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J Vet Intern Med. 2013 Jul-Aug;27(4):862-74. doi: 10.1111/jvim.12093. Epub 2013 May 10.

A comprehensive pathological survey of duodenal biopsies from dogs with diet-responsive chronic enteropathy.

Author information

1
Department of Clinical Sciences and Services, The Royal Veterinary College, Hatfield, UK.

Abstract

BACKGROUND:

The detailed pathological phenotype of diet-responsive chronic enteropathy (CE) and its modulation with dietary therapy remain poorly characterized.

HYPOTHESIS/OBJECTIVES:

Key mucosal lesions of diet-responsive CE resolve with dietary therapy.

METHODS:

This was a prospective observational study of 20 dogs with diet-responsive CE. Endoscopic duodenal biopsies collected before and 6 weeks after the start of a dietary trial were assessed by means of qualitative and quantitative histopathological, immunohistochemical, and ultrastructural criteria. Control duodenal biopsies were obtained from 10 healthy Beagle dogs on 1 occasion.

RESULTS:

Compared with control dogs, the CE dogs had higher villus stunting scores and higher overall WSAVA scores, a lower villus height-to-width ratio, and higher lamina propria density of eosinophils. The CE dogs also had ultrastructural lesions of the mitochondria and brush border. In common with other studies in which the disease and control populations are not matched for breed, age, sex, and environment, these comparisons should be interpreted with caution. Comparing biopsies collected at presentation and 6 weeks after starting the dietary trial, mean lamina propria mononuclear cell score and lamina propria densities of eosinophils and mononuclear cells decreased. Dietary therapy also improved ultrastructural lesions of the mitochondria and brush border, eliciting a decrease in intermicrovillar space and an increase in microvillus height.

CONCLUSIONS AND CLINICAL IMPORTANCE:

In dogs with diet-responsive CE, the remission of clinical signs with dietary therapy is associated with subtle decreases in lamina propria density of eosinophils and mononuclear cells, and resolution of ultrastructural lesions of the enterocyte.

KEYWORDS:

Eosinophil; Inflammatory bowel disease; Microscopy; Permeability; Ultrastructure; WSAVA standards

PMID:
23663231
DOI:
10.1111/jvim.12093
[Indexed for MEDLINE]
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