Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/111747
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Type: Journal article
Title: Plasma micronutrient levels and telomere length in children
Author: Milne, E.
O'Callaghan, N.
Ramankutty, P.
de Klerk, N.
Greenop, K.
Armstrong, B.
Miller, M.
Fenech, M.
Citation: Nutrition, 2015; 31(2):331-336
Publisher: Elsevier
Issue Date: 2015
ISSN: 0899-9007
1873-1244
Statement of
Responsibility: 
Elizabeth Milne, Nathan O’Callaghan, Padmaja Ramankutty, Nicholas H. de Klerk, Kathryn R. Greenop, Bruce K. Armstrong, Margaret Miller, Michael Fenech
Abstract: OBJECTIVE: Telomeres are long hexamer (TTAGGG) repeats at the ends of chromosomes, and contribute to maintenance of chromosomal stability. Telomere shortening has been linked to cancers and other chronic diseases in adults, although evidence for causal associations is limited. The aim of this study was to determine whether nutritional factors are associated with telomere length (TL) in children. METHODS: We conducted a cross-sectional study of nutritional factors and TL in 437 children between 2009 and 2011. Healthy children ages 3, 6, and 9 y provided blood samples, and their parents completed a food frequency questionnaire and a telephone interview about relevant environmental exposures. TL and blood micronutrient levels were measured, and genotyping at 10 loci was undertaken. Associations between the micronutrients and other variables were assessed using linear regression. RESULTS: No significant main or interactive effects of age or sex were seen. After adjustment for age, sex, parental education, and month of blood collection, TL was inversely associated with plasma zinc, and shorter in children with the homozygous mutant genotype of the RFC G80A (rs1051266) polymorphism. CONCLUSIONS: To the best of our knowledge, this is the first investigation of the association between telomere length and micronutrients in healthy children. The reason for the inverse relationship of TL with zinc is unknown but could be the result of an increase in telomere sequence deletions caused by labile zinc induction of oxidative stress. These findings should be corroborated in other studies before nutritional recommendations might be considered.
Keywords: DNA Damage
Zinc
Polymorphism
Nutrients
Nutrition
Pediatrics
Rights: © 2015 Elsevier Inc. All rights reserved.
DOI: 10.1016/j.nut.2014.08.005
Grant ID: http://purl.org/au-research/grants/nhmrc/572623
Appears in Collections:Aurora harvest 3
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