Chojdak-Łukasiewicz Justyna, Bizoń Anna, Kołtuniuk Aleksandra, Waliszewska-Prosół Marta, Budrewicz Sławomir, Piwowar Agnieszka, Pokryszko-Dragan Anna
Clinical Department of Neurology, Faculty of Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, Poland.
Department of Toxicology, Faculty of Pharmacy, Wroclaw Medical University, Borowska 211, 50-556 Wroclaw, Poland.
Biomedicines. 2024 Sep 5;12(9):2027. doi: 10.3390/biomedicines12092027.
SIRTs were demonstrated to play an important role in inflammatory, degenerative, and metabolic alterations, constituting the background of the central nervous system. Thus, they seem to be an appropriate object of investigation (as potential biomarkers of disease activity and/or novel therapeutic targets) in multiple sclerosis (MS), which has a complex etiology that comprises a cross-talk between all these processes. The aim of this study was to evaluate the levels of SIRT1 and SIRT2 in the serum of patients with the relapsing-remitting type of MS (RRMS), as well as their relationships with various aspects of MS-related disability.
A total of 115 patients with RRMS (78 women, 37 men, mean age 43 ± 9.9) and 39 healthy controls were included in the study. SIRT1 and SIRT2 were detected in the serum using the enzyme-linked immunoassay (ELISA) method. In the RRMS group, relationships were investigated between the SIRT 1 and 2 levels and the demographic data, MS-related clinical variables, and the results of tests evaluating fatigue, sleep problems, cognitive performance, autonomic dysfunction, and depression.
The levels of SIRT1 and SIRT2 in RRMS patients were significantly lower than in the controls (11.14 vs. 14. 23, = 0.04; 8.62 vs. 14.2, < 0.01). In the RRMS group, the level of both SIRTs was higher in men than in women (15.7 vs. 9.0; 11.3 vs. 7.3, = 0.002) and showed a significant correlation with the degree of disability (R = -0.25, = 0.018). No other relationships were found between SIRT levels and the analyzed data.
The serum levels of SIRT1 and 2 were decreased in the RRMS patients (especially in the female ones) and correlated with the degree of neurological deficit. The role of SIRTs as biomarkers of disease activity or mediators relevant for "invisible disability" in MS warrants further investigation.
已证明沉默调节蛋白(SIRTs)在炎症、退行性变和代谢改变中起重要作用,这些改变构成了中枢神经系统的背景。因此,它们似乎是多发性硬化症(MS)研究的合适对象(作为疾病活动的潜在生物标志物和/或新的治疗靶点),MS的病因复杂,包括所有这些过程之间的相互作用。本研究的目的是评估复发缓解型MS(RRMS)患者血清中SIRT1和SIRT2的水平,以及它们与MS相关残疾各方面的关系。
本研究共纳入115例RRMS患者(78例女性,37例男性,平均年龄43±9.9岁)和39名健康对照者。采用酶联免疫吸附测定(ELISA)法检测血清中的SIRT1和SIRT2。在RRMS组中,研究了SIRT1和2水平与人口统计学数据、MS相关临床变量以及评估疲劳、睡眠问题、认知表现、自主神经功能障碍和抑郁的测试结果之间的关系。
RRMS患者的SIRT1和SIRT2水平显著低于对照组(11.14对14.23,P = 0.04;8.62对14.2,P < 0.01)。在RRMS组中,男性的两种SIRTs水平均高于女性(15.7对9.0;11.3对7.3,P = 0.002),且与残疾程度呈显著相关(R = -0.25,P = 0.018)。未发现SIRT水平与分析数据之间的其他关系。
RRMS患者(尤其是女性患者)血清中SIRT1和2水平降低,且与神经功能缺损程度相关。SIRTs作为MS疾病活动生物标志物或与“隐性残疾”相关介质的作用值得进一步研究。