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Cognitive Function, Gait Speed Decline, and Comorbidities: The Health, Aging and Body Composition Study

Identifieur interne : 002343 ( Main/Corpus ); précédent : 002342; suivant : 002344

Cognitive Function, Gait Speed Decline, and Comorbidities: The Health, Aging and Body Composition Study

Auteurs : Hal H. Atkinson ; Caterina Rosano ; Eleanor M. Simonsick ; Jeff D. Williamson ; Cralen Davis ; Walter T. Ambrosius ; Stephen R. Rapp ; Matteo Cesari ; Anne B. Newman ; Tamara B. Harris ; Susan M. Rubin ; Kristine Yaffe ; Suzanne Satterfield ; Stephen B. Kritchevsky

Source :

RBID : ISTEX:6194D16518EA16C6D2F85E7B696D498D0097DDD2

Abstract

Background. Emerging evidence indicates an association between cognitive function and physical performance in late life. This study examines the relationship between cognitive function and subsequent gait speed decline among high-functioning older adults. Methods. Measures of global cognitive function (Modified Mini Mental State Examination [3MS]) and executive control function (ECF) (a clock drawing task [CLOX 1] and the 15-item Executive Interview [EXIT 15]) were obtained in the Health, Aging, and Body Composition Study in 1999–2000. Gait-speed (meters/second) was assessed over 20 meters at usual pace. Using a mixed model, we assessed the relationship between baseline cognitive function and gait-speed change over 3 years. Results. Two thousand, three hundred forty-nine older adults (mean age 75.6 ± 2.9 years) completed the assessments. After adjustment for baseline gait speed, a 1-standard-deviation (SD) lower performance on each cognitive test was associated with greater gait-speed decline over 3 years: 0.016 m/s for the 3MS (SD = 8.1), 0.009 m/s for CLOX 1 (SD = 2.4), and 0.012 m/s for EXIT 15 (SD = 4.1) (p <.0005 for all). After adjustment for comorbidities, the effect size was attenuated for 3MS and CLOX 1, and the association for EXIT 15 was no longer significant. Depression score was most strongly associated with the EXIT 15 effect reduction. Conclusion. Global and executive cognitive functions predict declines in gait speed. The association of ECF with gait speed decline is attenuated by comorbid conditions, particularly depression. Elucidation of the mechanisms underlying these associations may point to new pathways for the treatment of physical decline associated with diminished cognitive function.

Url:
DOI: 10.1093/gerona/62.8.844

Links to Exploration step

ISTEX:6194D16518EA16C6D2F85E7B696D498D0097DDD2

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<div type="abstract" xml:lang="en">Background. Emerging evidence indicates an association between cognitive function and physical performance in late life. This study examines the relationship between cognitive function and subsequent gait speed decline among high-functioning older adults. Methods. Measures of global cognitive function (Modified Mini Mental State Examination [3MS]) and executive control function (ECF) (a clock drawing task [CLOX 1] and the 15-item Executive Interview [EXIT 15]) were obtained in the Health, Aging, and Body Composition Study in 1999–2000. Gait-speed (meters/second) was assessed over 20 meters at usual pace. Using a mixed model, we assessed the relationship between baseline cognitive function and gait-speed change over 3 years. Results. Two thousand, three hundred forty-nine older adults (mean age 75.6 ± 2.9 years) completed the assessments. After adjustment for baseline gait speed, a 1-standard-deviation (SD) lower performance on each cognitive test was associated with greater gait-speed decline over 3 years: 0.016 m/s for the 3MS (SD = 8.1), 0.009 m/s for CLOX 1 (SD = 2.4), and 0.012 m/s for EXIT 15 (SD = 4.1) (p <.0005 for all). After adjustment for comorbidities, the effect size was attenuated for 3MS and CLOX 1, and the association for EXIT 15 was no longer significant. Depression score was most strongly associated with the EXIT 15 effect reduction. Conclusion. Global and executive cognitive functions predict declines in gait speed. The association of ECF with gait speed decline is attenuated by comorbid conditions, particularly depression. Elucidation of the mechanisms underlying these associations may point to new pathways for the treatment of physical decline associated with diminished cognitive function.</div>
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<surname>Satterfield</surname>
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<affiliation>Department of Preventive Medicine, University of Tennessee College of Medicine, Memphis.</affiliation>
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<forename type="first">Stephen B.</forename>
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<article-title>Cognitive Function, Gait Speed Decline, and Comorbidities: The Health, Aging and Body Composition Study</article-title>
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<contrib contrib-type="author">
<name>
<surname>Atkinson</surname>
<given-names>Hal H.</given-names>
</name>
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<xref rid="COR1"></xref>
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<contrib contrib-type="author">
<name>
<surname>Rosano</surname>
<given-names>Caterina</given-names>
</name>
<xref rid="AFF2"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Simonsick</surname>
<given-names>Eleanor M.</given-names>
</name>
<xref rid="AFF3"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Williamson</surname>
<given-names>Jeff D.</given-names>
</name>
<xref rid="AFF1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Davis</surname>
<given-names>Cralen</given-names>
</name>
<xref rid="AFF4"></xref>
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<contrib contrib-type="author">
<name>
<surname>Ambrosius</surname>
<given-names>Walter T.</given-names>
</name>
<xref rid="AFF4"></xref>
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<contrib contrib-type="author">
<name>
<surname>Rapp</surname>
<given-names>Stephen R.</given-names>
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<contrib contrib-type="author">
<name>
<surname>Cesari</surname>
<given-names>Matteo</given-names>
</name>
<xref rid="AFF6"></xref>
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<contrib contrib-type="author">
<name>
<surname>Newman</surname>
<given-names>Anne B.</given-names>
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<contrib contrib-type="author">
<name>
<surname>Harris</surname>
<given-names>Tamara B.</given-names>
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<surname>Rubin</surname>
<given-names>Susan M.</given-names>
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<given-names>Kristine</given-names>
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<name>
<surname>Kritchevsky</surname>
<given-names>Stephen B.</given-names>
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</contrib>
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<aff id="AFF1">
<label>1</label>
Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Claude D. Pepper Older Americans Independence Center and Roena Kulynych Center for Memory and Cognition Research, Sticht Center on Aging, Wake Forest University School of Medicine, Winston-Salem, North Carolina.</aff>
<aff id="AFF2">
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Department of Medicine, Division of Geriatrics, University of Pittsburgh Institute on Aging, Pennsylvania.</aff>
<aff id="AFF3">
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Intramural Research Program, National Institute on Aging, Baltimore and Bethesda, Maryland.</aff>
<aff>
<target target-type="aff" id="AFF4"></target>
<label>4</label>
Division of Public Health Sciences and
<target target-type="aff" id="AFF5"></target>
<label>5</label>
Department of Psychiatry and Behavioral Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.</aff>
<aff id="AFF6">
<label>6</label>
Department of Geriatrics and Aging Research, University of Florida, Gainesville.</aff>
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<target target-type="aff" id="AFF7"></target>
Departments of
<label>7</label>
Epidemiology and Biostatistics and
<target target-type="aff" id="AFF8"></target>
<label>8</label>
Psychiatry, Neurology and Epidemiology, University of California, San Francisco.</aff>
<aff id="AFF9">
<label>9</label>
Department of Preventive Medicine, University of Tennessee College of Medicine, Memphis.</aff>
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<author-notes>
<corresp id="COR1">Address correspondence to Hal H. Atkinson, MD, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157. E-mail:
<ext-link xlink:href="hatkinso@wfubmc.edu" ext-link-type="email">hatkinso@wfubmc.edu</ext-link>
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<pub-date pub-type="ppub">
<month>8</month>
<year>2007</year>
</pub-date>
<volume>62</volume>
<issue>8</issue>
<fpage>844</fpage>
<lpage>850</lpage>
<history>
<date date-type="accepted">
<day>8</day>
<month>11</month>
<year>2006</year>
</date>
<date date-type="received">
<day>30</day>
<month>6</month>
<year>2006</year>
</date>
</history>
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<copyright-statement>Copyright 2007 by The Gerontological Society of America</copyright-statement>
<copyright-year>2007</copyright-year>
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<p>
<bold>
<italic>Background.</italic>
</bold>
 Emerging evidence indicates an association between cognitive function and physical performance in late life. This study examines the relationship between cognitive function and subsequent gait speed decline among high-functioning older adults.</p>
<p>
<bold>
<italic>Methods.</italic>
</bold>
 Measures of global cognitive function (Modified Mini Mental State Examination [3MS]) and executive control function (ECF) (a clock drawing task [CLOX 1] and the 15-item Executive Interview [EXIT 15]) were obtained in the Health, Aging, and Body Composition Study in 1999–2000. Gait-speed (meters/second) was assessed over 20 meters at usual pace. Using a mixed model, we assessed the relationship between baseline cognitive function and gait-speed change over 3 years.</p>
<p>
<bold>
<italic>Results.</italic>
</bold>
 Two thousand, three hundred forty-nine older adults (mean age 75.6 ± 2.9 years) completed the assessments. After adjustment for baseline gait speed, a 1-standard-deviation (
<italic>SD</italic>
) lower performance on each cognitive test was associated with greater gait-speed decline over 3 years: 0.016 m/s for the 3MS (
<italic>SD</italic>
= 8.1), 0.009 m/s for CLOX 1 (
<italic>SD</italic>
= 2.4), and 0.012 m/s for EXIT 15 (
<italic>SD</italic>
= 4.1) (
<italic>p</italic>
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<p>
<bold>
<italic>Conclusion.</italic>
</bold>
Global and executive cognitive functions predict declines in gait speed. The association of ECF with gait speed decline is attenuated by comorbid conditions, particularly depression. Elucidation of the mechanisms underlying these associations may point to new pathways for the treatment of physical decline associated with diminished cognitive function.</p>
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