Movement Disorders (revue)

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Torpedoes in Parkinson's Disease, Alzheimer's Disease, Essential Tremor, and Control Brains

Identifieur interne : 001F31 ( PascalFrancis/Curation ); précédent : 001F30; suivant : 001F32

Torpedoes in Parkinson's Disease, Alzheimer's Disease, Essential Tremor, and Control Brains

Auteurs : Elan D. Louis [États-Unis] ; Phyllis L. Faust [États-Unis] ; Jean-Paul G. Vonsattel [États-Unis] ; Lawrence S. Honig [États-Unis] ; Alex Rajput [Canada] ; Ali Rajput [Canada] ; Rajesh Pahwa [États-Unis] ; Kelly E. Lyons [États-Unis] ; Webster G. Ross [États-Unis] ; Rodger J. Elble [États-Unis] ; Cordelia Erickson-Davis [États-Unis] ; Carol B. Moskowitz [États-Unis] ; Arlene Lawton [États-Unis]

Source :

RBID : Pascal:09-0386511

Descripteurs français

English descriptors

Abstract

Purkinje cell axonal swellings ("torpedoes"), described in several cerebellar disorders as well as essential tremor (ET), have not been quantified in common neurodegenerative conditions. The aim of this study was to quantify torpedoes Parkinson's disease (PD) and Alzheimer's disease (AD) compared with ET and control brains. Brains included 40 ET cases (34 cerebellar ET, 6 Lewy body variant of ET) and age-matched comparison brains (21 AD, 14 PD/diffuse Lewy body disease, 25 controls). Torpedoes were counted in 20 X 25 mm cerebellar cortical sections stained with Luxol Fast Blue/Hematoxylin and Eosin. The median number of torpedoes in cerebellar ET (12) was 12× higher than that of controls (1) and nearly 2.5× higher than in AD (5) or PD/ DLBD (5) (all P < 0.005). Furthermore, in a logistic regression model that adjusted for age and Alzheimer's-type changes, each torpedo more than doubled the odds of having cerebellar ET (Odds ratiocerebellar ET vs. control = 2.57, P = 0.006), indicating that the association between increased torpedoes and cerebellar ET was independent of these Alzheimer's-type changes. Although torpedoes are increased in AD and PD, as well as cerebellar ET, the magnitude of increase in cerebellar ET is greater, and cannot be accounted for by concomitant AD or PD pathology.
pA  
A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 24
A06       @2 11
A08 01  1  ENG  @1 Torpedoes in Parkinson's Disease, Alzheimer's Disease, Essential Tremor, and Control Brains
A11 01  1    @1 LOUIS (Elan D.)
A11 02  1    @1 FAUST (Phyllis L.)
A11 03  1    @1 VONSATTEL (Jean-Paul G.)
A11 04  1    @1 HONIG (Lawrence S.)
A11 05  1    @1 RAJPUT (Alex)
A11 06  1    @1 RAJPUT (Ali)
A11 07  1    @1 PAHWA (Rajesh)
A11 08  1    @1 LYONS (Kelly E.)
A11 09  1    @1 ROSS (Webster G.)
A11 10  1    @1 ELBLE (Rodger J.)
A11 11  1    @1 ERICKSON-DAVIS (Cordelia)
A11 12  1    @1 MOSKOWITZ (Carol B.)
A11 13  1    @1 LAWTON (Arlene)
A14 01      @1 GH Sergievsky Center, College of Physicians and Surgeons, Columbia University @2 New York, New York @3 USA @Z 1 aut. @Z 4 aut. @Z 11 aut. @Z 12 aut. @Z 13 aut.
A14 02      @1 Department of Neurology, College of Physicians and Surgeons, Columbia University @2 New York, New York @3 USA @Z 1 aut. @Z 4 aut. @Z 12 aut.
A14 03      @1 Taub Institute for Research on Alzheimer's Disease and the Aging Brain, College of Physicians and Surgeons, Columbia University @2 New York, New York @3 USA @Z 1 aut. @Z 3 aut. @Z 4 aut. @Z 13 aut.
A14 04      @1 Department of Epidemiology, Mailman School of Public Health, Columbia University @2 New York, New York @3 USA @Z 1 aut.
A14 05      @1 Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University @2 New York, New York @3 USA @Z 2 aut. @Z 3 aut.
A14 06      @1 Department of Neurology, Royal University Hospital @2 Saskatoon, Saskatchewan @3 CAN @Z 5 aut. @Z 6 aut.
A14 07      @1 Department of Neurology, University of Kansas Medical Center @2 Kansas City, Kansas @3 USA @Z 7 aut. @Z 8 aut.
A14 08      @1 Veterans Affairs Pacific Islands Health Care System, University of Hawaii, John A. Burns School of Medicine @2 Honolulu, Hawaii @3 USA @Z 9 aut.
A14 09      @1 Department of Medicine, University of Hawaii, John A. Burns School of Medicine @2 Honolulu, Hawaii @3 USA @Z 9 aut.
A14 10      @1 Department of Geriatrics, University of Hawaii, John A. Burns School of Medicine @2 Honolulu, Hawaii @3 USA @Z 9 aut.
A14 11      @1 Pacific Health Research Institute @2 Honolulu, Hawaii @3 USA @Z 9 aut.
A14 12      @1 Kuakini Medical Center/Honolulu-Asia Aging Study @2 Honolulu, Hawaii @3 USA @Z 9 aut.
A14 13      @1 Department of Neurology, Southern Illinois University School of Medicine @2 Springfield, Illinois @3 USA @Z 10 aut.
A20       @1 1600-1605
A21       @1 2009
A23 01      @0 ENG
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A60       @1 P
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C01 01    ENG  @0 Purkinje cell axonal swellings ("torpedoes"), described in several cerebellar disorders as well as essential tremor (ET), have not been quantified in common neurodegenerative conditions. The aim of this study was to quantify torpedoes Parkinson's disease (PD) and Alzheimer's disease (AD) compared with ET and control brains. Brains included 40 ET cases (34 cerebellar ET, 6 Lewy body variant of ET) and age-matched comparison brains (21 AD, 14 PD/diffuse Lewy body disease, 25 controls). Torpedoes were counted in 20 X 25 mm cerebellar cortical sections stained with Luxol Fast Blue/Hematoxylin and Eosin. The median number of torpedoes in cerebellar ET (12) was 12× higher than that of controls (1) and nearly 2.5× higher than in AD (5) or PD/ DLBD (5) (all P < 0.005). Furthermore, in a logistic regression model that adjusted for age and Alzheimer's-type changes, each torpedo more than doubled the odds of having cerebellar ET (Odds ratiocerebellar ET vs. control = 2.57, P = 0.006), indicating that the association between increased torpedoes and cerebellar ET was independent of these Alzheimer's-type changes. Although torpedoes are increased in AD and PD, as well as cerebellar ET, the magnitude of increase in cerebellar ET is greater, and cannot be accounted for by concomitant AD or PD pathology.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Maladie de Parkinson @2 NM @5 01
C03 01  X  ENG  @0 Parkinson disease @2 NM @5 01
C03 01  X  SPA  @0 Parkinson enfermedad @2 NM @5 01
C03 02  X  FRE  @0 Démence d'Alzheimer @5 02
C03 02  X  ENG  @0 Alzheimer disease @5 02
C03 02  X  SPA  @0 Demencia Alzheimer @5 02
C03 03  X  FRE  @0 Tremblement @5 03
C03 03  X  ENG  @0 Tremor @5 03
C03 03  X  SPA  @0 Temblor @5 03
C03 04  X  FRE  @0 Pathologie du système nerveux @5 04
C03 04  X  ENG  @0 Nervous system diseases @5 04
C03 04  X  SPA  @0 Sistema nervioso patología @5 04
C03 05  X  FRE  @0 Encéphale @5 09
C03 05  X  ENG  @0 Encephalon @5 09
C03 05  X  SPA  @0 Encéfalo @5 09
C03 06  X  FRE  @0 Cervelet @5 10
C03 06  X  ENG  @0 Cerebellum @5 10
C03 06  X  SPA  @0 Cerebelo @5 10
C03 07  X  FRE  @0 Anatomopathologie @5 11
C03 07  X  ENG  @0 Anatomic pathology @5 11
C03 07  X  SPA  @0 Anatomía patológica @5 11
C07 01  X  FRE  @0 Pathologie de l'encéphale @5 37
C07 01  X  ENG  @0 Cerebral disorder @5 37
C07 01  X  SPA  @0 Encéfalo patología @5 37
C07 02  X  FRE  @0 Syndrome extrapyramidal @5 38
C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Maladie dégénérative @5 39
C07 03  X  ENG  @0 Degenerative disease @5 39
C07 03  X  SPA  @0 Enfermedad degenerativa @5 39
C07 04  X  FRE  @0 Pathologie du système nerveux central @5 40
C07 04  X  ENG  @0 Central nervous system disease @5 40
C07 04  X  SPA  @0 Sistema nervosio central patología @5 40
C07 05  X  FRE  @0 Mouvement involontaire @5 42
C07 05  X  ENG  @0 Involuntary movement @5 42
C07 05  X  SPA  @0 Movimiento involuntario @5 42
C07 06  X  FRE  @0 Trouble neurologique @5 43
C07 06  X  ENG  @0 Neurological disorder @5 43
C07 06  X  SPA  @0 Trastorno neurológico @5 43
C07 07  X  FRE  @0 Système nerveux central @5 44
C07 07  X  ENG  @0 Central nervous system @5 44
C07 07  X  SPA  @0 Sistema nervioso central @5 44
N21       @1 278
N44 01      @1 OTO
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Pascal:09-0386511

Le document en format XML

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<title xml:lang="en" level="a">Torpedoes in Parkinson's Disease, Alzheimer's Disease, Essential Tremor, and Control Brains</title>
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<title level="j" type="main">Movement disorders</title>
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<front>
<div type="abstract" xml:lang="en">Purkinje cell axonal swellings ("torpedoes"), described in several cerebellar disorders as well as essential tremor (ET), have not been quantified in common neurodegenerative conditions. The aim of this study was to quantify torpedoes Parkinson's disease (PD) and Alzheimer's disease (AD) compared with ET and control brains. Brains included 40 ET cases (34 cerebellar ET, 6 Lewy body variant of ET) and age-matched comparison brains (21 AD, 14 PD/diffuse Lewy body disease, 25 controls). Torpedoes were counted in 20 X 25 mm cerebellar cortical sections stained with Luxol Fast Blue/Hematoxylin and Eosin. The median number of torpedoes in cerebellar ET (12) was 12× higher than that of controls (1) and nearly 2.5× higher than in AD (5) or PD/ DLBD (5) (all P < 0.005). Furthermore, in a logistic regression model that adjusted for age and Alzheimer's-type changes, each torpedo more than doubled the odds of having cerebellar ET (Odds ratio
<sub>cerebellar</sub>
<sub>ET</sub>
<sub>vs</sub>
. control =
<sup>2</sup>
.
<sup>57</sup>
,
<sup>P</sup>
<sup>=</sup>
0.006), indicating that the association between increased torpedoes and cerebellar ET was independent of these Alzheimer's-type changes. Although torpedoes are increased in AD and PD, as well as cerebellar ET, the magnitude of increase in cerebellar ET is greater, and cannot be accounted for by concomitant AD or PD pathology.</div>
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<s0>Purkinje cell axonal swellings ("torpedoes"), described in several cerebellar disorders as well as essential tremor (ET), have not been quantified in common neurodegenerative conditions. The aim of this study was to quantify torpedoes Parkinson's disease (PD) and Alzheimer's disease (AD) compared with ET and control brains. Brains included 40 ET cases (34 cerebellar ET, 6 Lewy body variant of ET) and age-matched comparison brains (21 AD, 14 PD/diffuse Lewy body disease, 25 controls). Torpedoes were counted in 20 X 25 mm cerebellar cortical sections stained with Luxol Fast Blue/Hematoxylin and Eosin. The median number of torpedoes in cerebellar ET (12) was 12× higher than that of controls (1) and nearly 2.5× higher than in AD (5) or PD/ DLBD (5) (all P < 0.005). Furthermore, in a logistic regression model that adjusted for age and Alzheimer's-type changes, each torpedo more than doubled the odds of having cerebellar ET (Odds ratio
<sub>cerebellar</sub>
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<sub>vs</sub>
. control =
<sup>2</sup>
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<sup>57</sup>
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<sup>P</sup>
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<s0>Sistema nervioso patología</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Encéphale</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Encephalon</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Encéfalo</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Cervelet</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Cerebellum</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Cerebelo</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Anatomopathologie</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Anatomic pathology</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Anatomía patológica</s0>
<s5>11</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Pathologie de l'encéphale</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Syndrome extrapyramidal</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Pathologie du système nerveux central</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Mouvement involontaire</s0>
<s5>42</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Involuntary movement</s0>
<s5>42</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Système nerveux central</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Central nervous system</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Sistema nervioso central</s0>
<s5>44</s5>
</fC07>
<fN21>
<s1>278</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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