Division of Neuroimmunology, Department of Neurology, Rostock University Medical Center, Gehlsheimer Str. 20, 18147 Rostock, Germany.
Department of Neurology, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Biomolecules. 2021 Oct 13;11(10):1510. doi: 10.3390/biom11101510.
Telomeres are protective structures at the ends of linear chromosomes. Shortened telomere lengths (TL) are an indicator of premature biological aging and have been associated with a wide spectrum of disorders, including multiple sclerosis (MS). MS is a chronic inflammatory, demyelinating and neurodegenerative disease of the central nervous system. The exact cause of MS is still unclear. Here, we provide an overview of genetic, environmental and lifestyle factors that have been described to influence TL and to contribute to susceptibility to MS and possibly disease severity. We show that several early-life factors are linked to both reduced TL and higher risk of MS, e.g., adolescent obesity, lack of physical activity, smoking and vitamin D deficiency. This suggests that the mechanisms underlying the disease are connected to cellular aging and senescence promoted by increased inflammation and oxidative stress. Additional prospective research is needed to clearly define the extent to which lifestyle changes can slow down disease progression and prevent accelerated telomere loss in individual patients. It is also important to further elucidate the interactions between shared determinants of TL and MS. In future, cell type-specific studies and advanced TL measurement methods could help to better understand how telomeres may be causally involved in disease processes and to uncover novel opportunities for improved biomarkers and therapeutic interventions in MS.
端粒是线性染色体末端的保护结构。端粒长度缩短(TL)是生物衰老过早的一个指标,与广泛的疾病有关,包括多发性硬化症(MS)。MS 是一种慢性炎症、脱髓鞘和中枢神经系统神经退行性疾病。MS 的确切病因仍不清楚。在这里,我们提供了遗传、环境和生活方式因素的概述,这些因素被描述为影响 TL,并有助于 MS 的易感性,可能还有疾病的严重程度。我们表明,有几个青春期的因素与 TL 缩短和 MS 风险增加有关,例如青少年肥胖、缺乏体育活动、吸烟和维生素 D 缺乏。这表明,疾病的机制与由炎症和氧化应激增加引起的细胞衰老和衰老有关。需要进一步的前瞻性研究来明确生活方式的改变在多大程度上可以减缓疾病的进展,并防止个体患者的端粒加速丢失。进一步阐明 TL 和 MS 的共同决定因素之间的相互作用也很重要。在未来,细胞类型特异性研究和先进的 TL 测量方法可以帮助更好地了解端粒如何可能在疾病过程中起因果作用,并为 MS 中改进的生物标志物和治疗干预措施提供新的机会。