Presynaptic Striatal Dopaminergic Function in Atypical Parkinsonism: A Metaanalysis of Imaging Studies

dc.contributor.authorValtteri Kaasinen
dc.contributor.authorTuomas Kankare
dc.contributor.authorJuho Joutsa
dc.contributor.authorTero Vahlberg
dc.contributor.organizationfi=PET-keskus|en=Turku PET Centre|
dc.contributor.organizationfi=biostatistiikka|en=Biostatistics|
dc.contributor.organizationfi=kliiniset neurotieteet|en=Clinical Neurosciences|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.74845969893
dc.contributor.organization-code1.2.246.10.2458963.20.89365200099
dc.converis.publication-id45500437
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/45500437
dc.date.accessioned2022-10-28T13:11:38Z
dc.date.available2022-10-28T13:11:38Z
dc.description.abstract<div>Background: Multiple-system atrophy (MSA), progressive supranuclear palsy (PSP), and corticobasal syndrome (CBS) have signs and symptoms overlapping those of Parkinson disease (PD), complicating their clinical diagnosis. Although presynaptic dopaminergic brain imaging with PET and SPECT is clinically widely used for patients with suspected PD, the benefit of functional imaging in atypical parkinsonism syndromes remains unclear. We compared striatal presynaptic dopaminergic function in MSA parkinsonism variant (MSA-P), MSA cerebellar variant (MSA-C), PSP, CBS, and PD using combined quantitative data from all published studies. Methods: The PubMed database was searched from inception to August 2018 for the terms "dopamine" OR "dopaminergic" AND "PET" OR "SPECT" OR "SPET" and keywords related to PD, MSA, PSP, and CBS. In total, 1,711 publications were identified. PET or SPECT studies comparing patients with atypical parkinsonism to another diagnostic group (PD, MSA, PSP, or CBS) were included. Tracers for dopamine transporter (DAT), aromatic amino acid decarboxylase (AADC), or vesicular monoamine type 2 were investigated. Tracer binding data were extracted from the original articles. Heterogeneity of the data was examined using I-2 statistics, and a random-effects model was used to summarize data. Hedges g was used as an estimator of effect size in group comparisons. Results are reported according to PRISMA guidelines. <br /></div><div><br /></div><div>Results: Thirty-five studies (29 DAT, 6 AADC, no vesicular monoamine type 2 studies) with 356 MSA-P patients, 204 PSP patients, 79 CBS patients, and 62 MSA-C patients were included in the meta-analysis. Caudate nucleus and putamen DAT function was clearly lower in PSP than in PD (caudate: 34.1% difference, g = -1.08, 95% confidence interval [CI] = -1.52 to -0.64; putamen: 18.2%, g = -0.86, 95% CI = -1.50 to -0.21) and MSA-P (striatum: 31.4%, g = -0.70, 95% CI = -1.21 to -0.19) and was clearly lower in MSA-P than in MSA-C (striatum: 46.0%, g = 1.46, 95% CI = 0.23 to 2.68). Although not significant because of limited data, aromatic L-AADC results paralleled the DAT findings. <br /></div><div>Conclusion: Striatal presynaptic DAT function is clearly lower in PSP patients than in PD and MSA-P patients and is clearly lower in MSA-P patients than in MSA-C patients.</div>
dc.format.pagerange1757
dc.format.pagerange1763
dc.identifier.jour-issn0161-5505
dc.identifier.olddbid180372
dc.identifier.oldhandle10024/163466
dc.identifier.urihttps://www.utupub.fi/handle/11111/38321
dc.identifier.urnURN:NBN:fi-fe2021042821683
dc.language.isoen
dc.okm.affiliatedauthorKaasinen, Valtteri
dc.okm.affiliatedauthorJoutsa, Juho
dc.okm.affiliatedauthorVahlberg, Tero
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.affiliatedauthorDataimport, 2609820 PET Tutkimus
dc.okm.discipline3124 Neurology and psychiatryen_GB
dc.okm.discipline3124 Neurologia ja psykiatriafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSOC NUCLEAR MEDICINE INC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.2967/jnumed.119.227140
dc.relation.ispartofjournalJournal of Nuclear Medicine
dc.relation.issue12
dc.relation.volume60
dc.source.identifierhttps://www.utupub.fi/handle/10024/163466
dc.titlePresynaptic Striatal Dopaminergic Function in Atypical Parkinsonism: A Metaanalysis of Imaging Studies
dc.year.issued2019

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