实用肝脏病杂志 ›› 2023, Vol. 26 ›› Issue (2): 185-188.doi: 10.3969/j.issn.1672-5069.2023.02.009

• 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RBP4和SREBP-1c水平变化分析*

范明芳, 田瑛, 周倩, 接贵涛, 刘淑芳   

  1. 276400 山东省临沂市 山东第一医科大学附属临沂医院检验科
  • 收稿日期:2022-06-22 出版日期:2023-03-10 发布日期:2023-03-21
  • 通讯作者: 刘淑芳,E-mail:liushufang626@163.com
  • 作者简介:范明芳,女,36岁,大学本科,主管技师。E-mail:fanmingfang1986@163.com
  • 基金资助:
    *山东省自然科学基金资助项目(编号:ZR201911070516)

Changes of serum RBP4 and SREBP-1c levels in patients with chronic hepatitis C and non-alcoholic fatty liver diseases

Fan Mingfang, Tian Ying, Zhou Qian, et al.   

  1. Clinical Laboratory, Central Hospital Affiliated to Shandong First Medical University, Linyi 276400, Shandong Province, China
  • Received:2022-06-22 Online:2023-03-10 Published:2023-03-21

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)患者血清视黄醇结合蛋白4(RBP4)和固醇调节元件结合蛋白-1c(SREBP-1c)水平变化及其临床意义。方法 2019年2月~2022年2月我院收治的CHC患者94例,接受肝穿刺活检和重组人干扰素-α2a联合利巴韦林治疗24周。使用全自动生化分析仪检测血生化指标,计算稳态模型胰岛素抵抗指数(HOMA-IR),采用ELISA法检测血清RBP4和SREBP-1c水平。结果 经组织病理学检查发现,在94例CHC患者中,合并NAFLD患者50例(53.2%),其中肝轻度脂肪变22例(44.0%)和中重度脂肪变28例(56.0%);CHC合并中重度脂肪变患者血清AST、ALT、ALP和GGT水平分别为(62.2±12.8)U/L、(87.2±11.5)U/L、(99.0±14.4)U/L和(69.4±10.3)U/L,显著高于CHC合并轻度脂肪变患者【分别为(53.6±10.1)U/L、(75.7±12.5)U/L、(83.8±12.7)U/L和(58.5±7.7)U/L,P<0.05】或CHC患者【分别为(51.7±8.5)U/L、(73.5±13.8)U/L、(81.6±10.9)U/L和(56.2±8.1)U/L,P<0.05】;CHC合并中重度脂肪变患者血清RBP4和SREBP-1c水平分别为(55.9±8.2)mg/L和(40.1±7.4)μg/L,显著高于合并轻度脂肪变患者【分别为(36.7±5.8)mg/L和(29.3±5.1)μg/L,P<0.05】或CHC患者【分别为(28.4±6.3)mg/L和(21.8±5.5)μg/L,P<0.05】;中重度脂肪变患者血清HbA1c和HOMA-IR水平分别为(5.7±0.5)%和(3.2±0.5),显著高于CHC合并轻度脂肪变患者【分别为(5.3±0.5)%和(2.5±0.4),P<0.05】或CHC患者【分别为(5.1±0.3)%和(1.9±0.3),P<0.05】;41例治疗应答组血清RBP4和SREBP-1c水平分别为(25.7±6.0)mg/L和(20.6±5.0)μg/L,显著低于53例治疗无应答组【分别为(48.5±7.4)mg/L和(35.5±6.3)μg/L,P<0.05】。结论 CHC合并NAFLD患者血清RBP4和SREBP-1c水平升高,可能影响对干扰素-α2a抗病毒治疗的应答,值得进一步研究。

关键词: 慢性丙型肝炎, 非酒精性脂肪性肝病, 干扰素-α2a, 视黄醇结合蛋白4, 固醇调节元件结合蛋白-1c, 应答

Abstract: Objective The aim of this study was to explore the implication of serum retinol-binding protein 4 (RBP4) and sterol regulatory element-binding protein-1c (SREBP-1c) in patients with chronic hepatitis C (CHC) and non-alcoholic fatty liver diseases (NAFLD). Methods A total of 94 patients with CHC were admitted to our hospital between February 2019 and February 2022, and all underwent liver biopsy and were treated with recombinant human interferon-α 2a and ribavirin for 24 weeks. The homeostasis model assessment of insulin resistance (HOMA-IR) was calculated. Serum RBP4 and SREBP-1c levels were detected by ELISA. Results The liver histopathological examination revealed NAFLD in 50 cases (53.2%), including 22 (44.0%) with mild and 28 (56.0%) with moderate-severe (M/S) steatosis in our series; serum AST, ALT, ALP and GGT levels in patients with M/S steatosis were(62.2±12.8)U/L, (87.2±11.5)U/L, (99.0±14.4)U/L and (69.4±10.3)U/L, much higher than [(53.6±10.1)U/L, (75.7±12.5)U/L, (83.8±12.7)U/L and (58.5±7.7)U/L, respectively, P<0.05] in patients with mild steatosis or [(51.7±8.5)U/L,(73.5±13.8)U/L,(81.6±10.9)U/L and (56.2±8.1)U/L, respectively, P<0.05] in patients with CHC; serum RBP4 and SREBP-1c levels in patients with M/S steatosis were (55.9±8.2) mg/L and (40.1±7.4)μg/L, significantly higher than [(36.7±5.8)mg/L and (29.3±5.1)μg/L, respectively, P<0.05] in patients with mild steatosis or [(28.4±6.3)mg/L and (21.8±5.5)μg/L, P<0.05] in patients with CHC; serum HbA1c and HOMA-IR in patients with M/S steatosis were (5.7±0.5)% and (3.2±0.5), both significantly higher than [(5.3±0.5)% and (2.5±0.4), P<0.05] in patients with mild steatosis or [(5.1±0.3)% and (1.9±0.3), P<0.05] in patients with CHC; serum RBP4 and SREBP-1c levels in 41 patients who responded to interferon-α 2a therapy were (25.7±6.0)mg/L and (20.6±5.0)μg/L, much lower than [(48.5±7.4)mg/L and (35.5±6.3)μg/L, P<0.05] in 53 patients who didn’t. Conclusion Serum RBP4 and SREBP-1c levels in patients with CHC and NAFLD increase, which might interferes with antiviral therapy, and warrants further investigation.

Key words: Hepatitis C, Non-alcoholic fatty liver diseases, Interferon-α 2a, Retinol-binding protein 4, Sterol regulatory element-binding protein-1c, Response