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Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

Identifieur interne : 000A60 ( Ncbi/Merge ); précédent : 000A59; suivant : 000A61

Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

Auteurs : A. C. Ludolph [Allemagne] ; J. Kassubek [Allemagne] ; B. G. Landwehrmeyer [Allemagne] ; E. Mandelkow [Allemagne] ; E.-M. Mandelkow [Allemagne] ; D. J. Burn [Royaume-Uni] ; D. Caparros-Lefebvre [France] ; K. A. Frey [États-Unis] ; J. G. De Yebenes [Espagne] ; T. Gasser [Allemagne] ; P. Heutink [Pays-Bas] ; G. Höglinger [Allemagne] ; Z. Jamrozik [Pologne] ; K. A. Jellinger [Autriche] ; A. Kazantsev [États-Unis] ; H. Kretzschmar [Allemagne] ; A. E. Lang [Canada] ; I. Litvan [États-Unis] ; J. J. Lucas [Espagne] ; P. L. Mcgeer [Canada] ; S. Melquist [États-Unis] ; W. Oertel [Allemagne] ; M. Otto [Allemagne] ; D. Paviour [Royaume-Uni] ; T. Reum [Allemagne] ; A. Saint-Raymond [Royaume-Uni] ; J. C. Steele ; M. Tolnay [Suisse] ; H. Tumani [Allemagne] ; J. C. Van Swieten [Pays-Bas] ; M. T. Vanier [France] ; J.-P. Vonsattel [États-Unis] ; S. Wagner [Allemagne] ; Z. K. Wszolek [États-Unis]

Source :

RBID : PMC:2847416

Abstract

Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments within the central nervous system. These pathologic characteristics suggest shared pathogenetic pathways and possible molecular targets for disease-modifying therapeutic interventions. Natural history studies, for instance, in progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17, corticobasal degeneration, and Niemann-Pick disease type C as well as in amyotrophic lateral sclerosis/Parkinson–dementia complex permit clinical characterization of the disease phenotypes and are crucial to the development and validation of biological markers for differential diagnostics and disease monitoring, for example, by use of neuroimaging or proteomic approaches. The wide pathologic and clinical spectrum of the tauopathies with parkinsonism is reviewed in this article, and perspectives on future advances in the understanding of the pathogenesis are given, together with potential therapeutic strategies.


Url:
DOI: 10.1111/j.1468-1331.2008.02513.x
PubMed: 19364361
PubMed Central: 2847416

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<name sortKey="Otto, M" sort="Otto, M" uniqKey="Otto M" first="M." last="Otto">M. Otto</name>
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<nlm:aff id="A1">Department of Neurology, University of Ulm, Ulm, Germany</nlm:aff>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurology, University of Ulm, Ulm</wicri:regionArea>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
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<region type="country">Angleterre</region>
</placeName>
<wicri:cityArea>National Hospital for Neurology, Dementia Research Centre, London</wicri:cityArea>
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<name sortKey="Reum, T" sort="Reum, T" uniqKey="Reum T" first="T." last="Reum">T. Reum</name>
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<name sortKey="Saint Raymond, A" sort="Saint Raymond, A" uniqKey="Saint Raymond A" first="A." last="Saint-Raymond">A. Saint-Raymond</name>
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<region type="country">Angleterre</region>
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<nlm:aff id="A24">University Hospital Rotterdam, Department of Neurology, Erasmus MC, Dr Molewaterplein, GD Rotterdam, the Netherlands</nlm:aff>
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<name sortKey="Wszolek, Z K" sort="Wszolek, Z K" uniqKey="Wszolek Z" first="Z. K." last="Wszolek">Z. K. Wszolek</name>
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<title level="j">European journal of neurology : the official journal of the European Federation of Neurological Societies</title>
<idno type="ISSN">1351-5101</idno>
<idno type="eISSN">1468-1331</idno>
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<div type="abstract" xml:lang="en">
<p id="P2">Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments within the central nervous system. These pathologic characteristics suggest shared pathogenetic pathways and possible molecular targets for disease-modifying therapeutic interventions. Natural history studies, for instance, in progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17, corticobasal degeneration, and Niemann-Pick disease type C as well as in amyotrophic lateral sclerosis/Parkinson–dementia complex permit clinical characterization of the disease phenotypes and are crucial to the development and validation of biological markers for differential diagnostics and disease monitoring, for example, by use of neuroimaging or proteomic approaches. The wide pathologic and clinical spectrum of the tauopathies with parkinsonism is reviewed in this article, and perspectives on future advances in the understanding of the pathogenesis are given, together with potential therapeutic strategies.</p>
</div>
</front>
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<journal-id journal-id-type="nlm-ta">Eur J Neurol</journal-id>
<journal-title>European journal of neurology : the official journal of the European Federation of Neurological Societies</journal-title>
<issn pub-type="ppub">1351-5101</issn>
<issn pub-type="epub">1468-1331</issn>
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<title-group>
<article-title>Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Ludolph</surname>
<given-names>A. C.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
<xref ref-type="author-notes" rid="FN1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kassubek</surname>
<given-names>J.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
<xref ref-type="author-notes" rid="FN1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Landwehrmeyer</surname>
<given-names>B. G.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
<xref ref-type="author-notes" rid="FN1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mandelkow</surname>
<given-names>E.</given-names>
</name>
<xref ref-type="aff" rid="A2">b</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mandelkow</surname>
<given-names>E.-M.</given-names>
</name>
<xref ref-type="aff" rid="A2">b</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Burn</surname>
<given-names>D. J.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Caparros-Lefebvre</surname>
<given-names>D.</given-names>
</name>
<xref ref-type="aff" rid="A4">d</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Frey</surname>
<given-names>K. A.</given-names>
</name>
<xref ref-type="aff" rid="A5">e</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>de Yebenes</surname>
<given-names>J. G.</given-names>
</name>
<xref ref-type="aff" rid="A6">f</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gasser</surname>
<given-names>T.</given-names>
</name>
<xref ref-type="aff" rid="A7">g</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Heutink</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="A8">h</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Höglinger</surname>
<given-names>G.</given-names>
</name>
<xref ref-type="aff" rid="A9">i</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jamrozik</surname>
<given-names>Z.</given-names>
</name>
<xref ref-type="aff" rid="A10">j</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jellinger</surname>
<given-names>K. A.</given-names>
</name>
<xref ref-type="aff" rid="A11">k</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kazantsev</surname>
<given-names>A.</given-names>
</name>
<xref ref-type="aff" rid="A12">l</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kretzschmar</surname>
<given-names>H.</given-names>
</name>
<xref ref-type="aff" rid="A13">m</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lang</surname>
<given-names>A. E.</given-names>
</name>
<xref ref-type="aff" rid="A14">n</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Litvan</surname>
<given-names>I.</given-names>
</name>
<xref ref-type="aff" rid="A15">o</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lucas</surname>
<given-names>J. J.</given-names>
</name>
<xref ref-type="aff" rid="A16">p</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>McGeer</surname>
<given-names>P. L.</given-names>
</name>
<xref ref-type="aff" rid="A17">q</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Melquist</surname>
<given-names>S.</given-names>
</name>
<xref ref-type="aff" rid="A18">r</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Oertel</surname>
<given-names>W.</given-names>
</name>
<xref ref-type="aff" rid="A9">i</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Otto</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Paviour</surname>
<given-names>D.</given-names>
</name>
<xref ref-type="aff" rid="A19">s</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Reum</surname>
<given-names>T.</given-names>
</name>
<xref ref-type="aff" rid="A20">t</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Saint-Raymond</surname>
<given-names>A.</given-names>
</name>
<xref ref-type="aff" rid="A21">u</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Steele</surname>
<given-names>J. C.</given-names>
</name>
<xref ref-type="aff" rid="A22">v</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tolnay</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="A23">w</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tumani</surname>
<given-names>H.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>van Swieten</surname>
<given-names>J. C.</given-names>
</name>
<xref ref-type="aff" rid="A24">x</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Vanier</surname>
<given-names>M. T.</given-names>
</name>
<xref ref-type="aff" rid="A25">y</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Vonsattel</surname>
<given-names>J.-P.</given-names>
</name>
<xref ref-type="aff" rid="A26">z</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wagner</surname>
<given-names>S.</given-names>
</name>
<xref ref-type="aff" rid="A27">aa</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wszolek</surname>
<given-names>Z. K.</given-names>
</name>
<xref ref-type="aff" rid="A28">bb</xref>
<xref ref-type="author-notes" rid="FN1">*</xref>
</contrib>
<contrib contrib-type="author">
<collab>for the Reisensburg Working Group for Tauopathies With Parkinsonism</collab>
</contrib>
</contrib-group>
<aff id="A1">
<label>a</label>
Department of Neurology, University of Ulm, Ulm, Germany</aff>
<aff id="A2">
<label>b</label>
Max Planck Unit for Structural Molecular Biology, c/o DESY, Notkestr, Hamburg, Germany</aff>
<aff id="A3">
<label>c</label>
Institute for Ageing and Health, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK</aff>
<aff id="A4">
<label>d</label>
Centre Hospitalier de Valenciennes, Résidence du Val d'Escaut, Avenue Desandrouin, Valenciennes, France</aff>
<aff id="A5">
<label>e</label>
University of Michigan Medical Center, 1500 E Medical Center Dr, Ann Arbor, MI, USA</aff>
<aff id="A6">
<label>f</label>
Hospital Ramon y Cajal, Neurology, Carretera Colmenar, Madrid, Spain</aff>
<aff id="A7">
<label>g</label>
Universitätsklinikum Tübingen, Zentrum für Neurologie, Hoppe-Seyler-Strasse, Tübingen, Germany</aff>
<aff id="A8">
<label>h</label>
VU University Medical Center, Department of Clinical Genetics and Anthropogenet, van der Boechorststraat, Amsterdam, the Netherlands</aff>
<aff id="A9">
<label>i</label>
Philipps-Universität, Neurologie, Rudolf-Bultmann-Strasse, Marburg, Germany</aff>
<aff id="A10">
<label>j</label>
Medical University of Warsaw, Neurology, Banacha, Warsaw, Poland</aff>
<aff id="A11">
<label>k</label>
Institute of Clinical Neurobiology, Kenyongasse, Vienna, Austria</aff>
<aff id="A12">
<label>l</label>
Massachusetts General Hospital, MIND/Harvard Medical School, Charlestown, MA, USA</aff>
<aff id="A13">
<label>m</label>
Institut für Neuropathologie, BrainNet (German Brain Bank), Feodor-Lynen-Strasse, Munich, Germany</aff>
<aff id="A14">
<label>n</label>
Toronto Western Hospital, Movement Disorders Center, Toronto, ON, Canada</aff>
<aff id="A15">
<label>o</label>
University of Louisville, School of Medicine/Department of Neurology, Louisville, KY, USA</aff>
<aff id="A16">
<label>p</label>
Centro de Biologica Molecular “Severo Ochoa,” Universidad Autonoma de Madrid and CiberNed, Cantoblanco, Madrid, Spain</aff>
<aff id="A17">
<label>q</label>
University of British Columbia, Kinsmen Laboratory of Neurological Research, Vancouver, BC, Canada</aff>
<aff id="A18">
<label>r</label>
Mayo Clinic, Department of Neuroscience, Jacksonville, FL, USA</aff>
<aff id="A19">
<label>s</label>
National Hospital for Neurology, Dementia Research Centre, London, England</aff>
<aff id="A20">
<label>t</label>
Bundesinstitut für Arzneimittel & Medizinprodukte, Wissenschaftlicher Service/Klinische Prüfungen, Georg-Kiesinger-Allee, Bonn, Germany</aff>
<aff id="A21">
<label>u</label>
European Medicines Agency (EMEA), Scientific Advice and Orphan Drugs Sector, 7 Westferry Circus, Canary Wharf, London, England</aff>
<aff id="A22">
<label>v</label>
Guam Memorial Hospital, Neurology, Carlos Camacho Way, Tamuning, Guam</aff>
<aff id="A23">
<label>w</label>
Institut für Pathologie, Schönbeinstrasse, Basel, Switzerland</aff>
<aff id="A24">
<label>x</label>
University Hospital Rotterdam, Department of Neurology, Erasmus MC, Dr Molewaterplein, GD Rotterdam, the Netherlands</aff>
<aff id="A25">
<label>y</label>
Institut National de la Santé et de la Recherche Médicale, Unit 820, Laeënnec Medical School, Lyon, France</aff>
<aff id="A26">
<label>z</label>
New York Brain Bank, Columbia University, Pathology, Babies Hospital, New York, NY, USA</aff>
<aff id="A27">
<label>aa</label>
Deutsche PSP-Gesellschaft e.V. (PSP Germany), c/o S. Wagner, Könneritzstrasse, Leipzig, Germany</aff>
<aff id="A28">
<label>bb</label>
Mayo Clinic, Department of Neurology, Jacksonville, FL, USA</aff>
<author-notes>
<corresp id="CR1">Correspondence: Prof Dr Albert C. Ludolph, Department of Neurology, University of Ulm, Oberer Eselsberg 45, 89081 Ulm, Germany (tel.: +49 731 1771200; fax: +49 731 1771202; e-mail:
<email>albert.ludolph@rku.de</email>
.).</corresp>
<fn id="FN1" fn-type="equal">
<label>*</label>
<p id="P1">These authors contributed equally to the work.</p>
</fn>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>21</day>
<month>5</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="ppub">
<month>3</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>30</day>
<month>3</month>
<year>2010</year>
</pub-date>
<volume>16</volume>
<issue>3</issue>
<fpage>297</fpage>
<lpage>309</lpage>
<permissions>
<copyright-statement>© 2009 EFNS</copyright-statement>
<copyright-year>2009</copyright-year>
</permissions>
<abstract>
<p id="P2">Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments within the central nervous system. These pathologic characteristics suggest shared pathogenetic pathways and possible molecular targets for disease-modifying therapeutic interventions. Natural history studies, for instance, in progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17, corticobasal degeneration, and Niemann-Pick disease type C as well as in amyotrophic lateral sclerosis/Parkinson–dementia complex permit clinical characterization of the disease phenotypes and are crucial to the development and validation of biological markers for differential diagnostics and disease monitoring, for example, by use of neuroimaging or proteomic approaches. The wide pathologic and clinical spectrum of the tauopathies with parkinsonism is reviewed in this article, and perspectives on future advances in the understanding of the pathogenesis are given, together with potential therapeutic strategies.</p>
</abstract>
<kwd-group>
<kwd>corticobasal degeneration</kwd>
<kwd>frontotemporal dementia with parkinsonism linked to chromosome 17</kwd>
<kwd>microtubule-associated protein tau, multiple system atrophy</kwd>
<kwd>Parkinson disease</kwd>
<kwd>parkinsonism</kwd>
<kwd>progressive supranuclear palsy</kwd>
<kwd>tauopathies</kwd>
</kwd-group>
<contract-num rid="AG1">P50 AG008702-11A19002 ||AG</contract-num>
<contract-sponsor id="AG1">National Institute on Aging : NIA</contract-sponsor>
</article-meta>
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<name sortKey="Mcgeer, P L" sort="Mcgeer, P L" uniqKey="Mcgeer P" first="P. L." last="Mcgeer">P. L. Mcgeer</name>
</country>
<country name="Suisse">
<noRegion>
<name sortKey="Tolnay, M" sort="Tolnay, M" uniqKey="Tolnay M" first="M." last="Tolnay">M. Tolnay</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Canada/explor/ParkinsonCanadaV1/Data/Ncbi/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000A60 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 000A60 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Canada
   |area=    ParkinsonCanadaV1
   |flux=    Ncbi
   |étape=   Merge
   |type=    RBID
   |clé=     PMC:2847416
   |texte=   Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i   -Sk "pubmed:19364361" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd   \
       | NlmPubMed2Wicri -a ParkinsonCanadaV1 

Wicri

This area was generated with Dilib version V0.6.29.
Data generation: Thu May 4 22:20:19 2017. Site generation: Fri Dec 23 23:17:26 2022