Cerebral White Matter and Slow Gait: Contribution of Hyperintensities and Normal-appearing Parenchyma
White matter hyperintensities (WMH), a common marker of cerebral small vessel disease, and lower microstructural integrity of normal-appearing white matter are associated with slower gait. How these cerebral measures interact in relation to slower gait is unknown. We assessed whether microstructural...
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creator | Rosario, Bedda L Rosso, Andrea L Aizenstein, Howard J Harris, Tamara Newman, Anne B Satterfield, Suzanne Studenski, Stephanie A Yaffe, Kristine Rosano, Caterina |
description | White matter hyperintensities (WMH), a common marker of cerebral small vessel disease, and lower microstructural integrity of normal-appearing white matter are associated with slower gait. How these cerebral measures interact in relation to slower gait is unknown. We assessed whether microstructural integrity of normal-appearing white matter, measured by fractional anisotropy (FA), moderates the association of higher WMH with slower gait.
WMH, FA, and gait speed were acquired for 265 community-dwelling older adults (average age = 82.9 years).
The inverse association between WMH and gait was robust to adjustment for age, gender, muscle strength, obesity, stroke, and hypertension (fully adjusted model: βs = -0.19, p = .001). The interaction between WMH and FA was significant; analyses stratified by FA showed that the inverse association between WMH and gait speed was significant only for those with low FA (FA < median, fully adjusted model: βs = -0.28, p = .001). Voxel-based results were similar for participants with FA less than median, there was an inverse association between gait speed and WMH which extended throughout the white matter (genu and body of corpus callosum, anterior limb of internal capsule, corona radiata, and superior longitudinal and fronto-occipital fasciculus). In contrast, for participants with FA ≥ median, the association was limited to the genu of corpus callosum, the cingulum, and the inferior longitudinal fasciculus.
Microstructural integrity is a moderating factor in the association between WMH and gait. Future studies should examine whether higher microstructural integrity represents a source of compensation in those with greater WMH burden to maintain function in late life. |
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WMH, FA, and gait speed were acquired for 265 community-dwelling older adults (average age = 82.9 years).
The inverse association between WMH and gait was robust to adjustment for age, gender, muscle strength, obesity, stroke, and hypertension (fully adjusted model: βs = -0.19, p = .001). The interaction between WMH and FA was significant; analyses stratified by FA showed that the inverse association between WMH and gait speed was significant only for those with low FA (FA < median, fully adjusted model: βs = -0.28, p = .001). Voxel-based results were similar for participants with FA less than median, there was an inverse association between gait speed and WMH which extended throughout the white matter (genu and body of corpus callosum, anterior limb of internal capsule, corona radiata, and superior longitudinal and fronto-occipital fasciculus). In contrast, for participants with FA ≥ median, the association was limited to the genu of corpus callosum, the cingulum, and the inferior longitudinal fasciculus.
Microstructural integrity is a moderating factor in the association between WMH and gait. Future studies should examine whether higher microstructural integrity represents a source of compensation in those with greater WMH burden to maintain function in late life.</description><identifier>ISSN: 1079-5006</identifier><identifier>ISSN: 1758-535X</identifier><identifier>EISSN: 1758-535X</identifier><identifier>DOI: 10.1093/gerona/glv224</identifier><identifier>PMID: 26755683</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Aged ; Aging - physiology ; Anisotropy ; Biomarkers ; Brain ; Corpus Callosum - diagnostic imaging ; Corpus Callosum - pathology ; Diffusion Tensor Imaging - methods ; Female ; Gait - physiology ; Gerontology ; Gyrus Cinguli - diagnostic imaging ; Gyrus Cinguli - pathology ; Humans ; Leukoencephalopathies - complications ; Leukoencephalopathies - pathology ; Leukoencephalopathies - physiopathology ; Male ; Medical disorders ; Mobility ; NMR ; Nuclear magnetic resonance ; Risk Factors ; Statistics as Topic ; Walking Speed - physiology ; White Matter - diagnostic imaging ; White Matter - pathology</subject><ispartof>The journals of gerontology. Series A, Biological sciences and medical sciences, 2016-07, Vol.71 (7), p.968-973</ispartof><rights>The Author 2016. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>Copyright Oxford University Press, UK Jul 2016</rights><rights>The Author 2016. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-dcc88b552797e32f093bc8115965ef16bdb566426630387e4770d118ff18c1c93</citedby><cites>FETCH-LOGICAL-c481t-dcc88b552797e32f093bc8115965ef16bdb566426630387e4770d118ff18c1c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26755683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosario, Bedda L</creatorcontrib><creatorcontrib>Rosso, Andrea L</creatorcontrib><creatorcontrib>Aizenstein, Howard J</creatorcontrib><creatorcontrib>Harris, Tamara</creatorcontrib><creatorcontrib>Newman, Anne B</creatorcontrib><creatorcontrib>Satterfield, Suzanne</creatorcontrib><creatorcontrib>Studenski, Stephanie A</creatorcontrib><creatorcontrib>Yaffe, Kristine</creatorcontrib><creatorcontrib>Rosano, Caterina</creatorcontrib><creatorcontrib>Health ABC Study</creatorcontrib><creatorcontrib>for the Health ABC Study</creatorcontrib><title>Cerebral White Matter and Slow Gait: Contribution of Hyperintensities and Normal-appearing Parenchyma</title><title>The journals of gerontology. Series A, Biological sciences and medical sciences</title><addtitle>J Gerontol A Biol Sci Med Sci</addtitle><description>White matter hyperintensities (WMH), a common marker of cerebral small vessel disease, and lower microstructural integrity of normal-appearing white matter are associated with slower gait. How these cerebral measures interact in relation to slower gait is unknown. We assessed whether microstructural integrity of normal-appearing white matter, measured by fractional anisotropy (FA), moderates the association of higher WMH with slower gait.
WMH, FA, and gait speed were acquired for 265 community-dwelling older adults (average age = 82.9 years).
The inverse association between WMH and gait was robust to adjustment for age, gender, muscle strength, obesity, stroke, and hypertension (fully adjusted model: βs = -0.19, p = .001). The interaction between WMH and FA was significant; analyses stratified by FA showed that the inverse association between WMH and gait speed was significant only for those with low FA (FA < median, fully adjusted model: βs = -0.28, p = .001). Voxel-based results were similar for participants with FA less than median, there was an inverse association between gait speed and WMH which extended throughout the white matter (genu and body of corpus callosum, anterior limb of internal capsule, corona radiata, and superior longitudinal and fronto-occipital fasciculus). In contrast, for participants with FA ≥ median, the association was limited to the genu of corpus callosum, the cingulum, and the inferior longitudinal fasciculus.
Microstructural integrity is a moderating factor in the association between WMH and gait. Future studies should examine whether higher microstructural integrity represents a source of compensation in those with greater WMH burden to maintain function in late life.</description><subject>Aged</subject><subject>Aging - physiology</subject><subject>Anisotropy</subject><subject>Biomarkers</subject><subject>Brain</subject><subject>Corpus Callosum - diagnostic imaging</subject><subject>Corpus Callosum - pathology</subject><subject>Diffusion Tensor Imaging - methods</subject><subject>Female</subject><subject>Gait - physiology</subject><subject>Gerontology</subject><subject>Gyrus Cinguli - diagnostic imaging</subject><subject>Gyrus Cinguli - pathology</subject><subject>Humans</subject><subject>Leukoencephalopathies - complications</subject><subject>Leukoencephalopathies - pathology</subject><subject>Leukoencephalopathies - physiopathology</subject><subject>Male</subject><subject>Medical disorders</subject><subject>Mobility</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Risk Factors</subject><subject>Statistics as Topic</subject><subject>Walking Speed - physiology</subject><subject>White Matter - diagnostic imaging</subject><subject>White Matter - pathology</subject><issn>1079-5006</issn><issn>1758-535X</issn><issn>1758-535X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUtv1DAUhS1ERR-wZIsisWET6kf8CAskNOoDqTwkQLCzHOdmxlVip7bTav49HqatgLvxle6no3N8EHpJ8FuCW3a6hhi8OV2Pt5Q2T9ARkVzVnPFfT8uOZVtzjMUhOk7pGu-G02fokArJuVDsCMEKInTRjNXPjctQfTI5Q6yM76tvY7irLozL76pV8Dm6bsku-CoM1eV2huh8Bp9cdpD-8J9DnMxYm3kGU47r6quJ4O1mO5nn6GAwY4IX9-8J-nF-9n11WV99ufi4-nBV20aRXPfWKtVxTmUrgdGh5OusIoS3gsNARNd3XIiGCsEwUxIaKXFPiBoGoiyxLTtB7_e689JN0Fsots2o5-gmE7c6GKf_vXi30etwq5sWC0ZZEXhzLxDDzQIp68klC-NoPIQlaVKccaYo3qGv_0OvwxJ9iaeJKv9MmJC0UPWesjGkFGF4NEOw3hWo9wXqfYGFf_V3gkf6oTH2G9Wwmbs</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Rosario, Bedda L</creator><creator>Rosso, Andrea L</creator><creator>Aizenstein, Howard J</creator><creator>Harris, Tamara</creator><creator>Newman, Anne B</creator><creator>Satterfield, Suzanne</creator><creator>Studenski, Stephanie A</creator><creator>Yaffe, Kristine</creator><creator>Rosano, Caterina</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160701</creationdate><title>Cerebral White Matter and Slow Gait: Contribution of Hyperintensities and Normal-appearing Parenchyma</title><author>Rosario, Bedda L ; 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Series A, Biological sciences and medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosario, Bedda L</au><au>Rosso, Andrea L</au><au>Aizenstein, Howard J</au><au>Harris, Tamara</au><au>Newman, Anne B</au><au>Satterfield, Suzanne</au><au>Studenski, Stephanie A</au><au>Yaffe, Kristine</au><au>Rosano, Caterina</au><aucorp>Health ABC Study</aucorp><aucorp>for the Health ABC Study</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebral White Matter and Slow Gait: Contribution of Hyperintensities and Normal-appearing Parenchyma</atitle><jtitle>The journals of gerontology. Series A, Biological sciences and medical sciences</jtitle><addtitle>J Gerontol A Biol Sci Med Sci</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>71</volume><issue>7</issue><spage>968</spage><epage>973</epage><pages>968-973</pages><issn>1079-5006</issn><issn>1758-535X</issn><eissn>1758-535X</eissn><abstract>White matter hyperintensities (WMH), a common marker of cerebral small vessel disease, and lower microstructural integrity of normal-appearing white matter are associated with slower gait. How these cerebral measures interact in relation to slower gait is unknown. We assessed whether microstructural integrity of normal-appearing white matter, measured by fractional anisotropy (FA), moderates the association of higher WMH with slower gait.
WMH, FA, and gait speed were acquired for 265 community-dwelling older adults (average age = 82.9 years).
The inverse association between WMH and gait was robust to adjustment for age, gender, muscle strength, obesity, stroke, and hypertension (fully adjusted model: βs = -0.19, p = .001). The interaction between WMH and FA was significant; analyses stratified by FA showed that the inverse association between WMH and gait speed was significant only for those with low FA (FA < median, fully adjusted model: βs = -0.28, p = .001). Voxel-based results were similar for participants with FA less than median, there was an inverse association between gait speed and WMH which extended throughout the white matter (genu and body of corpus callosum, anterior limb of internal capsule, corona radiata, and superior longitudinal and fronto-occipital fasciculus). In contrast, for participants with FA ≥ median, the association was limited to the genu of corpus callosum, the cingulum, and the inferior longitudinal fasciculus.
Microstructural integrity is a moderating factor in the association between WMH and gait. Future studies should examine whether higher microstructural integrity represents a source of compensation in those with greater WMH burden to maintain function in late life.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>26755683</pmid><doi>10.1093/gerona/glv224</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aging - physiology Anisotropy Biomarkers Brain Corpus Callosum - diagnostic imaging Corpus Callosum - pathology Diffusion Tensor Imaging - methods Female Gait - physiology Gerontology Gyrus Cinguli - diagnostic imaging Gyrus Cinguli - pathology Humans Leukoencephalopathies - complications Leukoencephalopathies - pathology Leukoencephalopathies - physiopathology Male Medical disorders Mobility NMR Nuclear magnetic resonance Risk Factors Statistics as Topic Walking Speed - physiology White Matter - diagnostic imaging White Matter - pathology |
title | Cerebral White Matter and Slow Gait: Contribution of Hyperintensities and Normal-appearing Parenchyma |
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