The Relation between Age, Gender and Apoptosis Regulator FasL Gene Expression in Multiple Sclerosis Patients

Atefeh Faraz, R. Yari, M. Taheri, M. Omrani, M. Saberi, M. Mazdeh, A. Sayad
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引用次数: 5

Abstract

"Multiple sclerosis (MS) is the most common chronic inflammatory demyelinating disease of the central nervous system (CNS). The exact immunopathogenic mechanisms are not known but there is some evidence that this severe disease is more likely to develop in genetically predisposed individuals, possibly in association with environmental factors Elimination of autoreactive T cells by activation induced cell-death (AICD) is considered to be one of major process in MS. The aim of this study were to evaluate expression level of FasL in whole blood from patients with Relapsing-Remitting (RR) form of MS, and to survey the association of FasL expression with risk, Expanded Disability Status Scale (EDSS) and duration of the disease. We compared FasL expression in 50 RR-MS patients with 50 healthy controls by Taqman Real time PCR technique. Albeit there was an expression decrease, no statistically significant difference was found between total RR-MS patients and controls. However, our results showed a clear association between decrease of FasL expression in females especially older than 40 years with risk of the disease (p= 0.04, 95% CI= 0.387-1.14; p= 0.003, 95% CI= 0.139-3.12, respectively). Moreover, there was not a significant correlation between EDSS and duration of the disease and FasL expression. This finding make a valuable question what is the principal concept for this significant association between FasL expression and risk of RR-MS in females who are older than 40 years. In this study, we failed to draw an exact expression– phenotype correlation which may be due to limited statistical confirmation as a result of the small sample size and needs more investigation. These findings may possibly reflect differences in the pathogenic mechanisms associated with the failure of AICD observed in this group of MS patients."
年龄、性别与多发性硬化症患者细胞凋亡调节因子FasL基因表达的关系
多发性硬化症(MS)是中枢神经系统(CNS)最常见的慢性炎症性脱髓鞘疾病。确切的免疫致病机制尚不清楚,但有证据表明,这种严重疾病更有可能在遗传易感个体中发展,可能与环境因素有关,激活诱导细胞死亡(AICD)消除自身反应性T细胞被认为是MS的主要过程之一。本研究的目的是评估复发缓解型(RR) MS患者全血中FasL的表达水平。并调查FasL表达与风险、扩展残疾状态量表(EDSS)和疾病持续时间的关系。我们用Taqman Real time PCR技术比较了50例RR-MS患者和50名健康对照者的FasL表达。虽然有表达减少,但总RR-MS患者与对照组之间无统计学差异。然而,我们的研究结果显示,FasL表达的降低在女性,尤其是40岁以上的女性中与疾病的风险有明显的关联(p= 0.04, 95% CI= 0.387-1.14;p= 0.003, 95% CI= 0.139-3.12)。此外,EDSS与病程和FasL表达之间无显著相关性。这一发现提出了一个有价值的问题,即FasL表达与40岁以上女性RR-MS风险之间的显著关联的主要概念是什么。在本研究中,我们未能得出准确的表达-表型相关性,这可能是由于样本量小,统计证实有限,需要进一步研究。这些发现可能反映了在这组MS患者中观察到的与AICD失败相关的致病机制的差异。”
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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