MDR1 Mutation
ABCB1 gene mutation
Tunnetaan myös nimellä: ABCB1 Mutation, MDR1 Gene Defect, P-glycoprotein Deficiency
Lyhyesti
The MDR1 mutation (ABCB1 gene defect) is a common hereditary condition in dogs, especially herding breeds, that causes life-threatening sensitivities to everyday medications. Learn how to identify at-risk dogs, recognize signs of drug toxicity, and safely manage your dog's healthcare with genetic testing.

TL;DR. Yleinen geenimutaatio paimenkoirilla poistaa suojaproteiinin toiminnan ja tekee tavallisista lääkkeistä myrkyllisiä tai hengenvaarallisia.
Shetland Sheepdogs are among the herding breeds highly predisposed to the MDR1 mutation.
Mikä se on?
The MDR1 (ABCB1) mutation is a hereditary defect that impairs P-glycoprotein, an efflux pump concentrated at the blood-brain barrier and in liver, kidney, and gut. Without a working pump, many drugs accumulate in sensitive tissues and cause neurologic or organ toxicity at ordinary doses.
Syyt ja riskitekijät
Autosomal incomplete dominant inheritance. Homozygous mutants lack functional P-glycoprotein; heterozygous carriers have reduced capacity and can still react at higher doses. Risk is breed-linked: Collie, Shetland Sheepdog, Australian Shepherd, Miniature American Shepherd, German Shepherd, Old English Sheepdog, Border Collie, English Shepherd, Whippet, Longhaired Whippet, Silken Windhound, and mixes with herding ancestry.
Oireet
- Vomiting, ataxia, lethargy, tremors, hypersalivation
- Depression, anorexia, mydriasis, diarrhea
- Bone marrow suppression (chemo substrates)
- Occasional: tachycardia, dehydration, seizures
"Common findings in dogs recorded in decreasing frequency included vomiting, ataxia, lethargy, tachycardia, hypersalivation, mydriasis, and seizures." - Plumb's Veterinary Drug Handbook, p.1982

Dilated pupils and severe lethargy are common clinical signs of drug toxicity in MDR1-affected dogs.
Miten eläinlääkärit diagnosoivat
One-time MDR1 genetic testing (cheek swab or blood) classifies clear, carrier, or affected. In acute toxicity: history of drug exposure, neurologic exam, CBC/chemistry for organ support and marrow effects.

Intravenous fat emulsion (lipid rescue therapy) is used to reverse severe lipophilic drug toxicities.
Hoito
No cure for the genotype. Acute exposure: decontamination if recent; Activated Charcoal; Intravenous Fat Emulsion for severe lipophilic toxicity (e.g. ivermectin); IV fluids, seizure control, intensive support. Lifelong: avoid or dose-adjust high-risk drugs (loperamide, high-dose ivermectin, some chemotherapeutics, acepromazine, butorphanol).
Ennuste
Excellent if never exposed to problem drugs. Guarded after high-dose toxicity depending on drug, dose, speed of care, and access to lipid rescue.
Ehkäisy
Test at-risk breeds and mixes before routine meds or chemo. Keep a contraindicated-drug list for every caretaker. Prefer MDR1-safe heartworm preventives when indicated.
Milloin soittaa eläinlääkärille
Emergency now: seizures, severe ataxia or inability to stand, stupor, non-reactive dilated pupils, uncontrolled drooling with vomiting after a suspect drug.
Tietyille roduille
Highest prevalence reported in Collies; also common in Shelties, Australian Shepherds, and Miniature American Shepherds. Appearance alone does not predict status; DNA test once.
Lähteet
- Plumb's Veterinary Drug Handbook, pages 1280, 1982, 2140.
- Small Animal Internal Medicine (5th Edition), page 1178.
- Small Animal Critical Care Medicine (2nd Edition), page 993.
My highlights & notes
Oireet ja merkit
Korkeamman riskin rodut
Miten se diagnosoidaan
- MDR1 Genetic TestingKultastandardi
Hoitotavat
Hoidon määrää lisensoitu eläinlääkäri. Tarkkoja annoksia ei näytetä tarkoituksella.
Usein kysytyt kysymykset
What is MDR1 Mutation?
The MDR1 mutation (ABCB1 gene defect) is a common hereditary condition in dogs, especially herding breeds, that causes life-threatening sensitivities to everyday medications. Learn how to identify at-risk dogs, recognize signs of drug toxicity, and safely manage your dog's healthcare with genetic testing.
What are the symptoms of MDR1 Mutation?
Loss of appetite、Ataxia (wobbly, unsteady walking)、Low mood and dullness、Diarrhoea、Excessive drooling、Lethargy、Mydriasis、Tremors (shaking, trembling)
How is MDR1 Mutation diagnosed?
MDR1 Genetic Testing
How is MDR1 Mutation treated?
Hoidon määrää lisensoitu eläinlääkäri. Tarkkoja annoksia ei näytetä tarkoituksella.
Lähteet
- Plumb · p. 1982
- Internal Medicine 5th · p. 1178
- Small Animal Critical Care Medicine, 2nd Edition (VetBooks.ir) · p. 993
- Plumb · p. 2140
- Plumb · p. 1280
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