Literature DB >> 22849680

Serum cobalamin, urine methylmalonic acid, and plasma total homocysteine concentrations in Border Collies and dogs of other breeds.

Sabina Lutz1, Adrian C Sewell, Beat Bigler, Barbara Riond, Claudia E Reusch, Peter H Kook.   

Abstract

OBJECTIVE: To determine reference ranges for serum cobalamin (Cbl), urine methylmalonic acid (uMMA), and plasma total homocysteine (tHcys) concentrations and to compare values for healthy control dogs with values for Border Collies (BCs), a breed in which hereditary cobalamin deficiency has been identified. ANIMALS: 113 BCs, 35 healthy control dogs fed a typical diet, and 12 healthy dogs fed a bone and raw food diet exclusively. PROCEDURES: Urine and blood samples were obtained from each dog and Cbl, uMMA, and tHcys concentrations were determined.
RESULTS: Reference ranges for Cbl (261 to 1,001 ng/L), uMMA (0 to 4.2 mmol/mol of creatinine), and tHcys (4.3 to 18.4 μmol/L) concentrations were determined. Four BCs had a Cbl concentration lower than the assay detection limit (150 ng/L); median uMMA and tHcys concentrations in these dogs were 4,064 mmol/mol of creatinine and 51.5 μmol/L, respectively. Clinical abnormalities included stunted growth, lethargy, anemia, and proteinuria. Abnormalities improved after administration of cobalamin. Of the 109 healthy BCs with Cbl and tHcys concentrations within reference ranges, 41 (37.6%) had a high uMMA concentration (range, 5 to 360 mmol/mol). Results for dogs fed raw food were similar to those for control dogs. CONCLUSIONS AND CLINICAL RELEVANCE: Hereditary cobalamin deficiency is a rare disease with various clinical signs. The finding of methylmalonic aciduria in healthy eucobalaminemic BCs and BCs with clinical signs of Cbl deficiency was surprising and indicated these dogs may have defects in intracellular processing of Cbl or intestinal Cbl malabsorption, respectively. Studies investigating Cbl absorption and metabolic pathways are warranted.

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Year:  2012        PMID: 22849680     DOI: 10.2460/ajvr.73.8.1194

Source DB:  PubMed          Journal:  Am J Vet Res        ISSN: 0002-9645            Impact factor:   1.156


  7 in total

1.  Serum Cobalamin (Vitamin B12) Concentrations in Rhesus Macaques (Macaca mulatta) and Pigtailed Macaques (Macaca nemestrina) with Chronic Idiopathic Diarrhea.

Authors:  Jessica M Izzi; Sarah E Beck; Robert J Adams; Kelly A Metcalf Pate; Eric K Hutchinson
Journal:  Comp Med       Date:  2016       Impact factor: 0.982

2.  Prospective long-term evaluation of parenteral hydroxocobalamin supplementation in juvenile beagles with selective intestinal cobalamin malabsorption (Imerslund-Gräsbeck syndrome).

Authors:  Peter Hendrik Kook; C E Reusch; M Hersberger
Journal:  J Vet Intern Med       Date:  2018-03-23       Impact factor: 3.333

3.  Daily oral cyanocobalamin supplementation in Beagles with hereditary cobalamin malabsorption (Imerslund-Gräsbeck syndrome) maintains normal clinical and cellular cobalamin status.

Authors:  Peter H Kook; Martin Hersberger
Journal:  J Vet Intern Med       Date:  2018-12-15       Impact factor: 3.333

Review 4.  Review of cobalamin status and disorders of cobalamin metabolism in dogs.

Authors:  Stefanie Kather; Niels Grützner; Peter H Kook; Franziska Dengler; Romy M Heilmann
Journal:  J Vet Intern Med       Date:  2019-11-23       Impact factor: 3.333

5.  Effect of oral or injectable supplementation with cobalamin in dogs with hypocobalaminemia caused by chronic enteropathy or exocrine pancreatic insufficiency.

Authors:  Chee-Hoon Chang; Jonathan A Lidbury; Jan S Suchodolski; Joerg M Steiner
Journal:  J Vet Intern Med       Date:  2022-08-31       Impact factor: 3.175

6.  A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).

Authors:  Marta Owczarek-Lipska; Vidhya Jagannathan; Cord Drögemüller; Sabina Lutz; Barbara Glanemann; Tosso Leeb; Peter H Kook
Journal:  PLoS One       Date:  2013-04-16       Impact factor: 3.240

7.  Degenerative liver disease in young Beagles with hereditary cobalamin malabsorption because of a mutation in the cubilin gene.

Authors:  P H Kook; M Drögemüller; T Leeb; J Howard; M Ruetten
Journal:  J Vet Intern Med       Date:  2014-01-27       Impact factor: 3.333

  7 in total

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