Moncho Francesc, Benlloch Salvador, Górriz Jose Luis
Department of Nephrology. University Clinical Hospital, INCLIVA, Valencia. RICORS Renal Instituto de salud Carlos III, Valencia. Spain.
Department of Digestive Medicine, Arnau de Vilanova Hospital, Valencia. CIBEREHD-Instituto de Salud Carlos III, Valencia. Spain.
Clin Kidney J. 2025 Aug 12;18(9):sfaf260. doi: 10.1093/ckj/sfaf260. eCollection 2025 Sep.
Metabolic dysfunction-associated steatotic liver disease (MASLD) has emerged as a major contributor to systemic metabolic dysfunction and is increasingly recognized as a risk enhancer for both cardiovascular disease (CVD) and chronic kidney disease (CKD). This review explores the complex interconnections between MASLD, CVD, and CKD, with emphasis on shared pathophysiological mechanisms and the clinical implications for risk assessment and management. We describe the crosstalk among the liver, heart, and kidneys, focusing on insulin resistance, chronic inflammation, and progressive fibrosis as key mediators. The severity of liver fibrosis in MASLD is independently associated with both cardiovascular and renal outcomes. Conventional cardiovascular risk scores may underestimate risk in MASLD-CKD populations, highlighting the need for integrated approaches that include hepatic, renal, and metabolic profiling. We also review current non-invasive diagnostic tools, including fibrosis scores and cardiovascular biomarkers, as well as emerging genetic and epigenetic markers that may enhance risk stratification. The therapeutic landscape is evolving, with promising results from lifestyle interventions and pharmacological agents such as GLP-1 receptor agonists, SGLT2 inhibitors, and novel antifibrotic compounds. We also propose a practical algorithm for the screening and risk stratification of MASLD in CKD patients, incorporating non-invasive fibrosis assessment and cardiometabolic risk evaluation. This stepwise approach supports early detection and personalized management, particularly in patients with CKD or type 2 diabetes. In conclusion, MASLD significantly amplifies cardiovascular and renal risk. Early, multidisciplinary intervention is essential to improve long-term outcomes in this high-risk population.
代谢功能障碍相关脂肪性肝病(MASLD)已成为全身代谢功能障碍的主要原因,并日益被认为是心血管疾病(CVD)和慢性肾脏病(CKD)的风险增强因素。本综述探讨了MASLD、CVD和CKD之间的复杂相互关系,重点关注共同的病理生理机制以及对风险评估和管理的临床意义。我们描述了肝脏、心脏和肾脏之间的相互作用,重点关注胰岛素抵抗、慢性炎症和进行性纤维化作为关键介质。MASLD中肝纤维化的严重程度与心血管和肾脏结局独立相关。传统的心血管风险评分可能低估MASLD-CKD人群的风险,这凸显了采用包括肝脏、肾脏和代谢分析在内的综合方法的必要性。我们还综述了当前的非侵入性诊断工具,包括纤维化评分和心血管生物标志物,以及可能增强风险分层的新兴遗传和表观遗传标志物。治疗格局正在不断发展,生活方式干预和药物治疗如GLP-1受体激动剂、SGLT2抑制剂和新型抗纤维化化合物已取得了令人鼓舞的结果。我们还提出了一种针对CKD患者MASLD筛查和风险分层的实用算法,纳入了非侵入性纤维化评估和心脏代谢风险评估。这种逐步方法支持早期检测和个性化管理,特别是在CKD或2型糖尿病患者中。总之,MASLD显著增加心血管和肾脏风险。早期多学科干预对于改善这一高危人群的长期结局至关重要。