Agah Elmira, Zardoui Arshia, Saghazadeh Amene, Ahmadi Mona, Tafakhori Abbas, Rezaei Nima
Students' Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran.
NeuroImmunology Research Association (NIRA), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
PLoS One. 2018 Jan 18;13(1):e0190252. doi: 10.1371/journal.pone.0190252. eCollection 2018.
Identifying a reliable biomarker may accelerate diagnosis of multiple sclerosis (MS) and lead to early management of the disease. Accumulating evidence suggest that cerebrospinal fluid (CSF) and peripheral blood concentration of osteopontin (OPN) may have diagnostic and prognostic value in MS. We conducted a systematic review and meta-analysis of studies that measured peripheral blood and CSF levels of OPN in MS patients and controls to evaluate the diagnostic potential of this biomarker better. We searched PubMed, Web of Science and Scopus databases to find articles that measured OPN concentration in peripheral blood and CSF samples from MS patients up to October 19, 2016. Q statistic tests and the I2 index were applied for heterogeneity assessment. If the I2 index was less than 40%, the fixed-effects model was used for meta-analysis. Random-effects meta-analysis was chosen if the I2 value was greater than 40%. After removal of duplicates, 918 articles were identified, and 27 of them fulfilled the inclusion criteria. We included 22 eligible studies in the final meta-analysis. MS patients, in general, had considerably higher levels of OPN in their CSF and blood when compared to all types of controls (p<0.05). When the comparisons were made between different subtypes of MS patients and controls, the results pointed to significantly higher levels of OPN in CSF of MS subgroups (p<0.05). All subtypes of MS patients, except CIS patients, had increased blood levels of OPN compared to controls (p<0.05). In the second set of meta-analyses, we compared the peripheral blood and CSF concentrations of OPN between MS patient subtypes. CIS patients had significantly lower levels of OPN both in their peripheral blood and CSF compared to patients with progressive subtypes of MS (p<0.05). CSF concentration of OPN was significantly higher among RRMS patients compared to the CIS patients and SPMS patients (P<0.05). Finally, patients with active MS had significantly higher OPN levels in their CSF compared to patients with stable disease (P = 0.007). The result of this study confirms that increased levels of OPN exist in CSF and peripheral blood of MS patients and strengthens the evidence regarding the clinical utility of OPN as a promising and validated biomarker for MS.
识别一种可靠的生物标志物可能会加速多发性硬化症(MS)的诊断并实现该疾病的早期管理。越来越多的证据表明,骨桥蛋白(OPN)在脑脊液(CSF)和外周血中的浓度可能在MS中具有诊断和预后价值。我们对测量MS患者和对照者外周血和CSF中OPN水平的研究进行了系统评价和荟萃分析,以更好地评估这种生物标志物的诊断潜力。我们检索了PubMed、科学网和Scopus数据库,以查找截至2016年10月19日测量MS患者外周血和CSF样本中OPN浓度的文章。应用Q统计检验和I2指数进行异质性评估。如果I2指数小于40%,则采用固定效应模型进行荟萃分析。如果I2值大于40%,则选择随机效应荟萃分析。在去除重复项后,共识别出918篇文章,其中27篇符合纳入标准。我们将22项符合条件的研究纳入最终的荟萃分析。总体而言,与所有类型的对照相比,MS患者脑脊液和血液中的OPN水平显著更高(p<0.05)。当在不同亚型的MS患者和对照之间进行比较时,结果表明MS亚组脑脊液中的OPN水平显著更高(p<0.05)。与对照相比,除临床孤立综合征(CIS)患者外,所有亚型的MS患者血液中的OPN水平均升高(p<0.05)。在第二组荟萃分析中,我们比较了MS患者亚型之间外周血和CSF中OPN的浓度。与进展型MS亚型患者相比,CIS患者外周血和CSF中的OPN水平均显著较低(p<0.05)。复发缓解型MS(RRMS)患者脑脊液中OPN的浓度显著高于CIS患者和继发进展型MS(SPMS)患者(P<0.05)。最后,与病情稳定的患者相比,活动期MS患者脑脊液中的OPN水平显著更高(P = 0.007)。本研究结果证实,MS患者脑脊液和外周血中OPN水平升高,并加强了关于OPN作为一种有前景且经过验证的MS生物标志物的临床效用的证据。