Ageing affects subtelomeric DNA methylation in blood cells from a large European population enrolled in the MARK-AGE study
Autor: | Michele Zampieri, Beatrix Grubeck-Loebenstein, Alexander Bürkle, Mikko Hurme, P. Eline Slagboom, Florence Debacq-Chainiaux, Olivier Toussaint, Maria A. Blasco, Tilman Grune, Claudio Franceschi, Ewa Sikora, Maria Giulia Bacalini, Antti Hervonen, Eugène H.J.M. Jansen, Stefano Tagliatesta, Valentina Aversano, Anna Reale, Martijn E.T. Dollé, Miriam Capri, Marco Malavolta, Maria Moreno-Villanueva, Efstathios S. Gonos, Christiane Schön, Nicolle Breusing, Fabio Ciccarone, Jürgen Bernhardt, Paola Caiafa |
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Přispěvatelé: | Bacalini M.G., Reale A., Malavolta M., Ciccarone F., Moreno-Villanueva M., Dolle M.E.T., Jansen E., Grune T., Gonos E.S., Schon C., Bernhardt J., Grubeck-Loebenstein B., Sikora E., Toussaint O., Debacq-Chainiaux F., Capri M., Hervonen A., Hurme M., Slagboom P.E., Breusing N., Aversano V., Tagliatesta S., Franceschi C., Blasco M.A., Burkle A., Caiafa P., Zampieri M. |
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Male Aging Offspring ageing subtelomere epigenetics DNA methylation Down syndrome centenarian offspring Population Context (language use) Centenarian offspring Biology 03 medical and health sciences 0302 clinical medicine ddc:570 Blood Cell Humans Epigenetics Settore BIO/10 education Cross-Sectional Studie Genetics Aged 80 and over education.field_of_study Subtelomere Blood Cells Epigenetic Methylation Europe Ageing 030104 developmental biology Cross-Sectional Studies 030220 oncology & carcinogenesis Female Original Article Geriatrics and Gerontology Human |
Zdroj: | Geroscience, 43(3), 1283-1302. SPRINGER GeroScience Bacalini, M G, Reale, A, Malavolta, M, Ciccarone, F, Moreno-Villanueva, M, Dollé, M E T, Jansen, E, Grune, T, Gonos, E S, Schön, C, Bernhardt, J, Grubeck-Loebenstein, B, Sikora, E, Toussaint, O, Debacq-Chainiaux, F, Capri, M, Hervonen, A, Hurme, M, Slagboom, P E, Breusing, N, Aversano, V, Tagliatesta, S, Franceschi, C, Blasco, M A, Bürkle, A, Caiafa, P & Zampieri, M 2021, ' Ageing affects subtelomeric DNA methylation in blood cells from a large European population enrolled in the MARK-AGE study ', GeroScience, vol. 43, no. 3, pp. 1283-1302 . https://doi.org/10.1007/s11357-021-00347-9 |
Popis: | Ageing leaves characteristic traces in the DNA methylation make-up of the genome. However, the importance of DNA methylation in ageing remains unclear. The study of subtelomeric regions could give promising insights into this issue. Previously reported associations between susceptibility to age-related diseases and epigenetic instability at subtelomeres suggest that the DNA methylation profile of subtelomeres undergoes remodelling during ageing. In the present work, this hypothesis has been tested in the context of the European large-scale project MARK-AGE. In this cross-sectional study, we profiled the DNA methylation of chromosomes 5 and 21 subtelomeres, in more than 2000 age-stratified women and men recruited in eight European countries. The study included individuals from the general population as well as the offspring of nonagenarians and Down syndrome subjects, who served as putative models of delayed and accelerated ageing, respectively. Significant linear changes of subtelomeric DNA methylation with increasing age were detected in the general population, indicating that subtelomeric DNA methylation changes are typical signs of ageing. Data also show that, compared to the general population, the dynamics of age-related DNA methylation changes are attenuated in the offspring of centenarian, while they accelerate in Down syndrome individuals. This result suggests that subtelomeric DNA methylation changes reflect the rate of ageing progression. We next attempted to trace the age-related changes of subtelomeric methylation back to the influence of diverse variables associated with methylation variations in the population, including demographics, dietary/health habits and clinical parameters. Results indicate that the effects of age on subtelomeric DNA methylation are mostly independent of all other variables evaluated. Supplementary Information The online version contains supplementary material available at 10.1007/s11357-021-00347-9. |
Databáze: | OpenAIRE |
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