Department of Systems Medicine, University of Rome Tor Vergata, Italy; Center for Atherosclerosis, Policlinico Tor Vergata, Rome, Italy.
Department of Systems Medicine, University of Rome Tor Vergata, Italy.
Atherosclerosis. 2018 Oct;277:179-185. doi: 10.1016/j.atherosclerosis.2018.06.014. Epub 2018 Jun 12.
We aimed to identify novel biomarkers for cardiovascular mortality through a non-targeted metabolomics approach in patients with established atherosclerotic disease from the Tor Vergata Atherosclerosis Registry (TVAR).
We compared the serum baseline metabolome of 19 patients with atherosclerosis suffering from cardiovascular death during follow-up with the baseline serum metabolome of 20 control patients matched for age, gender, body mass index (BMI) and atherosclerotic disease status, who survived during the observation period.
Three metabolites were significantly different in the cardiovascular mortality (CVM) group compared to controls: 2-hydroxycaproate, gluconate and sorbitol. 2-hydroxycaproate (otherwise known as alpha hydroxy caproate) was also significantly correlated with time to death. The metabolites performed better when combined together rather than singularly on the identification of CVM status.
Our analysis led to identify few metabolites potentially amenable of translation into the clinical practice as biomarkers for specific metabolic changes in the cardiovascular system in patients with established atherosclerotic disease.
我们旨在通过对来自 Tor Vergata 动脉粥样硬化注册研究(TVAR)的已确诊动脉粥样硬化患者进行非靶向代谢组学分析,确定心血管死亡率的新型生物标志物。
我们比较了 19 例在随访期间发生心血管死亡的动脉粥样硬化患者与 20 例年龄、性别、体重指数(BMI)和动脉粥样硬化疾病状态相匹配且在观察期间存活的对照组患者的基线血清代谢组。
与对照组相比,心血管死亡率(CVM)组有 3 种代谢物存在显著差异:2-羟基己酸、葡萄糖酸和山梨醇。2-羟基己酸(也称为α-羟基己酸)与死亡时间也呈显著相关。与单一标志物相比,这些代谢物联合使用在识别 CVM 状态方面表现更好。
我们的分析确定了一些潜在的代谢物,这些代谢物可能适用于将其转化为临床实践,作为已确诊动脉粥样硬化患者心血管系统特定代谢变化的生物标志物。