Ferré-González Laura, Peña-Bautista Carmen, Baquero Miguel, Cháfer-Pericás Consuelo
Alzheimer's Disease Research Group, Health Research Institute La Fe, 46026 Valencia, Spain.
Division of Neurology, University and Polytechnic Hospital La Fe, 46026 Valencia, Spain.
Antioxidants (Basel). 2022 Mar 14;11(3):551. doi: 10.3390/antiox11030551.
Alzheimer’s disease (AD) and other dementias are becoming increasingly common in the older population, and the number of people affected is expected to increase in a few years. Nowadays, biomarkers used in early AD diagnosis are expensive and invasive. Therefore, this research field is growing. In fact, peroxidation by-products derived from the oxidation of brain lipids (arachidonic (AA), docosahexanoic (DHA) and adrenic acid (AdA)) could be potential biomarkers, participating in the mechanisms of inflammation, neurotoxicity and cell death in AD pathology. Previous studies have shown specificity between lipid peroxidation compounds and other dementias (e.g., Lewy bodies (DLB), frontotemporal dementia (FTD)), but more research is required. Lipid peroxidation compounds (prostaglandins, isoprostanes, isofurans, neuroprostanes, neurofurans, dihomo-isoprostanes and dihomo-isofurans) were analysed by liquid chromatography and mass spectrometry in plasma samples from participants classified into a healthy group (n = 80), a mild cognitive impairment due to AD group (n = 106), a mild dementia due to AD group (n = 70), an advanced dementia due to AD group (n = 11) and a group of other non-AD dementias (n = 20). Most of these compounds showed statistically significant differences between groups (p < 0.05), showing higher levels for the healthy and non-AD groups than the AD groups. Then, a multivariate analysis was carried out on these compounds, showing good diagnosis indexes (AUC 0.77, sensitivity 81.3%, positive predictive value 81%). Moreover, evaluating AD disease prognosis, two compounds (15-F2t-IsoP and 14(RS)-14-F4t-NeuroP) and three total parameters (isoprostanes, isofurans and neurofurans) showed significant differences among groups. Some compounds derived from the oxidation of AA, DHA and AdA have demonstrated their potential use in differential AD diagnosis. Specifically, 15-F2t-IsoP, 14(RS)-14-F4t-NeuroP and the total parameters for isoprostanes, isofurans and neurofurans have shown prognostic value for AD from its earliest stages to its most severe form.
阿尔茨海默病(AD)和其他痴呆症在老年人群中越来越普遍,预计未来几年受影响的人数还会增加。目前,用于AD早期诊断的生物标志物价格昂贵且具有侵入性。因此,这一研究领域正在不断发展。事实上,脑脂质(花生四烯酸(AA)、二十二碳六烯酸(DHA)和肾上腺酸(AdA))氧化产生的过氧化副产物可能是潜在的生物标志物,参与AD病理过程中的炎症、神经毒性和细胞死亡机制。先前的研究已经表明脂质过氧化化合物与其他痴呆症(如路易体痴呆(DLB)、额颞叶痴呆(FTD))之间存在特异性,但仍需要更多的研究。通过液相色谱和质谱分析法,对分为健康组(n = 80)、AD所致轻度认知障碍组(n = 106)、AD所致轻度痴呆组(n = 70)、AD所致重度痴呆组(n = 11)和其他非AD痴呆症组(n = 20)的参与者血浆样本中的脂质过氧化化合物(前列腺素、异前列腺素、异呋喃、神经前列腺素、神经呋喃、二高异前列腺素和二高异呋喃)进行了分析。这些化合物中的大多数在组间显示出统计学上的显著差异(p < 0.05),健康组和非AD组的水平高于AD组。然后,对这些化合物进行多变量分析,显示出良好的诊断指标(AUC 0.77,灵敏度81.3%,阳性预测值81%)。此外,在评估AD疾病预后时,两种化合物(15-F2t-异前列腺素和14(RS)-14-F4t-神经前列腺素)以及三个总参数(异前列腺素、异呋喃和神经呋喃)在组间显示出显著差异。一些由AA、DHA和AdA氧化衍生的化合物已证明其在AD鉴别诊断中的潜在用途。具体而言,15-F2t-异前列腺素、14(RS)-14-F4t-神经前列腺素以及异前列腺素、异呋喃和神经呋喃的总参数从AD的最早阶段到最严重形式都显示出预后价值。