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Salivary Biomarker Evaluation of Chronic Pancreatitis Patients Reveals Alterations in Human Proteins, Cytokines, Prostaglandin E(2) Levels, and Bacterial Diversity

Chronic pancreatitis (CP) is a chronic fibroinflammatory condition of the pancreas difficult to diagnose in early stages. Novel biomarkers useful to facilitate early diagnosis or treatment responses may be found in biofluids. Although saliva can be easily and noninvasively collected from patients, u...

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Detalles Bibliográficos
Autores principales: Waldron, Richard T., Jones, Elaina K., Anani, Vincent I., Hines, Jolaine M., Zhao, Jing, Lugea, Aurelia, Diniz, Marcio A., Kim, Sungjin, Habtezion, Aida, Hoffman, Kristi L., Petrosino, Joseph F., Fisher, William E., Li, Liang, Lennon, Ryan J., Singh, Ravinder Jit, Vege, Santhi Swaroop, Pandol, Stephen J., Topazian, Mark D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9681020/
https://www.ncbi.nlm.nih.gov/pubmed/36395395
http://dx.doi.org/10.1097/MPA.0000000000002113
Descripción
Sumario:Chronic pancreatitis (CP) is a chronic fibroinflammatory condition of the pancreas difficult to diagnose in early stages. Novel biomarkers useful to facilitate early diagnosis or treatment responses may be found in biofluids. Although saliva can be easily and noninvasively collected from patients, useful salivary biomarkers from CP patients have not yet been identified. METHODS: Here, we analyzed the proteome by quantitative proteomics, cytokine/chemokine levels by Luminex analysis, prostaglandin E(2) (PGE(2)) levels by a mass spectrometry-based assay, and bacterial species diversity by 16S ribosomal ribonucleic acid sequencing in saliva samples from confirmed CP patients and healthy controls. RESULTS: Our results indicate the presence of various differentially expressed proteins, cytokines/chemokines, and a loss of oral bacterial diversity in the saliva of CP patients. The PGE(2) levels trend toward elevation in CP patients. Area under the receiver operating characteristic curve models for proteomic, cytokine, and PGE(2) assays ranged from 0.59 to 0.90. CONCLUSIONS: Collectively, our studies identify a range of putative CP biomarkers and alterations in human saliva requiring further validation. The biomarker discovery approaches we used might lead to identification of biomarkers useful for CP diagnosis and monitoring.