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早期神经传递损伤在非侵入性阿尔茨海默病检测中的作用。

Early neurotransmission impairment in non-invasive Alzheimer Disease detection.

机构信息

Neonatal Research Unit, Health Research Institute La Fe, Avda de Fernando Abril Martorell, 106; 46026, Valencia, Spain.

Neurology Unit, University and Polytechnic Hospital La Fe, Valencia, Spain.

出版信息

Sci Rep. 2020 Oct 2;10(1):16396. doi: 10.1038/s41598-020-73362-z.

Abstract

Alzheimer Disease (AD) is a pathology suffered by millions of people worldwide and it has a great social and economic impact. Previous studies reported a relationship between alterations in different amino acids and derivatives involved in neurotransmission systems and cognitive impairment. Therefore, in this study the neurotransmission impairment associated to early AD has been evaluated. For this purpose, different amino acids and derivatives were determined in saliva samples from AD patients and healthy subjects, by means of an analytical method based on chromatography coupled to tandem mass spectrometry. Results showed statistically significant differences in salivary levels for the compounds myo-inositol, creatine and acetylcholine; and other compounds (myo-inositol, glutamine, creatine, acetylcholine) showed significant correlations with some cognitive tests scores. Therefore, these compounds were included in a multivariate analysis and the corresponding diagnosis model showed promising indices (AUC 0.806, sensitivity 61%, specificity 92%). In conclusion, some amino acids and derivatives involved in neurotransmission impairment could be potential biomarkers in early and non-invasive AD detection.

摘要

阿尔茨海默病(AD)是一种影响全球数百万人的疾病,对社会和经济都有重大影响。先前的研究报告称,不同氨基酸及其神经递质系统相关衍生物的改变与认知障碍有关。因此,本研究评估了与早期 AD 相关的神经递质损伤。为此,通过基于色谱与串联质谱联用的分析方法,测定了 AD 患者和健康受试者唾液样本中的不同氨基酸及其衍生物。结果表明,在唾液水平上,化合物肌醇、肌酸和乙酰胆碱存在统计学显著差异;其他化合物(肌醇、谷氨酰胺、肌酸、乙酰胆碱)与某些认知测试分数显著相关。因此,这些化合物被纳入多元分析,相应的诊断模型显示出有前景的指标(AUC 为 0.806,灵敏度为 61%,特异性为 92%)。总之,一些参与神经递质损伤的氨基酸及其衍生物可能是早期和非侵入性 AD 检测的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34c/7532202/52690ad8e195/41598_2020_73362_Fig1_HTML.jpg

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