出 处:《中国糖尿病杂志》2018年第2期117-122,共6页Chinese Journal of Diabetes
基 金:国家自然科学基金(81660142);贵州省科技支撑计划项目社会发展攻关项目[黔科合SY字合(2013)3033号]
摘 要:目的探讨T2DM合并非酒精性脂肪肝(NAFLD)肝纤维化与血清25-羟维生素D[25-(OH)D]水平的关系。方法选取T2DM患者359例,其中单纯T2DM(T2DM组)患者158例,依据腹部超声诊断NAFLD的T2DM(T2DM+NAFLD)患者201例,再根据非酒精性脂肪肝肝纤维化评分(NFS)分为<-1.455亚组(可排除肝纤维化亚组)、-1.455~0.676亚组(不确定亚组)、>0.676亚组(肝纤维化亚组)。分别测定FPG、FIns、FC-P、HbA1c、血脂、肝功能、肾功能、血常规及血清25-(OH)D,计算BMI、胰岛素抵抗指数(HOMA-IR)、NFS。结果 T2DM+NAFLD组25-(OH)D、HDL-C、AST/ALT水平低于T2DM组(P<0.05);肝纤维化亚组25-(OH)D水平低于不确定亚组、可排除肝纤维化亚组[(9.78±3.39)、(11.85±4.34)vs(12.72±4.51)ng/ml,P<0.05]。NFS评分与病程、Scr、胱抑素C(Cys-C)呈正相关(r=0.328、0.160、0.354,P<0.05),与ALT、GGT、载脂蛋白B(ApoB)、25-(OH)D呈负相关(r=-0.306、-0.154、-0.235、-0.179,P<0.05)。BMI、25-(OH)D、HOMA-IR及SUA是NAFLD的影响因素;ALT(OR=0.965,P=0.045)、Cys-C(OR=1.005,P=0.006)、ApoB(OR=0.086,P=0.032)、25-(OH)D(OR=0.865,P=0.026)及病程(OR=1.171,P=0.006)是肝纤维化的影响因素。结论 T2DM合并NAFLD患者血清25-(OH)D水平的降低与肝纤维化相关,且低水平的25-(OH)D为NAFLD及肝纤维化的危险因素。Objective To investigate the relationship between hepatic fibrosis and serum 25-hydroxyvitamin D [ 25-( OH ) D] in type 2 diabetes mellitus (T2DM) patients complicated with nonalcoholic fatty liver disease (NAFLD). Methods 359 T2DM patients were divided simple T2DM group (n= 158)and T2DM+ NAFLD group (n= 201)according to abdominal ultrasound diagnosis. According to nonalcoholic fatty liver fibrosis score (NFS), 201 T2DM+ NAFLD were divided into three subgroups:45 without hepatic fibrosis (NFS^--I. 455), 52 with hepatic fibrosis(NFS^0. 676), 104 with uncertain hepatic fibrosis (NFS --1. 455~0. 676). Fasting blood glucose (FPG), fasting insulin (Fins), fasting C peptide (FC-P), glycosylated hemoglobin (HbA1 c), blood lipid, liver function, renal function, blood routine and serum 25-(OH)D were measured. The body mass (BMI), insulin resistance index (HOMA-IR)and NFS were calculated. Results The levels of 25-(OH)D, HDL-C and AST/ALT of T2DM+NAFLD group were significantly lower than those of T2DM group (P〈0.05). 25-(OH)D level of the liver fibrosis subgroup was significantly lower than patients with uncertain hepatic fibrosis and patients without hepatic fibrosis,[(9.78±3.39) vs (11.85±4.34) vs (12.72±4. 51)ng/ml,P〈0. 05]. NFS was positively correlated with course of disease, Scr and cystatin C (Cys-C), with r= 0. 328,0. 160 and 0. 354,respectively (P〈0.05), and negatively correlated with GGT, ALT, ApoB and 25-(OH) D, with r=-0. 306,--0. 154, -0. 235 and -0. 179, respectively (P%0.05). BMI, 25-(OH)D, HOMA-IR and SUA were influencing factors of NAFLD. ALT (OR = 0. 965, P = 0. 045), Cys-C (OR-- 1. 005, P = 0. 006) ,APOB(OR=O. 086,P=0. 032), 25-(OH)D(OR= 0. 865, P= 0. 026)and course of disease(OR= 1.171, P= 0. 006)were the related factors of hepatic fibrosis. Conclusion The decrease in serum 25-(OH)D levels was associated with hepatic fibrosis in patients with T2DM combin
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