Quiroga Borja, Díez Javier
Nephrology Department, IIS-La Princesa, Hospital Universitario de la Princesa, Madrid, Spain.
RICORS2040 Kidney Disease, Madrid, Spain.
Nephrol Dial Transplant. 2025 Feb 4;40(2):255-263. doi: 10.1093/ndt/gfae193.
Myokines are signalling moieties released by the skeletal muscle in response to acute and/or chronic exercise, which exert their beneficial or detrimental effects through paracrine and/or autocrine pathways on the skeletal muscle and through endocrine pathways in many other organs (e.g. the heart). Interestingly, alterations in myokines have been described in patients with heart failure (HF) that are associated with adverse structural and functional left ventricular remodelling and poor cardiac outcomes. Recent experimental and clinical studies have shown that the muscle regulation of a number of myokines is altered in chronic kidney disease (CKD) thus representing a new molecular aspect of the pathophysiology of skeletal myopathy present in patients with CKD. Muscle dysregulation of myokines may contribute to a number of disorders in non-dialysis and dialysis patients with CKD, including the high risk of developing HF. This possibility would translate into a range of new diagnostic and therapeutic options. In fact, the measurement of circulating myokines opens their possible usefulness as biomarkers to personalize exercise training and pharmacological therapies for the prevention and treatment of HF in patients with CKD and skeletal myopathy. This review will analyse information on some myokines that target the heart and are altered at the level of skeletal muscle and circulation in patients with CKD.
肌动蛋白是骨骼肌在急性和/或慢性运动时释放的信号分子,它们通过旁分泌和/或自分泌途径对骨骼肌发挥有益或有害作用,并通过内分泌途径作用于许多其他器官(如心脏)。有趣的是,心力衰竭(HF)患者体内的肌动蛋白发生了改变,这与左心室不良的结构和功能重塑以及不良的心脏预后有关。最近的实验和临床研究表明,慢性肾脏病(CKD)患者体内多种肌动蛋白的肌肉调节发生了改变,这代表了CKD患者骨骼肌病病理生理学的一个新的分子层面。肌动蛋白的肌肉调节异常可能导致CKD非透析和透析患者出现多种疾病,包括发生HF的高风险。这种可能性将转化为一系列新的诊断和治疗选择。事实上,循环肌动蛋白的检测揭示了它们作为生物标志物的潜在用途,可为CKD和骨骼肌病患者个性化运动训练和药物治疗以预防和治疗HF提供依据。本综述将分析一些针对心脏且在CKD患者骨骼肌和循环水平发生改变的肌动蛋白的相关信息。