[1] 温林. 非酒精性脂肪性肝病并发2型糖尿病患者血尿酸水平变化及其临床意义. 实用肝脏病杂志, 2021, 24(1):55-58. [2] Lee G, You H J, Bajaj J S, et al. Distinct signatures of gut microbiome and metabolites associated with significant fibrosis in non-obese NAFLD. Nat Commun, 2020, 11(1):4982. [3] 李珺. NAFLD患者TE成像特点与其病情严重程度及胰岛素抵抗的关系研究. 影像科学与光化学, 2020, 38(2):225-230. [4] Tanase D M, Gosav E M, Costea C F, et al. The intricate relationship between type 2 diabetes mellitus (T2DM), insulin resistance (IR), and nonalcoholic fatty liver disease (NAFLD. J Diabetes Res, 2020, 2020:3920196. [5] Mirabelli M, Chiefari E, Arcidiacono B, et al. Mediterranean diet nutrients to turn the tide against insulin resistance and related Diseases. Nutrients, 2020, 12(4):1066. [6] 中华医学会肝病学分会脂肪肝和酒精性肝病学组, 中国医师协会脂肪性肝病专家委员会, 范建高,等. 非酒精性脂肪性肝病防治指南(2018年更新版). 实用肝脏病杂志, 2018, 21(2):30-39. [7] Phillips PJ. Oral glucose tolerance testing. Aust Fam Physician, 2012, 41(6):391-393. [8] Gobato A O, Vasques A C, Zambon M P, et al. Prevalence of metabolic syndrome in obese Turkish children and adolescents. Rev Paul Pediatr, 2014, 32(1):55-62. [9] Angulo P, Hui J M, Marchesini G, et al. The NAFLD fibrosis score: a noninvasive system that identifies liver fibrosis in patients with NAFLD. Hepatology, 2007, 45(4):846-854. [10] Akshatha N S, Diwakar S, Santhekadur P K, et al. Extracellular vesicles as inflammatory drivers in NAFLD. Front Immunol, 2021, 11:627424. [11] 罗娟, 刘立伟, 刘纪民, 等. 非酒精性脂肪性肝病临床和病理特点及进展期纤维化危险因素性别差异的对比研究. 中华肝脏病杂志, 2021, 29(4):356-361. [12] Lomonaco R, Leiva E G, Bril F, et al. Advanced liver fibrosis is common in patients with type 2 diabetes followed in the outpatient setting: the need for systematic screening. Diabetes Care, 2021, 44(2):399-406. [13] Pierantonelli I, Svegliati-Baroni G. Nonalcoholic fatty liver disease: basic pathogenetic mechanisms in the progression from NAFLD to NASH. Transplantation, 2019, 103(1):e1-e13. [14] 杨燕, 姚艺璇, 洪秀韬, 等. 应用胰岛素抵抗替代指标评估2型糖尿病患者非酒精性脂肪肝及进展性肝纤维化的价值. 中华内分泌代谢杂志, 2021, 37(4):281-287. [15] Li C H, Chou Y T, Shen W C, et al. Increased risks of different grades of non-alcoholic fatty liver disease in prediabetic subjects with impaired fasting glucose and glucose tolerance, including the isolated glycosylated hemoglobin levels of 5.7-6.4% in a Chinese population. J Diabetes Investig, 2020, 11(5):1336-1343. [16] Li Y, Feng D, Esangbedo I C, et al. Insulin resistance, beta-cell function, adipokine profiles and cardiometabolic risk factors among Chinese youth with isolated impaired fasting glucose versus impaired glucose tolerance: the BCAMS study. BMJ Open Diabetes Res Care, 2020, 8(1):e000724. [17] Schwabe R F, Tabas I, Pajvani U B. Mechanisms of fibrosis development in nonalcoholic steatohepatitis. Gastroenterology, 2020, 158(7):1913-1928. [18] Stefano J T, Guedes L V, Souza A, et al. Usefulness of collagen type IV in the detection of significant liver fibrosis in nonalcoholic fatty liver disease. Ann hepatol, 2020, 20:100253. [19] Slimin Y, Hadi P. Diagnostic accuracy of glycoproteins in the assessment of liver fibrosis: A comparison between laminin, fibronectin, and hyaluronic acid. Turk J Gastroenterol, 2019, 30(6):524-531. [20] Govaere O, Cockell S, Tiniakos D, et al. Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis. Scie Transl Med, 2020, 12(572):eaba4448. [21] Fujii H, Imajo K, Yoneda M, et al. HOMA-IR: An independent predictor of advanced liver fibrosis in nondiabetic non-alcoholic fatty liver disease. J Gastroenterol Hepatol, 2019, 34(8):1390-1395. |