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HBV感染免疫耐受期肝组织炎症和纤维化的影响因素分析

刘春云 常丽仙 李俊义 祁燕伟 李卫昆 李惠敏 张映媛 高建鹏 刘立

引用本文:
Citation:

HBV感染免疫耐受期肝组织炎症和纤维化的影响因素分析

DOI: 10.3969/j.issn.1001-5256.2022.09.012
基金项目: 

云南省科技厅应用基础研究项目 (2017FH001-88)

伦理学声明:本研究方案于2015年1月1日经由昆明市第三人民医院伦理委员会审批,批号:昆三医伦2018030709,患者及家属均签署知情同意书。
利益冲突声明:本研究不存在研究者、伦理委员会成员、受试者监护人以及与公开研究成果有关的利益冲突。
作者贡献声明:刘春云负责资料收集、分析,撰写论文;常丽仙、李俊义、祁燕伟、李卫昆、李惠敏、张映媛负责资料收集; 刘立、高建鹏负责资料分析,指导写作思路并最后定稿。
详细信息
    通信作者:

    刘立,liuli197210@163.com

Influencing factors for liver inflammation and fibrosis in the immune-tolerant phase of HBV infection

Research funding: 

Yunnan Provincial Department of Science and Technology Applied Basic Research Project (2017FH001-88)

More Information
  • 摘要:   目的  对慢性HBV感染免疫耐受期患者进行肝脏损伤程度及肝纤维化的评价,为免疫耐受期患者的病情判断提供依据。  方法  随机选取昆明市第三人民医院2015年1月—2019年12月HBV DNA水平≥107 IU/mL、ALT≤40 U/L且临床资料完整者300例,收集其年龄、性别、感染HBV时间、血生化、HBsAg、HBV DNA等资料,并对患者的肝组织行病理检查,根据炎症分级分为两组(G<2组和G≥2组),根据纤维化程度分为两组(S<2组和S≥2组)。计量资料2组间比较采用t检验,使用单因素和多因素非条件logistic回归分析肝组织病理炎症活动≥G2和纤维化程度≥S2的影响因素。  结果  300例患者中,G≥2组213例(71%),S≥2组120例(40%),基线年龄(26.06±9.01)岁,男性占48%,感染时间(5.62±5.09)年。单因素分析显示,G<2组和G≥2组ALT、ALP、Alb、PLT、门静脉内径和脾脏厚度比较,差异均有统计学意义(t值分别为-26.677、-11.612、2.149、5.410、-6.092、-2.911,P值均<0.05);S<2组与S≥2组比较,感染时间、ALT、ALP、Alb、HBV DNA、PLT、门静脉内径和脾脏厚度比较,差异均有统计学意义(t值分别为-6.320、-6.694、-7.880、2.349、4.552、19.160、-5.782、-5.622,P值均<0.05)。多因素分析显示,ALT(OR=10.270,95%CI:2.212~47.672,P=0.003)、ALP(OR=1.097,95%CI:1.013~1.188,P=0.023)是免疫耐受期患者肝组织炎症≥G2的独立危险因子;ALP(OR=1.034,95%CI:1.015~1.054,P<0.001)、PLT(OR=0.913,95%CI:0.886~0.938,P<0.001)、HBV DNA(OR=0.198,95%CI:0.062~0.636,P=0.007)和感染时间(OR=1.176,95%CI:1.033~1.340,P=0.015)是免疫耐受期患者肝组织纤维化≥S2的独立影响因子。  结论  大多数免疫耐受期患者都有显著的肝组织学病变。ALT、ALP是免疫耐受期患者肝组织显著炎症的影响因素,ALP、HBV DNA、PLT和感染时间是免疫耐受期患者肝组织显著纤维化的影响因素。

     

  • 表  1  300例HBV感染免疫耐受期患者一般资料

    Table  1.   General information of 300 patients with hepatitis B (immune-tolerant phase)

    指标 数值
    男/女(例) 144/156
    年龄(岁) 26.06±9.01
    基因型(B/C/B和C/不详) 62/221/16/1
    感染时间(年) 5.62±5.09
    TBil(μmol/L) 15.79±8.09
    GGT(U/L) 19.51±14.80
    AST(U/L) 24.19±5.90
    ALT(U/L) 31.81±7.09
    ALP(U/L) 134.98±58.08
    Alb(g/L) 44.05±4.22
    Glo(g/L) 25.69±4.10
    HBsAg(lgIU/mL) 3.96±1.15
    HBV DNA(lgIU/mL) 8.03±0.54
    WBC(×109/L) 5.50±1.38
    PLT(×109/L) 174.14±63.16
    门静脉内径(mm) 11.39±1.88
    脾静脉内径(mm) 5.04±0.25
    脾脏厚度(mm) 30.35±4.62
    肝硬度(kPa) 5.67±2.07
    下载: 导出CSV

    表  2  300例HBV感染免疫耐受期患者肝组织炎症分级的分布及临床特征

    Table  2.   Distribution and clinical characteristics of liver tissue inflammation grades in 300 patients with hepatitis B (immune-tolerant phase)

    指标 G<2组(n=87) G≥2组(n=213) t P
    年龄(岁) 24.92±8.41 26.53±9.22 -1.403 0.162
    感染时间(年) 4.82±4.33 5.95±5.34 -1.759 0.080
    TBil(μmol/L) 15.08±6.28 16.08±8.72 -0.973 0.332
    GGT(U/L) 19.26±10.40 19.61±16.28 -0.183 0.855
    AST(U/L) 24.23±5.59 24.17±6.03 0.075 0.941
    ALT(U/L) 22.51±5.75 35.61±2.74 -26.677 <0.001
    ALP(U/L) 84.34±37.44 155.67±52.02 -11.612 <0.001
    Alb(g/L) 44.87±3.51 43.72±4.44 2.149 0.032
    Glo(g/L) 25.97±3.81 25.57±4.21 0.780 0.436
    HBV DNA(lgIU/mL) 8.08±0.56 8.01±0.53 1.091 0.276
    WBC(×109/L) 5.45±1.24 5.51±1.43 -0.330 0.741
    PLT(×109/L) 203.64±54.20 162.09±62.69 5.410 <0.001
    门静脉内径(mm) 10.41±1.00 11.79±2.01 -6.092 <0.001
    脾静脉内径(mm) 5.06±0.33 5.03±0.21 0.736 0.462
    脾脏厚度(mm) 29.15±4.55 30.84±4.56 -2.911 0.004
    肝硬度(kPa) 5.69±2.25 5.66±2.14 0.083 0.934
    下载: 导出CSV

    表  3  300例HBV感染免疫耐受期患者肝组织纤维化分级的分布及临床特征

    Table  3.   Distribution and clinical characteristics of liver fibrosis grades in 300 patients with hepatitis B (immune-tolerant phase)

    指标 S<2组(n=180) S≥2组(n=120) t P
    年龄(岁) 25.64±8.96 26.68±9.07 -0.978 0.329
    感染时间(年) 4.20±3.84 7.76±5.93 -6.320 <0.001
    TBil(μmol/L) 15.60±7.00 16.08±9.51 -0.502 0.616
    GGT(U/L) 20.06±17.26 18.69±10.06 0.781 0.435
    AST(U/L) 23.99±5.09 24.48±6.95 -0.702 0.483
    ALT(U/L) 29.72±7.78 34.94±4.34 -6.694 <0.001
    ALP(U/L) 115.32±57.92 164.48±44.33 -7.880 <0.001
    Alb(g/L) 44.51±3.60 43.36±4.94 2.349 0.019
    Glo(g/L) 25.90±4.13 25.36±4.04 1.123 0.263
    HBV DNA(lgIU/mL) 8.14±0.51 7.86±0.53 4.552 <0.001
    WBC(×109/L) 5.51±1.34 5.48±1.43 0.151 0.880
    PLT(×109/L) 212.39±53.38 116.77±14.31 19.160 <0.001
    门静脉内径(mm) 10.91±1.41 12.13±2.24 -5.782 <0.001
    脾静脉内径(mm) 5.03±0.23 5.05±0.27 -0.727 0.468
    脾脏厚度(mm) 29.18±4.80 32.10±3.71 -5.622 <0.001
    肝硬度(kPa) 5.80±2.25 5.48±2.04 1.221 0.223
    下载: 导出CSV
  • [1] TACHTATZIS PM, MARSHALL A, ARAVINTHAN A, et al. Correction: chronic hepatitis B virus infection: The relation between hepatitis B antigen expression, telomere length, senescence, inflammation and fibrosis[J]. PLoS One, 2015, 10(7): e0134315. DOI: 10.1371/journal.pone.0134315.
    [2] CHEN JD, ZHAI RR, LIU C, et al. Study on the correlation between serum core antibody of hepatitis B virus and glutamic pyruvic transaminase and nucleic acid copy number of hepatitis B virus in patients with chronic hepatitis B cirrhosis[J]. Clin J Med Offic, 2021, 49(8): 906-907. DOI: 10.16680/j.1671-3826.2021.08.18.

    陈家东, 翟荣荣, 刘灿, 等. 慢性乙肝肝硬化患者血清乙肝病毒核心抗体定量与谷丙转氨酶、乙肝病毒核酸拷贝数相关性研究[J]. 临床军医杂志, 2021, 49(8): 906-907. DOI: 10.16680/j.1671-3826.2021.08.18.
    [3] LEE HA, LEE HW, KIM IH, et al. Extremely low risk of hepatocellular carcinoma development in patients with chronic hepatitis B in immune-tolerant phase[J]. Aliment Pharmacol Ther, 2020, 52(1): 196-204. DOI: 10.1111/apt.15741.
    [4] CHEN Y, LI X, YE B, et al. Effect of telbivudine therapy on the cellular immune reponse in chronic hepatitis B[J]. Antiviral Res, 2011, 91: 23-31. DOI: 10.1016/j.antiviral.2011.04.008.
    [5] European Association for the Study of the Liver. EASL clinical practice guidelines: management of chronic hepatitis B virus infection[J]. J Hepatol, 2012, 57(1): 167-185. DOI: 10.1016/j.jhep.2012.02.010.
    [6] TRAN TT. Immune tolerant hepatitis B: a clinical dilemma[J]. Gastroenterol Hepatol (N Y), 2011, 7(8): 511-516. http://pdfs.semanticscholar.org/8cb9/7b4485e5ffef5819f2a569a08aeeca4fc4d1.pdf
    [7] ZONG L. Liver immune tolerance and HBV-induced liver cancer[D]. Hefei: University of Science and Technology of China, 2018.

    宗璐. 肝脏免疫耐受与HBV诱发肝癌[D]. 合肥: 中国科学技术大学, 2018.
    [8] Chinese Society of Infectious Diseases, Chinese Medical Association; Chinese Society of Hepatology, Chinese Medical Association. Guidelines for the prevention and treatment of chronic hepatitis B (version 2019)[J]. J Clin Hepatol, 2019, 35(12): 2648-2669. DOI: 10.3969/j.issn.1001-5256.2019.12.007.

    中华医学会感染病学分会, 中华医学会肝病学分会. 慢性乙型肝炎防治指南(2019年版)[J]. 临床肝胆病杂志, 2019, 35(12): 2648-2669. DOI: 10.3969/j.issn.1001-5256.2019.12.007.
    [9] NONG CL, LONG TH, GUO J. Histological characteristics and clinical analysis of chronic hepatitis B liver with normal ALT[J]. Shandong Med, 2012, 52(7): 51-53. DOI: 10.3969/j.issn.1002-266X.2012.07.020.

    农村立, 龙腾河, 郭堑. ALT正常的慢性乙型肝炎肝组织学特点与临床分析[J]. 山东医药, 2012, 52(7): 51-53. DOI: 10.3969/j.issn.1002-266X.2012.07.020.
    [10] GONG X, YANG J, TANG J, et al. A mechanistic assessment of the discordance between normal serum alanine aminotransferase levels and altered liver histology in chronic hepatitis B[J]. PLoS One, 2015, 10(7): e0134532. DOI: 10.1371/journal.pone.0134532.
    [11] WANG H, RU GQ, YAN R, et al. Histologic disease in Chinese chronic hepatitis B patients with low viral loads and persistently normal alanine aminotransferase levels[J]. J Clin Gastroenterol, 2016, 50(9): 790-796. DOI: 10.1097/MCG.0000000000000544.
    [12] ZHOU X, LI WZ, MA WT, et al. Correlation between liver histopathology and age, ALT and HBV DNA levels in patients with normal ALT and chronic HBV infection[J]. Chin Hepatol, 2019, 24(10): 1141-1144. DOI: 10.3969/j.issn.1008-1704.2019.10.016.

    周璇, 李维正, 马文婷, 等. ALT正常慢性HBV感染者肝组织病理与年龄、ALT和HBV DNA水平相关性研究[J]. 肝脏, 2019, 24(10): 1141-1144. DOI: 10.3969/j.issn.1008-1704.2019.10.016.
    [13] GUI HL, WANG H, YANG YH, et al. Significant histopathology in Chinese chronic hepatitis B patients with persistently high-normal alanine aminotransferase[J]. J Viral Hepat, 2010, 17 (Suppl 1): 44-50. DOI: 10.1111/j.1365-2893.2010.01270.x.
    [14] GÖBEL T, ERHARDT A, HERWIG M, et al. High prevalence of significant liver fibrosis and cirrhosis in chronic hepatitis B patients with normal ALT in central Europe[J]. J Med Virol, 2011, 83(6): 968-973. DOI: 10.1002/jmv.22048.
    [15] PARK JY, PARK YN, KIM DY, et al. High prevalence of significant histology in asymptomatic chronic hepatitis B patients with genotype C and high serum HBV DNA levels[J]. J Viral Hepat, 2008, 15(8): 615-621. DOI: 10.1111/j.1365-2893.2008.00989.x.
    [16] KUMAR M, SARIN SK, HISSAR S, et al. Virologic and histologic features of chronic hepatitis B virus-infected asymptomatic patients with persistently normal ALT[J]. Gastroenterology, 2008, 134(5): 1376-1384. DOI: 10.1053/j.gastro.2008.02.075.
    [17] NGUYEN MH, GARCIA RT, TRINH HN, et al. Histological disease in Asian-Americans with chronic hepatitis B, high hepatitis B virus DNA, and normal alanine aminotransferase levels[J]. Am J Gastroenterol, 2009, 104(9): 2206-2213. DOI: 10.1038/ajg.2009.248.
    [18] WANG C, DEUBNER H, SHUHART M, et al. High prevalence of significant fibrosis in patients with immunotolerance to chronic hepatitis B infection: (abstract)[J]. Hepatology, 2005, 42 (Suppl 1): 573A.
    [19] LIAO B, WANG Z, LIN S, et al. Significant fibrosis is not rare in Chinese chronic hepatitis B patients with persistent normal ALT[J]. PLoS One, 2013, 8(10): e78672. DOI: 10.1371/journal.pone.0078672.
    [20] ZHUANG H. Should patients in the immune tolerance stage of chronic hepatitis B virus infection be treated?[J]. J Clin Hepatol, 2021, 37(2): 272-277. DOI: 10.3969/j.issn.1001-5256.2021.02.007.

    庄辉. 慢性HBV感染免疫耐受期应否治疗?[J]. 临床肝胆病杂志, 2021, 37(2): 272-277. DOI: 10.3969/j.issn.1001-5256.2021.02.007.
    [21] HUANG Y. Patients in the immune-tolerant phase of chronic HBV infection should be actively treated with antiviral therapy[J]. J Clin Hepatol, 2021, 37(5): 1026. DOI: 10.3969/j.issn.1001-5256.2021.05.008.

    黄缘. 慢性HBV感染免疫耐受期患者应积极抗病毒治疗[J]. 临床肝胆病杂志, 2021, 37(5): 1026. DOI: 10.3969/j.issn.1001-5256.2021.05.008.
    [22] ZHUANG H. Correction note on the estimated number of patients in the immune-tolerant phase of hepatitis B virus infection in China and globally[J]. J Clin Hepatol, 2021, 37(4): 785-786. DOI: 10.3969/j.issn.1001-5256.2021.04.012.

    庄辉. 全球和我国HBV感染免疫耐受期患者人数估计更正说明[J]. 临床肝胆病杂志, 2021, 37(4): 785-786. DOI: 10.3969/j.issn.1001-5256.2021.04.012.
    [23] XING HQ, XIN SJ, ZHANG X, et al. Clinicopathological characteristics of patients with chronic hepatitis B virus infection in immune tolerance stage[J]. World Chin J Dig, 2006, 14(14): 1425-1429. DOI: 10.3969/j.issn.1009-3079.2006.14.018.

    邢汉前, 辛绍杰, 张欣, 等. 慢性乙型肝炎病毒感染免疫耐受期患者的临床病理特征[J]. 世界华人消化杂志, 2006, 14(14): 1425-1429. DOI: 10.3969/j.issn.1009-3079.2006.14.018.
    [24] LIN CL, LIAO LY, LIU CJ, et al. Hepatitis B viral factors in HBeAg-negative carriers with persistently normal serum alanine aminotransferase levels[J]. Hepatology, 2007, 45(5): 1193-1198. DOI: 10.1002/hep.21585.
    [25] BERTOLETTI A, KENNEDY PT. The immune tolerant phase of chronic HBV infection: new perspectives on an old concept[J]. Cell Mol Immunol, 2015, 12(3): 258-263. DOI: 10.1038/cmi.2014.79.
    [26] LIN Y, LI X. Research status of platelets in chronic liver disease[J]. J Clin Hepatol, 2017, 33(11): 2243-2246. DOI: 10.3969/j.issn.1001-5256.2017.11.043.

    林岩, 李汛. 血小板在慢性肝病中的研究现状[J]. 临床肝胆病杂志, 2017, 33(11): 2243-2246. DOI: 10.3969/j.issn.1001-5256.2017.11.043.
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