Neuromuscular determinants of maximum walking speed in well-functioning older adults

Maximum walking speed may offer an advantage over usual walking speed for clinical assessment of age-related declines in mobility function that are due to neuromuscular impairment. The objective of this study was to determine the extent to which maximum walking speed is affected by neuromuscular fun...

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Published inExperimental gerontology Vol. 48; no. 3; pp. 358 - 363
Main Authors Clark, David J., Manini, Todd M., Fielding, Roger A., Patten, Carolynn
Format Journal Article
LanguageEnglish
Published England Elsevier Inc 01.03.2013
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Abstract Maximum walking speed may offer an advantage over usual walking speed for clinical assessment of age-related declines in mobility function that are due to neuromuscular impairment. The objective of this study was to determine the extent to which maximum walking speed is affected by neuromuscular function of the lower extremities in older adults. We recruited two groups of healthy, well functioning older adults who differed primarily on maximum walking speed. We hypothesized that individuals with slower maximum walking speed would exhibit reduced lower extremity muscle size and impaired plantarflexion force production and neuromuscular activation during a rapid contraction of the triceps surae muscle group (soleus (SO) and gastrocnemius (MG)). All participants were required to have usual 10-meter walking speed of >1.0m/s. If the difference between usual and maximum 10m walking speed was <0.6m/s, the individual was assigned to the “Slower” group (n=8). If the difference between usual and maximum 10-meter walking speed was >0.6m/s, the individual was assigned to the “Faster” group (n=12). Peak rate of force development (RFD) and rate of neuromuscular activation (rate of EMG rise) of the triceps surae muscle group were assessed during a rapid plantarflexion movement. Muscle cross sectional area of the right triceps surae, quadriceps and hamstrings muscle groups was determined by magnetic resonance imaging. Across participants, the difference between usual and maximal walking speed was predominantly dictated by maximum walking speed (r=.85). We therefore report maximum walking speed (1.76 and 2.17m/s in Slower and Faster, p<.001) rather than the difference between usual and maximal. Plantarflexion RFD was 38% lower (p=.002) in Slower compared to Faster. MG rate of EMG rise was 34% lower (p=.01) in Slower than Faster, but SO rate of EMG rise did not differ between groups (p=.73). Contrary to our hypothesis, muscle CSA was not lower in Slower than Faster for the muscle groups tested, which included triceps surae (p=.44), quadriceps (p=.76) and hamstrings (p=.98). MG rate of EMG rise was positively associated with RFD and maximum 10m walking speed, but not the usual 10m walking speed. These findings support the conclusion that maximum walking speed is limited by impaired neuromuscular force and activation of the triceps surae muscle group. Future research should further evaluate the utility of maximum walking speed for use in clinical assessment to detect and monitor age-related functional decline. ► Maximum walking speed may be valuable for clinical assessment of mobility function. ► Capability to rapidly activate muscle is correlated with maximum walking speed. ► Lower extremity muscle size does not explain maximum walking speed. ► Deficient maximum walking speed reveals impaired muscle activation in healthy elders.
AbstractList Maximum walking speed may offer an advantage over usual walking speed for clinical assessment of age-related declines in mobility function that are due to neuromuscular impairment. The objective of this study was to determine the extent to which maximum walking speed is affected by neuromuscular function of the lower extremities in older adults. We recruited two groups of healthy, well functioning older adults who differed primarily on maximum walking speed. We hypothesized that individuals with slower maximum walking speed would exhibit reduced lower extremity muscle size and impaired plantarflexion force production and neuromuscular activation during a rapid contraction of the triceps surae muscle group (soleus (SO) and gastrocnemius (MG)). All participants were required to have usual 10-meter walking speed of >1.0m/s. If the difference between usual and maximum 10m walking speed was <0.6m/s, the individual was assigned to the "Slower" group (n=8). If the difference between usual and maximum 10-meter walking speed was >0.6m/s, the individual was assigned to the "Faster" group (n=12). Peak rate of force development (RFD) and rate of neuromuscular activation (rate of EMG rise) of the triceps surae muscle group were assessed during a rapid plantarflexion movement. Muscle cross sectional area of the right triceps surae, quadriceps and hamstrings muscle groups was determined by magnetic resonance imaging. Across participants, the difference between usual and maximal walking speed was predominantly dictated by maximum walking speed (r=.85). We therefore report maximum walking speed (1.76 and 2.17m/s in Slower and Faster, p<.001) rather than the difference between usual and maximal. Plantarflexion RFD was 38% lower (p=.002) in Slower compared to Faster. MG rate of EMG rise was 34% lower (p=.01) in Slower than Faster, but SO rate of EMG rise did not differ between groups (p=.73). Contrary to our hypothesis, muscle CSA was not lower in Slower than Faster for the muscle groups tested, which included triceps surae (p=.44), quadriceps (p=.76) and hamstrings (p=.98). MG rate of EMG rise was positively associated with RFD and maximum 10m walking speed, but not the usual 10m walking speed. These findings support the conclusion that maximum walking speed is limited by impaired neuromuscular force and activation of the triceps surae muscle group. Future research should further evaluate the utility of maximum walking speed for use in clinical assessment to detect and monitor age-related functional decline.
Maximum walking speed may offer an advantage over usual walking speed for clinical assessment of age-related declines in mobility function that are due to neuromuscular impairment. The objective of this study was to determine the extent to which maximum walking speed is affected by neuromuscular function of the lower extremities in older adults. We recruited two groups of healthy, well functioning older adults who differed primarily on maximum walking speed. We hypothesized that individuals with slower maximum walking speed would exhibit reduced lower extremity muscle size and impaired plantarflexion force production and neuromuscular activation during a rapid contraction of the triceps surae muscle group (soleus (SO) and gastrocnemius (MG)).
Maximum walking speed may offer an advantage over usual walking speed for clinical assessment of age-related declines in mobility function that are due to neuromuscular impairment. The objective of this study was to determine the extent to which maximum walking speed is affected by neuromuscular function of the lower extremities in older adults. We recruited two groups of healthy, well functioning older adults who differed primarily on maximum walking speed. We hypothesized that individuals with slower maximum walking speed would exhibit reduced lower extremity muscle size and impaired plantarflexion force production and neuromuscular activation during a rapid contraction of the triceps surae muscle group (soleus (SO) and gastrocnemius (MG)). All participants were required to have usual 10-meter walking speed >1.0 m/s. If the difference between usual and maximum 10m walking speed was < 0.6 m/s, the individual was assigned to the “ Slower ” group (n=8). If the difference between usual and maximum 10-meter walking speed was > 0.6 m/s, the individual was assigned to the “ Faster ” group (n=12). Peak rate of force development (RFD) and rate of neuromuscular activation (rate of EMG rise) of the triceps surae muscle group were assessed during a rapid plantarflexion movement. Muscle cross sectional area of the right triceps surae, quadriceps and hamstrings muscle groups was determined by magnetic resonance imaging. Across participants, the difference between usual and maximal walking speed was predominantly dictated by maximum walking speed (r=.85). We therefore report maximum walking speed (1.76 and 2.17 m/s in Slower and Faster , p<.001) rather than the difference between usual and maximal. Plantarflexion RFD was 38% lower (p=.002) in Slower compared to Faster . MG rate of EMG rise was 34% lower (p=.01) in Slower than Faster , but SO rate of EMG rise did not differ between groups (p=.73). Contrary to our hypothesis, muscle CSA was not lower in Slower than Faster for the muscle groups tested, which included triceps surae (p=.44), quadriceps (p=.76) and hamstrings (p=.98). MG rate of EMG rise was positively associated with RFD and maximum 10m walking speed, but not usual 10m walking speed. These findings support the conclusion that maximum walking speed is limited by impaired neuromuscular force and activation of the triceps surae muscle group. Future research should further evaluate the utility of maximum walking speed for use in clinical assessment to detect and monitor age-related functional decline.
Maximum walking speed may offer an advantage over usual walking speed for clinical assessment of age-related declines in mobility function that are due to neuromuscular impairment. The objective of this study was to determine the extent to which maximum walking speed is affected by neuromuscular function of the lower extremities in older adults. We recruited two groups of healthy, well functioning older adults who differed primarily on maximum walking speed. We hypothesized that individuals with slower maximum walking speed would exhibit reduced lower extremity muscle size and impaired plantarflexion force production and neuromuscular activation during a rapid contraction of the triceps surae muscle group (soleus (SO) and gastrocnemius (MG)). All participants were required to have usual 10-meter walking speed of >1.0m/s. If the difference between usual and maximum 10m walking speed was <0.6m/s, the individual was assigned to the “Slower” group (n=8). If the difference between usual and maximum 10-meter walking speed was >0.6m/s, the individual was assigned to the “Faster” group (n=12). Peak rate of force development (RFD) and rate of neuromuscular activation (rate of EMG rise) of the triceps surae muscle group were assessed during a rapid plantarflexion movement. Muscle cross sectional area of the right triceps surae, quadriceps and hamstrings muscle groups was determined by magnetic resonance imaging. Across participants, the difference between usual and maximal walking speed was predominantly dictated by maximum walking speed (r=.85). We therefore report maximum walking speed (1.76 and 2.17m/s in Slower and Faster, p<.001) rather than the difference between usual and maximal. Plantarflexion RFD was 38% lower (p=.002) in Slower compared to Faster. MG rate of EMG rise was 34% lower (p=.01) in Slower than Faster, but SO rate of EMG rise did not differ between groups (p=.73). Contrary to our hypothesis, muscle CSA was not lower in Slower than Faster for the muscle groups tested, which included triceps surae (p=.44), quadriceps (p=.76) and hamstrings (p=.98). MG rate of EMG rise was positively associated with RFD and maximum 10m walking speed, but not the usual 10m walking speed. These findings support the conclusion that maximum walking speed is limited by impaired neuromuscular force and activation of the triceps surae muscle group. Future research should further evaluate the utility of maximum walking speed for use in clinical assessment to detect and monitor age-related functional decline. ► Maximum walking speed may be valuable for clinical assessment of mobility function. ► Capability to rapidly activate muscle is correlated with maximum walking speed. ► Lower extremity muscle size does not explain maximum walking speed. ► Deficient maximum walking speed reveals impaired muscle activation in healthy elders.
Author Manini, Todd M.
Patten, Carolynn
Fielding, Roger A.
Clark, David J.
AuthorAffiliation 2 Institute on Aging, University of Florida, Gainesville FL, USA
1 Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville FL, USA
3 Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston MA, USA
4 Department of Physical Therapy, University of Florida, Gainesville FL, USA
AuthorAffiliation_xml – name: 1 Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville FL, USA
– name: 3 Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston MA, USA
– name: 4 Department of Physical Therapy, University of Florida, Gainesville FL, USA
– name: 2 Institute on Aging, University of Florida, Gainesville FL, USA
Author_xml – sequence: 1
  givenname: David J.
  surname: Clark
  fullname: Clark, David J.
  email: davidclark@ufl.edu
  organization: Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville FL, USA
– sequence: 2
  givenname: Todd M.
  surname: Manini
  fullname: Manini, Todd M.
  organization: Institute on Aging, University of Florida, Gainesville FL, USA
– sequence: 3
  givenname: Roger A.
  surname: Fielding
  fullname: Fielding, Roger A.
  organization: Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston MA, USA
– sequence: 4
  givenname: Carolynn
  surname: Patten
  fullname: Patten, Carolynn
  organization: Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville FL, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23376102$$D View this record in MEDLINE/PubMed
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Keywords Aging
Mobility
Walking
Muscle
Electromyography
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  year: 2013
  text: 2013-03-01
  day: 01
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Experimental gerontology
PublicationTitleAlternate Exp Gerontol
PublicationYear 2013
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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Snippet Maximum walking speed may offer an advantage over usual walking speed for clinical assessment of age-related declines in mobility function that are due to...
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SubjectTerms Aged
Aging
Aging - pathology
Aging - physiology
Electromyography
Electromyography - methods
Exercise Test - methods
Female
Geriatric Assessment - methods
Humans
Male
Mobility
Muscle
Muscle Contraction - physiology
Muscle, Skeletal - anatomy & histology
Muscle, Skeletal - innervation
Muscle, Skeletal - physiology
Neuromuscular Junction - physiology
Walking
Walking - physiology
Title Neuromuscular determinants of maximum walking speed in well-functioning older adults
URI https://dx.doi.org/10.1016/j.exger.2013.01.010
https://www.ncbi.nlm.nih.gov/pubmed/23376102
https://search.proquest.com/docview/1314706225
https://search.proquest.com/docview/1419367623
https://pubmed.ncbi.nlm.nih.gov/PMC3594593
Volume 48
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