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Safety of Plasma Infusions in Parkinson’s Disease

dc.contributor.authorParker, Jordan E.
dc.contributor.authorMartinez, Amaris
dc.contributor.authorDeutsch, Gayle K.
dc.contributor.authorPrabhakar, Varsha
dc.contributor.authorLising, Melanie
dc.contributor.authorKapphahn, Kristopher I.
dc.contributor.authorAnidi, Chioma M.
dc.contributor.authorNeuville, Raumin
dc.contributor.authorCoburn, Maria
dc.contributor.authorShah, Neil
dc.contributor.authorBronte‐stewart, Helen M.
dc.date.accessioned2020-12-02T14:36:09Z
dc.date.availableWITHHELD_12_MONTHS
dc.date.available2020-12-02T14:36:09Z
dc.date.issued2020-11
dc.identifier.citationParker, Jordan E.; Martinez, Amaris; Deutsch, Gayle K.; Prabhakar, Varsha; Lising, Melanie; Kapphahn, Kristopher I.; Anidi, Chioma M.; Neuville, Raumin; Coburn, Maria; Shah, Neil; Bronte‐stewart, Helen M. (2020). "Safety of Plasma Infusions in Parkinson’s Disease." Movement Disorders 35(11): 1905-1913.
dc.identifier.issn0885-3185
dc.identifier.issn1531-8257
dc.identifier.urihttps://hdl.handle.net/2027.42/163536
dc.description.abstractBackgroundYoung plasma infusions have emerged as a potential treatment for neurodegenerative disease, and convalescent plasma therapy has been used safely in the management of viral pandemics. However, the effect of plasma therapy in Parkinson’s disease (PD) is unknown.ObjectivesThe objective of this study was to determine the safety, tolerability, and feasibility of plasma infusions in people with PD.MethodsA total of 15 people with clinically established PD, at least 1 cognitive complaint, and on stable therapy received 1 unit of young fresh frozen plasma twice a week for 4- weeks. Assessments and adverse effects were performed/reported on and off therapy at baseline, immediately after, and 4- weeks after the infusions ended. Adverse effects were also assessed during infusions. The primary outcomes were safety, tolerability, and feasibility. Exploratory outcomes included Unified Parkinson’s Disease Rating Scale Part III off medication, neuropsychological battery, Parkinson’s Disease Questionnaire- 39, inflammatory markers (tumor necrosis factor- α, interleukin- 6), uric acid, and quantitative kinematics.ResultsAdherence rate was 100% with no serious adverse effects. There was evidence of improvement in phonemic fluency (P = 0.002) and in the Parkinson’s Disease Questionnaire- 39 stigma subscore (P = 0.013) that were maintained at the delayed evaluation. Elevated baseline tumor necrosis factor- α levels decreased 4- weeks after the infusions ended.ConclusionsYoung fresh frozen plasma was safe, feasible, and well tolerated in people with PD, without serious adverse effects and with preliminary evidence for improvements in phonemic fluency and stigma. The results of this study warrant further therapeutic investigations in PD and provide safety and feasibility data for plasma therapy in people with PD who may be at higher risk for severe complications of COVID- 19. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
dc.publisherJohn Wiley & Sons, Inc.
dc.subject.otherParkinson’s disease
dc.subject.otherplasma
dc.subject.otheryoung plasma
dc.subject.otherinfusions
dc.titleSafety of Plasma Infusions in Parkinson’s Disease
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/163536/2/mds28198.pdfen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/163536/1/mds28198_am.pdfen_US
dc.identifier.doi10.1002/mds.28198
dc.identifier.sourceMovement Disorders
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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