Effects of Continuous Dopaminergic Stimulation on Parkinson's Disease Gait: A Longitudinal Prospective Study with Levodopa Intestinal Gel Infusion.

Parkinson’s disease freezing of gait levodopa intestinal gel parkinsonian gait wearable sensors

Journal

Journal of Parkinson's disease
ISSN: 1877-718X
Titre abrégé: J Parkinsons Dis
Pays: Netherlands
ID NLM: 101567362

Informations de publication

Date de publication:
08 May 2024
Historique:
medline: 10 5 2024
pubmed: 10 5 2024
entrez: 10 5 2024
Statut: aheadofprint

Résumé

Gait issues, including reduced speed, stride length and freezing of gait (FoG), are disabling in advanced phases of Parkinson's disease (PD), and their treatment is challenging. Levodopa/carbidopa intestinal gel (LCIG) can improve these symptoms in PD patients with suboptimal control of motor fluctuations, but it is unclear if continuous dopaminergic stimulation can further improve gait issues, independently from reducing Off-time. To analyze before (T0) and after 3 (T1) and 6 (T2) months of LCIG initiation: a) the objective improvement of gait and balance; b) the improvement of FoG severity; c) the improvement of motor complications and their correlation with changes in gait parameters and FoG severity. This prospective, longitudinal 6-months study analyzed quantitative gait parameters using wearable inertial sensors, FoG with the New Freezing of Gait Questionnaire (NFoG-Q), and motor complications, as per the MDS-UPDRS part IV scores. Gait speed and stride length increased and duration of Timed up and Go and of sit-to-stand transition was significantly reduced comparing T0 with T2, but not between T0-T1. NFoG-Q score decreased significantly from 19.3±4.6 (T0) to 11.8±7.9 (T1) and 8.4±7.6 (T2) (T1-T0 p = 0.018; T2-T0 p <  0.001). Improvement of MDS-UPDRS-IV (T0-T2, p = 0.002, T0-T1 p = 0.024) was not correlated with improvement of gait parameters and NFoG-Q from T0 to T2. LEDD did not change significantly after LCIG initiation. Continuous dopaminergic stimulation provided by LCIG infusion progressively ameliorates gait and alleviates FoG in PD patients over time, independently from improvement of motor fluctuations and without increase of daily dosage of dopaminergic therapy.

Sections du résumé

Background UNASSIGNED
Gait issues, including reduced speed, stride length and freezing of gait (FoG), are disabling in advanced phases of Parkinson's disease (PD), and their treatment is challenging. Levodopa/carbidopa intestinal gel (LCIG) can improve these symptoms in PD patients with suboptimal control of motor fluctuations, but it is unclear if continuous dopaminergic stimulation can further improve gait issues, independently from reducing Off-time.
Objective UNASSIGNED
To analyze before (T0) and after 3 (T1) and 6 (T2) months of LCIG initiation: a) the objective improvement of gait and balance; b) the improvement of FoG severity; c) the improvement of motor complications and their correlation with changes in gait parameters and FoG severity.
Methods UNASSIGNED
This prospective, longitudinal 6-months study analyzed quantitative gait parameters using wearable inertial sensors, FoG with the New Freezing of Gait Questionnaire (NFoG-Q), and motor complications, as per the MDS-UPDRS part IV scores.
Results UNASSIGNED
Gait speed and stride length increased and duration of Timed up and Go and of sit-to-stand transition was significantly reduced comparing T0 with T2, but not between T0-T1. NFoG-Q score decreased significantly from 19.3±4.6 (T0) to 11.8±7.9 (T1) and 8.4±7.6 (T2) (T1-T0 p = 0.018; T2-T0 p <  0.001). Improvement of MDS-UPDRS-IV (T0-T2, p = 0.002, T0-T1 p = 0.024) was not correlated with improvement of gait parameters and NFoG-Q from T0 to T2. LEDD did not change significantly after LCIG initiation.
Conclusion UNASSIGNED
Continuous dopaminergic stimulation provided by LCIG infusion progressively ameliorates gait and alleviates FoG in PD patients over time, independently from improvement of motor fluctuations and without increase of daily dosage of dopaminergic therapy.

Identifiants

pubmed: 38728203
pii: JPD240003
doi: 10.3233/JPD-240003
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Gabriele Imbalzano (G)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Carlo Alberto Artusi (CA)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Claudia Ledda (C)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Elisa Montanaro (E)

SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Alberto Romagnolo (A)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Mario Giorgio Rizzone (MG)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Marco Bozzali (M)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Leonardo Lopiano (L)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Maurizio Zibetti (M)

Department of Neuroscience "Rita Levi Montalcini", University of Torino, Torino, Italy.
SC Neurologia 2U, AOU Città della Salute e della Scienza, Torino, Italy.

Classifications MeSH