Review on canine elbow dysplasia: pathogenesis, diagnosis, prevalence and genetic aspects.

Abstract

Elbow dysplasia (ED) is a progressive skeletal disease, which may comprise osteoarthrotic changes, incongruity of the joint, a fragmented medial coronoid process (FCP), osteochondrosis dissecans of the trochlea humeri (OCD), and an ununited anconeal process (UAP). Disturbances of enchondral ossification, as well as asynchronous growth of the antebrachial bones and an increased growth rate may provoke abnormal stresses on specific locations such as the medial coronoid process, the anconeal process of the ulna or the humeral trochlea, which may result in ED. Overnutrition with calcium, vitamin D and energy had important influence on rapidity of growth and proneness to ED. ED manifests most often in young dogs less than 1 1/2 year, causing clinical signs such as (intermittent) lameness, pain on movement and altered posture of the affected limb, and radiographically secondary osteoarthrotic changes such as osteophytes or the aforementioned primary lesions. As radiographic projection of the primary lesions FCP and OCD may be difficult in the commonly used mediolateral flexed and craniocaudal views, additional projections such as mediolateral extended or anteroposterior oblique views and alternative diagnostic means such as computed tomography (CT) may be worth considering. Cases of ED are reported in various breeds, though some breeds are especially predisposed and seem to be prone to specific primary lesions. For the German shepherd dog, a breed-predisposition for UAP may be explained by broad chondral junction in association with an accelerated pattern of skeletal maturation. Heritabilities were estimated in a variety of studies, depending strongly on the type of model used. The mode of inheritance is not yet ascertained, but recently the common assumption of a polygenic mode of inheritance for ED is doubted. Instead, genetic independence was supposed between different primary lesions, and also for ED as well as for FCP major gene influence was discussed. So long, phenotypic mass selection was accomplished in different countries most often resulting in a reduced prevalence of ED. The use of best linear unbiased prediction (BLUP) methods including information on relatives and separate evaluation of genetically independent primary lesions may further improve selection against ED.