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1000 Titel
  • Whole blood DNA methylation aging markers predict colorectal cancer survival: a prospective cohort study
1000 Autor/in
  1. Gao, Xin |
  2. Zhang, Yan |
  3. Boakye, Daniel |
  4. Li, Xiangwei |
  5. Chang-Claude, Jenny |
  6. Hoffmeister, Michael |
  7. Brenner, Hermann |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-11-30
1000 Erschienen in
1000 Quellenangabe
  • 12(1):184
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13148-020-00977-4 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708179/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Blood DNA methylation-based aging algorithms predict mortality in the general population. We investigated the prognostic value of five established DNA methylation aging algorithms for patients with colorectal cancer (CRC).!##!Methods!#!AgeAccelHorvath, AgeAccelHannum, DNAmMRscore, AgeAccelPheno and AgeAccelGrim were constructed using whole blood epi-genomic data from 2206 CRC patients. After a median follow-up of 6.2 years, 1079 deaths were documented, including 596 from CRC. Associations of the aging algorithms with survival outcomes were evaluated using the Cox regression and survival curves. Harrell's C-statistics were computed to investigate predictive performance.!##!Results!#!Adjusted hazard ratios (95% confidence intervals) of all-cause mortality for patients in the third compared to the first tertile were 1.66 (1.32, 2.09) for the DNAmMRscore, 1.35 (1.14, 1.59) for AgeAccelPheno and 1.65 (1.37, 2.00) for AgeAccelGrim, even after adjustment for age, sex and stage. AgeAccelHorvath and AgeAccelHannum were not associated with all-cause or CRC-specific mortality. In stage-specific analyses, associations were much stronger for patients with early or intermediate stage cancers (stages I, II and III) than for patients with metastatic (stage IV) cancers. Associations were weaker and less often statistically significant for CRC-specific mortality. Adding DNAmMRscore, AgeAccelPheno or AgeAccelGrim to models including age, sex and tumor stage improved predictive performance moderately.!##!Conclusions!#!DNAmMRscore, AgeAccelPheno and AgeAccelGrim could serve as non-invasive CRC prognostic biomarkers independent of other commonly used markers. Further research should aim for tailoring and refining such algorithms for CRC patients and to explore their value for enhanced prediction of treatment success and treatment decisions.
1000 Sacherschließung
lokal DNA Methylation/genetics [MeSH]
lokal Aged, 80 and over [MeSH]
lokal Aged [MeSH]
lokal Mortality/trends [MeSH]
lokal Genetic Markers/genetics [MeSH]
lokal Aging/blood [MeSH]
lokal Colorectal cancer
lokal Prognosis
lokal Aging
lokal Neoplasm Metastasis/pathology [MeSH]
lokal Mortality
lokal Male [MeSH]
lokal Whole blood
lokal Case-Control Studies [MeSH]
lokal DNA methylation
lokal Female [MeSH]
lokal Follow-Up Studies [MeSH]
lokal Adult [MeSH]
lokal Aging/genetics [MeSH]
lokal Humans [MeSH]
lokal Prospective Studies [MeSH]
lokal Predictive Value of Tests [MeSH]
lokal Middle Aged [MeSH]
lokal Epigenomics/methods [MeSH]
lokal CpG Islands/genetics [MeSH]
lokal Cancer epigenetics and diagnostics
lokal Research
lokal Colorectal Neoplasms/pathology [MeSH]
lokal Prognosis [MeSH]
lokal Neoplasm Metastasis/genetics [MeSH]
lokal Neoplasm Staging/methods [MeSH]
lokal Colorectal Neoplasms/genetics [MeSH]
lokal Colorectal Neoplasms/mortality [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-0108-6961|https://frl.publisso.de/adhoc/uri/WmhhbmcsIFlhbg==|https://frl.publisso.de/adhoc/uri/Qm9ha3llLCBEYW5pZWw=|https://frl.publisso.de/adhoc/uri/TGksIFhpYW5nd2Vp|https://frl.publisso.de/adhoc/uri/Q2hhbmctQ2xhdWRlLCBKZW5ueQ==|https://frl.publisso.de/adhoc/uri/SG9mZm1laXN0ZXIsIE1pY2hhZWw=|https://frl.publisso.de/adhoc/uri/QnJlbm5lciwgSGVybWFubg==
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1000 Erstellt am 2023-11-18T17:46:52.196+0100
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1000 Zuletzt bearbeitet 2024-04-03T13:44:41.161+0200
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