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Discovery of serum metabolites for diagnosis of progression of mild cognitive impairment to Alzheimer's disease using an optimized metabolomics method

机译:利用优化的代谢组种发现发现血清代谢物诊断对阿尔茨海默氏病的进展

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Mild cognitive impairment (MCI) is considered to represent early AD. Currently, there is a great need for sensitive tools to monitor the progression of MCI to AD. In this work, a nontargeted metabolomics approach was developed to examine metabolic differences in serum samples from the MCI subjects and the age-matched AD subjects. Based on principal component analysis, metabolic differences among AD and MCI subjects were identified. Nine metabolites in the serum of the AD subjects were significantly different from the MCI subjects. Two metabolites were selected as the candidate biomarkers and validated in separate and independent patient cohorts. The major contributors to the predictive model were upregulated sphinganine-1-phosphate and 7-ketocholesterol, which yielded satisfactory sensitivity, and specificity, indicating potential value for predicting the conversion of MCI to probable AD. The present study may provide a diagnosis tool to monitoring the progression of MCI to AD.
机译:轻度认知障碍(MCI)被认为代表早期广告。目前,很有需要对广告进行敏感工具来监控MCI的进展。在这项工作中,开发了一种不确定的代谢组种方法,以研究来自MCI受试者和年龄匹配的AD受试者的血清样本中的代谢差异。基于主成分分析,确定了广告和MCI受试者之间的代谢差异。在AD受试者的血清中九个代谢物与MCI受试者显着不同。选择两种代谢物作为候选生物标志物,并在单独和独立的患者队列中验证。预测模型的主要贡献者是上调的鞘氨氨酸-1-磷酸盐和7-酮化合物,其令人满意的敏感性和特异性,表明预测MCI转化为可能的广告的潜在价值。本研究可以提供监测MCI进展的诊断工具。

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