实用肝脏病杂志 ›› 2021, Vol. 24 ›› Issue (3): 347-350.doi: 10.3969/j.issn.1672-5069.2021.03.011

• 病毒性肝炎 • 上一篇    下一篇

慢性丙型肝炎合并非酒精性脂肪性肝病患者血清A-FABP水平变化及其临床意义

郝肖伟, 白娜, 郭小军, 陈永刚   

  1. 712000 陕西省咸阳市彩虹医院检验科(郝肖伟,白娜,郭小军);
    陕西中医药大学附属医院输血科(陈永刚)
  • 收稿日期:2020-08-06 出版日期:2021-05-30 发布日期:2021-04-30
  • 通讯作者: 陈永刚,E-mail:19947097@qq.com
  • 作者简介:郝肖伟,男,39岁,大学本科,主管检验师。E-mail:haoxiaowei33326561@163.com

Correlationof serum adipocyte type fatty acid binding protein levels to glucose-lipid metabolism in patients with chronic hepatitis C and non-alcoholic fatty liver diseases

Hao Xiaowei, Bai Na, Guo Xiaojun, et al   

  1. Clinical Laboratory, Rainbow Hospital,Xianyang 712000, Shaanxi Province,China
  • Received:2020-08-06 Online:2021-05-30 Published:2021-04-30

摘要: 目的 探讨慢性丙型肝炎(CHC)合并非酒精性脂肪性肝病(NAFLD)患者血清脂肪细胞型脂肪酸结合蛋白(A-FABP)水平变化及其与糖脂代谢的关系。方法 2017年4月~2020年4月我院收治85例CHC患者和同期体检者85例,CHC患者接受肝穿刺活检,采用ELISA法检测血清A-FABP水平,使用全自动生化分析仪检测血生化指标,应用稳态模型评价胰岛素抵抗指数(HOMA-IR),采用荧光定量PCR法检测丙型肝炎病毒(HCV)RNA载量。结果 在本组85例CHC患者中,经肝组织病理学检查,发现合并NAFLD患者42例;43例CHC血清A-FABP、ALT和AST水平分别为(13.1±2.9)μg/L、(74.8±14.8)U/L和(56.6±9.4)U/L,42例CHC合并NAFLD患者分别为(27.6±4.2)μg/L、(81.7±12.2)U/L和(58.2±8.1)U/L,均显著高于85例健康人【分别为(3.1±1.1)μg/L、(19.7±1.6)U/L和(27.8±3.5)U/L,P<0.05】;CHC患者血清FIN、FPG和HOMA-IR分别为(12.1±1.6)mIU/L、(6.0±1.3)mmol/L和(4.1±0.5),CHC合并NAFLD患者分别为(17.5±2.5)mIU/L、(6.2±1.3)mmol/L和(5.2±0.4),均显著高于健康人【分别为(4.2±0.9)mIU/L、(4.5±0.6)mmol/L和(1.6±0.2),P<0.05】;CHC患者血清TC、TG和LDL-C水平分别为(3.4±0.2)mmol/L、(1.0±0.2)mmol/L和(2.4±0.8)mmol/L,CHC合并NAFLD患者分别为(4.1±0.3)mmol/L、(1.9±0.2)mmol/L和(2.6±0.6)mmol/L,均显著高于健康人【分别为(2.5±0.3)mmol/L、(0.6±0.1)mmol/L和(1.7±0.2)mmol/L,P<0.05】。结论 CHC合并NAFLD患者血清A-FABP水平升高,可能与FIN、HOMA-IR和TG等糖脂代谢紊乱有关。

关键词: 慢性丙型肝炎, 非酒精性脂肪性肝病, 脂肪细胞型脂肪酸结合蛋白, 糖脂代谢

Abstract: Objective The aim of this study was to explore the correlation of serum adipocyte type fatty acid binding protein (A-FABP) levels to glucose-lipid metabolism in patients with chronic hepatitis C (CHC) and non-alcoholic fatty liver diseases (NAFLD). Methods During the period from April 2017 to April 2020, 85 patients with CHC and 85 healthy persons were recruited in this study, and all patients with CHC underwent liver biopsies. The levels of serum A-FABP was detected by enzyme-linked immunosorbent assay. The liver function and glucose-lipid metabolism indexes such as serum alanine aminotransferase (ALT), total bilirubin (TBIL), aspartate aminotransferase (AST), fasting blood glucose (FPG),fasting serum insulin (FIN), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), triacylglycerol (TG)] were detected by full-automatic biochemical analyzer. The homeostasis model assessment of insulin resistance (HOMA-IR) was evaluated by homeostasis model. The viral load of hepatitis C virus (HCV) was detected by fluorescent quantitative PCR. The correlation between serum A-FABP level and viral and glucose-lipid metabolism index in patients with CHC was analyzed. Results Out of 85 patients with CHC, 42 cases were found having NAFLD; serum A-FABP, ALT and AST levels in 43 patients with CHC were (13.1±2.9)μg/L, (74.8±14.8)U/L and (56.6±9.4)U/L, and they were(27.6±4.2)μg/L, (81.7±12.2)U/L and (58.2±8.1)U/L in 42 patients with CHC and NAFLD, all significantly higher than [(3.1±1.1)μg/L, (19.7±1.6)U/L and (27.8±3.5)U/L, respectively, P<0.05] in 85 healthy persons; blood FIN, FPG and HOMA-IR in patients with CHC were (12.1±1.6)mIU/L, (6.0±1.3) mmol/L and (4.1±0.5), and they were (17.5±2.5)mIU/L, (6.2±1.3)mmol/L and (5.2±0.4) in patients with CHC and NAFLD, all significantly higher than [(4.2±0.9)mIU/L,(4.5±0.6)mmol/L and (1.6±0.2), respectively, P<0.05] in healthy persons; blood TC, TG and LDL-C levels in patients with CHC were (3.4±0.2)mmol/L, (1.0±0.2)mmol/L and (2.4±0.8)mmol/L, and they were (4.1±0.3)mmol/L, (1.9±0.2)mmol/L and (2.6±0.6)mmol/L in patients with CHC and NAFLD, all significantly higher than [(2.5±0.3)mmol/L, (0.6±0.1)mmol/L and (1.7±0.2)mmol/L, P<0.05] in healthy persons. Conclusion Serum A-FABP levels increase in patients with CHC and NAFLD, which might be related to the imbalance of glucose-lipid metabolism.

Key words: Hepatitis C, Non-alcoholic fatty liver diseases, Adipocyte type fatty acid binding protein, Glucose-lipid metabolism