Subthalamic 85 Hz deep brain stimulation improves walking pace and stride length in Parkinson's disease patients.

Deep brain stimulation Gait Inertial measurement unit Low frequency Mobile sensors Nucleus subthalamicus Parkinson

Journal

Neurological research and practice
ISSN: 2524-3489
Titre abrégé: Neurol Res Pract
Pays: England
ID NLM: 101767802

Informations de publication

Date de publication:
10 Aug 2023
Historique:
received: 19 04 2023
accepted: 23 06 2023
medline: 10 8 2023
pubmed: 10 8 2023
entrez: 9 8 2023
Statut: epublish

Résumé

Mobile gait sensors represent a compelling tool to objectify the severity of symptoms in patients with idiopathic Parkinson's disease (iPD), but also to determine the therapeutic benefit of interventions. In particular, parameters of Deep Brain stimulation (DBS) with its short latency could be accurately assessed using sensor data. This study aimed at gaining insight into gait changes due to different DBS parameters in patients with subthalamic nucleus (STN) DBS. An analysis of various gait examinations was performed on 23 of the initially enrolled 27 iPD patients with chronic STN DBS. Stimulation settings were previously adjusted for either amplitude, frequency, or pulse width in a randomised order. A linear mixed effects model was used to analyse changes in gait speed, stride length, and maximum sensor lift. The findings of our study indicate significant improvements in gait speed, stride length, and leg lift measurable with mobile gait sensors under different DBS parameter variations. Notably, we observed positive results at 85 Hz, which proved to be more effective than often applied higher frequencies and that these improvements were traceable across almost all conditions. While pulse widths did produce some improvements in leg lift, they were less well tolerated and had inconsistent effects on some of the gait parameters. Our research suggests that using lower frequencies of DBS may offer a more tolerable and effective approach to enhancing gait in individuals with iPD. Our results advocate for lower stimulation frequencies for patients who report gait difficulties, especially those who can adapt their DBS settings remotely. They also show that mobile gait sensors could be incorporated into clinical practice in the near future.

Sections du résumé

BACKGROUND BACKGROUND
Mobile gait sensors represent a compelling tool to objectify the severity of symptoms in patients with idiopathic Parkinson's disease (iPD), but also to determine the therapeutic benefit of interventions. In particular, parameters of Deep Brain stimulation (DBS) with its short latency could be accurately assessed using sensor data. This study aimed at gaining insight into gait changes due to different DBS parameters in patients with subthalamic nucleus (STN) DBS.
METHODS METHODS
An analysis of various gait examinations was performed on 23 of the initially enrolled 27 iPD patients with chronic STN DBS. Stimulation settings were previously adjusted for either amplitude, frequency, or pulse width in a randomised order. A linear mixed effects model was used to analyse changes in gait speed, stride length, and maximum sensor lift.
RESULTS RESULTS
The findings of our study indicate significant improvements in gait speed, stride length, and leg lift measurable with mobile gait sensors under different DBS parameter variations. Notably, we observed positive results at 85 Hz, which proved to be more effective than often applied higher frequencies and that these improvements were traceable across almost all conditions. While pulse widths did produce some improvements in leg lift, they were less well tolerated and had inconsistent effects on some of the gait parameters. Our research suggests that using lower frequencies of DBS may offer a more tolerable and effective approach to enhancing gait in individuals with iPD.
CONCLUSIONS CONCLUSIONS
Our results advocate for lower stimulation frequencies for patients who report gait difficulties, especially those who can adapt their DBS settings remotely. They also show that mobile gait sensors could be incorporated into clinical practice in the near future.

Identifiants

pubmed: 37559161
doi: 10.1186/s42466-023-00263-7
pii: 10.1186/s42466-023-00263-7
pmc: PMC10413698
doi:

Types de publication

Journal Article

Langues

eng

Pagination

33

Informations de copyright

© 2023. The Author(s).

Références

Nervenarzt. 2019 Dec;90(12):1232-1238
pubmed: 31654235
Arch Neurol. 2011 Feb;68(2):165
pubmed: 20937936
Eur Rev Aging Phys Act. 2023 Mar 17;20(1):7
pubmed: 36932320
Arch Clin Neuropsychol. 2017 Nov 1;32(7):802-809
pubmed: 29028874
Lancet Neurol. 2019 Jul;18(7):697-708
pubmed: 30975519
J Parkinsons Dis. 2021;11(3):1455-1464
pubmed: 34057096
Lancet Neurol. 2009 Jan;8(1):67-81
pubmed: 19081516
Nat Rev Neurol. 2015 Feb;11(2):98-110
pubmed: 25582445
J Clin Med. 2021 Aug 05;10(16):
pubmed: 34441763
Mov Disord Clin Pract. 2021 Jul 19;8(7):1075-1082
pubmed: 34631943
PLoS One. 2013;8(2):e56956
pubmed: 23431395
NPJ Parkinsons Dis. 2022 Jun 2;8(1):69
pubmed: 35654835
Mov Disord. 2018 Jan;33(1):159-164
pubmed: 29150884
Neurology. 2020 Jul 28;95(4):e393-e401
pubmed: 32601120
J Neurol. 2013 Sep;260(9):2306-11
pubmed: 23749331
Sensors (Basel). 2017 Jun 28;17(7):
pubmed: 28657587
Neurology. 2008 Jul 8;71(2):80-4
pubmed: 18420482
IEEE Trans Biomed Circuits Syst. 2018 Dec;12(6):1230-1245
pubmed: 30418885
NPJ Parkinsons Dis. 2022 Oct 29;8(1):144
pubmed: 36309508
J Neuroeng Rehabil. 2021 Aug 10;18(1):125
pubmed: 34376190
Cureus. 2018 Oct 22;10(10):e3474
pubmed: 30648026
Clin Neurophysiol. 2021 Jul;132(7):1708-1713
pubmed: 33958263
Brain. 2010 Jun;133(Pt 6):1755-62
pubmed: 20371510
N Engl J Med. 2013 Feb 14;368(7):610-22
pubmed: 23406026
Mov Disord. 2014 Feb;29(2):270-4
pubmed: 24449169
Front Neurol. 2019 Feb 08;10:29
pubmed: 30800094
Neuromodulation. 2015 Dec;18(8):664-9
pubmed: 25833008
Sensors (Basel). 2015 Mar 17;15(3):6419-40
pubmed: 25789489
J Vis Exp. 2014 Jul 16;(89):
pubmed: 25077449
Neuromodulation. 2022 Feb;25(2):271-275
pubmed: 35125146
Mov Disord. 2008 Nov 15;23(15):2129-70
pubmed: 19025984
Biom J. 2008 Jun;50(3):346-63
pubmed: 18481363
Mov Disord. 2015 Oct;30(12):1591-601
pubmed: 26474316
Sensors (Basel). 2017 Aug 23;17(9):
pubmed: 28832511
Telemed J E Health. 2019 Mar;25(3):167-183
pubmed: 29969384
PLoS One. 2017 Oct 11;12(10):e0183989
pubmed: 29020012
J Neurol. 2018 Nov;265(11):2656-2665
pubmed: 30196324
Sci Rep. 2021 Jan 12;11(1):752
pubmed: 33436993
N Engl J Med. 1998 Oct 15;339(16):1105-11
pubmed: 9770557
J Intern Med. 2022 Nov;292(5):764-778
pubmed: 35798568
Brain Stimul. 2012 Jul;5(3):388-392
pubmed: 21824834
Front Hum Neurosci. 2022 May 16;16:806513
pubmed: 35652005
Br J Neurosurg. 2023 Feb;37(1):3-11
pubmed: 35603983
Front Aging Neurosci. 2020 Oct 15;12:577435
pubmed: 33192470

Auteurs

F Mügge (F)

Department of Neurology, University Hospital of Marburg, Baldingerstraße, Marburg, Germany.

U Kleinholdermann (U)

Department of Neurology, University Hospital of Marburg, Baldingerstraße, Marburg, Germany. kleinhol@med.uni-marburg.de.

A Heun (A)

Department of Neurology, University Hospital of Marburg, Baldingerstraße, Marburg, Germany.

M Ollenschläger (M)

Portabiles HealthCare Technologies, Henkestraße 91, 91052, Erlangen, Germany.

J Hannink (J)

Portabiles HealthCare Technologies, Henkestraße 91, 91052, Erlangen, Germany.

D J Pedrosa (DJ)

Department of Neurology, University Hospital of Marburg, Baldingerstraße, Marburg, Germany.
Center of Mind, Brain and Behaviour, Philipps University Marburg, Hans-Meerwein- Straße, Marburg, Germany.

Classifications MeSH