Sirtuin-1 level and gene polymorphisms in multiple sclerosis

Rania S. Nageeb, Amal Fawzy, Marwa Abdel-Monem Ateya, Aliaa Talaat
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Abstract

Sirtuin-1 (SIRT1) may affect multiple sclerosis (MS) disease. This study aimed to investigate the level of serum SIRT1, mRNA expression and genetic polymorphisms in Egyptian MS sufferers. Also, to assess its role as a possible biomarker in predicting the risk of MS and to evaluate the association between its levels and disability of MS. Measurement of SIRT1, serum level, mRNA expression level and genotyping for sirtuin-1 gene polymorphisms in 240 Egyptian subjects; 120 MS sufferers and 120 healthy control subjects. There was a significant diminishment of level of serum sirtuin-1, and sirtuin-1 mRNA expression in MS sufferers compared to control subjects. Different sirtuin-1 single nucleotide polymorphism frequencies were statistically significant in MS sufferers compared to the control subjects. Moreover, a negative correlation of serum level of sirtuin-1 in MS sufferers with MS disease duration, disability according to Expanded Disability Status Scale (EDSS) score, cholesterol, and triglyceride serum levels. Regarding the sirtuin-1 gene polymorphisms in MS sufferers, the rs7895833 GG genotype had significant higher cholesterol, and low-density lipoprotein (LDL) levels than the GA and AA genotypes and that the rs7069102 GG genotype had a higher LDL level than the CG and CC genotypes while the rs2273773 TT genotype was significantly associated with cholesterol, and LDL levels than the TC and CC genotypes. No significant difference was detected in EDSS score comparing different sirtuin-1 genotypes among MS sufferers. In MS sufferers, rs7895833 G allele can be independently associated with cholesterol, triglycerides, and LDL levels. rs7069102 C allele can be independently associated with LDL level. With regard to rs2273773, T allele, it can be independently associated with cholesterol and LDL levels. There was a significant association between different sirtuin-1 gene polymorphisms and dyslipidemia which may modulate the course of MS disease. Furthermore, serum sirtuin-1 level can be considered as a possible predictor of disability in multiple sclerosis sufferers.
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多发性硬化症患者的 Sirtuin-1 水平和基因多态性
Sirtuin-1(SIRT1)可能会影响多发性硬化症(MS)的病情。本研究旨在调查埃及多发性硬化症患者的血清 SIRT1 水平、mRNA 表达和基因多态性。同时,评估其作为预测多发性硬化症风险的可能生物标志物的作用,并评估其水平与多发性硬化症残疾之间的关联。在 240 名埃及受试者(120 名多发性硬化症患者和 120 名健康对照受试者)中测量 SIRT1、血清水平、mRNA 表达水平和 sirtuin-1 基因多态性基因分型。与对照组相比,多发性硬化症患者的血清sirtuin-1水平和sirtuin-1 mRNA表达量明显下降。与对照组相比,多发性硬化症患者体内不同的sirtuin-1单核苷酸多态性频率具有统计学意义。此外,多发性硬化症患者血清中的sirtuin-1水平与多发性硬化症的病程、残疾状况扩展量表(EDSS)评分、胆固醇和甘油三酯血清水平呈负相关。关于多发性硬化症患者的sirtuin-1基因多态性,rs7895833 GG基因型的胆固醇和低密度脂蛋白(LDL)水平明显高于GA和AA基因型,rs7069102 GG基因型的低密度脂蛋白水平高于CG和CC基因型,而rs2273773 TT基因型与胆固醇和低密度脂蛋白水平的相关性明显高于TC和CC基因型。在多发性硬化症患者中,比较不同的 sirtuin-1 基因型,EDSS 评分没有发现明显差异。在多发性硬化症患者中,rs7895833 G等位基因与胆固醇、甘油三酯和低密度脂蛋白水平独立相关,rs7069102 C等位基因与低密度脂蛋白水平独立相关。至于 rs2273773 T 等位基因,它与胆固醇和低密度脂蛋白水平独立相关。不同的sirtuin-1基因多态性与血脂异常之间存在明显的关联,而血脂异常可能会影响多发性硬化症的病程。此外,血清sirtuin-1水平可被视为多发性硬化症患者残疾的一个可能的预测指标。
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