4.4 Article

Association of fecal and serum microRNA profiles with gastrointestinal cancer and chronic inflammatory enteropathy in dogs

Journal

JOURNAL OF VETERINARY INTERNAL MEDICINE
Volume 36, Issue 6, Pages 1989-2001

Publisher

WILEY
DOI: 10.1111/jvim.16530

Keywords

biomarker; CIE; miRNA qPCR; neoplasia; RT-qPCR; small RNA sequencing

Funding

  1. Fondet [A5386]
  2. Independent Research Fund Denmark -Technology and Production [DFF-6111-00124]
  3. Danish Kennel Club

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This study found that specific microRNAs in feces and serum of dogs can be used as noninvasive biomarkers to differentiate gastrointestinal cancer from chronic inflammatory enteropathy. MiR-451 and miR-223 showed the best diagnostic performance, and combining them slightly improved the diagnostic effectiveness.
Background Reliable biomarkers to differentiate gastrointestinal cancer (GIC) from chronic inflammatory enteropathy (CIE) in dogs are needed. Fecal and serum microRNAs (miRNAs) have been proposed as diagnostic and prognostic markers of GI disease in humans and dogs. Hypothesis/Objectives Dogs with GIC have fecal and serum miRNA profiles that differ from those of dogs with CIE. Aims: (a) identify miRNAs that differentiate GIC from CIE, (b) use high-throughput reverse transcription quantitative real-time PCR (RT-qPCR) to establish fecal and serum miRNA panels to distinguish GIC from CIE in dogs. Animals Twenty-four dogs with GIC, 10 dogs with CIE, and 10 healthy dogs, all client-owned. Methods An international multicenter observational prospective case-control study. Small RNA sequencing was used to identify fecal and serum miRNAs, and RT-qPCR was used to establish fecal and serum miRNA panels with the potential to distinguish GIC from CIE. Results The best diagnostic performance for distinguishing GIC from CIE was fecal miR-451 (AUC: 0.955, sensitivity: 86.4%, specificity: 100%), miR-223 (AUC: 0.918, sensitivity: 90.9%, specificity: 80%), and miR-27a (AUC: 0.868, sensitivity: 81.8%, specificity: 90%) and serum miR-20b (AUC: 0.905, sensitivity: 90.5%, specificity: 90%), miR-148a-3p (AUC: 0.924, sensitivity: 85.7%, specificity: 90%), and miR-652 (AUC: 0.943, sensitivity: 90.5%, specificity: 90%). Slightly improved diagnostic performance was achieved when combining fecal miR-451 and miR-223 (AUC: 0.973, sensitivity: 95.5%, specificity: 90%). Conclusions and Clinical Importance When used as part of a diagnostic RT-qPCR panel, the abovementioned miRNAs have the potential to function as noninvasive biomarkers for the differentiation of GIC and CIE in dogs.

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