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Peer-reviewed veterinary case report

Blood microRNA tests for diagnosing and predicting dog Cushing's

By Karin Sanders et al.·Published in Frontiers in Veterinary Science·2021·Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, Netherlands, CH·View original on DOAJ

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Original publication title: Circulating MicroRNAs as Non-invasive Biomarkers for Canine Cushing's Syndrome

Species:
dog

Plain-English summary

A group of dogs with Cushing's syndrome, a condition caused by high cortisol levels, were tested to see if certain microRNAs in their blood could help diagnose the disease and predict if it would come back after treatment. Researchers found that specific microRNAs were present in different amounts in dogs with the disease compared to healthy dogs. Notably, one microRNA showed promise in indicating whether the disease might return after surgery. This suggests that testing for these microRNAs could help veterinarians make better decisions about treatment and follow-up care for dogs with Cushing's syndrome.

People also search for: dog Cushing's syndrome symptoms · dog blood test for Cushing's · microRNA biomarkers in dogs

Abstract

Canine Cushing's syndrome (hypercortisolism) can be caused by a pituitary tumor (pituitary-dependent hypercortisolism; PDH) or a cortisol-secreting adrenocortical tumor (csACT). For both cases, non-invasive biomarkers that could pre-operatively predict the risk of recurrence after surgery would greatly impact clinical decision making. The aim of this study was to determine whether circulating microRNAs (miRNAs) can be used as diagnostic (presence of PDH or csACT) and/or prognostic (disease recurrence, histological grade) non-invasive biomarkers for canine Cushing's syndrome. After a pilot study with 40 miRNAs in blood samples of healthy dogs (n = 3), dogs with PDH (n = 3) and dogs with a csACT (n = 4), we selected a total of 20 miRNAs for the definitive study. In the definitive study, these 20 miRNAs were analyzed in blood samples of healthy dogs (n = 6), dogs with PDH (n = 19, pre- and post-operative samples) and dogs with a csACT (n = 26, pre-operative samples). In dogs with PDH, six miRNAs (miR-122-5p, miR-126-5p, miR-141-3p, miR-222-3p, miR-375-3p and miR-483-3p) were differentially expressed compared to healthy dogs. Of one miRNA, miR-122-5p, the expression levels did not overlap between healthy dogs and dogs with PDH (p = 2.9x10−4), significantly decreased after hypophysectomy (p = 0.013), and were significantly higher (p = 0.017) in dogs with recurrence (n = 3) than in dogs without recurrence for at least one year after hypophysectomy (n = 7). In dogs with csACTs, two miRNAs (miR-483-3p and miR-223-3p) were differentially expressed compared to healthy dogs. Additionally, miR-141-3p was expressed significantly lower (p = 0.009) in dogs with csACTs that had a histopathological Utrecht score of ≥ 11 compared to those with a score of <11. These results indicate that circulating miRNAs have the potential to be non-invasive biomarkers in dogs with Cushing's syndrome that may contribute to clinical decision making.

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Original publication on DOAJ: https://doi.org/10.3389/fvets.2021.760487