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Published in: BMC Cancer 1/2024

Open Access 01-12-2024 | Research

Preoperative profiles of plasma amino acids and derivatives distinguish periampullary cancer and benign disease

Authors: Stina Margrethe Stålberg, Laxmi Silwal-Pandit, Nasser Ezzatkhah Bastani, Daniel Johan Hammer Nebdal, Ole Christian Lingjærde, Bjørn Steen Skålhegg, Elin Hegland Kure

Published in: BMC Cancer | Issue 1/2024

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Abstract

Periampullary cancers, including pancreatic ductal adenocarcinoma, ampullary-, cholangio-, and duodenal carcinoma, are frequently diagnosed in an advanced stage and are associated with poor overall survival. They are difficult to differentiate from each other and challenging to distinguish from benign periampullary disease preoperatively. To improve the preoperative diagnostics of periampullary neoplasms, clinical or biological markers are warranted.
In this study, 28 blood plasma amino acids and derivatives from preoperative patients with benign (N = 45) and malignant (N = 72) periampullary disease were analyzed by LC-MS/MS.
Principal component analysis and consensus clustering both separated the patients with cancer and the patients with benign disease. Glutamic acid had significantly higher plasma expression and 15 other metabolites significantly lower plasma expression in patients with malignant disease compared with patients having benign disease. Phenylalanine was the only metabolite associated with improved overall survival (HR = 0.50, CI 0.30–0.83, P < 0.01).
Taken together, plasma metabolite profiles from patients with malignant and benign periampullary disease were significantly different and have the potential to distinguish malignant from benign disease preoperatively.
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Metadata
Title
Preoperative profiles of plasma amino acids and derivatives distinguish periampullary cancer and benign disease
Authors
Stina Margrethe Stålberg
Laxmi Silwal-Pandit
Nasser Ezzatkhah Bastani
Daniel Johan Hammer Nebdal
Ole Christian Lingjærde
Bjørn Steen Skålhegg
Elin Hegland Kure
Publication date
01-12-2024
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2024
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-024-12320-8

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