| Literature DB >> 11777547 |
Francesca L Sciacca1, Cinzia Ferri, Fabrizio Veglia, Francesca Andreetta, Renato Mantegazza, Ferdinando Cornelio, Diego Franciotta, Giovanni Piccolo, Vittorio Cosi, Anna P Batocchi, Amelia Evoli, Luigi M E Grimaldi.
Abstract
Myasthenia gravis (MG) is a multifactorial autoimmune disease of the neuromuscular junction. We investigated the relation between four polymorphisms of the interleukin (IL)-1 gene cluster on 2q12-22, and MG susceptibility and clinical features in a large cohort of individuals. No polymorphism was associated with MG susceptibility. However, the IL-1A -889 CC genotype was associated with early disease onset (p=0.0044) in the whole MG group and the subgroup of CC males developed MG about 18 years earlier than males carrying other IL-1A -889 genotypes (p=0.022). This finding suggests that IL-1A is a disease modifier in MG, or is in linkage disequilibrium with an unknown locus on chromosome 2.Entities:
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Year: 2002 PMID: 11777547 DOI: 10.1016/s0165-5728(01)00449-0
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478