Using Clinical Scales and Digital Measures to Explore Falls in Patients with Lewy Body Dementia

dc.contributor.authorBattioui, Chakib
dc.contributor.authorMan, Albert
dc.contributor.authorPugh, Melissa
dc.contributor.authorWang, Jian
dc.contributor.authorDang, Xiangnan
dc.contributor.authorZhang, Hui
dc.contributor.authorArdayfio, Paul
dc.contributor.authorMunsie, Leanne
dc.contributor.authorHake, Ann Marie
dc.contributor.authorBiglan, Kevin
dc.contributor.departmentNeurology, School of Medicine
dc.date.accessioned2024-02-13T13:57:00Z
dc.date.available2024-02-13T13:57:00Z
dc.date.issued2023-06-21
dc.description.abstractIntroduction: PRESENCE was a phase 2 clinical trial assessing the efficacy of mevidalen, a D1 receptor positive allosteric modulator, for symptomatic treatment of Lewy body dementia (LBD). Mevidalen demonstrated improvements in motor and non-motor features of LBD, global functioning, and actigraphy-measured activity and daytime sleep. Adverse events (AEs) of fall were numerically increased in mevidalen-treated participants. Methods: A subset of PRESENCE participants wore a wrist actigraphy device for 2-week periods pre-, during, and posttreatment. Actigraphy sleep and activity measures were derived per period and analyzed to assess for their association with participants' reports of an AE of fall. Prespecified baseline and treatment-emergent clinical characteristics were also included in the retrospective analysis of falls. Independent-samples t test and χ2 test were performed to compare the means and proportions between individuals with/without falls. Results: A trend toward more falls was observed with mevidalen treatment (31/258 mevidalen-treated vs. 4/86 in placebo-treated participants: p = 0.12). Higher body mass index (BMI) (p < 0.05), more severe disease measured by baseline Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) part II (p < 0.05), and a trend toward improved Alzheimer's Disease Assessment Scale-Cognitive Subscale 13 (ADAS-Cog13) (p = 0.06) were associated with individuals with falls. No statistically significant associations with falls and treatment-emergent changes were observed. Conclusion: The association of falls with worse baseline disease severity and higher BMI and overall trend toward improvements on cognitive and motor scales suggest that falls in PRESENCE may be related to increased activity in mevidalen-treated participants at greater risk for falling. Future studies to confirm this hypothesis using fall diaries and digital assessments are necessary.
dc.eprint.versionFinal published version
dc.identifier.citationBattioui C, Man A, Pugh M, et al. Using Clinical Scales and Digital Measures to Explore Falls in Patients with Lewy Body Dementia. Digit Biomark. 2023;7(1):54-62. Published 2023 Jun 21. doi:10.1159/000529623
dc.identifier.urihttps://hdl.handle.net/1805/38419
dc.language.isoen_US
dc.publisherKarger
dc.relation.isversionof10.1159/000529623
dc.relation.journalDigital Biomarkers
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0
dc.sourcePMC
dc.subjectLewy body dementia
dc.subjectDigital measures
dc.subjectActigraphy
dc.subjectFalls
dc.subjectActivity
dc.subjectRisk factors
dc.titleUsing Clinical Scales and Digital Measures to Explore Falls in Patients with Lewy Body Dementia
dc.typeArticle
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