Differences in MicroRNA Expression in Aqueous Humor of Dogs Predisposed to Developing Primary Angle Closure Glaucoma: A Pilot Study
Hans D Westermeyer*, Jacklyn H Salmon and Michala de Linde Henriksen
North Carolina State University, College of Veterinary Medicine, Department of Clinical Sciences, Raleigh, NC
*Corresponding Author: Hans D Westermeyer, North Carolina State University, College of Veterinary Medicine, Department of Clinical Sciences, Raleigh, NC.
Received:
September 08, 2025; Published: October 06, 2025
Abstract
Purpose: The purpose of this pilot study was to explore the possibility of a common molecular pathway leading to the development of primary angle closure glaucoma (PACG) in dogs. This was done by comparing the aqueous humor (AH) microRNA (miRNA) profile of dogs predisposed to developing PACG to that of normal healthy dogs.
Material and Methods: The AH (250l) samples were collected under general anesthesia from the normal eye of dogs that had been diagnosed with PACG associated intraocular pressure (IOP) elevation in the opposite eye (study group; n=3 eyes). Aqueous humor from normal healthy eyes was also collected from purpose bred, beagle dogs immediately after euthanasia (control group; n=3 eyes). The AH samples were submitted to a commercial laboratory for miRNA sequencing and analysis.
Results: MicroRNA was successfully sequenced from all six AH samples. There were 19 sequences (16 novel and 3 known) which showed differential expression (13 upregulated and 6 downregulated) between eyes of the study group and the control group (P < 0.05). There were three sequences that were expressed in all study group dogs but not in any of the control group dogs (cfa-miRNA-206, NovelmiRNA-222, and NovelmiRNA-366).
Conclusions: There may be differences in miRNA expression in dog eyes predisposed to developing PACG prior to the onset of IOP elevation. Further investigation of these differences may lead to the discovery of the molecular mechanisms involved in IOP elevations in dogs with PACG and the development of novel diagnostic and treatment modalities.
Keywords: MicroRNA Expression; Aqueous Humor; Predisposed; Glaucoma
References
- Gelatt KN and MacKay EO. “Prevalence of the breed-related glaucomas in pure-bred dogs in North America”. Veterinary Ophthalmology 7 (2004): 97-111.
- Komáromy AM and Petersen-Jones SM. “Genetics of Canine Primary Glaucomas. Veterinary Clinics of North America: Small Animal Practice 45 (2015): 1159-1182.
- Graham KL., et al. “Genetic and Biochemical Biomarkers in Canine Glaucoma”. Veterinary Pathology 54 (2016): 194-203.
- Ahram DF., et al. “Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds”. PLoS One 10 (2015): e0126660.
- Kanemaki N., et al. “Dogs and Humans Share a Common Susceptibility Gene SRBD1 for Glaucoma Risk”. PLoS One 8 (2013): e74372.
- Greene KM., et al. “The role of microRNAs in glaucoma”. Experimental Eye Research 215 (2022): 108909.
- Benjamini Y and Hochberg Y. “Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing”. Journal of the Royal Statistical Society: Series B (Methodological) 57 (1995): 289-300.
- Durieux P., et al. “Tumor necrosis factor-alpha concentration in the aqueous humor of healthy and diseased dogs: A preliminary pilot study”. Journal Français d'Ophtalmologie 38 (2015): 288-294.
- Weinstein WL., et al. “Identification of ocular matrix metalloproteinases present within the aqueous humor and iridocorneal drainage angle tissue of normal and glaucomatous canine eyes”. Veterinary Ophthalmology 10 (2007): 108-116.
- Terhaar HM., et al. “Pro-inflammatory cytokines in aqueous humor from dogs with anterior uveitis and post-operative ocular hypertension following phacoemulsification, primary glaucoma, and normal healthy eyes”. PLoS One (2022): 17.
- Scott EM., et al. “Early histopathologic changes in the retina and optic nerve in canine primary angle-closure glaucoma”. Veterinary Ophthalmology 1 (2013): 79-86.
- Fick CM and Dubielzig RR. “Short posterior ciliary artery anatomy in normal and acutely glaucomatous dogs”. Veterinary Ophthalmology (2016): 43-49.
- Collins E., et al. “Pro-Inflammatory Cytokines in Aqueous Humor From ADAMTS10-Mutant Beagles at an Early Stage of Open-Angle Glaucoma”. Veterinary Ophthalmology (2025): 1-9.
- Jung SW and Bohan A. “Genome-wide sequencing and quantification of circulating microRNAs for dogs with congestive heart failure secondary to myxomatous mitral valve degeneration”. American Journal of Animal and Veterinary Sciences 79 (2018): 163-169.
- Zhou P., et al. “cfa-miR-143 Promotes Apoptosis via the p53 Pathway in Canine Influenza Virus H3N2-Infected Cells”. Viruses 9 (2017): 360.
- Zhang Y., et al. “MicroRNA Profiling of Atrial Fibrillation in Canines: MiR-206 Modulates Intrinsic Cardiac Autonomic Nerve Remodeling by Regulating SOD1”. PLoS One 10 (2015): e0122674.
- Soares MF., et al. “Differential expression of miRNAs in canine peripheral blood mononuclear cells (PBMC) exposed to Leishmania infantum in vitro”. Research in Veterinary Science 134 (2021): 58-63.
- Peng C., et al. “Characteristic Cytokine Profiles of Aqueous Humor in Glaucoma Secondary to Sturge-Weber Syndrome”. Frontiers in Immunology 11 (2020): 480347.
- Trivedi RH., et al. “Influence of Race and Age on Aqueous Humor Levels of Transforming Growth Factor-Beta 2 in Glaucomatous and Nonglaucomatous Eyes”. Journal of Ocular Pharmacology and Therapeutics 27 (2011): 477.
- Haq Z., et al. “Sex-Based Analysis of Potential Inflammation-Related Protein Biomarkers in the Aqueous Humor of Patients With Diabetes Mellitus”. Translational Vision Science and Technology 10 (2012): 12.
- Ferreira T., et al. “Exploring the role of microRNAs as diagnostic and prognostic biomarkers in canine mammary tumors”. GeroScience 46 (2024): 6641-6657.
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