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Comprehensive longi...
Comprehensive longitudinal study of epigenetic mutations in aging
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- Wang, Yunzhang (författare)
- Karolinska Institutet
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- Karlsson, Robert (författare)
- Karolinska Institutet
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- Jylhävä, Juulia (författare)
- Karolinska Institutet
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- Hedman, Åsa K. (författare)
- Karolinska Institutet
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- Almqvist, Catarina (författare)
- Karolinska Institutet
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- Karlsson, Ida K. (författare)
- Karolinska Institutet,Jönköping University,HHJ, Institutet för gerontologi,HHJ. ARN-J (Aging Research Network - Jönköping),Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden
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- Pedersen, Nancy L. (författare)
- Karolinska Institutet
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- Almgren, Malin (författare)
- Department of Clinical Neuroscience, Centrum for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden
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- Hägg, Sara (författare)
- Karolinska Institutet
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(creator_code:org_t)
- 2019-12-09
- 2019
- Engelska.
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Ingår i: Clinical Epigenetics. - : BioMed Central. - 1868-7083 .- 1868-7075. ; 11
- Relaterad länk:
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https://doi.org/10.1...
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https://clinicalepig...
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https://urn.kb.se/re...
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https://doi.org/10.1...
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http://kipublication...
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Abstract
Ämnesord
Stäng
- Background: The role of DNA methylation in aging has been widely studied. However, epigenetic mutations, here defined as aberrant methylation levels compared to the distribution in a population, are less understood. Hence, we investigated longitudinal accumulation of epigenetic mutations, using 994 blood samples collected at up to five time points from 375 individuals in old ages.Results: We verified earlier cross-sectional evidence on the increase of epigenetic mutations with age, and identified important contributing factors including sex, CD19+ B cells, genetic background, cancer diagnosis, and technical artifacts. We further classified epigenetic mutations into High/Low Methylation Outliers (HMO/LMO) according to their changes in methylation, and specifically studied methylation sites (CpGs) that were prone to mutate (frequently mutated CpGs). We validated four epigenetically mutated CpGs using pyrosequencing in 93 samples. Furthermore, by using twins, we concluded that the age-related accumulation of epigenetic mutations was not related to genetic factors, hence driven by stochastic or environmental effects.Conclusions: Here we conducted a comprehensive study of epigenetic mutation and highlighted its important role in aging process and cancer development.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
Nyckelord
- Aging
- Cancer
- Epigenetic mutation
- Twin study
- adult
- article
- artifact
- B lymphocyte
- cancer diagnosis
- epigenetics
- female
- genetic background
- human
- human cell
- human experiment
- human tissue
- longitudinal study
- major clinical study
- male
- methylation
- pyrosequencing
- stochastic model
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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