Objective: To explore the value of serum adiponectin(ADPN) and hepatocyte growth factor(HGF) levels in the diagnosis and severity assessment of non-alcoholic fatty liver disease(NAFLD). Methods: A total of 100 patients with diagnosed NAFLD who came to our hospital for treatment from May 2021 to May 2023 were selected as the disease group. They were separated into severe group(n=31), moderate group(n=33), and mild group(n=36) based on the severity of condition. In addition, 100 healthy patients in our hospital were selected as the control group during the same period. Serum ADPN and HGF levels were detected by using ELISA method; Logistic regression was applied to analyze the influencing factors of severe NAFLD; ROC curve was applied to analyze the diagnostic value of serum ADPN and HGF levels for NAFLD and severe NAFLD. Results: Compared with the control group, the serum ADPN level in the diseased group obviously decreased, while the HGF level obviously increased(P<0.05). The area under the curve(AUC) of the combined diagnosis of serum ADPN and HGF for NAFLD was higher than that of the individual diagnosis(0.859 vs 0.790, 0.744, Zcombined-ADPN=2.033, Zcombined-HGF=2.384, P=0.042, 0.017). As the severity of the disease increased, the proportion of diabetes, BMI, total cholesterol, triacylglycerol, HGF levels showed an upward trend, and the serum ADPN level showed a downward trend(P<0.05). ADPN was a protective factor that affected the occurrence of severe NAFLD(P<0.05), while total cholesterol and HGF were risk factors that affected the occurrence of severe NAFLD(P<0.05). The area under the curve(AUC) of the combined diagnosis of serum ADPN and HGF for severe NAFLD was higher than that of the two diagnoses alone(0.837 vs 0.674, 0.728, Zcombined-ADPN=2.393, Zcombined-HGF=2.092, P=0.017, 0.036). Conclusion: Serum ADPN level decreases and HGF level increases in patients with NAFLD, and the levels of ADPN and HGF are closely related to the severity of condition. The combination of the two has higher diagnostic value for NAFLD and severe NAFLD. |
[1] 张记,闫艳,李金燕.超声声衰减成像对不同程度非酒精性脂肪肝的诊断价值[J].临床超声医学杂志,2023,25(9):718-722.
[2] 杨可艺,黄雪芳,朱玉婧,等.体检人群非酒精性脂肪肝影响因素的双中心病例对照研究[J].国际检验医学杂志,2020,41(24):2966-2969.
[3] 陈利灵,郑宽勇,王亮,等.2型糖尿病合并非酒精性脂肪肝患者血清CMKLR1、STAT3表达与肝纤维化的关系[J].国际检验医学杂志,2023,44(16):1929-1933.
[4] STEFAN N,CUSI K.A global view of the interplay between non-alcoholic fatty liver disease and diabetes[J].Lancet Diabetes Endocrinol,2022,10(4):284-296.
[5] 蔡欣,辛春红,牛洪凯,等.代谢相关脂肪性肝病患者血清HIF-1α、Chemerin和脂联素水平变化及临床意义探讨[J].实用肝脏病杂志,2023,26(5):654-657.
[6] 段琪,李思玥,李清兰,等.肝细胞生长因子对CCl4致肝细胞损伤相关炎性因子的影响[J].海南医学院学报,2023,29(18):1383-1388.
[7] DE SILVA D M,ROY A,KATO T,et al.Targeting the hepatocyte growth factor/Met pathway in cancer[J].Biochem Soc Trans,2017,45(4):855-870.
[8] 何清,李阳,邓盼盼,等.Toll样受体4、肝细胞生长因子水平对肝细胞癌患者切除术后预后的影响[J].实用临床医药杂志,2021,25(24):43-47.
[9] 童丽.肝脏彩色多普勒超声在非酒精性脂肪肝病情程度评估中的应用[J].基层医学论坛,2023,27(25):110-112.
[10] 南月敏,付娜,李文聪,等.2017美国非酒精性脂肪性肝病诊断与管理指南解读[J].中华肝脏病杂志,2017,25(9):687-694.
[11] 丰萍璐,刘若男,李坤,等.成年健康体检人群幽门螺旋杆菌感染与超重/肥胖、血脂、血糖及非酒精性脂肪肝的关系研究[J].现代预防医学,2022,49(8):1375-1378.
[12] 曾媛,袁姝倩,谢铭,等.超重/肥胖成人局部脂肪量与非酒精性脂肪肝发生风险的关系[J].卫生研究,2022,51(5):753-760.
[13] 孙娜,何明海,杨文翔,等.血清25-羟维生素D3与2型糖尿病合并非酒精性脂肪肝患者糖代谢、肝功能及病情进展的相关性[J].实用临床医药杂志,2022,26(1):89-94.
[14] CAI G S,SU H,ZHANG J.Protective effect of probiotics in patients with non-alcoholic fatty liver disease[J].Medicine(Baltimore),2020,99(32):21464-21475.
[15] 胡红琳,刘瑞侠,孙蓉,等.脂联素与2型糖尿病乳腺癌发生的相关性及其机制研究[J].中华糖尿病杂志,2021,13(2):162-168.
[16] MAVILIA M G,WU G Y.Liver and serum adiponectin levels in non-alcoholic fatty liver disease[J].J Dig Dis,2021,22(4):214-221.
[17] 徐亮,钟燕,苏淑婷,等.反应性氧化物、脂联素在慢性乙型肝炎病毒感染合并非酒精性脂肪性肝病中的研究[J].中华肝脏病杂志,2020,28(3):247-253.
[18] 刘田田,滕军放,张敏,等.颈动脉斑块中血管生长因子表达与新生微血管密度的研究[J].中华老年心脑血管病杂志,2022,24(6):571-574.
[19] 王玉慧,赵芳,王瑷,等.老年脑动脉粥样硬化患者继发血管性认知功能障碍的风险预测因子研究[J].中华保健医学杂志,2022,24(1):26-29.
[20] 沈晓燕,种亚楠,狄海莉,等.颈内动脉海绵窦钙化水平与脑动脉粥样硬化的相关性[J].中西医结合心脑血管病杂志,2022,20(14):2657-2660.
[21] 李颖,张晓燕,李庆利.血清HGF、ADPN、miR-126在脑动脉粥样硬化患者中的表达及临床意义探讨[J].临床研究,2023,31(5):25-28. |