Literature DB >> 20609838

Vascular function in older adults with depressive disorder.

Raghupathy Paranthaman1, Adam S Greenstein, Alistair S Burns, J Kennedy Cruickshank, Anthony M Heagerty, Alan Jackson, Rayaz A Malik, Marietta L J Scott, Robert C Baldwin.   

Abstract

BACKGROUND: Cerebrovascular disease plays an important role in depressive disorder, especially in older adults. An understanding of vascular function in depression is important etiologically and to develop innovative treatments that may improve prognosis by ameliorating vascular damage.
METHODS: This study assessed endothelial function, arterial stiffness, and atherosclerosis in a variety of vessel beds in 25 elderly subjects with depressive disorder compared with 21 nondepressed control subjects. Subjects underwent pulse wave velocity, pulse wave analysis, carotid intima media thickness analysis, and magnetic resonance imaging. A subset (16 patients and 15 control subjects) had assessment of biopsied small artery dilatation to acetylcholine to further assess endothelial function.
RESULTS: The mean sample age was 72.4 years with an average age at onset for depression of 60 years. Mean carotid intima media thickness was significantly higher in depressed subjects (p < .01). Pulse wave velocity was 1.6 m/sec higher in depressed subjects (borderline significance). There was a significant reduction in the dilatation response to acetylcholine in preconstricted small arteries (p = .01). On magnetic resonance imaging, depressed subjects had significantly more dilated Virchow-Robin spaces in the basal ganglia (p = .01). Depressed subjects had greater volume of white matter lesions in all regions, but this did not reach statistical significance. There were no baseline differences in vascular risk.
CONCLUSIONS: Depression in the elderly is associated with poorer endothelial function and more atherosclerosis. This is associated with a greater white matter hyperintensities lesion load and basal ganglia microangiopathy. The use of vasoprotective drugs to improve endothelial function or retard atherosclerosis as depression-modifying agents should be explored. Crown Copyright 2010. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20609838     DOI: 10.1016/j.biopsych.2010.04.017

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


  33 in total

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7.  Neural correlates of apathy in late-life depression: a pilot [18 F]FDDNP positron emission tomography study.

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8.  Frontocingulate cerebral blood flow and cerebrovascular reactivity associated with antidepressant response in late-life depression.

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Review 10.  Association of Microvascular Dysfunction With Late-Life Depression: A Systematic Review and Meta-analysis.

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