Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/205337
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dc.contributor.authorRodríguez Fernández, Blanca-
dc.contributor.authorGispert, Juan Domingo-
dc.contributor.authorGuigo, Roderic-
dc.contributor.authorNavarro, Arcadi-
dc.contributor.authorVilor Tejedor, Natalia-
dc.contributor.authorCrous Bou, Marta-
dc.date.accessioned2024-01-08T14:52:51Z-
dc.date.available2024-01-08T14:52:51Z-
dc.date.issued2022-08-05-
dc.identifier.issn2001-0370-
dc.identifier.urihttps://hdl.handle.net/2445/205337-
dc.description.abstractTelomere length (TL) is a biomarker of biological aging. Shorter telomeres have been associated with mortality and increased rates of age-related diseases. However, observational studies are unable to conclude whether TL is causally associated with those outcomes. Mendelian randomization (MR) was developed for assessing causality using genetic variants in epidemiological research. The objective of this study was to test the potential causal role of TL in neurodegenerative disorders and life expectancy through MR analysis. Summary level data were extracted from the most recent genome-wide association studies for TL, Alzheimer's disease (AD), Parkinson's disease, Frontotemporal dementia, Amyotrophic Lateral Sclerosis, Progressive Supranuclear Palsy and life expectancy. MR estimates revealed that longer telomeres inferred a protective effect on risk of AD (OR = 0.964; adjusted p-value = 0.039). Moreover, longer telomeres were significantly associated with increased life expectancy (beta(IVW) = 0.011; adjusted p-value = 0.039). Sensitivity analyses suggested evidence for directional pleiotropy in AD analyses. Our results showed that genetically predicted longer TL may increase life expectancy and play a protective causal effect on AD. We did not observe significant causal relationships between longer TL and other neurodegenerative diseases. This suggests that the involvement of TL on specific biological mechanisms might differ between AD and life expectancy, with respect to that in other neurodegenerative diseases. Moreover, the presence of pleiotropy may reflect the complex interplay between TL homeostasis and AD pathophysiology. Further observational studies are needed to confirm these results. (C) 2022 The Author(s). Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).-
dc.format.extent6 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier BV-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.csbj.2022.08.006-
dc.relation.ispartofComputational and Structural Biotechnology Journal, 2022, vol. 20, p. 4251-4256-
dc.relation.urihttps://doi.org/10.1016/j.csbj.2022.08.006-
dc.rightscc by-nc-nd (c) Rodríguez Fernández, Blanca et al., 2022-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationMalalties neurodegeneratives-
dc.subject.classificationTelòmer-
dc.subject.otherNeurodegenerative Diseases-
dc.subject.otherTelomere-
dc.titleGenetically predicted telomere length and its relationship with neurodegenerative diseases and life expectancy-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2023-12-13T13:29:13Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid36051868-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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