONCLUSIONS: Our results suggest individuals who have LLD with PCI have decreased activation in the similar neural networks associated with the development of Alzheimer disease among nondepressed individuals. Measuring neural activity in these regions in individuals with LLD may help identify patients at-risk for cognitive impairment.

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Year:  2012        PMID: 22157280      PMCID: PMC3337345          DOI: 10.1097/JGP.0b013e31823e2cc7

Source DB:  PubMed          Journal:  Am J Geriatr Psychiatry        ISSN: 1064-7481            Impact factor:   4.105


  45 in total

1.  Amygdala activation to sad pictures during high-field (4 tesla) functional magnetic resonance imaging.

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2.  A total score for the CERAD neuropsychological battery.

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3.  Prefrontal mechanisms for executive control over emotional distraction are altered in major depression.

Authors:  Lihong Wang; Kevin S LaBar; Moria Smoski; M Zachary Rosenthal; Florin Dolcos; Thomas R Lynch; Ranga R Krishnan; Gregory McCarthy
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4.  Depressive state- and disease-related alterations in neural responses to affective and executive challenges in geriatric depression.

Authors:  Lihong Wang; K Ranga Krishnan; David C Steffens; Guy G Potter; Florin Dolcos; Gregory McCarthy
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Review 5.  Functional abnormalities of the medial temporal lobe memory system in mild cognitive impairment and Alzheimer's disease: insights from functional MRI studies.

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6.  Imaging Alzheimer pathology in late-life depression with PET and Pittsburgh Compound-B.

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Review 10.  Pathways linking late-life depression to persistent cognitive impairment and dementia.

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1.  Amygdala network dysfunction in late-life depression phenotypes: Relationships with symptom dimensions.

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Review 2.  Depression in cognitive impairment.

Authors:  Laurel D Pellegrino; Matthew E Peters; Constantine G Lyketsos; Christopher M Marano
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3.  Imbalanced hippocampal functional networks associated with remitted geriatric depression and apolipoprotein E ε4 allele in nondemented elderly: a preliminary study.

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Review 5.  Depression and cognitive impairment in older adults.

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Review 8.  Disruption of Neural Homeostasis as a Model of Relapse and Recurrence in Late-Life Depression.

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9.  Depressive-like behavior observed with a minimal loss of locus coeruleus (LC) neurons following administration of 6-hydroxydopamine is associated with electrophysiological changes and reversed with precursors of norepinephrine.

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Review 10.  The age-by-disease interaction hypothesis of late-life depression.

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