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@ARTICLE{Vieregge:1049996,
author = {Vieregge, Magdalena and Kuzkina, Anastasia and Janzen,
Annette and Oertel, Wolfgang H. and Sommerauer, Michael and
Volkmann, Jens and Doppler, Kathrin},
title = {{D}ermal {A}lpha‐{S}ynuclein {A}ggregation in {S}eed
{A}mplification {A}ssays for {P}arkinson's {D}isease
{S}ubtype {D}ifferentiation},
journal = {European journal of neurology},
volume = {32},
number = {12},
issn = {1351-5101},
address = {Oxford [u.a.]},
publisher = {Wiley-Blackwell},
reportid = {FZJ-2025-05710},
pages = {e70453},
year = {2025},
note = {This work was supported by German Federal Ministry of
Education and Research (BMBF). We thank Andrea
Sauer-Weckertand Antonia Kohl for expert
technicalassistance. Kathrin Doppler is supported by grants
from theInterdisciplinary Center of Clinical Research of the
University HospitalWürzburg and by the German Research
Foundation as a member of theClinical Research Unit
ResolvePain. Brain lysates were kindly providedby Camelia
Monoranu. Michael Sommerauer receives funding from
theprogram “Netzwerke 2021”, an initiative of the
Ministry of Culture andScience of the State of
Northrhine-Westphalia,and from the FederalMinistry of
Education and Research (BMBF) within the frameworkof the
funding programme ACCENT (funding code 01EO2107). OpenAccess
funding enabled and organized by Projekt DEAL.},
abstract = {Skin biopsies and seed amplification assays (SAA) provide a
sensitive and potentially quantitative method to detect
alpha‐synuclein (a‐syn) aggregation in peripheral nerve
fibers in Parkinson's disease (PD). Relating to the
previously published hypothesis that PD may either originate
in the peripheral (body‐first) or central (brain‐first)
nervous system, we investigated whether patients with
clinical features that have been reported to be associated
with a suspected body‐first subtype of PD exhibit higher
levels of a‐syn aggregation in dermal nerve fibers
compared to those without these features. Patients with
isolated REM sleep behavior disorder (iRBD) representing a
suspected premotor stage of body‐first PD were studied in
comparison to the PD cohort.MethodsPatients were categorized
on the basis of clinical features, and SAA parameters such
as lag time, number of positive curves, and titers were
analyzed and correlated with clinical
features.ResultsAlthough patients with clinical features of
suspected body‐first PD showed slightly higher titers,
significant differences were mainly observed between iRBD
patients and PD patients.},
cin = {INM-3},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406},
pnm = {5252 - Brain Dysfunction and Plasticity (POF4-525)},
pid = {G:(DE-HGF)POF4-5252},
typ = {PUB:(DE-HGF)16},
doi = {10.1111/ene.70453},
url = {https://juser.fz-juelich.de/record/1049996},
}