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Relationship between periventricular and deep white matter lesions and depressive symptoms in older people. The LADIS Study

✍ Scribed by Mani S Krishnan; John T O'Brien; Michael J Firbank; Leonardo Pantoni; Giovanna Carlucci; Timo Erkinjuntti; Anders Wallin; Lars-Olof Wahlund; Philip Scheltens; Elisabeth C.W. van Straaten; Domenico Inzitari


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
120 KB
Volume
21
Category
Article
ISSN
0885-6230

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✦ Synopsis


Abstract

Background

Both types of cerebral white matter hyperintensities, periventricular (PVL) and deep white matter lesions (DWML) have been previously associated with the development of depression in older subjects. However, it remains controversial as to whether PVL, DWML, or both are most strongly associated with depression and this was the aim of the current study.

Methods

In a pan‐European multicentre study of 626 older subjects, we examined the relationship between PVL and DWML, depressive symptoms (GDS quintile), cognitive status (MMSE), hypertension and history of stroke.

Results

In univariate analysis we found that depressive symptoms as assessed by GDS were associated with both types of white matter lesions (Spearman rho = 0.12 p = 0.002 for DWML and rho = 0.09 p = 0.01 for PVL). Using ordinal logistic regression analysis the total DWML score (p = 0.041), rather than PVL (p = 0.9) was found to predict GDS scores.

Conclusions

DWML, but not PVL, were most strongly associated with depressive symptoms in this sample. As DWML (unlike PVL) are associated with vascular ischaemic damage, our findings are consistent with the ‘vascular depression’ hypothesis. Longitudinal studies are needed to clarify the time course of these relationships, in particular, whether modifying DWML alters the natural history of depression. Copyright © 2006 John Wiley & Sons, Ltd.


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## Background: Cerebral white matter hyperintensities on magnetic resonance imaging (mri) scans have been associated with vascular disease and late-life depression, both in the general population and in psychiatric patients. therefore, a cerebrovascular etiology for late-onset depression has been h