Abstract
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.
Highlights
Division of Neuroimmunology, Department of Neurology, Rostock University Medical Center, Department of Neurology, Medical University of Vienna, Währinger Gürtel 18–20, 1090 Vienna, Austria
We present an overview of genetic, environmental and lifestyle factors that have been described to be associated with risk and possibly severity of multiple sclerosis (MS), on the one hand, and with telomere lengths (TL), on the other hand
Evidence is accumulating that leukocyte telomere length (LTL) provides an indication of immunocompetence
Summary
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Biobank indicated that longer telomeres are related to a higher risk of developing MS later in life (adjusted hazard ratio (HR) per standard deviation (SD) longer LTL = 1.27) [33]. This somewhat contradictory finding may suggest that shortened TLs in MS patients result from a higher rate of telomere attrition and/or as a consequence of pathophysiological processes. A better understanding of TL variation across human tissues and cell types may help to further delineate the relationship with age and the role of telomere-mediated mechanisms in disease risk
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.