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Freezing of gait in idiopathic normal pressure hydrocephalus
Umeå University, Faculty of Medicine, Department of Clinical Sciences.
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.ORCID iD: 0000-0001-6451-1940
Edmond J. Safra Program in Parkinson’s Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, UHN, ON, Toronto, Canada; Division of Neurology, University of Toronto, ON, Toronto, Canada; Krembil Brain Institute, ON, Toronto, Canada; Center for Advancing Neurotechnological Innovation to Application (CRANIA), ON, Toronto, Canada.
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.
2024 (English)In: Fluids and Barriers of the CNS, E-ISSN 2045-8118, Vol. 21, no 1, article id 22Article in journal (Refereed) Published
Abstract [en]

Background: Reports of freezing of gait (FoG) in idiopathic normal pressure hydrocephalus (iNPH) are few and results are variable. This study's objective was to evaluate the frequency of FoG in a large cohort of iNPH patients, identify FoG-associated factors, and assess FoG’s responsiveness to shunt surgery.

Methods: Videotaped standardized gait protocols with iNPH patients pre- and post-shunt surgery (n = 139; median age 75 (71–79) years; 48 women) were evaluated for FoG episodes by two observers (Cohens kappa = 0.9, p < 0.001). FoG episodes were categorized. Mini-mental state examination (MMSE) and MRI white matter hyperintensities (WMH) assessment using the Fazekas scale were performed. CSF was analyzed for Beta-amyloid, Tau, and Phospho-tau. Patients with and without FoG were compared.

Results: Twenty-two patients (16%) displayed FoG at baseline, decreasing to seven (8%) after CSF shunt surgery (p = 0.039). The symptom was most frequently exhibited during turning (n = 16, 73%). Patients displaying FoG were older (77.5 vs. 74.6 years; p = 0.029), had a slower walking speed (0.59 vs. 0.89 m/s; p < 0.001), a lower Tinetti POMA score (6.8 vs. 10.8; p < 0.001), lower MMSE score (21.3 vs. 24.0; p = 0.031), and longer disease duration (4.2 vs. 2.3 years; p < 0.001) compared to patients not displaying FoG. WMH or CSF biomarkers did not differ between the groups.

Conclusions: FoG is occurring frequently in iNPH patients and may be considered a typical feature of iNPH. FoG in iNPH was associated with higher age, longer disease duration, worse cognitive function, and a more unstable gait. Shunt surgery seems to improve the symptom.

Place, publisher, year, edition, pages
BioMed Central (BMC), 2024. Vol. 21, no 1, article id 22
Keywords [en]
Cerebrospinal fluid shunts, Gait disorders, Neurologic, Hydrocephalus, normal pressure, Parkinson disease, Parkinsonian disorders
National Category
Neurology
Identifiers
URN: urn:nbn:se:umu:diva-222428DOI: 10.1186/s12987-024-00522-yISI: 001181184300001PubMedID: 38454478Scopus ID: 2-s2.0-85187136335OAI: oai:DiVA.org:umu-222428DiVA, id: diva2:1845670
Available from: 2024-03-19 Created: 2024-03-19 Last updated: 2024-03-19Bibliographically approved

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Malm, JanBäckström, David C

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