Mild Parkinsonian Signs are Associated with Lower Olfactory Test Scores in the Community-dwelling Elderly
Identifieur interne : 000023 ( Pmc/Curation ); précédent : 000022; suivant : 000024Mild Parkinsonian Signs are Associated with Lower Olfactory Test Scores in the Community-dwelling Elderly
Auteurs : Elan D. Louis [États-Unis] ; Karen Marder [États-Unis] ; Matthias H. Tabert [États-Unis] ; D. P. Devanand [États-Unis]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2008.
Abstract
Mild Parkinsonian signs (MPS, impaired gait, rigidity, bradykinesia, rest tremor) are commonly found during the clinical examination of older people and may be a precursor to Parkinson’s disease (PD) or Alzheimer’s disease (AD). Marked deficits in olfaction occur in PD and AD.
To determine whether University of Pennsylvania Smell Test (UPSIT) scores were lower in non-demented community-dwelling elderly with vs. without MPS.
Non-demented persons age ≥65 years without PD in Washington Heights-Inwood, NY were evaluated with an abbreviated motor Unified Parkinson’s Disease Rating Scale and a 40-item UPSIT. Lower UPSIT and higher transformed UPSIT score (square root [UPSIT — 41]) indicated greater olfactory dysfunction.
One-hundred-seventy-seven (16.4%) of 1,078 participants had MPS. Mean UPSIT scores (MPS vs. without MPS) were 24.3±7.1 vs. 26.4±6.8, p< 0.001. In a logistic regression analysis adjusting for age and education, transformed UPSIT score was associated with MPS (OR 1.25, 95% CI 1.04 – 1.52, p = 0.02). In an adjusted logistic regression analysis, participants with higher transformed UPSIT scores (based on a median split) were 1.55 times more likely to have MPS than were those with lower scores (p = 0.01). Within transformed UPSIT score quartiles, the odds of having MPS were 1.0 (reference), 1.35, 2.02, and 2.20 (p < 0.05). The association with transformed UPSIT scores was similar across MPS sub-types (axial dysfunction, rigidity, tremor).
MPS were associated with a mild reduction in olfactory function. These observations further support the view of MPS as a marker of emerging degenerative brain pathologies.
Url:
DOI: 10.1002/mds.21777
PubMed: 18098296
PubMed Central: 2679986
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
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<front><div type="abstract" xml:lang="en"><sec id="S1"><title>Background</title>
<p id="P1">Mild Parkinsonian signs (MPS, impaired gait, rigidity, bradykinesia, rest tremor) are commonly found during the clinical examination of older people and may be a precursor to Parkinson’s disease (PD) or Alzheimer’s disease (AD). Marked deficits in olfaction occur in PD and AD.</p>
</sec>
<sec id="S2"><title>Objective</title>
<p id="P2">To determine whether University of Pennsylvania Smell Test (UPSIT) scores were lower in non-demented community-dwelling elderly with vs. without MPS.</p>
</sec>
<sec sec-type="methods" id="S3"><title>Methods</title>
<p id="P3">Non-demented persons age ≥65 years without PD in Washington Heights-Inwood, NY were evaluated with an abbreviated motor Unified Parkinson’s Disease Rating Scale and a 40-item UPSIT. Lower UPSIT and higher transformed UPSIT score (square root [UPSIT — 41]) indicated greater olfactory dysfunction.</p>
</sec>
<sec id="S4"><title>Results</title>
<p id="P4">One-hundred-seventy-seven (16.4%) of 1,078 participants had MPS. Mean UPSIT scores (MPS vs. without MPS) were 24.3±7.1 vs. 26.4±6.8, p< 0.001. In a logistic regression analysis adjusting for age and education, transformed UPSIT score was associated with MPS (OR 1.25, 95% CI 1.04 – 1.52, p = 0.02). In an adjusted logistic regression analysis, participants with higher transformed UPSIT scores (based on a median split) were 1.55 times more likely to have MPS than were those with lower scores (p = 0.01). Within transformed UPSIT score quartiles, the odds of having MPS were 1.0 (reference), 1.35, 2.02, and 2.20 (p < 0.05). The association with transformed UPSIT scores was similar across MPS sub-types (axial dysfunction, rigidity, tremor).</p>
</sec>
<sec id="S5"><title>Conclusions</title>
<p id="P5">MPS were associated with a mild reduction in olfactory function. These observations further support the view of MPS as a marker of emerging degenerative brain pathologies.</p>
</sec>
</div>
</front>
</TEI>
<pmc article-type="research-article" xml:lang="EN"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front><journal-meta><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>
<journal-title>Movement disorders : official journal of the Movement Disorder Society</journal-title>
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<article-id pub-id-type="doi">10.1002/mds.21777</article-id>
<article-id pub-id-type="manuscript">NIHMS112686</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Mild Parkinsonian Signs are Associated with Lower Olfactory Test Scores in the Community-dwelling Elderly</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Louis</surname>
<given-names>Elan D.</given-names>
</name>
<degrees>MD, MSc</degrees>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A2">2</xref>
<xref ref-type="aff" rid="A3">3</xref>
<xref ref-type="aff" rid="A6">6</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Marder</surname>
<given-names>Karen</given-names>
</name>
<degrees>MD, MPH</degrees>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A2">2</xref>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Tabert</surname>
<given-names>Matthias H.</given-names>
</name>
<degrees>PhD</degrees>
<xref ref-type="aff" rid="A4">4</xref>
<xref ref-type="aff" rid="A7">7</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Devanand</surname>
<given-names>D. P.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="A5">5</xref>
<xref ref-type="aff" rid="A7">7</xref>
</contrib>
</contrib-group>
<aff id="A1"><label>1</label>
The Gertrude H. Sergievsky Center, College of Physicians and Surgeons, Columbia University, New York, N.Y., U.S.A.</aff>
<aff id="A2"><label>2</label>
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, N.Y., U.S.A.</aff>
<aff id="A3"><label>3</label>
Taub Institute for Research of Alzheimer’s Disease and the Aging Brain, College of Physicians and Surgeons, Columbia University, New York, N.Y., U.S.A.</aff>
<aff id="A4"><label>4</label>
Department of Geriatric Psychiatry, College of Physicians and Surgeons, Columbia University, New York, N.Y., U.S.A.</aff>
<aff id="A5"><label>5</label>
Department of Biological Psychiatry, College of Physicians and Surgeons, Columbia University, New York, N.Y., U.S.A.</aff>
<aff id="A6"><label>6</label>
Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, N.Y., U.S.A.</aff>
<aff id="A7"><label>7</label>
New York State Psychiatric Institute, New York, N.Y., U.S.A.</aff>
<author-notes><corresp id="CR1"><bold>Correspondence:</bold>
Dr. Elan Louis, Unit 198, Neurological Institute, 710 West 168th Street, New York, NY, 10032, USA. Tel: (212) 305 - 9194, FAX: (212) 305 -1304, Email: <email>EDL2@columbia.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted"><day>24</day>
<month>4</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="ppub"><day>15</day>
<month>3</month>
<year>2008</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>11</day>
<month>5</month>
<year>2009</year>
</pub-date>
<volume>23</volume>
<issue>4</issue>
<fpage>524</fpage>
<lpage>530</lpage>
<abstract><sec id="S1"><title>Background</title>
<p id="P1">Mild Parkinsonian signs (MPS, impaired gait, rigidity, bradykinesia, rest tremor) are commonly found during the clinical examination of older people and may be a precursor to Parkinson’s disease (PD) or Alzheimer’s disease (AD). Marked deficits in olfaction occur in PD and AD.</p>
</sec>
<sec id="S2"><title>Objective</title>
<p id="P2">To determine whether University of Pennsylvania Smell Test (UPSIT) scores were lower in non-demented community-dwelling elderly with vs. without MPS.</p>
</sec>
<sec sec-type="methods" id="S3"><title>Methods</title>
<p id="P3">Non-demented persons age ≥65 years without PD in Washington Heights-Inwood, NY were evaluated with an abbreviated motor Unified Parkinson’s Disease Rating Scale and a 40-item UPSIT. Lower UPSIT and higher transformed UPSIT score (square root [UPSIT — 41]) indicated greater olfactory dysfunction.</p>
</sec>
<sec id="S4"><title>Results</title>
<p id="P4">One-hundred-seventy-seven (16.4%) of 1,078 participants had MPS. Mean UPSIT scores (MPS vs. without MPS) were 24.3±7.1 vs. 26.4±6.8, p< 0.001. In a logistic regression analysis adjusting for age and education, transformed UPSIT score was associated with MPS (OR 1.25, 95% CI 1.04 – 1.52, p = 0.02). In an adjusted logistic regression analysis, participants with higher transformed UPSIT scores (based on a median split) were 1.55 times more likely to have MPS than were those with lower scores (p = 0.01). Within transformed UPSIT score quartiles, the odds of having MPS were 1.0 (reference), 1.35, 2.02, and 2.20 (p < 0.05). The association with transformed UPSIT scores was similar across MPS sub-types (axial dysfunction, rigidity, tremor).</p>
</sec>
<sec id="S5"><title>Conclusions</title>
<p id="P5">MPS were associated with a mild reduction in olfactory function. These observations further support the view of MPS as a marker of emerging degenerative brain pathologies.</p>
</sec>
</abstract>
<kwd-group><kwd>Mild parkinsonian signs</kwd>
<kwd>olfaction</kwd>
<kwd>elderly</kwd>
<kwd>population</kwd>
<kwd>epidemiology</kwd>
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<contract-num rid="NS1">R01 NS042859-05</contract-num>
<contract-num rid="NS1">R01 NS042859-04</contract-num>
<contract-num rid="NS1">R01 NS042859-03</contract-num>
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<contract-num rid="AG1">P01 AG007232-190010</contract-num>
<contract-num rid="AG1">P01 AG007232-180010</contract-num>
<contract-num rid="AG1">P01 AG007232-170010</contract-num>
<contract-num rid="AG1">P01 AG007232-160010</contract-num>
<contract-sponsor id="NS1">National Institute of Neurological Disorders and Stroke : NINDS</contract-sponsor>
<contract-sponsor id="AG1">National Institute on Aging : NIA</contract-sponsor>
</article-meta>
</front>
</pmc>
</record>
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