IMPLEMENTACIÓN DE UN ALGORITMO PREDICTIVO MULTIESCALA, MEDIANTE LA INTEGRACIÓN DE TECNOLOGÍAS -ÓMICAS HUMANAS Y MICROBIANAS, PARA LA DETECCIÓN TEMPRANA, DIAGNÓSTICO Y SEGUIMIENTO DE LA SARCOPENIA
PMPTA23/00012
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Nombre agencia financiadora Instituto de Salud Carlos III
Acrónimo agencia financiadora ISCIII
Programa Programa Estatal para Impulsar la Investigación Científico-Técnica y su Transferencia
Subprograma Subprograma Estatal de Transferencia de Conocimiento
Convocatoria Proyectos de Medicina Personalizada y Terapias Avanzadas
Año convocatoria 2023
Unidad de gestión Plan Estatal de Investigación Científica, Técnica y de Innovación 2021-2023
Centro beneficiario UNIVERSIDAD AUTONOMA DE MADRID
Centro realización UNIVERSIDAD AUTONOMA DE MADRID
Identificador persistente http://dx.doi.org/10.13039/501100004587
Publicaciones
Resultados totales (Incluyendo duplicados): 1Encontrada(s) 1 página(s)
Differential association of selenium exposure with insulin resistance and ß-cell function in middle age and older adults
Zaguán. Repositorio Digital de la Universidad de Zaragoza
- Rodriguez-Hernandez, Zulema
- Bel-Aguilar, Javier
- Moreno-Franco, Belen
- Grau-Perez, Maria
- Redon, Josep
- Gomez-Ariza, Jose L.
- Garcia-Barrera, Tamara
- Olmedo, Pablo
- Gil, Fernando
- Cenarro, Ana
- Civeira, Fernando
- Puzo, Jose
- Casasnovas, Jose A.
- Banegas, Jose R.
- Sotos-Prieto, Mercedes
- Ortola, Rosario
- Laclaustra, Martin
- Rodriguez-Artalejo, Fernando
- Garcia-Esquinas, Esther
- Tellez-Plaza, Maria
- Pastor-Barriuso, Roberto
Objective
To assess whether the role of selenium on pre-diabetes is differential by age, given comorbidities and decreased β-cell function in older adults.
Research design and methods
We evaluated the cross-sectional association of blood selenium with the homeostatic model assessment for insulin resistance (HOMA-IR) and β-cell function (HOMA-β) in middle-aged (Aragon Workers Health Study [AWHS], N = 1186), and older (Seniors ENRICA [Study on Nutrition and Cardiovascular Risk in Spain]-2 [SEN-2], N = 915) diabetes-free adults. A subsample of participants from AWHS (N = 571) and SEN-2 (N = 603) had glucose and insulin repeated measurements for longitudinal analysis. We validated the cross-sectional dose–response associations in the 2011–2018 National Health and Nutrition Examination Survey (NHANES, N = 1317 middle age and N = 960 older) participants. Selenium was measured in whole blood with ICP-MS in AWHS, SEN-2 and NHANES.
Results
The cross-sectional geometric mean ratios (95% confidence intervals) per two-fold selenium increase were 1.09 (1.01, 1.19) for HOMA-IR and 1.15 (1.06, 1.24) for HOMA-β in AWHS; and 1.13 (0.98, 1.31) and 1.03 (0.90, 1.18), in SEN-2. The cross-sectional dose-response associations were consistent in NHANES, with mostly increasingly positive trends for both HOMA endpoints in younger adults and a plateau at levels >~150 μg/L in older adults. The longitudinal dose–response consistently showed positive associations at high selenium dose for both HOMA endpoints in the younger, but not the older, study population.
Conclusions
Increased blood selenium was associated with increased insulin resistance and β-cell function in middle-aged, but not in older individuals, especially for β-cell function. The results suggest that selenium-associated insulin resistance might induce compensatory increased β-cell function at younger ages, being this compensatory capacity decreased with aging.
To assess whether the role of selenium on pre-diabetes is differential by age, given comorbidities and decreased β-cell function in older adults.
Research design and methods
We evaluated the cross-sectional association of blood selenium with the homeostatic model assessment for insulin resistance (HOMA-IR) and β-cell function (HOMA-β) in middle-aged (Aragon Workers Health Study [AWHS], N = 1186), and older (Seniors ENRICA [Study on Nutrition and Cardiovascular Risk in Spain]-2 [SEN-2], N = 915) diabetes-free adults. A subsample of participants from AWHS (N = 571) and SEN-2 (N = 603) had glucose and insulin repeated measurements for longitudinal analysis. We validated the cross-sectional dose–response associations in the 2011–2018 National Health and Nutrition Examination Survey (NHANES, N = 1317 middle age and N = 960 older) participants. Selenium was measured in whole blood with ICP-MS in AWHS, SEN-2 and NHANES.
Results
The cross-sectional geometric mean ratios (95% confidence intervals) per two-fold selenium increase were 1.09 (1.01, 1.19) for HOMA-IR and 1.15 (1.06, 1.24) for HOMA-β in AWHS; and 1.13 (0.98, 1.31) and 1.03 (0.90, 1.18), in SEN-2. The cross-sectional dose-response associations were consistent in NHANES, with mostly increasingly positive trends for both HOMA endpoints in younger adults and a plateau at levels >~150 μg/L in older adults. The longitudinal dose–response consistently showed positive associations at high selenium dose for both HOMA endpoints in the younger, but not the older, study population.
Conclusions
Increased blood selenium was associated with increased insulin resistance and β-cell function in middle-aged, but not in older individuals, especially for β-cell function. The results suggest that selenium-associated insulin resistance might induce compensatory increased β-cell function at younger ages, being this compensatory capacity decreased with aging.