No Relation Between Cognitive Impairment, Physical Disability and Serum Biomarkers in a Cohort of Progressive Multiple Sclerosis Patients

被引:1
作者
Gajewski, Bartosz [1 ]
Karlinska, Iwona [1 ]
Domowicz, Malgorzata [1 ]
Bednarski, Igor [1 ]
Swiderek-Matysiak, Mariola [1 ]
Stasiolek, Mariusz [1 ]
机构
[1] Med Univ Lodz, Dept Neurol, Kopcinskiego 22, PL-90153 Lodz, Poland
关键词
progressive multiple sclerosis; biomarkers; cognitive impairment; progression; neurofilament light chain; chitanse-3; like-protein-1; Brief International Cognitive Assessment for Multiple Sclerosis; NEUROFILAMENT LIGHT-CHAIN; YKL-40; CXCL13; DYSFUNCTION; VALIDATION; DIAGNOSIS; ATROPHY; LEVEL; RISK; MS;
D O I
10.3390/biom15010068
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite significant efforts, there is still an existing need to identify diagnostic tools that would enable fast and reliable detection of the progressive stage of multiple sclerosis (MS) and help in monitoring the disease course and/or treatment effects. The aim of this prospective study in a group of people with progressive MS was to determine whether changes in the levels of selected serum biomarkers and in cognitive function may predict disease progression, and therefore refine the decision-making process in the evaluation of MS patients. Forty two (42) patients with progressive MS completed all the study procedures; the mean duration of follow-up was 12.97 months. During the observation period, serum concentration of chitinase-3 like-protein-1 (CHI3L1/YKL-40) decreased significantly in the whole study group (from 4034.95 +/- 262.62 to 2866.43 +/- 173.37; p = 0.0005), as well as in subgroups of people with secondary progressive and primary progressive MS (SPMS: from 3693.81 +/- 388.68 to 2542.76 +/- 256.59; p = 0.0207; and PPMS: from 4376.09 +/- 353.27 to 3190.09 +/- 233.22; p = 0.0089, respectively). A significant worsening of Brief International Cognitive Assessment for Multiple Sclerosis (BICAMS) scores was detected in the whole study group (from 1.18 +/- 0.14 to 1.34 +/- 0.15; p = 0.0331) as well as in the PPMS subgroup (from 1.04 +/- 0.18 to 1.26 +/- 0.20; p = 0.0216). No correlations between the analyzed molecular parameters or the results of neuropsychological tests and physical disability were observed. In conclusion, an emphasis should be placed on furthering the search for multimodal biomarkers of disease progression, especially in the PMS population, based on simultaneous analysis of several factors, such as blood biomarkers and cognitive profiles.
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页数:19
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