Amyotrophic Lateral Sclerosis
- 1 March 1986
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 43 (3) , 234-238
- https://doi.org/10.1001/archneur.1986.00520030026007
Abstract
• We examined the family history and associated diseases in 58 patients with amyotrophic lateral sclerosis (ALS), as well as the T-cell phenotypes and functions in 46 consecutive patients with this disorder. A family history of thyroid disease was present in 19%, and an additional 21% of patients described family members with other possible autoimmune disorders. In 19% of the patients with ALS either past or present thyroid disease was documented. Eleven of 47 additional patients with ALS had significant elevations of microsomal and/or thyroglobulin antibody levels. The T-cell phenotypes and functions were comparable in the ALS and control groups, with the exception of the presence of Ia antigen. In patients with ALS, 11.9% of the T cells were positive for the Ia antigen, while in both a normal control population and a non-ALS neurologic disease population, only 6.4% of T cells have this antigenic determinant. These data support involvement of autoimmune mechanisms in ALS.This publication has 27 references indexed in Scilit:
- Thyroid Function in 44 Patients With Amyotrophic Lateral SclerosisArchives of Neurology, 1982
- The clinical spectrum of hexosaminidase deficiency diseasesNeurology, 1981
- Histocompatibility antigens associated with motor neurone diseaseJournal of the Neurological Sciences, 1977
- Epidemiology of Motor-Neuron DiseasesNew England Journal of Medicine, 1973
- Amyotrophic Lateral Sclerosis: Effect of Serum on Anterior Horn Cells in Tissue CultureScience, 1973
- Spinal muscular atrophy secondary to macroglobulinemiaNeurology, 1968
- Toxicity of motor neurone disease serum for myelin in tissue culture.BMJ, 1965
- Functional Studies of Cultured Brain Tissues as Related to "Demyelinative Disorders"Science, 1965
- Amyotrophic lateral sclerosis with progressive dementiaNeurology, 1962
- A syndrome clinically resembling amyotrophic lateral sclerosis following chronic mercurialismNeurology, 1961