Markianos Manolis, Koutsis Georgios, Evangelopoulos Maria-Eleftheria, Mandellos Dimitrios, Karahalios Georgios, Sfagos Constantin
Department of Neurology, Athens University Medical School, Eginition Hospital, Athens, Greece.
J Neurochem. 2009 Jan;108(1):158-64. doi: 10.1111/j.1471-4159.2008.05750.x. Epub 2008 Nov 12.
Axonal degeneration and brain tissue loss occur during disease progression in multiple sclerosis (MS) and are expected to influence neurotransmitter activities, with consequences on neurologic and psychiatric symptomatology. We searched for relationships of disease duration, disability, and severity of MS patients to CSF levels of the major metabolites of noradrenaline, dopamine, and serotonin, MHPG, methoxyhydroxyphenylglycol (MHPG), homovanillic acid, and 5-hydroxyindoleacetic acid (5-HIAA), respectively, in 39 patients with relapsing-remitting (RR) MS in remission, and 26 patients with progressive (PR) MS. Disability and Disease Severity were assessed by the Expanded Disability Status Scale (EDSS) and the Multiple Sclerosis Severity Score (MSSS). Compared with the levels of 50 control subjects, MHPG levels were not different in either MS group, correlated negatively to duration of illness and number of relapses in the RRMS group, but not to EDSS score or to MSSS. Homovanillic acid levels were significantly lower only in the PRMS group, with a negative correlation to duration of illness, and a strong negative correlation to EDSS score, but not to MSSS. 5-HIAA was significantly lower in both RRMS and PRMS groups. In the RRMS group, 5-HIAA levels were negatively related to EDSS and to MSSS. Multiple regression analyses revealed a significant association of MHPG to duration of illness, and a strong negative association of 5-HIAA to MSSS rather than to EDSS. The strong negative correlation of MSSS to CSF 5-HIAA levels in RRMS group of patients indicates that deficits in central serotonergic activity are related to the rate of disability accumulation in RRMS, and could be linked to the reported reduction of disease activity by serotonergic drugs.
在多发性硬化症(MS)的疾病进展过程中会发生轴突变性和脑组织损失,预计这会影响神经递质活性,进而对神经和精神症状产生影响。我们研究了39例缓解期复发缓解型(RR)MS患者和26例进展型(PR)MS患者的疾病持续时间、残疾程度以及MS严重程度与脑脊液中去甲肾上腺素、多巴胺和血清素主要代谢产物水平,即3-甲氧基-4-羟基苯乙二醇(MHPG)、甲氧基羟基苯乙二醇(MHPG)、高香草酸和5-羟基吲哚乙酸(5-HIAA)之间的关系。通过扩展残疾状态量表(EDSS)和多发性硬化症严重程度评分(MSSS)评估残疾和疾病严重程度。与50名对照受试者的水平相比,两个MS组的MHPG水平均无差异,在RRMS组中,MHPG水平与疾病持续时间和复发次数呈负相关,但与EDSS评分或MSSS无关。仅PRMS组的高香草酸水平显著降低,与疾病持续时间呈负相关,与EDSS评分呈强负相关,但与MSSS无关。RRMS组和PRMS组的5-HIAA均显著降低。在RRMS组中,5-HIAA水平与EDSS和MSSS呈负相关。多元回归分析显示,MHPG与疾病持续时间存在显著关联,5-HIAA与MSSS呈强负相关,而非与EDSS。RRMS组患者中MSSS与脑脊液5-HIAA水平的强负相关表明,中枢5-羟色胺能活性缺陷与RRMS中残疾累积率相关,并且可能与血清素能药物报道的疾病活动减少有关。