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尿代谢特征反映了年轻人、中年人和老年人的心血管风险。

Urinary metabolic signatures reflect cardiovascular risk in the young, middle-aged, and elderly populations.

机构信息

Department of Immunology, Immunoallergy and Proteomics Laboratory, IIS-Fundación Jiménez Díaz, UAM, Avenida Reyes Católicos 2, 28040, Madrid, Spain.

CAI-RMN, Universidad Complutense de Madrid, Madrid, Spain.

出版信息

J Mol Med (Berl). 2020 Nov;98(11):1603-1613. doi: 10.1007/s00109-020-01976-x. Epub 2020 Sep 11.

Abstract

The predictive value of traditional cardiovascular risk estimators is limited, and young and elderly populations are particularly underrepresented. We aimed to investigate the urine metabolome and its association with cardiovascular risk to identify novel markers that might complement current estimators based on age. Urine samples were collected from 234 subjects categorized into three age-grouped cohorts: 30-50 years (cohort I, young), 50-70 years (cohort II, middle-aged), and > 70 years (cohort III, elderly). Each cohort was further classified into three groups: (a) control, (b) individuals with cardiovascular risk factors, and (c) those who had a previous cardiovascular event. Novel urinary metabolites linked to cardiovascular risk were identified by nuclear magnetic resonance in cohort I and then evaluated by target mass spectrometry quantification in all cohorts. A previously identified metabolic fingerprint associated with atherosclerosis was also analyzed and its potential risk estimation investigated in the three aged cohorts. Three different metabolic signatures were identified according to age: 2-hydroxybutyrate, gamma-aminobutyric acid, hypoxanthine, guanidoacetate, oxaloacetate, and serine in young adults; citrate, cyclohexanol, glutamine, lysine, pantothenate, pipecolate, threonine, and tyramine shared by middle-aged and elderly adults; and trimethylamine N-oxide and glucuronate associated with cardiovascular risk in all three cohorts. The urinary metabolome contains a metabolic signature of cardiovascular risk that differs across age groups. These signatures might serve to complement existing algorithms and improve the accuracy of cardiovascular risk prediction for personalized prevention. KEY MESSAGES: • Cardiovascular risk in the young and elderly is underestimated. • The urinary metabolome reflects cardiovascular risk across all age groups. • Six metabolites constitute a metabolic signature of cardiovascular risk in young adults. • Middle-aged and elderly adults share a cardiovascular risk metabolic signature. • TMAO and glucuronate levels reflect cardiovascular risk across all age groups.

摘要

传统心血管风险评估器的预测价值有限,且年轻人和老年人的代表性不足。我们旨在研究尿液代谢组及其与心血管风险的关联,以确定可能补充基于年龄的现有评估器的新型标志物。收集了来自 234 名受试者的尿液样本,这些受试者分为三个年龄组队列:30-50 岁(队列 I,年轻)、50-70 岁(队列 II,中年)和>70 岁(队列 III,老年)。每个队列进一步分为三组:(a)对照组,(b)有心血管危险因素的个体,和(c)有先前心血管事件的个体。通过对队列 I 中的核磁共振识别与心血管风险相关的新型尿液代谢物,然后通过靶向质谱定量评估所有队列中的这些代谢物。还分析了与动脉粥样硬化相关的先前鉴定的代谢指纹,并研究了其在三个年龄队列中的潜在风险估计。根据年龄确定了三种不同的代谢特征:年轻成年人中的 2-羟丁酸、γ-氨基丁酸、次黄嘌呤、胍基乙酸、草酰乙酸和丝氨酸;中年和老年人共有的柠檬酸、环己醇、谷氨酰胺、赖氨酸、泛酸、哌啶酸、苏氨酸和酪胺;以及与所有三个队列中的心血管风险相关的三甲胺 N-氧化物和葡萄糖醛酸。尿液代谢组包含一个随年龄组而异的心血管风险代谢特征。这些特征可能有助于补充现有算法并提高心血管风险预测的准确性,以实现个性化预防。主要发现:•年轻人和老年人的心血管风险被低估。•尿液代谢组反映了所有年龄组的心血管风险。•六种代谢物构成了年轻成年人心血管风险的代谢特征。•中年和老年人共享心血管风险的代谢特征。•TMAO 和葡萄糖醛酸盐水平反映了所有年龄组的心血管风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cb5/7591416/bee259661ea4/109_2020_1976_Fig1_HTML.jpg

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