TY - JOUR
T1 - Coordination and control of forces during multifingered grasping in Parkinson's disease
AU - Rearick, Matthew P.
AU - Stelmach, George E.
AU - Leis, Berta
AU - Santello, Marco
N1 - Funding Information:
The authors thank Amparo Casares for assisting with the data collection, Dr. Mitchell Longstaff for insight regarding the analyses, and Dr. John F. Soechting for use of the grip apparatus. This work was partially supported by NIH Grants R01 NS39352-02 and R01 NS33173-08 (GES) and a USPHS Training Grant, NS07309 (MPR).
PY - 2002
Y1 - 2002
N2 - In this study, we focused on how subjects with Parkinson's disease (PD) grasp and lift with five-digits of the hand. This task provided the opportunity to simultaneously examine (a) the coordination of multiple segments (i.e., digits), (b) the sequencing of multiple tasks (i.e., force development, object lift, and hold), and (c) the control of force output. We found that PD patients coordinated and controlled five-digit forces comparable to that of age-matched controls. Specifically, these groups developed and maintained similar force amplitudes and force sharing patterns across all grasping phases. In addition, PD patients demonstrated similar levels of variability both within and across trials. In the frequency domain, however, some differences were observed across groups, especially in PD patients exhibiting obvious action tremor (AT) at a single modal frequency. In these subjects (four of nine PD patients), there was a systematic disruption, i.e., a phase-shifting away from ∼0°, in-phase force synchronization patterns normally observed between digits. This disruption typically occurred at and around the AT frequency, while at many other frequencies synchronization patterns were maintained. The composite of these findings implies that although global features observed in five-digit grasping in PD patients are preserved, more subtle aspects of the coordination between digits, as revealed by frequency domain analysis, are not. These results are discussed in relation to the neural mechanisms that might underlie physiological synchronization of forces and its pathological disruption.
AB - In this study, we focused on how subjects with Parkinson's disease (PD) grasp and lift with five-digits of the hand. This task provided the opportunity to simultaneously examine (a) the coordination of multiple segments (i.e., digits), (b) the sequencing of multiple tasks (i.e., force development, object lift, and hold), and (c) the control of force output. We found that PD patients coordinated and controlled five-digit forces comparable to that of age-matched controls. Specifically, these groups developed and maintained similar force amplitudes and force sharing patterns across all grasping phases. In addition, PD patients demonstrated similar levels of variability both within and across trials. In the frequency domain, however, some differences were observed across groups, especially in PD patients exhibiting obvious action tremor (AT) at a single modal frequency. In these subjects (four of nine PD patients), there was a systematic disruption, i.e., a phase-shifting away from ∼0°, in-phase force synchronization patterns normally observed between digits. This disruption typically occurred at and around the AT frequency, while at many other frequencies synchronization patterns were maintained. The composite of these findings implies that although global features observed in five-digit grasping in PD patients are preserved, more subtle aspects of the coordination between digits, as revealed by frequency domain analysis, are not. These results are discussed in relation to the neural mechanisms that might underlie physiological synchronization of forces and its pathological disruption.
KW - Finger force synergies
KW - Force control
KW - Grasping
KW - Human hand
KW - Parkinson's disease
KW - Tremor
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U2 - 10.1006/exnr.2002.8003
DO - 10.1006/exnr.2002.8003
M3 - Article
C2 - 12429189
AN - SCOPUS:0036433455
SN - 0014-4886
VL - 177
SP - 428
EP - 442
JO - Neurodegeneration
JF - Neurodegeneration
IS - 2
ER -