Rohun Justyna, Dudzik Danuta, Raczak-Gutknecht Joanna, Wabich Elżbieta, Młodziński Krzysztof, Markuszewski Michał J, Daniłowicz-Szymanowicz Ludmiła
Department of Cardiology and Electrotherapy, Faculty of Medicine, Medical University of Gdansk, 80-214 Gdańsk, Poland.
Department of Biopharmaceutics and Pharmacodynamics, Faculty of Pharmacy, Medical University of Gdansk, 80-416 Gdańsk, Poland.
J Clin Med. 2024 Dec 25;14(1):34. doi: 10.3390/jcm14010034.
Atrial fibrillation (AF) is the most frequent arrhythmia in the adult population associated with a high rate of severe consequences leading to significant morbidity and mortality worldwide. Therefore, its prompt recognition is of high clinical importance. AF detection often remains challenging due to unspecific symptoms and a lack of reliable biomarkers for its prediction. Herein, novel bioanalytical methodologies, such as metabolomics, offer new opportunities for a better understanding of the underlying pathological mechanisms of cardiovascular diseases, including AF. The metabolome, considered a complete set of small molecules present in the organism, directly reflects the current phenotype of the studied system and is highly sensitive to any changes, including arrhythmia's onset. A growing body of evidence suggests that metabolite profiling has prognostic value in AF prediction, highlighting its potential role not only in early diagnosis but also in guiding therapeutic interventions. By identifying specific metabolites as a disease biomarker or recognising particular metabolomic pathways involved in the AF pathomechanisms, metabolomics could be of great clinical value for further clinical decision-making, risk stratification, and an individual personalised approach. The presented narrative review aims to summarise the current state of knowledge on metabolomics in AF with a special emphasis on its implications for clinical practice and personalised medicine.
心房颤动(AF)是成年人群中最常见的心律失常,在全球范围内导致严重后果的发生率很高,从而导致显著的发病率和死亡率。因此,对其进行及时识别具有高度的临床重要性。由于症状不具特异性且缺乏用于预测的可靠生物标志物,AF检测往往仍具有挑战性。在此,代谢组学等新型生物分析方法为更好地理解包括AF在内的心血管疾病的潜在病理机制提供了新机会。代谢组被认为是生物体中存在的一整套小分子,它直接反映了所研究系统的当前表型,并且对任何变化(包括心律失常的发作)高度敏感。越来越多的证据表明,代谢物谱分析在AF预测中具有预后价值,突出了其不仅在早期诊断中而且在指导治疗干预方面的潜在作用。通过将特定代谢物鉴定为疾病生物标志物或识别参与AF发病机制的特定代谢组学途径,代谢组学对于进一步的临床决策、风险分层和个体化的个性化方法可能具有巨大的临床价值。本叙述性综述旨在总结目前关于AF中代谢组学的知识状态,特别强调其对临床实践和个性化医学的影响。