La maladie de Parkinson au Canada (serveur d'exploration)

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Correlates of Excessive Daytime Sleepiness in De Novo Parkinson's Disease: A Case Control Study

Identifieur interne : 000845 ( Pmc/Curation ); précédent : 000844; suivant : 000846

Correlates of Excessive Daytime Sleepiness in De Novo Parkinson's Disease: A Case Control Study

Auteurs : Tanya Simuni [États-Unis] ; Chelsea Caspell-Garcia [États-Unis] ; Christopher Coffey [États-Unis] ; Lama M. Chahine [États-Unis] ; Shirley Lasch [États-Unis] ; Wolfgang H. Oertel [Allemagne] ; Geert Mayer ; Birgit Högl [Autriche] ; Ron Postuma [Canada] ; Aleksandar Videnovic [États-Unis] ; Amy Willis Amara [États-Unis] ; Ken Marek [États-Unis]

Source :

RBID : PMC:4822999

Abstract

Objective

This study was undertaken to determine the frequency and correlates of excessive daytime sleepiness in de novo, untreated Parkinson's disease (PD) patients compared with the matched healthy controls.

Methods

Data were obtained from the Parkinson's Progression Markers Initiative, an international study of de novo, untreated PD patients and healthy controls. At baseline, participants were assessed with a wide range of motor and nonmotor scales, including the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS). Excessive daytime sleepiness was assessed based on the Epworth Sleepiness scale (ESS), with a cutoff of 10.

Results

Four hundred twenty-three PD subjects and 196 healthy controls were recruited into the study. Mean ESS (min, max) score was 5.8 (0, 20) for the PD subjects and 5.6 (0, 19) for healthy controls (P = 0.54). Sixty-six (15.6%) PD subjects and 24 (12%) healthy controls had ESS of at least 10 (P = 0.28). No difference was seen in demographic characteristics, age of onset, disease duration, PD subtype, cognitive status, or utilization of sedatives between the PD sleepiness-positive versus the negative group. The sleepiness-positive group had higher MDS-UPDRS Part I and II but not III scores, and higher depression and autonomic dysfunction scores. Sleepiness was associated with a marginal reduction of A-beta (P = 0.05) but not alpha-synuclein spinal fluid levels in PD.

Conclusions

This largest case control study demonstrates no difference in prevalence of excessive sleepiness in subjects with de novo untreated PD compared with healthy controls. The only clinical correlates of sleepiness were mood and autonomic dysfunction. Ongoing longitudinal analyses will be essential to further examine clinical and biological correlates of sleepiness in PD and specifically the role of dopaminergic therapy.


Url:
DOI: 10.1002/mds.26248
PubMed: 26095202
PubMed Central: 4822999

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PMC:4822999

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Geert Mayer
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<title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<sec id="S1">
<title>Objective</title>
<p id="P1">This study was undertaken to determine the frequency and correlates of excessive daytime sleepiness in de novo, untreated Parkinson's disease (PD) patients compared with the matched healthy controls.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Data were obtained from the Parkinson's Progression Markers Initiative, an international study of de novo, untreated PD patients and healthy controls. At baseline, participants were assessed with a wide range of motor and nonmotor scales, including the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS). Excessive daytime sleepiness was assessed based on the Epworth Sleepiness scale (ESS), with a cutoff of 10.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Four hundred twenty-three PD subjects and 196 healthy controls were recruited into the study. Mean ESS (min, max) score was 5.8 (0, 20) for the PD subjects and 5.6 (0, 19) for healthy controls (
<italic>P</italic>
= 0.54). Sixty-six (15.6%) PD subjects and 24 (12%) healthy controls had ESS of at least 10 (
<italic>P</italic>
= 0.28). No difference was seen in demographic characteristics, age of onset, disease duration, PD subtype, cognitive status, or utilization of sedatives between the PD sleepiness-positive versus the negative group. The sleepiness-positive group had higher MDS-UPDRS Part I and II but not III scores, and higher depression and autonomic dysfunction scores. Sleepiness was associated with a marginal reduction of A-beta (
<italic>P</italic>
= 0.05) but not alpha-synuclein spinal fluid levels in PD.</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">This largest case control study demonstrates no difference in prevalence of excessive sleepiness in subjects with de novo untreated PD compared with healthy controls. The only clinical correlates of sleepiness were mood and autonomic dysfunction. Ongoing longitudinal analyses will be essential to further examine clinical and biological correlates of sleepiness in PD and specifically the role of dopaminergic therapy.</p>
</sec>
</div>
</front>
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<journal-id journal-id-type="nlm-journal-id">8610688</journal-id>
<journal-id journal-id-type="pubmed-jr-id">5937</journal-id>
<journal-id journal-id-type="nlm-ta">Mov Disord</journal-id>
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<article-title>Correlates of Excessive Daytime Sleepiness in De Novo Parkinson's Disease: A Case Control Study</article-title>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Simuni</surname>
<given-names>Tanya</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A1">1</xref>
<xref rid="FN1" ref-type="author-notes">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Caspell-Garcia</surname>
<given-names>Chelsea</given-names>
</name>
<degrees>MS</degrees>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Coffey</surname>
<given-names>Christopher</given-names>
</name>
<degrees>PhD</degrees>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chahine</surname>
<given-names>Lama M.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lasch</surname>
<given-names>Shirley</given-names>
</name>
<degrees>MBA</degrees>
<xref ref-type="aff" rid="A4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Oertel</surname>
<given-names>Wolfgang H.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mayer</surname>
<given-names>Geert</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A6">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Högl</surname>
<given-names>Birgit</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A7">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Postuma</surname>
<given-names>Ron</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Videnovic</surname>
<given-names>Aleksandar</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Amara</surname>
<given-names>Amy Willis</given-names>
</name>
<degrees>MD, PhD</degrees>
<xref ref-type="aff" rid="A10">10</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Marek</surname>
<given-names>Ken</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A4">4</xref>
</contrib>
<on-behalf-of>for the PPMI Sleep Working group on behalf of the PPMI Investigators</on-behalf-of>
</contrib-group>
<aff id="A1">
<label>1</label>
Northwestern University Feinberg School of Medicine, Chicago, IL, USA</aff>
<aff id="A2">
<label>2</label>
The University of Iowa, Iowa City, IA, USA</aff>
<aff id="A3">
<label>3</label>
The University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA</aff>
<aff id="A4">
<label>4</label>
Institute for Neurodegenerative Disorders, New Haven, CT, USA</aff>
<aff id="A5">
<label>5</label>
Charitable Hertie Foundation, Frankfurt/Main, Germany</aff>
<aff id="A6">
<label>6</label>
Hephata-Klinik, Hephata Hessisches Diakoniezentrum e. V</aff>
<aff id="A7">
<label>7</label>
Innsbruck Medical University, Innsbruck, Austria</aff>
<aff id="A8">
<label>8</label>
McGill University, Montréal, Québec, Canada</aff>
<aff id="A9">
<label>9</label>
Massachusetts General Hospital, Boston, MA, USA</aff>
<aff id="A10">
<label>10</label>
UAB School of Medicine, Birmingham, AL, USA</aff>
<author-notes>
<corresp id="FN1">
<label>*</label>
Correspondence to: Dr. Tanya Simuni, MD, Department of Neurology, Northwestern University Feinberg School of Medicine, 710 North Lake Shore Drive, 1126, Chicago, IL 60611,
<email>tsimuni@nmff.org</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>1</day>
<month>4</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>11</day>
<month>6</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="ppub">
<month>9</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>01</day>
<month>9</month>
<year>2016</year>
</pub-date>
<volume>30</volume>
<issue>10</issue>
<fpage>1371</fpage>
<lpage>1381</lpage>
<pmc-comment>elocation-id from pubmed: 10.1002/mds.26248</pmc-comment>
<abstract>
<sec id="S1">
<title>Objective</title>
<p id="P1">This study was undertaken to determine the frequency and correlates of excessive daytime sleepiness in de novo, untreated Parkinson's disease (PD) patients compared with the matched healthy controls.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Data were obtained from the Parkinson's Progression Markers Initiative, an international study of de novo, untreated PD patients and healthy controls. At baseline, participants were assessed with a wide range of motor and nonmotor scales, including the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS). Excessive daytime sleepiness was assessed based on the Epworth Sleepiness scale (ESS), with a cutoff of 10.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Four hundred twenty-three PD subjects and 196 healthy controls were recruited into the study. Mean ESS (min, max) score was 5.8 (0, 20) for the PD subjects and 5.6 (0, 19) for healthy controls (
<italic>P</italic>
= 0.54). Sixty-six (15.6%) PD subjects and 24 (12%) healthy controls had ESS of at least 10 (
<italic>P</italic>
= 0.28). No difference was seen in demographic characteristics, age of onset, disease duration, PD subtype, cognitive status, or utilization of sedatives between the PD sleepiness-positive versus the negative group. The sleepiness-positive group had higher MDS-UPDRS Part I and II but not III scores, and higher depression and autonomic dysfunction scores. Sleepiness was associated with a marginal reduction of A-beta (
<italic>P</italic>
= 0.05) but not alpha-synuclein spinal fluid levels in PD.</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">This largest case control study demonstrates no difference in prevalence of excessive sleepiness in subjects with de novo untreated PD compared with healthy controls. The only clinical correlates of sleepiness were mood and autonomic dysfunction. Ongoing longitudinal analyses will be essential to further examine clinical and biological correlates of sleepiness in PD and specifically the role of dopaminergic therapy.</p>
</sec>
</abstract>
<kwd-group>
<kwd>Parkinson's disease</kwd>
<kwd>daytime somnolence</kwd>
<kwd>biomarkers</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

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