TY - JOUR
T1 - Associations Between Amantadine Usage, Gait, and Cognition in PSP
T2 - A post-hoc Analysis of the Davunetide Trial
AU - The AL-108-231 investigators
AU - Dale, Marian L.
AU - Brumbach, Barbara H.
AU - Boxer, Adam L.
AU - Hiller, Amie L.
N1 - Funding Information:
Funding. MD received a pilot grant from the Parkinson Center of Oregon, an OCTRI KL2 Scholarship Award (KL2TR002370), a Collins Medical Trust Pilot Project Award, and a Loan Repayment Program (LRP) award from NIH-NINDS for projects examining cerebellar TMS in progressive supranuclear palsy. AB receives research support from NIH, the Tau Research Consortium, the Association for Frontotemporal Degeneration, Bluefield Project to Cure Frontotemporal Dementia, Corticobasal Degeneration Solutions, the Association for Frontotemporal Degeneration, and the Alzheimer's Association. He has served as a consultant for Abbvie, AGTC, Alector, Arkuda, Arvinas, Asceneuron, AZTherapeutics, Bioage, Eisai, Ionis, Lundbeck, Passage BIO, Pinteon, Regeneron, Samumed, Third Rock,Transposon and UCB, and received research support from Biogen, Eisai, Eli Lilly, Genentech, Novartis, Roche, and TauRx. AH received a pilot grant from the Huntington's Disease Society of America examining psychological stress and salivary cortisol in Huntington's disease and a grant from Adamas Pharmaceuticals to examine the effects of extended release amantadine on gait and balance in Parkinson's disease.
Funding Information:
MD received a pilot grant from the Parkinson Center of Oregon, an OCTRI KL2 Scholarship Award (KL2TR002370), a Collins Medical Trust Pilot Project Award, and a Loan Repayment Program (LRP) award from NIH-NINDS for projects examining cerebellar TMS in progressive supranuclear palsy. AB receives research support from NIH, the Tau Research Consortium, the Association for Frontotemporal Degeneration, Bluefield Project to Cure Frontotemporal Dementia, Corticobasal Degeneration Solutions, the Association for Frontotemporal Degeneration, and the Alzheimer’s Association. He has served as a consultant for Abbvie, AGTC, Alector, Arkuda, Arvinas, Asceneuron, AZTherapeutics, Bioage, Eisai, Ionis, Lundbeck, Passage BIO, Pinteon, Regeneron, Samumed, Third Rock,Transposon and UCB, and received research support from Biogen, Eisai, Eli Lilly, Genentech, Novartis, Roche, and TauRx. AH received a pilot grant from the Huntington’s Disease Society of America examining psychological stress and salivary cortisol in Huntington’s disease and a grant from Adamas Pharmaceuticals to examine the effects of extended release amantadine on gait and balance in Parkinson’s disease.
Publisher Copyright:
© Copyright © 2020 Dale, Brumbach, Boxer and Hiller.
PY - 2020/12/21
Y1 - 2020/12/21
N2 - Introduction: Amantadine anecdotally improves gait in progressive supranuclear palsy (PSP) but definitive data is lacking. We investigated associations between amantadine usage, gait, cognition, and activities of daily living in 310 subjects with PSP using data from the davunetide trial. Method: We compared baseline demographics, PSP Rating Scale (PSPRS), Repeat Battery for the Assessment of Neuropsychological Status (RBANS), and Schwab and England Activities of Daily Living (SEADL) scores between subjects taking vs. not taking amantadine using chi-square tests for categorical variables and independent sample t-tests for continuous variables. Using the general linear model (GLM), we tested whether group status predicted total PSPRS, PSPRS-gait and midline, total RBANS, RBANS-attention, and SEADL before and after the 52-weeks follow-up. Results: Subjects taking vs. not taking amantadine were similar at baseline, except subjects taking amantadine had a higher Clinical Global Impression (CGI) Score (p = 0.01). However, the CGI change score did not differ between groups at week 52 (p = 0.10). Using GLM models (controlling for covariates), we found that subjects taking vs. not taking amantadine did not significantly predict total PSPRS, PSPRS-gait and midline, total RBANS, RBANS-attention, or SEADL at baseline, week 52, or the change score between baseline and week 52. Discussion: This post-hoc analysis of the davunetide trial did not find an association between amantadine and gait or cognitive measures in PSP, but was not powered to find such a difference. Future studies should still examine amantadine for symptomatic benefit in multiple PSP subtypes.
AB - Introduction: Amantadine anecdotally improves gait in progressive supranuclear palsy (PSP) but definitive data is lacking. We investigated associations between amantadine usage, gait, cognition, and activities of daily living in 310 subjects with PSP using data from the davunetide trial. Method: We compared baseline demographics, PSP Rating Scale (PSPRS), Repeat Battery for the Assessment of Neuropsychological Status (RBANS), and Schwab and England Activities of Daily Living (SEADL) scores between subjects taking vs. not taking amantadine using chi-square tests for categorical variables and independent sample t-tests for continuous variables. Using the general linear model (GLM), we tested whether group status predicted total PSPRS, PSPRS-gait and midline, total RBANS, RBANS-attention, and SEADL before and after the 52-weeks follow-up. Results: Subjects taking vs. not taking amantadine were similar at baseline, except subjects taking amantadine had a higher Clinical Global Impression (CGI) Score (p = 0.01). However, the CGI change score did not differ between groups at week 52 (p = 0.10). Using GLM models (controlling for covariates), we found that subjects taking vs. not taking amantadine did not significantly predict total PSPRS, PSPRS-gait and midline, total RBANS, RBANS-attention, or SEADL at baseline, week 52, or the change score between baseline and week 52. Discussion: This post-hoc analysis of the davunetide trial did not find an association between amantadine and gait or cognitive measures in PSP, but was not powered to find such a difference. Future studies should still examine amantadine for symptomatic benefit in multiple PSP subtypes.
KW - amantadine
KW - balance
KW - cognition
KW - gait
KW - progressive supranuclear palsy
UR - http://www.scopus.com/inward/record.url?scp=85098784804&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85098784804&partnerID=8YFLogxK
U2 - 10.3389/fneur.2020.606925
DO - 10.3389/fneur.2020.606925
M3 - Article
AN - SCOPUS:85098784804
SN - 1664-2295
VL - 11
JO - Frontiers in Neurology
JF - Frontiers in Neurology
M1 - 606925
ER -