TY - JOUR
T1 - Associations of fat-soluble micronutrients and redox biomarkers with frailty status in the FRAILOMIC initiative
AU - Kochlik, Bastian
AU - Stuetz, Wolfgang
AU - Pérès, Karine
AU - Pilleron, Sophie
AU - Féart, Catherine
AU - García García, Francisco José
AU - Bandinelli, Stefania
AU - Gomez-Cabrero, David
AU - Rodriguez-Mañas, Leocadio
AU - Grune, Tilman
AU - Weber, Daniela
N1 - Funding Information:
This work was supported by the European Union's Seventh Framework Programme (FP7-HEALTH; grant number 305483, FRAILOMIC Project). The 3-C Study is conducted under a partnership agreement between the Institut National de la Santé et de la Recherche Médicale (INSERM), Victor Segalen–Bordeaux2 University, and Sanofi-Synthélabo. Fondation pour la Recherche Médicale funded the preparation and beginning of the study. The 3-C Study is sponsored by the Caisse Nationale Maladie des Travailleurs Salariés, Direction Générale de la Santé, Conseils Régionaux of Aquitaine and Bourgogne, Fondation de France, Ministry of Research-INSERM Program Cohortes et collections de données biologiques, Fondation Plan Alzheimer (FCS 2009-2012), and Caisse Nationale pour la Solidarité et l'Autonomie (CNSA) and ‘Programme Longévité et vieillissement' (COGICARE 07-LVIE 003 01). The AMI project was funded by AGRICA (CAMARCA, CRCCA, CCPMA PREVOYANCE, CPCEA, and AGRI PREVOYANCE), la Mutualité Sociale Agricole (MSA) de Gironde, and la Caisse Centrale de la Mutualité Sociale Agricole (CCMSA). The InCHIANTI study baseline (1998–2000) was supported as a ‘targeted project' (ICS110.1/RF97.71) by the Italian Ministry of Health and in part by the U.S. National Institute on Aging (Contracts: 263 MD 9164 and 263 MD 821336); the Follow-up 1 (2001–2003) was funded by the U.S. National Institute on Aging (Contracts: N.1-AG-1-1 and N.1-AG-1-2111); the Follow-ups 2 and 3 (2004–2010) were financed by the U.S. National Institute on Aging (Contract: N01-AG-5-0002) and supported in part by the Intramural research program of the National Institute on Aging, National Institutes of Health, Baltimore, Maryland. The TSHA cohort was funded by grants PI07/90637, PI10/01532, and CB16/10/00456 from the Instituto de Salud Carlos III (Ministerio de Economía y Competitividad, Spain), 03031-00 from the Instituto de Ciencias de la Salud de Castilla la Mancha, and PI2010/020 from FISCAM.5. The authors certify that they comply with the Ethical guidelines for authorship and publishing in the Journal of Cachexia, Sarcopenia and Muscle.
Publisher Copyright:
© 2019 The Authors Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Background: A poor fat-soluble micronutrient (FMN) and a high oxidative stress status are associated with frailty. Our aim was to determine the cross-sectional association of FMNs and oxidative stress biomarkers [protein carbonyls (PrCarb) and 3-nitrotyrosine] with the frailty status in participants older than 65 years. Methods: Plasma levels of vitamins A (retinol), D3, E (α-tocopherol and γ-tocopherol) and carotenoids (α-carotene and β-carotene, lycopene, lutein/zeaxanthin, and β-cryptoxanthin), PrCarb, and 3-nitrotyrosine were measured in 1450 individuals of the FRAILOMIC initiative. Participants were classified into robust, pre-frail, and frail using Fried's frailty criteria. Associations between biomarkers and frailty status were assessed by general linear and logistic regression models, both adjusted for cohort, season of blood sampling, gender, age, height, weight, and smoking. Results: Robust participants had significantly higher vitamin D3 and lutein/zeaxanthin concentrations than pre-frail and frail subjects; had significantly higher γ-tocopherol, α-carotene, β-carotene, lycopene, and β-cryptoxanthin concentrations than frail subjects, and had significantly lower PrCarb concentrations than frail participants in multivariate linear models. Frail subjects were more likely to be in the lowest than in the highest tertile for vitamin D3 (adjusted odds ratio: 2.15; 95% confidence interval: 1.42–3.26), α-tocopherol (2.12; 1.39–3.24), α-carotene (1.69; 1.00–2.88), β-carotene (1.84; 1.13–2.99), lycopene (1.94; 1.24–3.05), lutein/zeaxanthin (3.60; 2.34–5.53), and β-cryptoxanthin (3.02; 1.95–4.69) and were more likely to be in the highest than in the lowest tertile for PrCarb (2.86; 1.82–4.49) than robust subjects in multivariate regression models. Conclusions: Our study indicates that both low FMN and high PrCarb concentrations are associated with pre-frailty and frailty.
AB - Background: A poor fat-soluble micronutrient (FMN) and a high oxidative stress status are associated with frailty. Our aim was to determine the cross-sectional association of FMNs and oxidative stress biomarkers [protein carbonyls (PrCarb) and 3-nitrotyrosine] with the frailty status in participants older than 65 years. Methods: Plasma levels of vitamins A (retinol), D3, E (α-tocopherol and γ-tocopherol) and carotenoids (α-carotene and β-carotene, lycopene, lutein/zeaxanthin, and β-cryptoxanthin), PrCarb, and 3-nitrotyrosine were measured in 1450 individuals of the FRAILOMIC initiative. Participants were classified into robust, pre-frail, and frail using Fried's frailty criteria. Associations between biomarkers and frailty status were assessed by general linear and logistic regression models, both adjusted for cohort, season of blood sampling, gender, age, height, weight, and smoking. Results: Robust participants had significantly higher vitamin D3 and lutein/zeaxanthin concentrations than pre-frail and frail subjects; had significantly higher γ-tocopherol, α-carotene, β-carotene, lycopene, and β-cryptoxanthin concentrations than frail subjects, and had significantly lower PrCarb concentrations than frail participants in multivariate linear models. Frail subjects were more likely to be in the lowest than in the highest tertile for vitamin D3 (adjusted odds ratio: 2.15; 95% confidence interval: 1.42–3.26), α-tocopherol (2.12; 1.39–3.24), α-carotene (1.69; 1.00–2.88), β-carotene (1.84; 1.13–2.99), lycopene (1.94; 1.24–3.05), lutein/zeaxanthin (3.60; 2.34–5.53), and β-cryptoxanthin (3.02; 1.95–4.69) and were more likely to be in the highest than in the lowest tertile for PrCarb (2.86; 1.82–4.49) than robust subjects in multivariate regression models. Conclusions: Our study indicates that both low FMN and high PrCarb concentrations are associated with pre-frailty and frailty.
KW - 3-Nitrotyrosine
KW - Carotenoids
KW - Fat-soluble micronutrients
KW - Frail
KW - Protein carbonyls
UR - http://www.scopus.com/inward/record.url?scp=85070982121&partnerID=8YFLogxK
U2 - 10.1002/jcsm.12479
DO - 10.1002/jcsm.12479
M3 - Article
C2 - 31436047
AN - SCOPUS:85070982121
VL - 10
SP - 1339
EP - 1346
JO - Journal of Cachexia, Sarcopenia and Muscle
JF - Journal of Cachexia, Sarcopenia and Muscle
SN - 2190-5991
IS - 6
ER -