AI Article Synopsis

  • A systematic literature review was conducted to assess the impact of neuromuscular rate of force development (RFD), maximal muscle strength (Fmax), and physical function in neurodegenerative conditions like Parkinson's, Alzheimer's, Multiple Sclerosis, and Stroke.
  • The review found that individuals with neurodegenerative diseases showed significant deficits in RFD (-31%) and physical function (-26%), both of which were worse than those seen in Fmax (-21%).
  • It concluded that RFD is more sensitive to changes in neuromuscular function due to neurodegeneration than Fmax and could be a valuable biomarker for monitoring these changes in physical function.

Article Abstract

We systematically reviewed existing literature regarding lower extremity neuromuscular rate of force development (RFD), maximal muscle strength (Fmax), and physical function in neurodegenerative populations, and to what extent these outcomes are affected and/or associated. Following PRISMA guidelines, 4 databases (Pubmed, Embase, SPORTDiscus, Web of Science) were searched. Across aging, Parkinson Disease (PD), Alzheimer's Disease (AD), Multiple Sclerosis (MS), or Stroke, included studies should report (Part 1) deficits in lower extremity RFD, Fmax, and physical function (~ individuals having inferior vs. superior physical function), and/or (Part 2) associations between RFD (or Fmax) and physical function. A total of N=32 studies (n=1087 participants) were included. Part 1: deficits in RFD (-31%, ; N=22) were comparable to deficits in physical function (-26%; N=7), yet both deficits exceeded that of Fmax (-21%; N=20). Part 2: associations between RFD and physical function (r=0.13, ; N=16) were comparable to associations between Fmax and physical function ((r=0.15; N=12). Lower extremity RFD is (1) particularly sensitive (i.e. adapts earlier and/or more extensively) towards neurodegeneration, and more so than Fmax, and (2) of importance for physical function but apparently not superior to Fmax. RFD could serve as a useful indicator/biomarker of changes in neuromuscular function elicited by neurodegeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716292PMC

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