Skip to main content
padlock icon - secure page this page is secure

Progression of multiple sclerosis is associated with exon 1 CTLA-4 gene polymorphism

Buy Article:

$52.00 + tax (Refund Policy)

Bilińska M, Frydecka I, Noga L, Dobosz T, Żołędziewska M, Suwalska K, Tutak A, Pokryszko-Dragan A. Progression of multiple sclerosis is associated with exon 1 CTLA-4 gene polymorphism.

Acta Neurol Scand 2004 DOI: 10.1111/j.1600-0404.2004.00271.x © Blackwell Munksgaard 2004. Objectives –

Multiple sclerosis (MS) is a chronic demyelinating disease of the central nervous system which is widely believed to have a T-cell-mediated etiology. The cytotoxic T-lymphocyte antigen-4 (CTLA-4) antigen molecule plays a key role in the downregulation of T-cell responses. To examine the genetic association of the CTLA-4 gene locus with MS, we analyzed an exon 1 (A49G) transition. Material and methods –

One hundred and fifty-two MS patients and 154 controls were examined. The A/G transition was genotyped by a polymerase chain reaction followed by labeling with a SNaPshot kit and detection using a capillary genetic analyzer. Results –

The genotype, allele and phenotype frequencies did not differ significantly between MS patients and controls. Those MS patients with AA and AG genotypes had 4.36 times greater risk of progressing from the relapsing–remitting to the secondary progressive form of the disease than those with the GG genotype. Conclusion –

The results of our study indicate that CTLA-4 (A49G) exon 1 polymorphism is associated with MS progression.
No References
No Citations
No Supplementary Data
No Article Media
No Metrics

Keywords: CTLA-4 (A49G) exon 1 polymorphism; clinical course; multiple sclerosis

Document Type: Research Article

Affiliations: 1: Department of Neurology, Wrocław Medical University, Poland 2: Pathophysiology 3: Institute of Forensic Medicine, Wrocław Medical University, Wrocław, Poland 4: Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland

Publication date: July 1, 2004

  • Access Key
  • Free content
  • Partial Free content
  • New content
  • Open access content
  • Partial Open access content
  • Subscribed content
  • Partial Subscribed content
  • Free trial content
Cookie Policy
Cookie Policy
Ingenta Connect website makes use of cookies so as to keep track of data that you have filled in. I am Happy with this Find out more