Personal aging markers and ageotypes revealed by deep longitudinal profiling
The molecular changes that occur with aging are not well understood 1 – 4 . Here, we performed longitudinal and deep multiomics profiling of 106 healthy individuals from 29 to 75 years of age and examined how different types of ‘omic’ measurements, including transcripts, proteins, metabolites, cytok...
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Published in | Nature medicine Vol. 26; no. 1; pp. 83 - 90 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.01.2020
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | The molecular changes that occur with aging are not well understood
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. Here, we performed longitudinal and deep multiomics profiling of 106 healthy individuals from 29 to 75 years of age and examined how different types of ‘omic’ measurements, including transcripts, proteins, metabolites, cytokines, microbes and clinical laboratory values, correlate with age. We identified both known and new markers that associated with age, as well as distinct molecular patterns of aging in insulin-resistant as compared to insulin-sensitive individuals. In a longitudinal setting, we identified personal aging markers whose levels changed over a short time frame of 2–3 years. Further, we defined different types of aging patterns in different individuals, termed ‘ageotypes’, on the basis of the types of molecular pathways that changed over time in a given individual. Ageotypes may provide a molecular assessment of personal aging, reflective of personal lifestyle and medical history, that may ultimately be useful in monitoring and intervening in the aging process.
Longitudinal multiomics profiling of a cohort of healthy people reveals distinct aging patterns—termed ageotypes—in different individuals. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 M. Ashland and W.Z. managed the cohort and coordinated clinical visits. A.B. and M.S. obtained funding and provided additional study resources. S.A., W.Z., A.B., S.M.S.-F.R. and M.S. wrote and revised the manuscript. M.S. supervised the overall study. S.A., W.Z., M.R.S., K.C. and M. Avina performed experimental bench work and collected data. W.Z. and S.A. analyzed the data and generated results, with contributions from S.M.S.-F.R. M. Avina managed and coordinated the biobank sample inventory. Author contributions |
ISSN: | 1078-8956 1546-170X 1546-170X |
DOI: | 10.1038/s41591-019-0719-5 |