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Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs

To evaluate the ability of serum glial fibrillary acidic protein (GFAP) concentration as a diagnostic marker for canine central nervous system (CNS) disorders, sera from dogs with various CNS (n=47) and non-CNS (n=56) disorders were measured for GFAP by using an ELISA kit. Healthy Beagles (n=15) and...

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Autores principales: MIYAKE, Hizuru, INOUE, Akiko, TANAKA, Miho, MATSUKI, Naoaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942992/
https://www.ncbi.nlm.nih.gov/pubmed/23856761
http://dx.doi.org/10.1292/jvms.13-0252
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author MIYAKE, Hizuru
INOUE, Akiko
TANAKA, Miho
MATSUKI, Naoaki
author_facet MIYAKE, Hizuru
INOUE, Akiko
TANAKA, Miho
MATSUKI, Naoaki
author_sort MIYAKE, Hizuru
collection PubMed
description To evaluate the ability of serum glial fibrillary acidic protein (GFAP) concentration as a diagnostic marker for canine central nervous system (CNS) disorders, sera from dogs with various CNS (n=47) and non-CNS (n=56) disorders were measured for GFAP by using an ELISA kit. Healthy Beagles (n=15) and Pug dogs (n=12) were also examined as controls. Interestingly, only Pug dogs with necrotizing meningoencephalitis (NME) showed elevated serum GFAP concentrations (<0.01 to 1.14 ng/ml), while other breeds of dogs with NME did not. Among the Pug dogs with NME, serum GFAP concentrations did not correlate with their clinical features, such as ages or survival times. Our data indicate the usefulness of serum GFAP as a novel marker for Pug dogs with NME.
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spelling pubmed-39429922014-04-22 Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs MIYAKE, Hizuru INOUE, Akiko TANAKA, Miho MATSUKI, Naoaki J Vet Med Sci Clinical Pathology To evaluate the ability of serum glial fibrillary acidic protein (GFAP) concentration as a diagnostic marker for canine central nervous system (CNS) disorders, sera from dogs with various CNS (n=47) and non-CNS (n=56) disorders were measured for GFAP by using an ELISA kit. Healthy Beagles (n=15) and Pug dogs (n=12) were also examined as controls. Interestingly, only Pug dogs with necrotizing meningoencephalitis (NME) showed elevated serum GFAP concentrations (<0.01 to 1.14 ng/ml), while other breeds of dogs with NME did not. Among the Pug dogs with NME, serum GFAP concentrations did not correlate with their clinical features, such as ages or survival times. Our data indicate the usefulness of serum GFAP as a novel marker for Pug dogs with NME. The Japanese Society of Veterinary Science 2013-07-12 2013-11 /pmc/articles/PMC3942992/ /pubmed/23856761 http://dx.doi.org/10.1292/jvms.13-0252 Text en ©2013 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Clinical Pathology
MIYAKE, Hizuru
INOUE, Akiko
TANAKA, Miho
MATSUKI, Naoaki
Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs
title Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs
title_full Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs
title_fullStr Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs
title_full_unstemmed Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs
title_short Serum Glial Fibrillary Acidic Protein as a Specific Marker for Necrotizing Meningoencephalitis in Pug Dogs
title_sort serum glial fibrillary acidic protein as a specific marker for necrotizing meningoencephalitis in pug dogs
topic Clinical Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942992/
https://www.ncbi.nlm.nih.gov/pubmed/23856761
http://dx.doi.org/10.1292/jvms.13-0252
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