Plasma proteomic signature of age in healthy humans

被引:369
作者
Tanaka, Toshiko [1 ]
Biancotto, Angelique [2 ]
Moaddel, Ruin [3 ]
Moore, Ann Zenobia [1 ]
Gonzalez-Freire, Marta [1 ]
Aon, Miguel A. [4 ]
Candia, Julian [2 ]
Zhang, Pingbo [5 ]
Cheung, Foo [2 ]
Fantoni, Giovanna [2 ]
Semba, Richard D. [5 ]
Ferrucci, Luigi [1 ]
机构
[1] NIA, Longitudinal Study Sect, Translat Gerontol Branch, NIH, 251 Bayview Blvd,Room 10B121, Baltimore, MD 21224 USA
[2] NIH, Trans NIH Ctr Human Immunol Autoimmun & Inflammat, Bldg 10, Bethesda, MD 20892 USA
[3] NIA, Lab Clin Invest, NIH, Baltimore, MD 21224 USA
[4] NIA, Lab Cardiovasc Sci, NIH, Baltimore, MD USA
[5] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA
关键词
aging; aptamers; healthy aging; humans; plasma; proteomics; INFLAMMATORY MARKERS; BIOMARKER; CANCER; CELLS; ASSOCIATION; EXPRESSION; PHENOTYPE; DISCOVERY; GROWTH; RISK;
D O I
10.1111/acel.12799
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To characterize the proteomic signature of chronological age, 1,301 proteins were measured in plasma using the SOMAscan assay (SomaLogic, Boulder, CO, USA) in a population of 240 healthy men and women, 22-93 years old, who were disease- and treatment-free and had no physical and cognitive impairment. Using a p <= 3.83 x 10(-5) significance threshold, 197 proteins were positively associated, and 20 proteins were negatively associated with age. Growth differentiation factor 15 (GDF15) had the strongest, positive association with age (GDF15; 0.018 +/- 0.001, p = 7.49 x 10(-56)). In our sample, GDF15 was not associated with other cardiovascular risk factors such as cholesterol or inflammatory markers. The functional pathways enriched in the 217 age-associated proteins included blood coagulation, chemokine and inflammatory pathways, axon guidance, peptidase activity, and apoptosis. Using elastic net regression models, we created a proteomic signature of age based on relative concentrations of 76 proteins that highly correlated with chronological age (r = 0.94). The generalizability of our findings needs replication in an independent cohort.
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页数:13
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