实用肝脏病杂志 ›› 2022, Vol. 25 ›› Issue (1): 58-61.doi: 10.3969/j.issn.1672-5069.2022.01.015

• 酒精性肝病 • 上一篇    下一篇

酒精性肝病患者血清IL-17水平及其基因-197A/G位点单核苷酸多态性分析*

冯宇, 杜振元, 李艳彬, 刘红   

  1. 122000 辽宁省朝阳市第二医院检验科(冯宇,杜振元,李艳彬);锦州医科大学附属第一医院肝病科(刘红)
  • 收稿日期:2021-01-29 发布日期:2022-01-12
  • 作者简介:冯宇,男,34岁,大学本科,主管检验师。E-mail:lgfengyu@163.com
  • 基金资助:
    * 辽宁省自然科学基金资助项目(编号:2017020257)

Serum IL-17 levels and single nucleotide polymorphism of its gene at -197A/G locus in patients with alcoholic liver diseases

Feng Yu, Du Zhenyuan, Li Yanbin, et al   

  1. Clinical Laboratory, Second Hospital, Chaoyang 122000, Liaoning Province, China
  • Received:2021-01-29 Published:2022-01-12

摘要: 目的 探讨酒精性肝病(ALD)患者血清白细胞介素-17(IL-17)水平及其基因-197A/G位点单核苷酸多态性的变化。方法 2015年10月~2020年10月我院收治的酒精性脂肪肝患者44例、酒精性肝炎患者40例、酒精性肝硬化患者34例和ALD相关性肝癌患者18例,采用ELISA法检测血清IL-17水平,采用单核苷酸检测试剂盒检测外周血IL-17-197A/G位点基因多态性。结果 肝癌患者血清IL-17水平为(8.7±1.4)pg/mL,显著高于酒精性脂肪肝、酒精性肝炎和酒精性肝硬化患者【分别为(3.7±0.3)pg/mL、(4.0±0.6)pg/mL和(6.9±0.8)pg/mL,均P<0.05】;肝癌患者血清ALT、AST、GGT和ALB水平分别为(54.3±13.3)U/L、(53.8±13.7)U/L、(262.2±17.9)U/L和(33.9±13.8)g/L,酒精性肝硬化患者分别为(39.8±8.8)U/L、(40.1±7.2)U/L、(251.1±7.9)U/L和(31.1±2.6)g/L,酒精性肝炎患者分别为(84.0±7.5)U/L、(75.4±6.8)U/L、(245.1±5.6)U/L和(43.1±5.7)g/L,与酒精性脂肪肝患者【分别为(29.5±5.2)U/L、(30.5±7.8)U/L、(142.7±5.2)U/L和(42.7±3.2)g/L,均P<0.05】比,差异显著;肝癌和酒精性肝硬化患者AA基因型分布频率分别为77.9%和64.7%,显著高于酒精性脂肪肝和酒精性肝炎患者(分别为22.7%和27.5%,均P<0.05),A等位基因分布频率分别为83.3%和75.0%,显著高于酒精性脂肪肝和酒精性肝炎患者(分别为26.1%和33.8%,均P<0.05)。结论 高水平的血清IL-17可能与ALD病情进展相关,外周血IL-17-197A/G位点AA基因型和A等位基因是ALD发生的易感基因,可能增加酒精性肝硬化甚至肝癌发生的风险。

关键词: 酒精性肝病, 白细胞介素-17, IL-17-197A/G位点, 基因多态性

Abstract: Objective The aim of this study was to investigate serum interleukin-17 (IL-17) levels and the single nucleotide polymorphism (SNP) of its gene at -197A/G locus in patients with alcoholic liver diseases (ALD). Methods 44 patients with alcoholic fatty liver, 40 with alcoholic hepatitis, 34 with alcoholic cirrhosis and 18 with ALD-related liver cancer were recruited in this study between October 2015 and October 2020, and serum IL-17 level was detected by ELISA. The gene polymorphisms at -197A/G locus were detected by single nucleotide test kits. Results Serum IL-17 level in patients with liver cancer was (8.7±1.4) pg/mL, significantly higher than [(3.7±0.3) pg/mL, (4.0±0.6) pg/mL and (6.9±0.8) pg/mL, respectively, P<0.05] in patients with alcoholic fatty liver, alcoholic hepatitis and alcoholic cirrhosis; serum ALT, AST, GGT and ALB levels in patients with liver cancer were (54.3±13.3)U/L,(53.8±13.7)U/L,(262.2±17.9)U/L and (33.9±13.8)g/L, those in patients with alcoholic liver cirrhosis were (39.8±8.8)U/L,(40.1±7.2)U/L, (251.1±7.9)U/L and (31.1±2.6)g/L, in alcoholic hepatitis were (84.0±7.5)U/L,(75.4±6.8)U/L, (245.1±5.6)U/L and (43.1±5.7)g/L, all significantly different compared to(29.5±5.2)U/L,(30.5±7.8)U/L, (142.7±5.2)U/L and (42.7±3.2)g/L, respectively, P<0.05] in patients with alcoholic fatty liver; the distribution frequencies of AA genotype of IL-17 gene at -197A/G locus in patients with liver cancer and alcoholic cirrhosis were 77.9% and 64.7%, significantly higher than 22.7% and 27.5% (P<0.05) in patients with alcoholic fatty liver and alcoholic hepatitis, and the distribution frequencies of A allele in patients with liver cancer and alcoholic cirrhosis were 83.3% and 75.0%, significantly higher than 26.1% and 33.8% (P<0.05) in patients with alcoholic fatty liver and alcoholic hepatitis. Conclusion High serum level of IL-17 might be related with the progression of ALDs and the AA genotype and A allele of IL-17 at -197A/G locus could be the susceptibility genes of patients with ALD, which might increase the risk of alcoholic liver cirrhosis and even liver cancer.

Key words: Alcoholic liver diseases, Interleukin-17, IL-17 gene at -197A/G locus, Gene polymorphism