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The following 4 article abstracts report on effects of Deep Brain
Stimulation on functions such as working memory, speed of mental
processing, bimanual motor speed and coordination, speech. The first
study found some negative results, especially in patients over age 69.
Does anyone have more information about this or know  of similar studies?
I will see if I can obtain the full article.

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From: WE MOVE <[log in to unmask]>
To: <[log in to unmask]>
Date: Fri, 8 Dec 2000 17:09:52 -0600
Subject: Effects of DBS in Parkinson's disease
Message-ID: <[log in to unmask]>

1. Neuropsychological consequences of chronic bilateral stimulation of
the
subthalamic nucleus in Parkinson's disease
JA Saint-Cyr, LL Trepanier, R Kumar, AM Lozano, AE Lang
Brain 2000;123:2091-2108

Deep brain stimulation of the subthalamic nucleus can lead to long term
declines in neuropsychological measures, especially in older patients,
according to this study.

Eleven PD patients, including 6 older than age 69, received bilateral DBS
to the STN. In both younger and older patients at 12 months
post-operation, UPDRS motor scores had improved and levodopa daily doses
had declined, with greater changes in younger patients for both measures
(Kumar 1998). Neuropsychological evaluations were performed at baseline
and postoperatively both at early (3-6 months) and late (9-12 months)
time
points. At the early time point, results showed significant declines in
working memory, speed of mental processing, bimanual motor speed and
coordination, and other areas, with more consistent decline in older
patients. By the late time point, only learning based on multiple trials
had recovered to baseline values. The authors state, "Tasks reliant on
the
integrity of frontal striatal circuitry either did not recover or
gradually worsened."


2. An investigation of the effects of subthalamic stimulation on acoustic
measures of voice
C Dromey, R Kumar, AE Lang, AM Lozano
Movement Disorders 2000;15:1132-1138

DBS to the STN produces little significant improvement in speech
variables, according to this report.

A variety of speech-related variables were measured both on and off
medication in 7 PD patients before and 6 months after bilateral STN
electrode implantation. At 6 months for the group as a whole, no
significant change was seen in any of the measures of speech production
in
the off-med on-stim state. In the on-med on-stim state, there were small
increases in sound pressure level and fundamental frequency variability.
The authors state, "These findings are consistent with several other
studies that have reported disparity between limb and speech improvements
after neurosurgical intervention for Parkinson's disease."


3. Effect of bilateral deep-brain stimulation on oral control of patients
with parkinsonism
M Gentil, P Garcia-Ruiz, P Pollak, AL Benabid
European Neurology 2000;44:147-152

Deep brain stimulation of the STN improves force and control of the
articulatory organs, while stimulation of the ventral intermediate
nucleus
(VIM) does not, according to this study.

Force generation and control in the tongue, upper lip, and lower lip were
measured in 10 STN patients and 4 VIM patients on and off stimulation
after at least 10 hours off medication. STN stimulation significantly
improved maximal voluntary force in all three organs by at least 50% over
no stimulation, while VIM stimulation had no significant effect. STN
stimulation improved target force precision as well, while VIM
stimulation
either had no effect or worsened it (in the tongue). STN stimulation
improved speech as measured by UPDRS Item 18, while VIM stimulation
worsened it.


4. No tissue damage by chronic deep brain stimulation in Parkinson's
disease
C Haberler, F Alesch, PR Mazal, P Pilz, K Jellinger, MM Pinter, JA
Hainfellner, H Budka
Ann Neurol 2000;48:372-376

Brains were examined from 8 patients who had received DBS to either the
STN (2) or the VIM (6), and who had died of unrelated causes. Patients
had
received stimulation for 3-69 months prior to death, except for 1 patient
who died 2 days after implantation of myocardial infarction. In all but
this last patient, a thin inner capsule of connective tissue was found
around the lead track, whose thickness was not correlated with duration
of
stimulation. No difference was seen in tissue changes surrounding active
contacts versus those surrounding insulated parts of the lead. Other
changes noted in some patients included slight microglial activation
around the lead track. The authors state, "We conclude that chronic DBS
does not cause damage to adjacent brain parenchyma."

Copyright 2000 WE MOVE
Editor: Richard Robinson ([log in to unmask])

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