<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Bogdanski AM</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>New methods are needed to detect pancreatic ductal adenocarcinoma (PDAC) earlier to improve outcomes. We previously reported that a panel of protein N-glycosylation traits (NGTs) discriminated PDAC from healthy-controls with an area under the curve (AUC) of 0.81-0.88. However, it remained unclear whether this panel accurately differentiates PDAC from other benign pancreatic disorders. Our study aims to evaluate the performance of the NGT panel in combination with CA19-9, in a diverse cohort, including PDAC cases, healthy-controls and controls with benign pancreatic disorders.&lt;h4>Methods&lt;/h4>Protein N-glycosylation profiles were determined in plasma samples using an in-house developed mass spectrometry assay. CA19-9 levels were measured using routine immunoassay test. Res</pubmed_abstract><journal>Pancreas</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12419019</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Protein N-Glycosylation Traits Combined with CA19-9 Accurately Distinguish Pancreatic Cancer Cases From Healthy Controls and Benign Pancreatic Diseases.</pubmed_title><pmcid>PMC12419019</pmcid><pubmed_authors>Ballieux BEPB</pubmed_authors><pubmed_authors>Cobbaert CM</pubmed_authors><pubmed_authors>Clift KE</pubmed_authors><pubmed_authors>Mesker WE</pubmed_authors><pubmed_authors>Klatte DCF</pubmed_authors><pubmed_authors>Wallace MB</pubmed_authors><pubmed_authors>van der Burgt YEM</pubmed_authors><pubmed_authors>van Leerdam ME</pubmed_authors><pubmed_authors>van Hooft JE</pubmed_authors><pubmed_authors>Bogdanski AM</pubmed_authors><pubmed_authors>Wuhrer M</pubmed_authors><pubmed_authors>Bi Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protein N-Glycosylation Traits Combined with CA19-9 Accurately Distinguish Pancreatic Cancer Cases From Healthy Controls and Benign Pancreatic Diseases.</name><description>&lt;h4>Objectives&lt;/h4>New methods are needed to detect pancreatic ductal adenocarcinoma (PDAC) earlier to improve outcomes. We previously reported that a panel of protein N-glycosylation traits (NGTs) discriminated PDAC from healthy-controls with an area under the curve (AUC) of 0.81-0.88. However, it remained unclear whether this panel accurately differentiates PDAC from other benign pancreatic disorders. Our study aims to evaluate the performance of the NGT panel in combination with CA19-9, in a diverse cohort, including PDAC cases, healthy-controls and controls with benign pancreatic disorders.&lt;h4>Methods&lt;/h4>Protein N-glycosylation profiles were determined in plasma samples using an in-house developed mass spectrometry assay. CA19-9 levels were measured using routine immunoassay test. Res</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-06-02T01:01:54.347Z</modification><creation>2026-05-24T03:07:36.603Z</creation></dates><accession>S-EPMC12419019</accession><cross_references><pubmed>40403287</pubmed><doi>10.1097/MPA.0000000000002517</doi></cross_references></HashMap>