Boulos Mariana, Mousa Rabia S, Jeries Nizar, Simaan Elias, Alam Klode, Bulus Bulus, Assy Nimer
Internal Medicine Department, Galilee Medical Centre, Nahariya 221001, Israel.
The Azrieli Faculty of Medicine, Bar-Ilan University, Safed 1311502, Israel.
Int J Mol Sci. 2025 Apr 7;26(7):3448. doi: 10.3390/ijms26073448.
Metabolic syndrome (MetS) and metabolic dysfunction-associated steatotic liver disease (MASLD) are closely related, with rapidly increasing prevalence globally, driving significant public health concerns. Both conditions share common pathophysiological mechanisms such as insulin resistance (IR), adipose tissue dysfunction, oxidative stress, and gut microbiota dysbiosis, which contribute to their co-occurrence and progression. While the clinical implications of this overlap, including increased cardiovascular, renal, and hepatic risk, are well recognized, current diagnostic and therapeutic approaches remain insufficient due to the clinical and individuals' heterogeneity and complexity of these diseases. This review aims to provide an in-depth exploration of the molecular mechanisms linking MetS and MASLD, identify critical gaps in our understanding, and highlight existing challenges in early detection and treatment. Despite advancements in biomarkers and therapeutic interventions, the need for a comprehensive, integrated approach remains. The review also discusses emerging therapies targeting specific pathways, the potential of precision medicine, and the growing role of artificial intelligence in enhancing research and clinical management. Future research is urgently needed to combine multi-omics data, precision medicine, and novel biomarkers to better understand the complex interactions between MetS and MASLD. Collaborative, multidisciplinary efforts are essential to develop more effective diagnostic tools and therapies to address these diseases on a global scale.
代谢综合征(MetS)与代谢功能障碍相关脂肪性肝病(MASLD)密切相关,在全球范围内患病率迅速上升,引发了重大的公共卫生问题。这两种病症具有共同的病理生理机制,如胰岛素抵抗(IR)、脂肪组织功能障碍、氧化应激和肠道微生物群失调,这些因素导致了它们的共同出现和进展。虽然这种重叠的临床影响,包括心血管、肾脏和肝脏风险增加,已得到充分认识,但由于这些疾病的临床和个体异质性及复杂性,目前的诊断和治疗方法仍然不足。本综述旨在深入探讨连接MetS和MASLD的分子机制,识别我们理解中的关键差距,并突出早期检测和治疗中的现有挑战。尽管生物标志物和治疗干预取得了进展,但仍需要一种全面、综合的方法。该综述还讨论了针对特定途径的新兴疗法、精准医学的潜力以及人工智能在加强研究和临床管理方面日益重要的作用。迫切需要未来的研究将多组学数据、精准医学和新型生物标志物结合起来,以更好地理解MetS和MASLD之间的复杂相互作用。合作、多学科的努力对于开发更有效的诊断工具和疗法以在全球范围内应对这些疾病至关重要。
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