Bokhari Syed Faqeer Hussain, Umais Muhammad, Faizan Sattar Syed Muhammad, Mehboob Umair, Iqbal Asma, Amir Maaz, Bakht Danyal, Ali Khawar, Hasan Abdul Haseeb, Javed Muhammad Arsham, Dost Wahidullah
Department of Medicine and Surgery, King Edward Medical University, Lahore 54000, Punjab, Pakistan.
Department of Curative Medicine, Kabul University of Medical Sciences, Kabul 10001, Afghanistan.
World J Cardiol. 2025 Jul 26;17(7):106561. doi: 10.4330/wjc.v17.i7.106561.
Cardiovascular diseases (CVDs) remain the leading cause of morbidity and mortality worldwide, necessitating innovative diagnostic and prognostic strategies. Traditional biomarkers like C-reactive protein, uric acid, troponin, and natriuretic peptides play crucial roles in CVD management, yet they are often limited by sensitivity and specificity constraints. This narrative review critically examines the emerging landscape of cardiac biomarkers and advocates for a multiple-marker approach to enhance early detection, prognosis, and risk stratification of CVD. In recent years, several novel biomarkers have shown promise in revolutionizing CVD diagnostics. Gamma-glutamyltransferase, microRNAs, endothelial microparticles, placental growth factor, trimethylamine N-oxide, retinol-binding protein 4, copeptin, heart-type fatty acid-binding protein, galectin-3, growth differentiation factor-15, soluble suppression of tumorigenicity 2, fibroblast growth factor 23, and adrenomedullin have emerged as significant indicators of CV health. These biomarkers provide insights into various pathophysiological processes, such as oxidative stress, endothelial dysfunction, inflammation, metabolic disturbances, and myocardial injury. The integration of these novel biomarkers with traditional ones offers a more comprehensive understanding of CVD mechanisms. This multiple-marker approach can improve diagnostic accuracy, allowing for better risk stratification and more personalized treatment strategies. This review underscores the need for continued research to validate the clinical utility of these biomarkers and their potential incorporation into routine clinical practice. By leveraging the strengths of both traditional and novel biomarkers, precise therapeutic plans can be developed, thereby improving the management and prognosis of patients with CVDs. The ongoing exploration and validation of these biomarkers are crucial for advancing CV care and addressing the limitations of current diagnostic tools.
心血管疾病(CVDs)仍然是全球发病和死亡的主要原因,因此需要创新的诊断和预后策略。传统生物标志物如C反应蛋白、尿酸、肌钙蛋白和利钠肽在心血管疾病管理中发挥着关键作用,但它们往往受到敏感性和特异性的限制。这篇叙述性综述批判性地审视了心脏生物标志物的新领域,并提倡采用多标志物方法来加强心血管疾病的早期检测、预后评估和风险分层。近年来,几种新型生物标志物在革新心血管疾病诊断方面显示出了前景。γ-谷氨酰转移酶、微小RNA、内皮微粒、胎盘生长因子、氧化三甲胺、视黄醇结合蛋白4、 copeptin、心型脂肪酸结合蛋白、半乳糖凝集素-3、生长分化因子-15、可溶性肿瘤抑制因子2、成纤维细胞生长因子23和肾上腺髓质素已成为心血管健康的重要指标。这些生物标志物为氧化应激、内皮功能障碍、炎症、代谢紊乱和心肌损伤等各种病理生理过程提供了见解。将这些新型生物标志物与传统生物标志物相结合,能更全面地了解心血管疾病的机制。这种多标志物方法可以提高诊断准确性,实现更好的风险分层和更个性化的治疗策略。本综述强调需要持续研究以验证这些生物标志物的临床效用及其纳入常规临床实践的潜力。通过利用传统和新型生物标志物的优势,可以制定精确治疗方案,从而改善心血管疾病患者的管理和预后。对这些生物标志物的持续探索和验证对于推进心血管护理及克服当前诊断工具的局限性至关重要。