Gradenigo Hospital, University of Turin, Turin, Italy.
Department of Medical Sciences, San Giovanni Battista Hospital, University of Turin, Turin, Italy.
Trends Mol Med. 2015 Oct;21(10):645-662. doi: 10.1016/j.molmed.2015.08.005.
Mounting evidence connects non-alcoholic fatty liver disease (NAFLD) to chronic kidney disease (CKD). We review emerging mechanistic links between NAFLD and CKD, including altered activation of angiotensin converting enzyme (ACE)-2, nutrient/energy sensors sirtuin-1 and AMP-activated kinase, as well as impaired antioxidant defense mediated by nuclear factor erythroid 2-related factor-2 (Nrf2). Dietary fructose excess may also contribute to NAFLD and CKD. NAFLD affects renal injury through lipoprotein dysmetabolism and altered secretion of the hepatokines fibroblast growth factor-21, fetuin-A, insulin-like growth factor-1, and syndecan-1. CKD may mutually aggravate NAFLD and associated metabolic disturbances through altered intestinal barrier function and microbiota composition, the accumulation of uremic toxic metabolites, and alterations in pre-receptor glucocorticoid metabolism. We conclude by discussing the implications of these findings for the treatment of NAFLD and CKD.
越来越多的证据表明非酒精性脂肪性肝病(NAFLD)与慢性肾脏病(CKD)有关。我们综述了 NAFLD 和 CKD 之间新出现的机制联系,包括血管紧张素转换酶(ACE)-2、营养/能量传感器 Sirtuin-1 和 AMP 激活的蛋白激酶的激活改变,以及核因子红细胞 2 相关因子-2(Nrf2)介导的抗氧化防御受损。饮食果糖过量也可能导致 NAFLD 和 CKD。NAFLD 通过脂蛋白代谢紊乱和肝分泌因子成纤维细胞生长因子-21、胎球蛋白-A、胰岛素样生长因子-1 和 syndecan-1 的改变影响肾脏损伤。CKD 可能通过改变肠道屏障功能和微生物群落组成、尿毒症毒性代谢物的积累以及前受体糖皮质激素代谢的改变,相互加重 NAFLD 和相关代谢紊乱。最后,我们讨论了这些发现对 NAFLD 和 CKD 治疗的意义。