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Journal Article

Motor segmentation: a key neuromuscular impairment in people with parkinson’s disease

Rebecca J. Daniels; Christopher A. Knight
Experimental Brain Research · Vol. 243, Issue 12 · 2025

Abstract

Healthy adults (OA) achieve rapid isometric force production with a brief, high amplitude burst of neural excitation. In some people with Parkinson’s disease (PwPD), transient reductions in neural excitation (motor segmentation) reduce rates of force development (RFD) and prolong contractions. Segmentation has strong relationships with time and rate-based measures of slowing in rapid contractions and is reliably measured from the second derivative of force (F”(t)). We sought more information about how segmentation affects neuromuscular control in PwPD. Aim 1 was to determine the prevalence of PwPD with segmentation (PD Seg ). Aim 2 was to determine how force performance differs in PD Seg , PwPD without segmentation (PD NoSeg ), and OA. Aim 3 was to quantify force segment durations. Fifty-seven PwPD ON medication and 22 OA performed rapid isometric finger abduction contractions to 20–60% of maximal voluntary contraction force. The median number of force segments to 90% of peak force were measured from F”(t) zero crossings. Additional outcomes included median times to peak force (tPF) and peak RFD (tRFD), and peak RFD (RFDpk). 68% of PwPD had segmentation (median segments ≥ 2, 95% CI [0.55 0.80]). PD Seg had slower tPF, tRFD and RFDpk than PD NoSeg and OA (all p ≤ 0.012, 0.38 ≤ r ≤ 0.85). PD NoSeg and OA did not have statistically different tPF, tRFD, or RFDpk ( p > 0.05). PD Seg had consistent segment durations (coefficient of variation ≤ 25.5%) and shorter first segment durations compared to PD NoSeg and OA ( p < 0.001, r ≥ 0.68), indicating PD Seg had reduced neuromuscular excitation prior to peak force. Segmentation identifies specific pathophysiology in neuromuscular control that exacerbates slowing in isometric force production.

Bibliographic Information

JournalExperimental Brain Research
PublisherSpringer
Publication Date2025-12-01
Publication Year2025
Volume243
Issue12
Document TypeJournal Article
Print ISSN0014-4819
eISSN1432-1106
DOI10.1007/s00221-025-07189-3

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NARA Access Coverage1966-01-01~Current
Journal Homepagehttps://www.springer.com/journal/221
Publisher PageOpen Publisher Page
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