非认知障碍健康老年受试者血浆代谢组显著的年龄相关改变

Xiaobei Pan, P. Passmore, S. Graham, S. Todd, B. McGuinness, B. Green
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引用次数: 2

摘要

背景:年龄是大多数常见神经退行性疾病的主要危险因素。尽管越来越多的研究关注衰老疾病,但关于健康老年人衰老血液中代谢物变化的信息很少。这些信息可以帮助我们了解与衰老相关的神经认知变化,并进一步提高神经退行性疾病未来代谢物生物标志物的有效性和再现性。材料和方法:本研究的目的是评估非认知障碍老年参与者的代谢组学特征如何随着年龄的增长而变化。本研究采用靶向液相色谱-质谱/MS代谢组学方法,检测了17名非认知障碍老年参与者(T0;78.10±6.30 y小型精神状态检查=29.29±0.85),同样的17名受试者在~5年后进行了随访(T5;83.29±6.13 y迷你精神状态检查=27.47±1.62)。结果:使用测定的187种血浆代谢产物的浓度建立偏最小二乘判别模型,发现从基线(T0)起5年(T5)的代谢组学特征明显不同(R2=0.95;Q2=0.90)。当将T5的代谢产物水平与T0进行比较时,40个酰基肉毒碱中的25个和14个溶血磷脂酰胆碱中的2个增加,而14个溶血磷酰胆碱中3个和14种鞘磷脂中2个减少。此外,42种氨基酸中的20种在两个时间点之间存在显著差异。T5时14个氨基酸增加,而6个氨基酸减少。结论:老年非认知障碍受试者的血浆代谢组随年龄变化,这可能有助于开发有效和敏感的人类疾病代谢生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Significant age-related alterations in the blood plasma metabolome of noncognitively impaired healthy elderly subjects
Background: Age is a major risk factor for most common neurodegenerative diseases. Although an increased research focus on diseases of aging, there is little information regarding the metabolite changes in the aging blood in healthy older adults. Such information could help us to understand neurocognitive changes associated with aging and also further improve the validity and reproducibility of future metabolite biomarkers for neurodegenerative diseases. Materials and Methods: The purpose of this study was to assess how the metabolomic profiles of noncognitively impaired elderly participants changes with aging. Using a targeted liquid chromatography-mass spectrometry/MS metabolomics approach, this study examined 17 noncognitively impaired elderly participants (T0; 78.10±6.30 y; mini-mental state exam=29.29±0.85) and the same 17 subjects were followed-up ∼5 years later (T5; 83.29±6.13 y; mini-mental state exam=27.47±1.62). Results: The concentrations of 187 plasma metabolites determined were used to build a partial least squares-discriminant model which found that metabolomic profiles taken 5 years (T5) from baseline (T0) were distinctly different (R2=0.95; Q2=0.90). When metabolites levels at T5 were compared with T0, 68 of the 73 phosphatidylcholines, 25 of the 40 acylcarnitines, and 2 of the 14 lysophosphatidylcholines were increased, whereas 3 of the 14 lysophosphatidylcholines and 2 of the 14 sphingomyelins were decreased. Moreover, 20 of the 42 amino acids concentrations were significantly different between the 2 time points. Fourteen amino acids were increased at T5, whereas 6 amino acids were decreased. Conclusions: The plasma metabolome changes with age in elderly, noncognitively impaired subjects, and this could aid in developing valid and sensitive metabolite biomarkers for human disease.
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