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Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds
BACKGROUND: An inherited basis for congenital extrahepatic portosystemic shunts (EHPSS) has been demonstrated in several small dog breeds. If in general both portocaval and porto-azygous shunts occur in breeds predisposed to portosystemic shunts then this could indicate a common genetic background....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602064/ https://www.ncbi.nlm.nih.gov/pubmed/22784395 http://dx.doi.org/10.1186/1746-6148-8-112 |
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author | Van den Bossche, Lindsay van Steenbeek, Frank G Favier, Robert P Kummeling, Anne Leegwater, Peter AJ Rothuizen, Jan |
author_facet | Van den Bossche, Lindsay van Steenbeek, Frank G Favier, Robert P Kummeling, Anne Leegwater, Peter AJ Rothuizen, Jan |
author_sort | Van den Bossche, Lindsay |
collection | PubMed |
description | BACKGROUND: An inherited basis for congenital extrahepatic portosystemic shunts (EHPSS) has been demonstrated in several small dog breeds. If in general both portocaval and porto-azygous shunts occur in breeds predisposed to portosystemic shunts then this could indicate a common genetic background. This study was performed to determine the distribution of extrahepatic portocaval and porto-azygous shunts in purebred dog populations. RESULTS: Data of 135 client owned dogs diagnosed with EHPSS at the Faculty of Veterinary Medicine of Utrecht University from 2001 – 2010 were retrospectively analyzed. The correlation between shunt localization, sex, age, dog size and breed were studied. The study group consisted of 54 males and 81 females from 24 breeds. Twenty-five percent of dogs had porto-azygous shunts and 75% had portocaval shunts. Of the dogs with porto-azygous shunts only 27% was male (P = 0.006). No significant sex difference was detected in dogs with a portocaval shunt. Both phenotypes were present in almost all breeds represented with more than six cases. Small dogs are mostly diagnosed with portocaval shunts (79%) whereas both types are detected. The age at diagnosis in dogs with porto-azygous shunts was significantly higher than that of dogs with portocaval shunts (P < 0.001). CONCLUSION: The remarkable similarity of phenotypic variation in many dog breeds may indicate common underlying genes responsible for EHPSS across breeds. The subtype of EHPSS could be determined by a minor genetic component or modulating factors during embryonic development. |
format | Online Article Text |
id | pubmed-3602064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36020642013-03-20 Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds Van den Bossche, Lindsay van Steenbeek, Frank G Favier, Robert P Kummeling, Anne Leegwater, Peter AJ Rothuizen, Jan BMC Vet Res Research Article BACKGROUND: An inherited basis for congenital extrahepatic portosystemic shunts (EHPSS) has been demonstrated in several small dog breeds. If in general both portocaval and porto-azygous shunts occur in breeds predisposed to portosystemic shunts then this could indicate a common genetic background. This study was performed to determine the distribution of extrahepatic portocaval and porto-azygous shunts in purebred dog populations. RESULTS: Data of 135 client owned dogs diagnosed with EHPSS at the Faculty of Veterinary Medicine of Utrecht University from 2001 – 2010 were retrospectively analyzed. The correlation between shunt localization, sex, age, dog size and breed were studied. The study group consisted of 54 males and 81 females from 24 breeds. Twenty-five percent of dogs had porto-azygous shunts and 75% had portocaval shunts. Of the dogs with porto-azygous shunts only 27% was male (P = 0.006). No significant sex difference was detected in dogs with a portocaval shunt. Both phenotypes were present in almost all breeds represented with more than six cases. Small dogs are mostly diagnosed with portocaval shunts (79%) whereas both types are detected. The age at diagnosis in dogs with porto-azygous shunts was significantly higher than that of dogs with portocaval shunts (P < 0.001). CONCLUSION: The remarkable similarity of phenotypic variation in many dog breeds may indicate common underlying genes responsible for EHPSS across breeds. The subtype of EHPSS could be determined by a minor genetic component or modulating factors during embryonic development. BioMed Central 2012-07-11 /pmc/articles/PMC3602064/ /pubmed/22784395 http://dx.doi.org/10.1186/1746-6148-8-112 Text en Copyright ©2012 Van den Bossche et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Van den Bossche, Lindsay van Steenbeek, Frank G Favier, Robert P Kummeling, Anne Leegwater, Peter AJ Rothuizen, Jan Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds |
title | Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds |
title_full | Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds |
title_fullStr | Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds |
title_full_unstemmed | Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds |
title_short | Distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds |
title_sort | distribution of extrahepatic congenital portosystemic shunt morphology in predisposed dog breeds |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602064/ https://www.ncbi.nlm.nih.gov/pubmed/22784395 http://dx.doi.org/10.1186/1746-6148-8-112 |
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