6533b7d8fe1ef96bd1269a77

RESEARCH PRODUCT

Trace elements levels in centenarian ‘dodgers’

Fabian Sanchis-gomarCarmen Fiuza-lucesRafael AlisRafael AlisHelios Pareja-galeanoEnzo EmanueleAlejandro LuciaAlejandro Santos-lozanoNuria Garatachea

subject

0301 basic medicineGerontologyMalemedicine.medical_specialtyAgingGerontologíaLongevityAncianoPredictor variablesEthnic originBiologyLogistic regressionBiochemistryInorganic Chemistry03 medical and health sciencesSelenium0302 clinical medicineInternal medicinemedicineHumansHealthy agingAged 80 and overSuccessful agingLifespanTrace elementTrace ElementsGeriatría030104 developmental biologyEndocrinologyROC CurveHealthCohortMultivariate AnalysisMolecular MedicineFemaleCentenarian030217 neurology & neurosurgeryCopper

description

Trace element bioavailability can play a role in several metabolic and physiological pathways known to be altered during the aging process. We aimed to explore the association of trace elements with increased lifespan by analyzing the circulating levels of seven trace elements (Cr, Cu, Fe, Mn, Mo, Se and Zn) in a cohort of healthy centenarians or ‘dodgers’ (≥100 years, free of major age-related diseases) in comparison with sex-matched younger elderly controls. Centenarians showed significant lower Cu (783.7 (76.7, 1608.9) vs 962.5 (676.3, 2064.4) μg/mL, P < 0.001), but higher Fe (1.3 (0.4, 4.7) vs 1.1 (0.5, 8.4) μg/mL, P = 0.003) and Se (85.7 (43.0, 256.7) vs 77.8 (24.3, 143.8) ng/mL, P = 0.002) values compared with elderly controls. The logistic regression analysis identified the combination of Cu and Se as significant predictor variables associated with successful aging (P = 0.001), while receiver operating characteristic (ROC) analysis confirmed that Cu and Se (either alone or in combination) were independent variables associated with healthy aging. An ‘improved’ trace element profile (reduced Cu and elevated Se, which are involved in key physiological processes) could play a role in the resistance to disease showed by centenarian ‘dodgers’, and, therefore, at least partly, be involved in the healthy aging phenotype shown by these subjects. These results should be confirmed in larger cohorts of other geographic/ethnic origin and the potential cause–effect association tested in mechanistic experimental settings. PI15/00558 3.225 JCR (2016) Q2, 65/138 Endocrinology and Metabolism, 118/290 Biochemistry and Molecular Biology 0.774 SJR (2016) Q2, 213/451 Biochemistry, 21/72 Inorganic Chemistry; Q3, 100/183 Molecular Medicine No data IDR 2016 UEM

10.1016/j.jtemb.2016.02.002https://hdl.handle.net/11268/5037