Ultrasound imaging in an experimental model of fatty liver disease and cirrhosis in rats

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dc.contributor.authorLessa, Andréia S
dc.contributor.authorParedes, Bruno D
dc.contributor.authorDias, Juliana V
dc.contributor.authorCarvalho, Adriana B
dc.contributor.authorQuintanilha, Luiz Fernando
dc.contributor.authorTakiya, Christina M
dc.contributor.authorTura, Bernardo R
dc.contributor.authorRezende, Guilherme F M
dc.contributor.authorCarvalho, Antonio C Campos de
dc.contributor.authorResende, Célia M C
dc.contributor.authorGoldenberg, Regina C S
dc.date.accessioned2024-01-05T12:27:12Z
dc.date.available2024-01-05T12:27:12Z
dc.date.issued2010
dc.description.abstractBackground: Domestic dogs and cats are very well known to develop chronic hepatic diseases, including hepatic lipidosis and cirrhosis. Ultrasonographic examination is extensively used to detect them. However, there are still few reports on the use of the ultrasound B-mode scan in correlation with histological findings to evaluate diffuse hepatic changes in rodents, which represent the most important animal group used in experimental models of liver diseases. The purpose of this study was to determine the reliability of ultrasound findings in the assessment of fatty liver disease and cirrhosis when compared to histological results in Wistar rats by following up a murine model of chronic hepatic disease. Results: Forty Wistar rats (30 treated, 10 controls) were included. Liver injury was induced by dual exposure to CCl4 and ethanol for 4, 8 and 15 weeks. Liver echogenicity, its correlation to the right renal cortex echogenicity, measurement of portal vein diameter (PVD) and the presence of ascites were evaluated and compared to histological findings of hepatic steatosis and cirrhosis. Liver echogenicity correlated to hepatic steatosis when it was greater or equal to the right renal cortex echogenicity, with a sensitivity of 90%, specificity of 100%, positive and negative predictive values of 100% and 76.9% respectively, and accuracy of 92.5%. Findings of heterogeneous liver echogenicity and irregular surface correlated to liver cirrhosis with a sensitivity of 70.6%, specificity of 100%, positive and negative predictive values of 100% and 82.1% respectively, and accuracy of 87.5%. PVD was significantly increased in both steatotic and cirrhotic rats; however, the later had greater diameters. PVD cut-off point separating steatosis from cirrhosis was 2.1 mm (sensitivity of 100% and specificity of 90.5%). One third of cirrhotic rats presented with ascites. Conclusion: The use of ultrasound imaging in the follow-up of murine diffuse liver disease models is feasible and efficient, especially when the studied parameters are used in combination. The potential implication of this study is to provide a non-invasive method that allows follow-up studies of fatty liver disease and cirrhosis of individual rats for pre-clinical drug or cell based therapies.
dc.identifier.citationLessa AS, Paredes BD, Dias JV, Carvalho AB, Quintanilha LF, Takiya CM, Tura BR, Rezende GF, Campos de Carvalho AC, Resende CM, Goldenberg RC. Ultrasound imaging in an experimental model of fatty liver disease and cirrhosis in rats. BMC Vet Res. 2010 Jan 29;6:6. doi: .
dc.identifier.otherDOI: 10.1186/1746-6148-6-6
dc.identifier.urihttps://dspace.inc.saude.gov.br/handle/123456789/388
dc.language.isoen
dc.publisherBMC Veterinary Research
dc.subject.meshAnimalsen
dc.subject.meshAscites / pathologyen
dc.subject.meshCarbon Tetrachlorideen
dc.subject.meshDisease Models, Animalen
dc.subject.meshEthanolen
dc.subject.meshFatty Liver / chemically induceden
dc.subject.meshFatty Liver / diagnostic imaging*en
dc.subject.meshFatty Liver / pathologyen
dc.subject.meshFemaleen
dc.subject.meshLiver Cirrhosis / chemically induceden
dc.subject.meshLiver Cirrhosis / diagnostic imaging*en
dc.subject.meshLiver Cirrhosis / pathologyen
dc.subject.meshPortal Vein / pathologyen
dc.subject.meshRatsen
dc.subject.meshReproducibility of Resultsen
dc.subject.meshSpleen / pathologyen
dc.subject.meshUltrasonographyen
dc.titleUltrasound imaging in an experimental model of fatty liver disease and cirrhosis in rats
dc.typeArticle
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