<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Beach TG</submitter><funding>National Institute of Neurological Disorders and Stroke</funding><funding>National Brain and Tissue Resource for Parkinson’s Disease and Related Disorders</funding><funding>NIA NIH HHS</funding><funding>Arizona Alzheimer’s Disease Core Center</funding><funding>NINDS NIH HHS</funding><funding>National Institute on Aging</funding><funding>Michael J. Fox Foundation for Parkinson’s Research</funding><pagination>793-802</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6097838</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>77(9)</volume><pubmed_abstract>Immunohistochemical (IHC) α-synuclein (Asyn) pathology in peripheral biopsies may be a biomarker of Parkinson disease (PD). The multi-center Systemic Synuclein Sampling Study (S4) is evaluating IHC Asyn pathology within skin, colon and submandibular gland biopsies from 60 PD and 20 control subjects. Asyn pathology is being evaluated by a blinded panel of specially trained neuropathologists. Preliminary work assessed 2 candidate immunoperoxidase methods using a set of PD and control autopsy-derived sections from formalin-fixed, paraffin-embedded blocks of the 3 tissues. Both methods had 100% specificity; one, utilizing the 5C12 monoclonal antibody, was more sensitive in skin (67% vs 33%), and was chosen for further use in S4. Four trainee neuropathologists were trained to perform S4 histopa</pubmed_abstract><journal>Journal of neuropathology and experimental neurology</journal><pubmed_title>Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4).</pubmed_title><pmcid>PMC6097838</pmcid><funding_grant_id>U24 NS072026</funding_grant_id><funding_grant_id>P30 AG019610</funding_grant_id><funding_grant_id>P30 AG19610</funding_grant_id><pubmed_authors>Purri R</pubmed_authors><pubmed_authors>Jennings D</pubmed_authors><pubmed_authors>Noyes-Lloyd C</pubmed_authors><pubmed_authors>Coffey CS</pubmed_authors><pubmed_authors>Dziadek S</pubmed_authors><pubmed_authors>Munoz DG</pubmed_authors><pubmed_authors>Linder C</pubmed_authors><pubmed_authors>Duffy A</pubmed_authors><pubmed_authors>Akhtar R</pubmed_authors><pubmed_authors>Kremer T</pubmed_authors><pubmed_authors>Corbille AG</pubmed_authors><pubmed_authors>Ecklund D</pubmed_authors><pubmed_authors>Goßmann J</pubmed_authors><pubmed_authors>Amara A</pubmed_authors><pubmed_authors>Russell D</pubmed_authors><pubmed_authors>Letournel F</pubmed_authors><pubmed_authors>Foroud T</pubmed_authors><pubmed_authors>Seibyl J</pubmed_authors><pubmed_authors>White CL</pubmed_authors><pubmed_authors>Konig F</pubmed_authors><pubmed_authors>Chahine L</pubmed_authors><pubmed_authors>Riss H</pubmed_authors><pubmed_authors>Dave KD</pubmed_authors><pubmed_authors>Mollenhauer B</pubmed_authors><pubmed_authors>Crary JF</pubmed_authors><pubmed_authors>Marras C</pubmed_authors><pubmed_authors>Glass MJ</pubmed_authors><pubmed_authors>Lott D</pubmed_authors><pubmed_authors>Walker JE</pubmed_authors><pubmed_authors>Potter M</pubmed_authors><pubmed_authors>Keshavarzian A</pubmed_authors><pubmed_authors>Visanji N</pubmed_authors><pubmed_authors>Riley L</pubmed_authors><pubmed_authors>Canamero M</pubmed_authors><pubmed_authors>Sue LI</pubmed_authors><pubmed_authors>Guilmette L</pubmed_authors><pubmed_authors>Case R</pubmed_authors><pubmed_authors>Smith D</pubmed_authors><pubmed_authors>Cresswell M</pubmed_authors><pubmed_authors>Adler CH</pubmed_authors><pubmed_authors>Rothberg B</pubmed_authors><pubmed_authors>Serrano GE</pubmed_authors><pubmed_authors>Blair C</pubmed_authors><pubmed_authors>Schneider J</pubmed_authors><pubmed_authors>Arnedo V</pubmed_authors><pubmed_authors>Systemic Synuclein Sampling Study (S4)</pubmed_authors><pubmed_authors>Hogarth P</pubmed_authors><pubmed_authors>Derkinderen P</pubmed_authors><pubmed_authors>Intorcia AJ</pubmed_authors><pubmed_authors>Kopil CM</pubmed_authors><pubmed_authors>Mitchell C</pubmed_authors><pubmed_authors>Beach TG</pubmed_authors><pubmed_authors>Oza V</pubmed_authors><pubmed_authors>Sade H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4).</name><description>Immunohistochemical (IHC) α-synuclein (Asyn) pathology in peripheral biopsies may be a biomarker of Parkinson disease (PD). The multi-center Systemic Synuclein Sampling Study (S4) is evaluating IHC Asyn pathology within skin, colon and submandibular gland biopsies from 60 PD and 20 control subjects. Asyn pathology is being evaluated by a blinded panel of specially trained neuropathologists. Preliminary work assessed 2 candidate immunoperoxidase methods using a set of PD and control autopsy-derived sections from formalin-fixed, paraffin-embedded blocks of the 3 tissues. Both methods had 100% specificity; one, utilizing the 5C12 monoclonal antibody, was more sensitive in skin (67% vs 33%), and was chosen for further use in S4. Four trainee neuropathologists were trained to perform S4 histopa</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Sep</publication><modification>2026-04-07T16:57:33.969Z</modification><creation>2019-09-04T07:01:29Z</creation></dates><accession>S-EPMC6097838</accession><cross_references><pubmed>30107604</pubmed><doi>10.1093/jnen/nly056</doi></cross_references></HashMap>