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 inNature medicine Vol. 26; no. 1; pp. 83 - 90
Main Authors Ahadi, Sara, Zhou, Wenyu, Schüssler-Fiorenza Rose, Sophia Miryam, Sailani, M. Reza, Contrepois, Kévin, Avina, Monika, Ashland, Melanie, Brunet, Anne, Snyder, Michael
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.01.2020
Nature Publishing Group
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Summary: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, 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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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