Undulating changes in human plasma proteome profiles across the lifespan.
cross_sectional · Level IV
Where this comes from
- Record sourced from PubMed, PMID 31806903.
- Also identified by DOI 10.1038/s41591-019-0673-2 and PMC identifier 7062043.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Aging is a predominant risk factor for several chronic diseases that limit healthspan<sup>1</sup>. Mechanisms of aging are thus increasingly recognized as potential therapeutic targets. Blood from young mice reverses aspects of aging and disease across multiple tissues<sup>2-10</sup>, which supports a hypothesis that age-related molecular changes in blood could provide new insights into age-related disease biology. We measured 2,925 plasma proteins from 4,263 young adults to nonagenarians (18-95 years old) and developed a new bioinformatics approach that uncovered marked non-linear alterations in the human plasma proteome with age. Waves of changes in the proteome in the fourth, seventh and eighth decades of life reflected distinct biological pathways and revealed differential associations with the genome and proteome of age-related diseases and phenotypic traits. This new approach to the study of aging led to the identification of unexpected signatures and pathways that might offer potential targets for age-related diseases.
Medical subject headings
- Aging
- Blood Proteins
- Longevity
- Proteome