Centre for Advanced Discovery and Experimental Therapeutics (CADET), Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
Biometals. 2018 Apr;31(2):267-276. doi: 10.1007/s10534-018-0089-3. Epub 2018 Mar 7.
Sporadic 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 (R = - 0.03, R = 0.65; P = 0.009), and copper-calcium (R = - 0.01, R = 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.
散发性阿尔茨海默病(AD)是一种神经退行性疾病,导致最常见的与年龄相关的痴呆症,但其发病机制仍不清楚。尽管迄今为止关于这些中枢神经系统扰动如何反映在外周血液中的数据不一致,但在 AD 大脑中,金属,特别是全脑铜缺乏的调节改变,以及其他金属更局部的扰动,是突出的。为了评估金属失调在 AD 中产生生物标志物的潜力,我们对 AD 和匹配对照病例的样本进行了七项必需金属和硒的病例对照研究,通过电感耦合等离子体质谱法测量。金属为钠、钾、钙、镁、铁、锌和铜。在整个研究组和女性参与者中,病例和对照组之间的血浆金属水平没有差异。相比之下,在男性中,有中度证据表明,锌水平在 AD 中趋于升高[10.8(10.2-11.5)]µmol/L,平均值(±95%CI;P=0.021)与对照组相比[10.2(9.6-10.4)]。因此,AD 中男性的血浆锌水平改变存在性别差异。在相关性分析中,AD 病例中有更多“强”金属共调节的证据,并且金属对的差异共调节:铜-钠(R=-0.03,R=0.65;P=0.009)和铜-钙(R=-0.01,R=0.65;P=0.01)在 AD 男性中具有统计学意义,这可能与 AD 中严重受损脑区铜失调的报告证据一致。总之,我们的数据表明,血浆中金属共调节的测量可能提供 AD 大脑中发生的那些金属扰动的有用表示,因此可能作为基于血浆的生物标志物有用。