Gastroenterology, Department of Clinical Medicine, Sapienza University of Rome, Rome, Italy.
Liver Int. 2013 May;33(5):714-21. doi: 10.1111/liv.12128. Epub 2013 Feb 24.
Chronic diseases, including cirrhosis, are often accompanied by protein-energy malnutrition and muscle loss, which in turn negatively affect quality of life, morbidity and mortality. Unlike other chronic conditions, few data are available on the molecular mechanisms underlying muscle wasting in this clinical setting.
To assess mechanisms of muscle atrophy in patients with cirrhosis.
Nutritional [subjective global assessment (SGA) and anthropometry] and metabolic assessment was performed in 30 cirrhotic patients awaiting liver transplantation. Rectus abdominis biopsies were obtained intraoperatively in 22 cirrhotic patients and in 10 well-nourished subjects undergoing elective surgery for non-neoplastic disease, as a control group. Total RNA was extracted and mRNA for atrogenes (MuRF-1, Atrogin-1/MAFbx), myostatin (MSTN), GSK3β and IGF-1 was assayed.
A total of 50% of cirrhotic patients were malnourished based on SGA, while 53% were muscle-depleted according to mid-arm muscle area (MAMA<5th percentile). MuRF-1 RNA expression was significantly increased in malnourished cirrhotic patients (SGA-B/C) vs. well-nourished patients (SGA-A) (P = 0.01). The phosphorylation of GSK3β was up-regulated in cirrhotic patients with hepatocellular carcinoma (HCC) vs. patients without tumour (P < 0.05).
Muscle loss is frequently found in end-stage liver disease patients. Molecular factors pertaining to signalling pathways known to be involved in the regulation of muscle mass are altered during cirrhosis and HCC.
慢性疾病,包括肝硬化,常伴有蛋白质-能量营养不良和肌肉损失,这反过来又会对生活质量、发病率和死亡率产生负面影响。与其他慢性疾病不同,关于这种临床情况下肌肉减少的分子机制的数据很少。
评估肝硬化患者肌肉萎缩的机制。
对 30 名等待肝移植的肝硬化患者进行营养(主观整体评估(SGA)和人体测量)和代谢评估。在 22 名肝硬化患者和 10 名营养良好的因非肿瘤疾病接受择期手术的患者中,在手术过程中获得了腹直肌活检作为对照组。提取总 RNA,检测肌萎缩基因(MuRF-1、Atrogin-1/MAFbx)、肌肉生长抑制素(MSTN)、GSK3β 和 IGF-1 的 mRNA。
根据 SGA,50%的肝硬化患者存在营养不良,而根据上臂中部肌肉面积(MAMA<5%),53%的患者存在肌肉消耗。营养不良的肝硬化患者(SGA-B/C)与营养良好的患者(SGA-A)相比,MuRF-1 RNA 表达显著增加(P=0.01)。肝癌(HCC)患者的 GSK3β磷酸化水平高于无肿瘤患者(P<0.05)。
终末期肝病患者常出现肌肉损失。与肌肉质量调节相关的信号通路中的分子因子在肝硬化和 HCC 期间发生改变。