Neuroaxonal dystrophy associated with vitamin E deficiency in two Haflinger horses.
Abstract: Neuroaxonal dystrophy and minimal diffuse degenerative myelopathy was diagnosed in two female full sibling, 1- and 2-year-old, Haflinger horses. Both animals developed slowly progressive ataxia from the age of 4 months. Clinical signs, which were more prominent in the hind legs, included hypermetria and dysmetria. Histological examination revealed neuroaxonal dystrophy characterized by spheroid formation, vacuolation, astrogliosis and lipofuscin pigment deposition in macrophages and neuronal perikarya. These changes were restricted to the gracilis and cuneate nuclei, nucleus of the solitary tract, nucleus intermediomedialis in the sacral and the seventh segment of the cervical spinal cord and Stilling-Clarke's column in both horses and the medial vestibular nucleus in the older horse. Both diseased Haflingers had significantly reduced serum alpha- and gamma-tocopherol values. No significant alteration in serum total lipid concentrations and serum selenium values were observed. It is likely that the condition has a familial hereditary basis. It is unclear whether there is a link between the observed neuroaxonal dystrophy and vitamin E deficiency and further investigations are warranted.
Publication Date: 1990-07-01 PubMed ID: 2394844
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Summary
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The study reveals neuroaxonal dystrophy, a kind of neurological disorder, and minimal diffuse degenerative myelopathy in two young Haflinger horses likely associated with vitamin E deficiency. The horses exhibited specific symptoms, and researchers concluded that the condition might be inherited but more investigation is needed to confirm if the disorder is directly linked to the vitamin deficiency.
Study Subject and Diagnosis
- The study was conducted on two female Haflinger horses, aged 1 and 2 years, who were full siblings.
- Both the horses had been developing slow progressive ataxia or loss of control of bodily movements since they were 4 months old.
- More prominent symptoms were observed in the hind legs including hypermetria and dysmetria which relate to miscalculations in distance and speed of movements.
- Through a histological examination, the horses were diagnosed with neuroaxonal dystrophy, characterized by certain abnormalities in nervous tissue structures.
Disease Manifestation and Symptoms
- Abnormalities caused by neuroaxonal dystrophy included spheroid formation, vacuolation (formation of vacuoles or cavity), astrogliosis (increased activity of astrocytes in the central nervous system), and deposition of lipofuscin pigment (a sign of aging or damage) in macrophages (a type of white blood cell) and neuronal cell bodies.
- These changes were confined to specific areas of the nervous system, including the gracilis and cuneate nuclei, nucleus of the solitary tract, nucleus intermediomedialis in the sacral and the seventh segment of the cervical spinal cord and, additionally, in the medial vestibular nucleus in the older horse.
Biochemical Observations
- It was found that both the horses had significantly less serum alpha- and gamma-tocopherol, forms of vitamin E.
- The total lipid concentrations and serum selenium values in their blood were found to be normal.
Possible Causes of the Disorder
- A potential hereditary basis for the condition in these horses was proposed by the researchers due to the familial relationship of the subjects.
- A link between neuroaxonal dystrophy and vitamin E deficiency was suggested but not confirmed. The researchers indicated a need for further studies to establish the correlation definitively.
Cite This Article
APA
Baumgärtner W, Frese K, Elmadfa I.
(1990).
Neuroaxonal dystrophy associated with vitamin E deficiency in two Haflinger horses.
J Comp Pathol, 103(1), 114-119.
Publication
Researcher Affiliations
- Institut für Veterinär-Pathologie, Fustus-Liebig-Universität, Giessen, F.R.G.
MeSH Terms
- Animals
- Ataxia / etiology
- Ataxia / pathology
- Ataxia / veterinary
- Brain Diseases / etiology
- Brain Diseases / pathology
- Brain Diseases / veterinary
- Chromatography, High Pressure Liquid
- Female
- Hindlimb
- Horse Diseases / etiology
- Horse Diseases / pathology
- Horses
- Spinal Cord Diseases / etiology
- Spinal Cord Diseases / pathology
- Spinal Cord Diseases / veterinary
- Vitamin E / analysis
- Vitamin E Deficiency / complications
- Vitamin E Deficiency / pathology
- Vitamin E Deficiency / veterinary
Citations
This article has been cited 3 times.- Powers A, Peek SF, Reed S, Donnelly CG, Tinkler S, Gasper D, Woolard KD, Finno CJ. Equine neuroaxonal dystrophy/degenerative myeloencephalopathy in Gypsy Vanner horses. J Vet Intern Med 2024 May-Jun;38(3):1792-1798.
- Ma Y, Peng S, Donnelly CG, Ghosh S, Miller AD, Woolard K, Finno CJ. Genetic polymorphisms in vitamin E transport genes as determinants for risk of equine neuroaxonal dystrophy. J Vet Intern Med 2024 Jan-Feb;38(1):417-423.
- Finno CJ, Famula T, Aleman M, Higgins RJ, Madigan JE, Bannasch DL. Pedigree analysis and exclusion of alpha-tocopherol transfer protein (TTPA) as a candidate gene for neuroaxonal dystrophy in the American Quarter Horse. J Vet Intern Med 2013 Jan-Feb;27(1):177-85.
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