Recent advances in cardiovascular disease research driven by metabolomics technologies in the context of systems biology

Boyao Zhang, Thierry Schmidlin
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Abstract

Traditional risk factors and biomarkers of cardiovascular diseases (CVD) have been mainly discovered through clinical observations. Nevertheless, there is still a gap in knowledge in more sophisticated CVD risk factor stratification and more reliable treatment outcome prediction, highlighting the need for a more comprehensive understanding of disease mechanisms at the molecular level. This need has been addressed by integrating information derived from multiomics studies, which provides systematic insights into the different layers of the central dogma in molecular biology. With the advancement of technologies such as NMR and UPLC-MS, metabolomics have become a powerhouse in pharmaceutical and clinical research for high-throughput, robust, quantitative characterisation of metabolic profiles in various types of biospecimens. In this review, we highlight the versatile value of metabolomics spanning from targeted and untargeted identification of novel biomarkers and biochemical pathways, to tracing drug pharmacokinetics and drug-drug interactions for more personalised medication in CVD research (Fig. 1).

Abstract Image

系统生物学背景下代谢组学技术推动心血管疾病研究的最新进展
心血管疾病(CVD)的传统风险因素和生物标志物主要是通过临床观察发现的。尽管如此,在更复杂的心血管疾病风险因素分层和更可靠的治疗结果预测方面仍存在知识空白,这凸显了从分子水平更全面地了解疾病机制的必要性。通过整合多组学研究获得的信息,可以系统地了解分子生物学中心教条的不同层面,从而满足这一需求。随着核磁共振(NMR)和超高效液相色谱质谱(UPLC-MS)等技术的发展,代谢组学已成为制药和临床研究中对各类生物样本的代谢谱进行高通量、稳健和定量表征的重要手段。在这篇综述中,我们将重点介绍代谢组学的多功能价值,包括有针对性和无针对性地鉴定新型生物标记物和生化途径,以及追踪药物药代动力学和药物间相互作用,从而在心血管疾病研究中实现更个性化的用药(图 1)。
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