Peer-reviewed veterinary case report
Neurological toxicosis in cats with MDR1 mutation after eprinomectin
By Mealey, Katrina L et al.·Published in Journal of veterinary pharmacology and therapeutics·2024·Washington State University, United States·View original on PubMed →
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Original publication title: Application of eprinomectin-containing parasiticides at label doses causes neurological toxicosis in cats homozygous for ABCB11930_1931del TC.
- Species:
- cat
Plain-English summary
A group of cats with a specific genetic mutation (ABCB11930_1931delTC) experienced serious neurological problems after being treated with a topical flea medication containing eprinomectin. Out of the eight affected cats with this mutation, three sadly died, while five recovered. The study found that this mutation is more common in cats than previously thought, which raises concerns about the safety of using eprinomectin in these cats. It's important for pet owners to discuss their cat's genetic background with their veterinarian before using this medication to avoid potential toxicity.
People also search for: cat neurological problems after flea treatment · eprinomectin toxicity in cats · ABCB1 mutation in cats · safe flea medication for cats with genetic mutation
Abstract
The feline MDR1 mutation (ABCB11930_1931delTC) has been associated with neurological toxicosis after topical application of eprinomectin products labeled for feline use. Information was collected from veterinarians who submitted samples for ABCB11930_1931delTC genotyping. In most cases, the submission form indicated an adverse event involving eprinomectin, in other cases submitting veterinarians were contacted to determine whether the patient had experienced an adverse drug event involving eprinomectin. If so, additional information was obtained to determine whether the case met inclusion criteria. 14 cases were highly consistent with eprinomectin toxicosis. Eight cats were homozygous for ABCB11930_1931del TC (3 died; 5 recovered). Six cats were homozygous wildtype (2 died; 4 recovered). The observed ABCB11930_1931delTC frequency (57%) was higher than the expected frequency (≤1%) in the feline population (Fisher Exact test, p < 0.01). Among wildtype cats, four were concurrently treated with potential competitive inhibitors of P-glycoprotein. Results indicate that topical eprinomectin products, should be avoided in cats homozygous for ABCB11930_1931delTC. This is a serious, preventable adverse event occurring in an identifiable subpopulation treated with FDA-approved products in accordance with label directions. Acquired P-glycoprotein deficiency resulting from drug interactions may enhance susceptibility to eprinomectin-induced neurological toxicosis in any cat, regardless of ABCB1 genotype.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/38366723/