We studied genetic polymorphisms in the promoter region at position -511 of the interleukin (IL) -1beta gene (IL-1B-511) and at position -889 of the IL-1alpha gene (IL-1A-889), in 111 Japanese patients with multiple system atrophy (MSA) and 160 controls. The distribution of IL-1B-511 was significant
Interleukin-1A (−889) genetic polymorphism increases the risk of multiple system atrophy
✍ Scribed by Onofre Combarros; Jon Infante; Javier Llorca; José Berciano
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 45 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0885-3185
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✦ Synopsis
Abstract
In a case‐control study using a clinically well‐defined group of 30 multiple system atrophy (MSA) patients and 110 control subjects, homozygosity for interleukin‐1A (IL‐1A) allele 2 (high secretor of proinflammatory cytokine) in the regulatory region (‐889) of the IL‐1A gene was associated with a fivefold increased risk for MSA. © 2003 Movement Disorder Society
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