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MDR1 Mutation

ABCB1 gene mutation

Tunnetaan myös nimellä: ABCB1 Mutation, MDR1 Gene Defect, P-glycoprotein Deficiency

Eläinlääkärin tarkistamaDogKiireellisyys: LowKuinka yleinen: Common

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.

Shetland Sheepdog looking alert
Shetland Sheepdogs are among the herding breeds highly predisposed to the MDR1 mutation.

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

Lethargic German Shepherd with dilated pupils
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 bag on an IV pole
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

  1. Plumb · p. 1982
  2. Internal Medicine 5th · p. 1178
  3. Small Animal Critical Care Medicine, 2nd Edition (VetBooks.ir) · p. 993
  4. Plumb · p. 2140
  5. Plumb · p. 1280

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