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自身免疫性肝炎诊断和治疗指南(2021)

中华医学会肝病学分会

引用本文:
Citation:

自身免疫性肝炎诊断和治疗指南(2021)

DOI: 10.3760/cma.j.cn112138-20211112-00796
利益冲突声明:所有作者均声明不存在利益冲突。

    通信作者:马雄, 上海交通大学医学院附属仁济医院消化内科, 上海市消化疾病研究所, maxiongmd@163.com

Guidelines on the diagnosis and management of autoimmune hepatitis (2021)

  • 摘要: 自身免疫性肝炎(autoimmune hepatitis, AIH)患者的临床特点包括血清氨基转移酶水平升高、高免疫球蛋白G血症、血清自身抗体阳性, 肝组织学上存在中重度界面性肝炎等。早期诊断和恰当治疗可显著改善AIH患者的生存期和生活质量, 减轻社会医疗负担。《自身免疫性肝炎诊断和治疗共识(2015)》在规范我国AIH的诊断和治疗方面发挥了积极作用。在此基础上, 2021年底中华医学会肝病分会组织有关专家结合最新进展制定本部指南, 旨在进一步提高我国AIH诊治水平。

     

  • 图  1  AIH的药物治疗

    注:*建议有条件时在使用前检测TPMT和NUDT15基因型和/或活性, 启动糖皮质激素2周后添加硫唑嘌呤(50~100 mg/d), 并注意监测血常规。失代偿期肝硬化患者不建议使用硫唑嘌呤。* *对于经泼尼松(龙)治疗后副作用严重者, 布地奈德可作为替代药物。但布地奈德在肝硬化患者中失去首过效应的优势, 有增加门静脉血栓形成的风险, 此外在急性重症AIH或急性肝功能衰竭中治疗作用未知, 因此上述情况下不建议使用。

    表  1  推荐意见的证据等级和推荐强度等级

    级别 详细说明
    证据质量
      高(A) 进一步研究不可能改变对该疗效评估结果的可信度
      中(B) 进一步研究有可能影响该疗效评估结果的可信度, 且可能改变该评估结果
      低或非常低(C) 进一步研究很有可能影响该疗效评估结果的可信度, 且很可能改变该评估结果
    推荐强度
      强(1) 明确显示干预措施利大于弊或弊大于利
      弱(2) 利弊不确定或无论质量高低的证据均显示利弊相当
    下载: 导出CSV

    表  2  AIH综合诊断积分系统(1999年)

    参数/临床特征 计分 参数/临床特征 计分
    女性 +2 药物史
    ALP(正常上限倍数)与AST(或ALT)(正常上限倍数)的比值   阳性 -4
      阴性 +1
      <1.5 +2 平均乙醇摄入量(g/d)
      1.5~3.0 0   <25 +2
      >3.0 -2   >60 -2
    血清γ-球蛋白或IgG与正常值的比值 肝组织学检查
      >2.0 +3   界面性肝炎 +3
      1.5~2.0 +2   主要为淋巴-浆细胞浸润 +1
      1.0~1.5 +1   肝细胞呈玫瑰花环样改变 +1
      <1.0 0   无上述表现 -5
    ANA, ASMA或LKM-1滴度 胆管改变 -3
      >1∶80 +3 其他改变 -3
      1∶80 +2 其他免疫性疾病 +2
      1∶40 +1 其他可用的参数
      <1∶40 0   其他特异性自身抗体(SLA/LP、LC-1、ASGPR、pANCA)阳性 +2
      AMA阳性 -4 HLA-DR3或DR4 +1
    肝炎病毒标志物 对治疗的反应
      阳性 -3   完全 +2
      阴性 +3   复发 +3
    总积分的解释
    治疗前 治疗后
      明确的AIH ≥16   明确的AIH ≥18
      可能的AIH 10~15   可能的AIH 12~17
    下载: 导出CSV

    表  3  IAIHG的AIH简化诊断标准

    变量 标准 分值 备注
    ANA或SMA 1∶40 1 相当于我国常用的ANA 1∶100的最低滴度
    ANA或SMA 1∶80 2 多项同时出现时最多2分
    LKM-1 1∶40 2
    SLA 阳性 2
    IgG >正常值上限 1
    >1.1倍正常值上限 2
    肝组织学 符合AIH 1 界面性肝炎、汇管区和小叶内淋巴-浆细胞浸润、肝细胞玫瑰样花环以及穿入现象被认为是特征性肝组织学改变, 4项中具备3项为典型表现
    典型AIH表现 2
    排除病毒性肝炎 2
    注:分值= 6分:AIH可能;分值≥7分:确诊AIH。
    下载: 导出CSV

    表  4  AIH的鉴别诊断

    疾病 临床表现和实验室检查 病理学表现
    HCV感染 血清ANA可低滴度阳性或LKM-1阳性, IgG水平轻度升高;抗-HCV抗体和HCV RNA阳性 肝细胞脂肪变性、淋巴滤泡形成、肉芽肿形成
    药物性肝损伤 药物史明确, 停用药物后好转;血清氨基转移酶水平升高和/或胆汁淤积表现 汇管区中性粒细胞和嗜酸粒细胞浸润、肝细胞大泡脂肪变性、肝细胞胆汁淤积, 纤维化程度一般较轻(低于S2)
    代谢相关性脂肪性肝病 1/3患者血清ANA可低滴度阳性, 血清氨基转移酶轻度升高, 胰岛素抵抗表现 肝细胞呈大泡脂肪变性、肝窦纤维化、汇管区炎症较轻
    Wilson病 血清ANA可阳性, 血清铜蓝蛋白低, 24 h尿铜升高, 可有角膜色素环(K-F环)阳性 存在肝细胞脂肪变性、空泡状核形成、汇管区炎症, 可伴界面炎, 可有大量铜沉着
    下载: 导出CSV
  • [1] 中华医学会肝病学分会, 中华医学会消化病学分会, 中华医学会感染病学分会. 自身免疫性肝炎诊断和治疗共识(2015)[J]. 临床肝胆病杂志, 2016, 32(1): 9-22. DOI: 10.3969/j.issn.1001-5256.2016.01.002.
    [2] de BOER YS, GERUSSI A, van den BRAND FF, et al. Association between black race and presentation and liver-related outcomes of patients with autoimmune hepatitis[J]. Clin Gastroenterol Hepatol, 2019, 17(8): 1616-1624. e2. DOI: 10.1016/j.cgh.2018.11.028.
    [3] WANG QX, YAN L, MA X. Autoimmune hepatitis in the Asia-Pacific Area[J]. J Clin Transl Hepatol, 2018, 6(1): 48-56. DOI: 10.14218/JCTH.2017.00032.
    [4] LAMBA M, NGU JH, STEDMAN C. Trends in incidence of autoimmune liver diseases and increasing incidence of autoimmune hepatitis[J]. Clin Gastroenterol Hepatol, 2021, 19(3): 573-579. e1. DOI: 10.1016/j.cgh.2020.05.061.
    [5] TANAKA A, MORI M, MATSUMOTO K, et al. Increase trend in the prevalence and male-to-female ratio of primary biliary cholangitis, autoimmune hepatitis, and primary sclerosing cholangitis in Japan[J]. Hepatol Res, 2019, 49(8): 881-889. DOI: 10.1111/hepr.13342.
    [6] TANAKA A. Autoimmune Hepatitis: 2019 Update[J]. Gut Liver, 2020, 14(4): 430-438. DOI: 10.5009/gnl19261.
    [7] LI Y, YAN L, WANG R, et al. Serum immunoglobulin G levels predict biochemical and histological remission of autoimmune hepatitis type 1: A single-center experience and literature review[J]. Clin Rev Allergy Immunol, 2021. DOI: 10.1007/s12016-021-08833-w.[Online ahead of print]
    [8] WANG QX, JIANG WJ, MIAO Q, et al. Clinical and histological features of autoantibody-negative autoimmune hepatitis in Chinese patients: A single center experience[J]. J Dig Dis, 2013, 14(4): 175-180. DOI: 10.1111/1751-2980.12022.
    [9] DHALIWAL HK, HOEROLDT BS, DUBE AK, et al. Long-term prognostic significance of persisting histological activity despite biochemical remission in autoimmune hepatitis[J]. Am J Gastroenterol, 2015, 110(7): 993-999. DOI: 10.1038/ajg.2015.139.
    [10] GURUNG A, ASSIS DN, MCCARTY TR, et al. Histologic features of autoimmune hepatitis: A critical appraisal[J]. Hum Pathol, 2018, 82: 51-60. DOI: 10.1016/j.humpath.2018.07.014.
    [11] MIAO Q, BIAN Z, TANG R, et al. Emperipolesis mediated by CD8 T cells is a characteristic histopathologic feature of autoimmune hepatitis[J]. Clin Rev Allergy Immunol, 2015, 48(2-3): 226-235. DOI: 10.1007/s12016-014-8432-0.
    [12] STRAVITZ RT, LEFKOWITCH JH, FONTANA RJ, et al. Autoimmune acute liver failure: Proposed clinical and histological criteria[J]. Hepatology, 2011, 53(2): 517-526. DOI: 10.1002/hep.24080
    [13] TAKAHASHI A, ARINAGA-HINO T, OHIRA H, et al. Autoimmune hepatitis in Japan: Trends in a nationwide survey[J]. J Gastroenterol, 2017, 52(5): 631-640. DOI: 10.1007/s00535-016-1267-0.
    [14] ALVAREZ F, BERG PA, BIANCHI FB, et al. International Autoimmune Hepatitis Group Report: Review of criteria for diagnosis of autoimmune hepatitis[J]. J Hepatol, 1999, 31(5): 929-938. DOI: 10.1016/s0168-8278(99)80297-9.
    [15] HENNES EM, ZENIYA M, CZAJA AJ, et al. Simplified criteria for the diagnosis of autoimmune hepatitis[J]. Hepatology, 2008, 48(1): 169-176. DOI: 10.1002/hep.22322.
    [16] QIU D, WANG Q, WANG H, et al. Validation of the simplified criteria for diagnosis of autoimmune hepatitis in Chinese patients[J]. J Hepatol, 2011, 54(2): 340-347. DOI: 10.1016/j.jhep.2010.06.032.
    [17] GALASKI J, WEILER-NORMANN C, SCHAKAT M, et al. Update of the simplified criteria for autoimmune hepatitis: Evaluation of the methodology for immunoserological testing[J]. J Hepatol, 2021, 74(2): 312-320. DOI: 10.1016/j.jhep.2020.07.032.
    [18] CHEN RL, WANG QX, MA X. Precision medicine for autoimmune hepatitis[J]. J Dig Dis, 2019, 20(7): 331-337. DOI: 10.1111/1751-2980.12786.
    [19] WANG Z, SHENG L, YANG Y, et al. The management of autoimmune hepatitis patients with decompensated cirrhosis: Real-world experience and a comprehensive review[J]. Clin Rev Allergy Immunol, 2017, 52(3): 424-435. DOI: 10.1007/s12016-016-8583-2.
    [20] PEISELER M, LIEBSCHER T, SEBODE M, et al. Efficacy and limitations of budesonide as a second-line treatment for patients with autoimmune hepatitis[J]. Clin Gastroenterol Hepatol, 2018, 16(2): 260-267. e1. DOI: 10.1016/j.cgh.2016.12.040.
    [21] MANNS MP, WOYNAROWSKI M, KREISEL W, et al. Budesonide induces remission more effectively than prednisone in a controlled trial of patients with autoimmune hepatitis[J]. Gastroenterology, 2010, 139(4): 1198-1206. DOI: 10.1053/j.gastro.2010.06.046.
    [22] WOYNAROWSKI M, NEMETH A, BARUCH Y, et al. Budesonide versus prednisone with azathioprine for the treatment of autoimmune hepatitis in children and adolescents[J]. J Pediatr, 2013, 163(5): 1347-1353. e1. DOI: 10.1016/j.jpeds.2013.05.042.
    [23] EFE C, HAGSTRÖM H, YTTING H, et al. Efficacy and safety of mycophenolate mofetil and tacrolimus as second-line therapy for patients with autoimmune hepatitis[J]. Clin Gastroenterol Hepatol, 2017, 15(12): 1950-1956. e1. DOI: 10.1016/j.cgh.2017.06.001.
    [24] LIBERAL R, de BOER YS, ANDRADE RJ, et al. Expert clinical management of autoimmune hepatitis in the real world[J]. Aliment Pharmacol Ther, 2017, 45(5): 723-732. DOI: 10.1111/apt.13907.
    [25] DE LEMOS-BONOTTO M, VALLE-TOVO C, COSTABEBER AM, et al. A systematic review and meta-analysis of second-line immunosuppressants for autoimmune hepatitis treatment[J]. Eur J Gastroenterol Hepatol, 2018, 30(2): 212-216. DOI: 10.1097/MEG.0000000000001019.
    [26] HANOUNEH M, RITCHIE MM, ASCHA M, et al. A review of the utility of tacrolimus in the management of adults with autoimmune hepatitis[J]. Scand J Gastroenterol, 2019, 54(1): 76-80. DOI: 10.1080/00365521.2018.1551498.
    [27] MONTANO-LOZA AJ, BHANJI RA, WASILENKO S, et al. Systematic review: Recurrent autoimmune liver diseases after liver transplantation[J]. Aliment Pharmacol Ther, 2017, 45(4): 485-500. DOI: 10.1111/apt.13894.
    [28] MACK CL, ADAMS D, ASSIS DN, et al. Diagnosis and management of autoimmune hepatitis in adults and children: 2019 practice guidance and guidelines from the American Association for the Study of Liver Diseases[J]. Hepatology, 2020, 72(2): 671-722. DOI: 10.1002/hep.31065.
    [29] KERKAR N, YANNI G. 'De novo' and 'recurrent' autoimmune hepatitis after liver transplantation: A comprehensive review[J]. J Autoimmun, 2016, 66: 17-24. DOI: 10.1016/j.jaut.2015.08.017.
    [30] MORIYAMA T, NISHⅡ R, PEREZ-ANDREU V, et al. NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity[J]. Nat Genet, 2016, 48(4): 367-373. DOI: 10.1038/ng.3508.
    [31] LOHSE AW, SEBODE M, J∅RGENSEN MH, et al. Second-line and third-line therapy for autoimmune hepatitis: A position statement from the European Reference Network on Hepatological Diseases and the International Autoimmune Hepatitis Group[J]. J Hepatol, 2020, 73(6): 1496-1506. DOI: 10.1016/j.jhep.2020.07.023.
    [32] XU Q, SHENG L, BAO H, et al. Evaluation of transient elastography in assessing liver fibrosis in patients with autoimmune hepatitis[J]. J Gastroenterol Hepatol, 2017, 32(3): 639-644. DOI: 10.1111/jgh.13508.
    [33] HARTL J, EHLKEN H, SEBODE M, et al. Usefulness of biochemical remission and transient elastography in monitoring disease course in autoimmune hepatitis[J]. J Hepatol, 2018, 68(4): 754-763. DOI: 10.1016/j.jhep.2017.11.020.
    [34] FIX OK, BLUMBERG EA, CHANG KM, et al. American Association for the Study of Liver Diseases Expert Panel consensus statement: Vaccines to prevent coronavirus disease 2019 infection in patients with liver disease[J]. Hepatology, 2021, 74(2): 1049-1064. DOI: 10.1002/hep.31751.
    [35] CORNBERG M, BUTI M, EBERHARDT CS, et al. EASL position paper on the use of COVID-19 vaccines in patients with chronic liver diseases, hepatobiliary cancer and liver transplant recipients[J]. J Hepatol, 2021, 74(4): 944-951. DOI: 10.1016/j.jhep.2021.01.032.
    [36] BIEWENGA M, INDERSON A, TUSHUIZEN ME, et al. Early predictors of short-term prognosis in acute and acute severe autoimmune hepatitis[J]. Liver Transpl, 2020, 26(12): 1573-1581. DOI: 10.1002/lt.25906.
    [37] ZACHOU K, ARVANITI P, AZARIADIS K, et al. Prompt initiation of high-dose i. v. corticosteroids seems to prevent progression to liver failure in patients with original acute severe autoimmune hepatitis[J]. Hepatol Res, 2019, 49(1): 96-104. DOI: 10.1111/hepr.13252.
    [38] YEOMAN AD, WESTBROOK RH, ZEN Y, et al. Prognosis of acute severe autoimmune hepatitis (AS-AIH): The role of corticosteroids in modifying outcome[J]. J Hepatol, 2014, 61(4): 876-882. DOI: 10.1016/j.jhep.2014.05.021.
    [39] REDDY HG, SCHNEIDER BJ, TAI AW. Immune checkpoint inhibitor-associated colitis and hepatitis[J]. Clin Transl Gastroenterol, 2018, 9(9): 180. DOI: 10.1038/s41424-018-0049-9.
    [40] CZAJA AJ. Immune inhibitory proteins and their pathogenic and therapeutic implications in autoimmunity and autoimmune hepatitis[J]. Autoimmunity, 2019, 52(4): 144-160. DOI: 10.1080/08916934.2019.1641200.
    [41] LOOMBA R, LIANG TJ. Hepatitis B reactivation associated with immune suppressive and biological modifier therapies: Current concepts, management strategies, and future directions[J]. Gastroenterology, 2017, 152(6): 1297-1309. DOI: 10.1053/j.gastro.2017.02.009.
    [42] LIN XQ, SHENG L, XIAO X, et al. Analysis of clinical diagnosis and treatment in chronic hepatitis B combined with autoimmune hepatitis[J]. Chin J Hepatol, 2020, 28(4): 351-356. DOI: 10.3760/cma.j.cn501113-20190120-00020.

    林小钦, 盛黎, 肖潇, 等. 慢性乙型肝炎合并自身免疫性肝炎的临床诊治分析[J]. 中华肝脏病杂志, 2020, 28(4): 351-356. DOI: 10.3760/cma.j.cn501113-20190120-00020.
    [43] MIELI-VERGANI G, VERGANI D, BAUMANN U, et al. Diagnosis and management of pediatric autoimmune liver disease: ESPGHAN hepatology committee position statement[J]. J Pediatr Gastroenterol Nutr, 2018, 66(2): 345-360. DOI: 10.1097/MPG.0000000000001801.
    [44] NASTASIO S, SCIVERES M, MATARAZZO L, et al. Long-term follow-up of children and young adults with autoimmune hepatitis treated with cyclosporine[J]. Dig Liver Dis, 2019, 51(5): 712-718. DOI: 10.1016/j.dld.2018.10.018.
    [45] EFE C, TAⅡ HA, YTTING H, et al. Tacrolimus and mycophenolate mofetil as second-line therapies for pediatric patients with autoimmune hepatitis[J]. Dig Dis Sci, 2018, 63(5): 1348-1354. DOI: 10.1007/s10620-018-5011-x.
    [46] WANG Q, QIU D, MA X. Early normalisation of aminotransferase predicts complete biochemical remission in autoimmune hepatitis patients[J]. Aliment Pharmacol Ther, 2011, 34(1): 107-109. DOI: 10.1111/j.1365-2036.2011.04690.x.
    [47] TANSEL A, KATZ LH, EL-SERAG HB, et al. Incidence and determinants of hepatocellular carcinoma in autoimmune hepatitis: A systematic review and Meta-analysis[J]. Clin Gastroenterol Hepatol, 2017, 15(8): 1207-1217. e4. DOI: 10.1016/j.cgh.2017.02.006.
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