1
Institute of Biological Chemistry and Nutrition, University of Hohenheim, Stuttgart 70599, Germany
2
Institute of Nutrition, Friedrich-Schiller-University, Jena 07743, Germany
3
Department of Molecular Toxicology, German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), Nuthetal 14558, Germany
4
National Institute of Public Health and the Environment (RIVM), BA Bilthoven 3721, The Netherlands
5
Institute for Biomedical Aging Research, Leipold-Franzens-University, Innsbruck 6020, Austria
6
Institute for Nutritional Sciences and Physiology, University for Health Sciences, Hall in Tirol 6060, Austria
7
Unit of Cellular Biochemistry and Biology, University of Namur, Namur 5000, Belgium
8
BioTeSys GmbH, Esslingen 73728, Germany
9
Institute of Biological Research and Biotechnology, National Hellenic Research Foundation (NHRF), Athens 11635, Greece
10
Department of Experimental Pathology, University of Bologna, Bologna 40126, Italy
11
Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw 02-093, Poland
12
Molecular Toxicology, Department of Biology, University of Konstanz, Konstanz 78457, Germany
13
Department of Applied Nutritional Science/Dietetics, Institute of Nutritional Medicine, University of Hohenheim, Stuttgart 70599, Germany
14
German Center for Diabetes Research (DZD), Munich-Neuherberg 85764, Germany
15
German Center for Cardiovascular Research (DZHK), Berlin 13357, Germany
16
NutriAct-Competence Cluster Nutrition Research Berlin-Potsdam, Nuthetal 14458, Germany
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Abstract
Blood micronutrient status may change with age. We analyzed plasma carotenoids, α-/γ-tocopherol, and retinol and their associations with age, demographic characteristics, and dietary habits (assessed by a short food frequency questionnaire) in a cross-sectional study of 2118 women and men (age-stratified from 35
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Blood micronutrient status may change with age. We analyzed plasma carotenoids, α-/γ-tocopherol, and retinol and their associations with age, demographic characteristics, and dietary habits (assessed by a short food frequency questionnaire) in a cross-sectional study of 2118 women and men (age-stratified from 35 to 74 years) of the general population from six European countries. Higher age was associated with lower lycopene and α-/β-carotene and higher β-cryptoxanthin, lutein, zeaxanthin, α-/γ-tocopherol, and retinol levels. Significant correlations with age were observed for lycopene (
r = −0.248), α-tocopherol (
r = 0.208), α-carotene (
r = −0.112), and β-cryptoxanthin (
r = 0.125; all
p < 0.001). Age was inversely associated with lycopene (−6.5% per five-year age increase) and this association remained in the multiple regression model with the significant predictors (covariables) being country, season, cholesterol, gender, smoking status, body mass index (BMI (kg/m
2)), and dietary habits. The positive association of α-tocopherol with age remained when all covariates including cholesterol and use of vitamin supplements were included (1.7% vs. 2.4% per five-year age increase). The association of higher β-cryptoxanthin with higher age was no longer statistically significant after adjustment for fruit consumption, whereas the inverse association of α-carotene with age remained in the fully adjusted multivariable model (−4.8% vs. −3.8% per five-year age increase). We conclude from our study that age is an independent predictor of plasma lycopene, α-tocopherol, and α-carotene.
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