Functional brain changes in sarcopenia: evidence for differential central neural mechanisms in dynapenic older women
Background The European Working Group on Sarcopenia in Older People (EWGSOP2) recently revised its definition and diagnostic criteria for sarcopenia, placing muscle strength at the forefront. The pathogenesis of dynapenia (or low muscle strength) is still not fully understood, but there is emerging...
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Veröffentlicht in: | Aging clinical and experimental research 2023-05, Vol.35 (5), p.1015-1025 |
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description | Background
The European Working Group on Sarcopenia in Older People (EWGSOP2) recently revised its definition and diagnostic criteria for sarcopenia, placing muscle strength at the forefront. The pathogenesis of dynapenia (or low muscle strength) is still not fully understood, but there is emerging evidence that central neural factors constitute critical determinants.
Methods
Our cross-sectional study included 59 community-dwelling older women (mean age 73.1 ± 4.9 years). Participants underwent detailed skeletal muscle assessments for muscle strength defined by handgrip strength and chair rise time measurements using the recently published EWGSOP2 cut-off points. Functional magnetic resonance imaging (fMRI) was assessed during the performance of a cognitive dual-task paradigm, consisting of a baseline, two single-tasks (motor and arithmetic) and one dual-task (motor and arithmetic combined).
Results
Forty-seven percent (28/59) of participants were classified as dynapenic. fMRI results revealed a differential recruitment of motor circuits in the brain during the dual-task condition in dynapenic as compared with non-dynapenic participants. In particular, while the brain activity during the single-tasks did not differ between the two groups, only during the dual-task non-dynapenic participants showed significant increased activation in dorsolateral prefrontal and premotor cortex, and in supplementary motor area as compared to dynapenic participants.
Conclusion
Our results point to a dysfunctional involvement of brain networks associated with motor control in dynapenia in a multi-tasking paradigm. A better knowledge of the link between dynapenia and brain functions could provide new impulses in the diagnosis and interventions for sarcopenia. |
doi_str_mv | 10.1007/s40520-023-02391-1 |
format | Article |
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The European Working Group on Sarcopenia in Older People (EWGSOP2) recently revised its definition and diagnostic criteria for sarcopenia, placing muscle strength at the forefront. The pathogenesis of dynapenia (or low muscle strength) is still not fully understood, but there is emerging evidence that central neural factors constitute critical determinants.
Methods
Our cross-sectional study included 59 community-dwelling older women (mean age 73.1 ± 4.9 years). Participants underwent detailed skeletal muscle assessments for muscle strength defined by handgrip strength and chair rise time measurements using the recently published EWGSOP2 cut-off points. Functional magnetic resonance imaging (fMRI) was assessed during the performance of a cognitive dual-task paradigm, consisting of a baseline, two single-tasks (motor and arithmetic) and one dual-task (motor and arithmetic combined).
Results
Forty-seven percent (28/59) of participants were classified as dynapenic. fMRI results revealed a differential recruitment of motor circuits in the brain during the dual-task condition in dynapenic as compared with non-dynapenic participants. In particular, while the brain activity during the single-tasks did not differ between the two groups, only during the dual-task non-dynapenic participants showed significant increased activation in dorsolateral prefrontal and premotor cortex, and in supplementary motor area as compared to dynapenic participants.
Conclusion
Our results point to a dysfunctional involvement of brain networks associated with motor control in dynapenia in a multi-tasking paradigm. A better knowledge of the link between dynapenia and brain functions could provide new impulses in the diagnosis and interventions for sarcopenia.</description><identifier>ISSN: 1720-8319</identifier><identifier>ISSN: 1594-0667</identifier><identifier>EISSN: 1720-8319</identifier><identifier>DOI: 10.1007/s40520-023-02391-1</identifier><identifier>PMID: 37029271</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Aged ; Brain - diagnostic imaging ; Cross-Sectional Studies ; Female ; Geriatrics/Gerontology ; Hand Strength - physiology ; Humans ; Medicine ; Medicine & Public Health ; Muscle strength ; Muscle Strength - physiology ; Original ; Original Article ; Sarcopenia ; Sarcopenia - diagnosis</subject><ispartof>Aging clinical and experimental research, 2023-05, Vol.35 (5), p.1015-1025</ispartof><rights>The Author(s) 2023. corrected publication 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. corrected publication 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-8dcda7e919394108dc620fcec66ce44faefe998b9991d3ea851aa536c25fba053</citedby><cites>FETCH-LOGICAL-c475t-8dcda7e919394108dc620fcec66ce44faefe998b9991d3ea851aa536c25fba053</cites><orcidid>0000-0003-4885-1042 ; 0000-0002-0540-7024</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s40520-023-02391-1$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40520-023-02391-1$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37029271$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Trost, Wiebke</creatorcontrib><creatorcontrib>Hars, Mélany</creatorcontrib><creatorcontrib>Fernandez, Natalia</creatorcontrib><creatorcontrib>Herrmann, François</creatorcontrib><creatorcontrib>Chevalley, Thierry</creatorcontrib><creatorcontrib>Ferrari, Serge</creatorcontrib><creatorcontrib>Gold, Gabriel</creatorcontrib><creatorcontrib>Rizzoli, René</creatorcontrib><creatorcontrib>Vuilleumier, Patrik</creatorcontrib><creatorcontrib>Trombetti, Andrea</creatorcontrib><title>Functional brain changes in sarcopenia: evidence for differential central neural mechanisms in dynapenic older women</title><title>Aging clinical and experimental research</title><addtitle>Aging Clin Exp Res</addtitle><addtitle>Aging Clin Exp Res</addtitle><description>Background
The European Working Group on Sarcopenia in Older People (EWGSOP2) recently revised its definition and diagnostic criteria for sarcopenia, placing muscle strength at the forefront. The pathogenesis of dynapenia (or low muscle strength) is still not fully understood, but there is emerging evidence that central neural factors constitute critical determinants.
Methods
Our cross-sectional study included 59 community-dwelling older women (mean age 73.1 ± 4.9 years). Participants underwent detailed skeletal muscle assessments for muscle strength defined by handgrip strength and chair rise time measurements using the recently published EWGSOP2 cut-off points. Functional magnetic resonance imaging (fMRI) was assessed during the performance of a cognitive dual-task paradigm, consisting of a baseline, two single-tasks (motor and arithmetic) and one dual-task (motor and arithmetic combined).
Results
Forty-seven percent (28/59) of participants were classified as dynapenic. fMRI results revealed a differential recruitment of motor circuits in the brain during the dual-task condition in dynapenic as compared with non-dynapenic participants. In particular, while the brain activity during the single-tasks did not differ between the two groups, only during the dual-task non-dynapenic participants showed significant increased activation in dorsolateral prefrontal and premotor cortex, and in supplementary motor area as compared to dynapenic participants.
Conclusion
Our results point to a dysfunctional involvement of brain networks associated with motor control in dynapenia in a multi-tasking paradigm. A better knowledge of the link between dynapenia and brain functions could provide new impulses in the diagnosis and interventions for sarcopenia.</description><subject>Aged</subject><subject>Brain - diagnostic imaging</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Geriatrics/Gerontology</subject><subject>Hand Strength - physiology</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Muscle strength</subject><subject>Muscle Strength - physiology</subject><subject>Original</subject><subject>Original Article</subject><subject>Sarcopenia</subject><subject>Sarcopenia - diagnosis</subject><issn>1720-8319</issn><issn>1594-0667</issn><issn>1720-8319</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9UcFu1TAQtBCoLW1_gAOKxIVLYNdO4pgLQhUFpEpc4Gz5OevWVWI_7KRV_x6n77UUDhys2fXOzq49jL1CeIcA8n1uoOVQAxfrUVjjM3aEslz1AtXzJ_Ehe5nzNUCDJTlgh0ICV1ziEZvPl2BnH4MZq00yPlT2yoRLylUJs0k2bil486GiGz9QsFS5mKrBO0eJwuxLmy2YCgZaVphoVfB5upcY7oJZFWwVx4FSdRsnCifshTNjptM9HrOf559_nH2tL75_-Xb26aK2jWznuh_sYCQpVEI1CCXtODhLtussNY0z5EipfqOUwkGQ6Vs0phWd5a3bGGjFMfu4090um4mG_aJ6m_xk0p2Oxuu_K8Ff6ct4oxGwUU23KrzdK6T4a6E868lnS-NoAsUlay5VL7ETHAr1zT_U67ik8q-F1YOUUgnAwuI7lk0x50TucRsEvbqqd67q4qi-d1WvTa-fvuOx5cHGQhA7Qi6l4l76M_s_sr8BUfCwTQ</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Trost, Wiebke</creator><creator>Hars, Mélany</creator><creator>Fernandez, Natalia</creator><creator>Herrmann, François</creator><creator>Chevalley, Thierry</creator><creator>Ferrari, Serge</creator><creator>Gold, Gabriel</creator><creator>Rizzoli, René</creator><creator>Vuilleumier, Patrik</creator><creator>Trombetti, Andrea</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4885-1042</orcidid><orcidid>https://orcid.org/0000-0002-0540-7024</orcidid></search><sort><creationdate>20230501</creationdate><title>Functional brain changes in sarcopenia: evidence for differential central neural mechanisms in dynapenic older women</title><author>Trost, Wiebke ; Hars, Mélany ; Fernandez, Natalia ; Herrmann, François ; Chevalley, Thierry ; Ferrari, Serge ; Gold, Gabriel ; Rizzoli, René ; Vuilleumier, Patrik ; Trombetti, Andrea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-8dcda7e919394108dc620fcec66ce44faefe998b9991d3ea851aa536c25fba053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aged</topic><topic>Brain - diagnostic imaging</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Geriatrics/Gerontology</topic><topic>Hand Strength - physiology</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Muscle strength</topic><topic>Muscle Strength - physiology</topic><topic>Original</topic><topic>Original Article</topic><topic>Sarcopenia</topic><topic>Sarcopenia - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trost, Wiebke</creatorcontrib><creatorcontrib>Hars, Mélany</creatorcontrib><creatorcontrib>Fernandez, Natalia</creatorcontrib><creatorcontrib>Herrmann, François</creatorcontrib><creatorcontrib>Chevalley, Thierry</creatorcontrib><creatorcontrib>Ferrari, Serge</creatorcontrib><creatorcontrib>Gold, Gabriel</creatorcontrib><creatorcontrib>Rizzoli, René</creatorcontrib><creatorcontrib>Vuilleumier, Patrik</creatorcontrib><creatorcontrib>Trombetti, Andrea</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Aging clinical and experimental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trost, Wiebke</au><au>Hars, Mélany</au><au>Fernandez, Natalia</au><au>Herrmann, François</au><au>Chevalley, Thierry</au><au>Ferrari, Serge</au><au>Gold, Gabriel</au><au>Rizzoli, René</au><au>Vuilleumier, Patrik</au><au>Trombetti, Andrea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional brain changes in sarcopenia: evidence for differential central neural mechanisms in dynapenic older women</atitle><jtitle>Aging clinical and experimental research</jtitle><stitle>Aging Clin Exp Res</stitle><addtitle>Aging Clin Exp Res</addtitle><date>2023-05-01</date><risdate>2023</risdate><volume>35</volume><issue>5</issue><spage>1015</spage><epage>1025</epage><pages>1015-1025</pages><issn>1720-8319</issn><issn>1594-0667</issn><eissn>1720-8319</eissn><abstract>Background
The European Working Group on Sarcopenia in Older People (EWGSOP2) recently revised its definition and diagnostic criteria for sarcopenia, placing muscle strength at the forefront. The pathogenesis of dynapenia (or low muscle strength) is still not fully understood, but there is emerging evidence that central neural factors constitute critical determinants.
Methods
Our cross-sectional study included 59 community-dwelling older women (mean age 73.1 ± 4.9 years). Participants underwent detailed skeletal muscle assessments for muscle strength defined by handgrip strength and chair rise time measurements using the recently published EWGSOP2 cut-off points. Functional magnetic resonance imaging (fMRI) was assessed during the performance of a cognitive dual-task paradigm, consisting of a baseline, two single-tasks (motor and arithmetic) and one dual-task (motor and arithmetic combined).
Results
Forty-seven percent (28/59) of participants were classified as dynapenic. fMRI results revealed a differential recruitment of motor circuits in the brain during the dual-task condition in dynapenic as compared with non-dynapenic participants. In particular, while the brain activity during the single-tasks did not differ between the two groups, only during the dual-task non-dynapenic participants showed significant increased activation in dorsolateral prefrontal and premotor cortex, and in supplementary motor area as compared to dynapenic participants.
Conclusion
Our results point to a dysfunctional involvement of brain networks associated with motor control in dynapenia in a multi-tasking paradigm. A better knowledge of the link between dynapenia and brain functions could provide new impulses in the diagnosis and interventions for sarcopenia.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>37029271</pmid><doi>10.1007/s40520-023-02391-1</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4885-1042</orcidid><orcidid>https://orcid.org/0000-0002-0540-7024</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Brain - diagnostic imaging Cross-Sectional Studies Female Geriatrics/Gerontology Hand Strength - physiology Humans Medicine Medicine & Public Health Muscle strength Muscle Strength - physiology Original Original Article Sarcopenia Sarcopenia - diagnosis |
title | Functional brain changes in sarcopenia: evidence for differential central neural mechanisms in dynapenic older women |
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