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复发性缓解型多发性硬化症患者血浆游离 DNA 的甲基化模式。

Methylation patterns of cell-free plasma DNA in relapsing-remitting multiple sclerosis.

机构信息

Rush University Medical Center, Department of Neurological Sciences, Multiple Sclerosis Center, Chicago, IL 60612, USA.

出版信息

J Neurol Sci. 2010 Mar 15;290(1-2):16-21. doi: 10.1016/j.jns.2009.12.018. Epub 2010 Jan 12.

Abstract

BACKGROUND

There is growing interest for identification of new targets for biomarker development in multiple sclerosis (MS). The goal of this study was to compare the concentration and the methylation patterns of cell-free plasma DNA (cfpDNA) in patients with relapsing-remitting multiple sclerosis (RRMS) and healthy individuals.

METHODS

Three 30-patient cohorts were examined: patients with RRMS, in either remission or exacerbation, and healthy individuals as controls. Concentration of cfpDNA was determined using a standard fluorometric assay. Patterns of methylation in 56 gene promoters were determined by a microarray-based assay (MethDet-56). The data were analyzed to identify statistically relevant differences among the study groups.

RESULTS

The concentration of cfpDNA in patients with RRMS was four to eight-fold higher compared to healthy controls. Significant differences in cfpDNA methylation patterns were detected in all three comparisons: RRMS patients in remission versus healthy controls were recognized with 79.2% sensitivity and 92.9% specificity; RRMS patients in exacerbation versus healthy controls were recognized with 75.9% sensitivity and 91.5% specificity; and RRMS patients in exacerbation versus those in remission were recognized with 70.8% sensitivity and 71.2% specificity.

CONCLUSION

Based on our findings, we conclude that patients with RRMS display unique disease- and state-specific changes of cfpDNA. Our findings are of clinical significance as they could be used in the development of potentially new biomarkers for MS. This is the first report in our knowledge describing such changes of cfpDNA in patients with MS.

摘要

背景

人们越来越有兴趣在多发性硬化症(MS)中寻找新的生物标志物开发靶点。本研究的目的是比较缓解期和活动期复发缓解型多发性硬化症(RRMS)患者与健康个体的循环无细胞血浆 DNA(cfpDNA)的浓度和甲基化模式。

方法

检查了三个 30 例患者队列:缓解期或恶化期 RRMS 患者,以及健康个体作为对照。使用标准荧光测定法确定 cfpDNA 的浓度。通过基于微阵列的测定法(MethDet-56)确定 56 个基因启动子的甲基化模式。对数据进行分析,以确定研究组之间存在统计学差异。

结果

RRMS 患者的 cfpDNA 浓度比健康对照组高四到八倍。在所有三种比较中均检测到 cfpDNA 甲基化模式的显着差异:缓解期 RRMS 患者与健康对照组的识别率为 79.2%,特异性为 92.9%;恶化期 RRMS 患者与健康对照组的识别率为 75.9%,特异性为 91.5%;恶化期 RRMS 患者与缓解期 RRMS 患者的识别率为 70.8%,特异性为 71.2%。

结论

基于我们的发现,我们得出结论,RRMS 患者显示出独特的疾病和状态特异性 cfpDNA 变化。我们的发现具有临床意义,因为它们可用于开发潜在的 MS 新生物标志物。这是我们所知的第一个描述 MS 患者 cfpDNA 发生这种变化的报告。

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