Excessive early-life dietary exposure: a potential source of elevated brain iron and a risk factor for Parkinson's disease

被引:26
作者
Hare, Dominic J. [1 ,2 ,3 ]
Cardoso, Barbara Rita [2 ,4 ]
Raven, Erika P. [5 ,6 ]
Double, Kay L. [7 ,8 ]
Finkelstein, David I. [2 ]
Szymlek-Gay, Ewa A. [9 ]
Biggs, Beverley-Ann [1 ,10 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Doherty Inst, Dept Med, Melbourne, Vic, Australia
[2] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[3] Univ Technol Sydney, Elemental Bioimaging Facil, Broadway, NSW, Australia
[4] Univ Sao Paulo, Dept Food & Expt Nutr, Dept Pharmaceut Sci, Sao Paulo, Brazil
[5] Georgetown Univ, Med Ctr, Ctr Funct & Mol Imaging, Washington, DC 20007 USA
[6] NINDS, Adv Magnet Resonance Imaging Sect, Lab Funct & Mol Imaging, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
[7] Univ Sydney, Sydney Med Sch, Darlington, NSW, Australia
[8] Univ Sydney, Brain & Mind Ctr, Camperdown, NSW, Australia
[9] Deakin Univ, Sch Exercise & Nutr Sci, Inst Phys Act & Nutr, Geelong, Vic, Australia
[10] Royal Melbourne Hosp, Victorian Infect Dis Serv, Melbourne, Vic, Australia
基金
美国国家科学基金会;
关键词
TRANSCRANIAL ULTRASOUND; HEMOCHROMATOSIS GENE; SUBSTANTIA-NIGRA; UNITED-STATES; DIAGNOSIS; INFANTS; POLYMORPHISMS; FORTIFICATION; ASSOCIATION; MORTALITY;
D O I
10.1038/s41531-016-0004-y
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Iron accumulates gradually in the ageing brain. In Parkinson's disease, iron deposition within the substantia nigra is further increased, contributing to a heightened pro-oxidant environment in dopaminergic neurons. We hypothesise that individuals in high-income countries, where cereals and infant formulae have historically been fortified with iron, experience increased early-life iron exposure that predisposes them to age-related iron accumulation in the brain. Combined with genetic factors that limit iron regulatory capacity and/or dopamine metabolism, this may increase the risk of Parkinson's diseases. We propose to (a) validate a retrospective biomarker of iron exposure in children; (b) translate this biomarker to adults; (c) integrate it with in vivo brain iron in Parkinson's disease; and (d) longitudinally examine the relationships between early-life iron exposure and metabolism, brain iron deposition and Parkinson's disease risk. This approach will provide empirical evidence to support therapeutically addressing brain iron deposition in Parkinson's diseases and produce a potential biomarker of Parkinson's disease risk in preclinical individuals.
引用
收藏
页数:5
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