Ontology type: schema:ScholarlyArticle Open Access: True
2018-03-07
AUTHORSJingshu Xu, Stephanie J. Church, Stefano Patassini, Paul Begley, Katherine A. B. Kellett, Emma R. L. C. Vardy, Richard D. Unwin, Nigel M. Hooper, Garth J. S. Cooper
ABSTRACTSporadic Alzheimer’s disease (AD) is a neurodegenerative disorder that causes the most prevalent form of age-related dementia but its pathogenesis remains obscure. Altered regulation of metals, particularly pan-cerebral copper deficiency, and more regionally-localized perturbation of other metals, are prominent in AD brain although data on how these CNS perturbations are reflected in the peripheral bloodstream are inconsistent to date. To assess the potential use of metal dysregulation to generate biomarkers in AD, we performed a case–control study of seven essential metals and selenium, measured by inductively coupled plasma mass-spectrometry, in samples from AD and matched control cases. Metals were sodium, potassium, calcium, magnesium, iron, zinc, and copper. In the whole study-group and in female participants, plasma metal levels did not differ between cases and controls. In males by contrast, there was moderate evidence that zinc levels trended towards increase in AD [10.8 (10.2–11.5)] µmol/L, mean (± 95% CI; P = 0.021) compared with controls [10.2 (9.6–10.4)]. Thus alterations in plasma zinc levels differed between genders in AD. In correlational analysis, there was evidence for an increased number of ‘strong’ metal co-regulations in AD cases and differential co-modulations of metal pairs: copper-sodium (Rcontrol = − 0.03, RAD = 0.65; P = 0.009), and copper-calcium (Rcontrol = − 0.01, RAD = 0.65; P = 0.01) were significant in AD males, potentially consistent with reported evidence for dysregulation of copper in severely damaged brain regions in AD. In conclusion, our data suggest that the measurement of metals co-regulation in plasma may provide a useful representation of those metal perturbations taking place in the AD brain and therefore might be useful as plasma-based biomarkers.Graphical Abstract More... »
PAGES267-276
http://scigraph.springernature.com/pub.10.1007/s10534-018-0089-3
DOIhttp://dx.doi.org/10.1007/s10534-018-0089-3
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PUBMEDhttps://www.ncbi.nlm.nih.gov/pubmed/29516299
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