Literature DB >> 23208772

Morphometric analysis of vascular pathology in the orbitofrontal cortex of older subjects with major depression.

Jose Javier Miguel-Hidalgo1, Wei Jiang, Lisa Konick, James C Overholser, George J Jurjus, Craig A Stockmeier, David C Steffens, K Ranga R Krishnan, Grazyna Rajkowska.   

Abstract

OBJECTIVE: Late-life depression has been associated with risk for cerebrovascular pathology, as demonstrated in neuroimaging studies of older depressed patients, as well as mood disorder following cerebrovascular accidents. However, more research is needed on neuroanatomical changes in late-life depression, where there has been no clearly documented link to brain injury. Such studies should examine morphological changes in medium and small sized vessels that supply the cortical gray and white matter.
METHODS: The present study used a non-specific histological Nissl staining and a more vessel-specific immunolabeling with endothelial marker von Willebrand Factor (vWF) to estimate density and size of blood vessel segments in the orbitofrontal cortex of 16 older subjects with major depressive disorder (MDD) and 9 non-psychiatric comparison subjects.
RESULTS: The density of Nissl-stained vessel segments and of segments with perivascular spaces was higher in subjects with MDD than in comparison subjects in gray (GM) and white matter (WM). In GM, the density of vWF-immunoreactive segments with cross-sectional areas greater than 800 µm2 was higher in MDD. In WM, only the density of vWF-immunoreactive segments with patent perivascular spaces and diameters larger than 60 µm was higher in subjects with MDD. Also in the WM, only subjects with late-onset MDD presented a significantly higher density of vWF-positive segments than comparison subjects.
CONCLUSIONS: In older subjects with MDD, there appear to be morphological changes that increase visibility of medium-sized vessel segments with some labeling techniques, and this increased visibility may be related to increased patency of perivascular spaces around arterioles.
Copyright © 2012 John Wiley & Sons, Ltd.

Entities:  

Keywords:  blood vessels; depression; morphometry; prefrontal cortex

Mesh:

Year:  2012        PMID: 23208772      PMCID: PMC3679255          DOI: 10.1002/gps.3911

Source DB:  PubMed          Journal:  Int J Geriatr Psychiatry        ISSN: 0885-6230            Impact factor:   3.485


  46 in total

1.  Immunohistochemistry of neural markers for the study of the laminar architecture in celloidin sections from the human cerebral cortex.

Authors:  J J Miguel-Hidalgo; G Rajkowska
Journal:  J Neurosci Methods       Date:  1999-10-30       Impact factor: 2.390

2.  A neuropathological study of vascular factors in late-life depression.

Authors:  A J Thomas; I N Ferrier; R N Kalaria; R H Perry; A Brown; J T O'Brien
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-01       Impact factor: 10.154

3.  Evidence of white matter tract disruption in MRI hyperintensities.

Authors:  W D Taylor; M E Payne; K R Krishnan; H R Wagner; J M Provenzale; D C Steffens; J R MacFall
Journal:  Biol Psychiatry       Date:  2001-08-01       Impact factor: 13.382

4.  Cell adhesion molecule expression in the dorsolateral prefrontal cortex and anterior cingulate cortex in major depression in the elderly.

Authors:  Alan J Thomas; I Nicol Ferrier; Rajesh N Kalaria; Sue Davis; John T O'Brien
Journal:  Br J Psychiatry       Date:  2002-08       Impact factor: 9.319

5.  Reduction of orbital frontal cortex volume in geriatric depression.

Authors:  T Lai; M E Payne; C E Byrum; D C Steffens; K R Krishnan
Journal:  Biol Psychiatry       Date:  2000-11-15       Impact factor: 13.382

6.  Medial orbital frontal lesions in late-onset depression.

Authors:  J R MacFall; M E Payne; J E Provenzale; K R Krishnan
Journal:  Biol Psychiatry       Date:  2001-05-01       Impact factor: 13.382

Review 7.  Depression as a contributing factor in cerebrovascular disease.

Authors:  K R Krishnan
Journal:  Am Heart J       Date:  2000-10       Impact factor: 4.749

8.  Low gene expression of bone morphogenetic protein 7 in brainstem astrocytes in major depression.

Authors:  Gregory A Ordway; Attila Szebeni; Michelle J Chandley; Craig A Stockmeier; Lianbin Xiang; Samuel S Newton; Gustavo Turecki; Michelle M Duffourc; Meng-Yang Zhu; Hobart Zhu; Katalin Szebeni
Journal:  Int J Neuropsychopharmacol       Date:  2011-09-06       Impact factor: 5.176

9.  Localization of age-associated white matter hyperintensities in late-life depression.

Authors:  Warren D Taylor; James R MacFall; David C Steffens; Martha E Payne; James M Provenzale; K Ranga Rama Krishnan
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2003-05       Impact factor: 5.067

10.  Ischemic basis for deep white matter hyperintensities in major depression: a neuropathological study.

Authors:  Alan J Thomas; John T O'Brien; Sue Davis; Clive Ballard; Robert Barber; Rajesh N Kalaria; Robert H Perry
Journal:  Arch Gen Psychiatry       Date:  2002-09
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  3 in total

Review 1.  The vascular depression hypothesis: mechanisms linking vascular disease with depression.

Authors:  W D Taylor; H J Aizenstein; G S Alexopoulos
Journal:  Mol Psychiatry       Date:  2013-02-26       Impact factor: 15.992

2.  Fluoxetine Requires the Endfeet Protein Aquaporin-4 to Enhance Plasticity of Astrocyte Processes.

Authors:  Barbara Di Benedetto; Victoria A Malik; Salina Begum; Lena Jablonowski; Gabriela B Gómez-González; Inga D Neumann; Rainer Rupprecht
Journal:  Front Cell Neurosci       Date:  2016-02-02       Impact factor: 5.505

3.  Molecular and Genetic Characterization of Depression: Overlap with other Psychiatric Disorders and Aging.

Authors:  Ying Ding; Lun-Ching Chang; Xingbin Wang; Jean-Philippe Guilloux; Jenna Parrish; Hyunjung Oh; Beverly J French; David A Lewis; George C Tseng; Etienne Sibille
Journal:  Mol Neuropsychiatry       Date:  2015-05
  3 in total

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