[1] 武丹, 马向鹰. 非酒精性脂肪性肝病肝硬化患者胰岛素抵抗水平与颈动脉硬化程度和左心室功能研究. 实用肝脏病杂志, 2019, 22(6): 876-879.
[2] Alessandro F, Tublin ME, Chopra KB, et al. Comparison of 2D shear wave elastography, transient elastography, and MR elastography for the diagnosis of fibrosis in patients with nonalcoholic fatty liver disease. Am Roent, 2020, 214(1): 21-25.
[3] Bao LC, Yin J, Gao W, et al. A long-acting FGF21 alleviates hepatic steatosis and inflammation in a mouse model of non-alcoholic steatohepatitis partly through an FGF21-adiponectin-IL17A pathway. Br J Pharmacol, 2018, 175(16): 3379-3393.
[4] Singhal G, Kumar G, Chan S, et al. Deficiency of fibroblast growth factor 21 (FGF21) promotes hepatocellular carcinoma (HCC) in mice on a long term obesogenic diet. Mol Metab, 2018,13(11): 56-66.
[5] Zhu SL, Wu YZ, Ye XL, et al. FGF21 ameliorates nonalcoholic fatty liver disease by inducing autophagy. Mol cell bio, 2016, 420(1): 1450-1455.
[6] 中华医学会肝病学分会脂肪肝和酒精性肝病学组, 中国医师协会脂肪肝专家委员会. 非酒精性脂肪性肝病诊疗指南(2018年版). 实用肝脏病杂志, 2018, 21(2): 177-186.
[7] Antonio F, Guido C, Anna A, et al. The contribution of the adipose tissue-liver axis in pediatric patients with nonalcoholic fatty liver disease after laparoscopic sleeve gastrectomy. Pediatrics, 2020, 216(3): 321-325.
[8] 田军伟, 肖远力, 王艳超. 应用血清TG/HDL-C比值早期诊断非酒精性脂肪性肝病患者临床价值探讨. 实用肝脏病杂志, 2017, 20(4): 416-419.
[9] Wu GY, Li HT, Fang QC, et al. Complementary role of fibroblast growth factor 21 and cytokeratin 18 in monitoring the different stages of nonalcoholic fatty liver disease. Sci Rep, 2017, 7(10): 5095-5096.
[10] Li Y, Wong K, Walsh K, et al. Retinoic acid receptor β stimulates hepatic induction of fibroblast growth factor 21 to promote fatty acid oxidation and control whole-body energy homeostasis in mice. J Biol Chem, 2017, 288(15): 10490-10504.
[11] 关阳, 陈金军, 邓红. 非酒精性脂肪性肝病患者人体脂肪成分指标的变化. 实用肝脏病杂志, 2018, 21(2): 229-232.
[12] Grimaudo S, Pipitone RM, Pennisi G, et al. Association between pnpla3 rs738409 c>g variant and liver-related outcomes in patients with nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol, 2019, 10(11):24-37.
[13] Weslie YK, Benjamin JC, Sudathip S, et al. Lambert. mitigation of nonalcoholic fatty liver disease in high-fat-fed mice by the combination of decaffeinated green tea extract and voluntary exercise. Nut Biochemist, 2020, 76(10): 25-28.
[14] Ampuero J, Pais R, Aller R, et al. Development and validation of hepamet fibrosis scoring system–a simple, noninvasive test to identify patients with nonalcoholic fatty liver disease with advanced fibrosis. Clin Gastroenterol Hepatol, 2020, 18(1): 55-58.
[15] 信丰智, 曹海霞, 范建高. 胰高血糖素样肽-1改善非酒精性脂肪性肝病作用机制研究进.实用肝脏病杂志, 2018, 21(2): 313-316.
[16] Haidari F, Hojhabrimanesh A, Helli B, et al. An energy-restricted high-protein diet supplemented with β -cryptoxanthin alleviated oxidative stress and inflammation in nonalcoholic fatty liver disease: a randomized controlled trial. Nutrit Res, 2020, 73(5): 13-15.
[17] Kopp MA, Watzlawick R, Martus P, et al. Long-term functional outcome in patients with acquired infections after acute spinal cord injury. Neurology, 2017, 88(9): 892-900.
[18] Desai BN, Singhal G, Watanabe M, et al. Fibroblast growth factor 21 (FGF21) is robustly induced by ethanol and has a protective role in ethanol associated liver injury. Mol Metab, 2017, 6(11): 1395-1406.
[19] Rusli F, Deelen J, Andriyani E, et al. Fibroblast growth factor 21 reflects liver fat accumulation and dysregulation of signalling pathways in the liver of C57BL/6J mice. Sci Rep, 2016, 6(29): 30484-30485. |