Serum Proteomic Signatures of Common Health Outcomes among Older Adults

Author:

Roberts Jackson A.,Basu-Roy Sayantani,Shin Jong,Varma Vijay R.,Williamson Andrew,Blackshear Chad,Griswold Michael E.,Candia Julián,Elango Palchamy,Karikkineth Ajoy C.,Tanaka Toshiko,Ferrucci Luigi,Thambisetty Madhav

Abstract

<b><i>Introduction:</i></b> In aging populations, the coexistence of multiple health comorbidities represents a significant challenge for clinicians and researchers. Leveraging advances in omics techniques to characterize these health conditions may provide insight into disease pathogenesis as well as reveal biomarkers for monitoring, prognostication, and diagnosis. Researchers have previously established the utility of big data approaches with respect to comprehensive health outcome measurements in younger populations, identifying protein markers that may provide significant health information with a single blood sample. <b><i>Methods:</i></b> Here, we employed a similar approach in two cohorts of older adults, the Baltimore Longitudinal Study of Aging (mean age = 76.12 years) and InCHIANTI Study (mean age = 66.05 years), examining the relationship between levels of serum proteins and 5 key health outcomes: kidney function, fasting glucose, physical activity, lean body mass, and percent body fat. <b><i>Results:</i></b> Correlations between proteins and health outcomes were primarily shared across both older adult cohorts. We further identified that most proteins associated with health outcomes in the older adult cohorts were not associated with the same outcomes in a prior study of a younger population. A subset of proteins, adiponectin, MIC-1, and NCAM-120, were associated with at least three health outcomes in both older adult cohorts but not in the previously published younger cohort, suggesting that they may represent plausible markers of general health in older adult populations. <b><i>Conclusion:</i></b> Taken together, these findings suggest that comprehensive protein health markers have utility in aging populations and are distinct from those identified in younger adults, indicating unique mechanisms of disease with aging.

Publisher

S. Karger AG

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