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Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis.
Xin, Lei; Gao, Jun; Wang, Dan; Lin, Jin-Huan; Liao, Zhuan; Ji, Jun-Tao; Du, Ting-Ting; Jiang, Fei; Hu, Liang-Hao; Li, Zhao-Shen.
Afiliación
  • Xin L; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Gao J; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Wang D; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Lin JH; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Liao Z; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Ji JT; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Du TT; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Jiang F; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Hu LH; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
  • Li ZS; Department of Gastroenterology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
Sci Rep ; 7: 40019, 2017 01 11.
Article en En | MEDLINE | ID: mdl-28074846
ABSTRACT
Chronic pancreatitis (CP) is an inflammatory disease characterized by progressive fibrosis of pancreas. Early diagnosis will improve the prognosis of patients. This study aimed to obtain serum miRNA biomarkers for early diagnosis of CP. In the current study, we analyzed the differentially expressed miRNAs (DEmiRs) of CP patients from Gene Expression Omnibus (GEO), and the DEmiRs in plasma of early CP patients (n = 10) from clinic by miRNA microarrays. Expression levels of DEmiRs were further tested in clinical samples including early CP patients (n = 20), late CP patients (n = 20) and healthy controls (n = 18). The primary endpoints were area under curve (AUC) and expression levels of DEmiRs. Four DEmiRs (hsa-miR-320a-d) were obtained from GEO CP, meanwhile two (hsa-miR-221 and hsa-miR-130a) were identified as distinct biomarkers of early CP by miRNA microarrays. When applied on clinical serum samples, hsa-miR-320a-d were accurate in predicting late CP, while hsa-miR-221 and hsa-miR-130a were accurate in predicting early CP with AUC of 100.0% and 87.5%. Our study indicates that miRNA expression profile is different in early and late CP. Hsa-miR-221 and hsa-miR-130a are biomarkers of early CP, and the panel of the above 6 serum miRNAs has the potential to be applied clinically for early diagnosis of CP.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: MicroARNs / Pancreatitis Crónica Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: MicroARNs / Pancreatitis Crónica Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: China