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慢性乙型肝炎免疫耐受期患者显著肝损伤的列线图模型及其预测价值分析

王春艳 杨武才 谭文辉 邓亚 郭畅 张珊 王建军 陈国凤 纪冬

引用本文:
Citation:

慢性乙型肝炎免疫耐受期患者显著肝损伤的列线图模型及其预测价值分析

DOI: 10.3969/j.issn.1001-5256.2021.07.010
基金项目: 

解放军总医院医疗大数据与人工智能研发项目 (2019MBD-024);

首都临床特色应用研究特色课题 (Z181100001718034);

菊梅肝胆病防治能力建设专项基金重点项目 (2018JM12603003)

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:王春艳、邓亚、纪冬负责课题设计,资料分析,撰写论文;王春艳、杨武才、谭文辉、邓亚、郭畅、张珊、王建军、陈国凤、纪冬参与收集数据,修改论文;王春艳、纪冬负责拟定写作思路,指导撰写文章并最后定稿。
详细信息
    通信作者:

    纪冬,jidg302@126.com

  • 中图分类号: R512.62;R575.2

Value of a nomogram model in predicting significant liver injury in patients with immune-tolerant phase chronic hepatitis B

Research funding: 

Medical Big Data and Artificial Intelligence Development Fund of Chinese PLA General Hospital (2019MBD-024)

the Capital Characteristic Clinic Project of Beijing Municipal Science and Technology Commission (Z181100001718034)

Key Project of Jumei Special Fund for Hepatobiliary Disease Prevention and Treatment (2018JM12603003)

  • 摘要:   目的  分析慢性HBV感染免疫耐受期(IT-CHB)患者显著肝损伤的高危因素并建立列线图预测模型。  方法  回顾性分析2002年8月—2017年12月在解放军总医院第五医学中心接受肝活检的382例慢性HBV感染者的资料,按照肝组织是否存在显著肝损伤分为2组,显著肝损伤组(≥G2或S2,n=82)和非显著肝损伤组(n=300)。正态分布的计量数据2组间比较采用独立样本t检验;非正态分布数据2组间比较采用Mann- Whitney U检验; 多组比较采用Kruskal-Wallis H检验;计数资料2组间比较采用χ2检验。相关性分析采用Spearman秩相关。采用单/多因素logistic回归方法筛选高危因素,并建立列线图模型,用C-指数、ROC曲线、校准曲线以及Bootstrap法来评价列线图的区分度及校准度。  结果  2组年龄、HBV DNA载量、ALT、AST、PLT比较差异均有统计学意义(t=-7.071,Z值别为-4.924、-3.693、-6.945、-0.585、-5.723,P值均<0.001)。Logistic回归分析显示年龄(OR=1.074,95%CI: 1.043~1.107,P<0.001),HBV DNA载量(OR=0.442,95%CI: 0.314~0.624,P<0.001),AST(OR=1.096,95%CI: 1.051~1.142,P<0.001),PLT(OR=0.992,95%CI: 0.986~0.998,P=0.006)是显著肝损伤的高危因素。基于以上因素建立列线图模型,预测显著肝损伤的C-指数为0.845,并且有拟合度高的校正曲线,其ROC曲线下面积(AUC)为0.845(95%CI: 0.795~0.895),显著优于APRI(AUC=0.781,95%CI: 0.723~0.840)以及FIB-4 (AUC=0.802,95%CI: 0.746~0.859)。  结论  免疫耐受期具有显著肝损伤的患者比例并不少见,基于年龄、HBV DNA、AST、PLT构建的列线图模型具有良好的预测准确性,可用于个体化预测IT-CHB患者的显著肝损伤,减少肝活检,为抗病毒的精准治疗提供参考。

     

  • 图  1  不同年龄段与肝组织病理炎症及纤维化的关系

    图  2  HBV DNA载量与不同阶段肝组织病理炎症及纤维化的关系

    图  3  预测IT-CHB患者显著肝损伤的列线图

    表  1  患者基线的一般资料

    指标 总体(n=382) 非显著肝损伤组(n=300) 显著肝损伤组(n=82) 统计值 P
    男性[例(%)] 261(68.3) 201(67.0) 60(73.2) χ2=1.133 0.287
    年龄(岁) 33.3±10.2 31.5±9.1 39.9±11.2 t=-7.071 <0.001
    年龄段[例(%)] χ2=56.472 <0.001
      <30岁 161(42.1) 147(49.0) 14(17.1)
      30~39岁 130(34.0) 106(35.3) 24(29.3)
      40~49岁 64(16.8) 35(11.7) 29(35.4)
      ≥50岁 27(7.1) 12(4.0) 15(18.3)
    乙型肝炎家族史[例(%)] 221(57.9) 173(57.7) 48(58.5) χ2=0.020 0.888
    BMI(kg/m2) 23.2±3.53 23.0±3.4 23.7±3.9 t=-1.021 0.308
    HBV DNA(log10IU/ml) 8.4(7.8~8.8) 8.4(8.0~8.8) 7.9(6.9~8.5) Z=-4.924 <0.001
    ALT(U/L) 23.0(18.0~28.0) 23.0(18.0~28.0) 25.5(21.0~32.0) Z=-3.693 <0.001
    AST(U/L) 23.0(19.0~27.0) 21.0(19.0~26.0) 28.0(23.0~34.0) Z=-6.945 <0.001
    TBil(μmol/L) 11.1(8.3~15.3) 10.9(8.3~15.3) 11.5(8.6~15.4) Z=-0.585 0.559
    PLT(×109/L) 202(164~234) 208(176~239) 161(137~209) Z=-5.723 <0.001
    下载: 导出CSV

    表  2  显著肝损伤的logistic回归分析

    因素 单因素分析 多因素分析
    OR(95%CI) P OR(95%CI) P
    年龄 1.084 (1.057~1.113) <0.001 1.074(1.043~1.107) <0.001
    HBV DNA 0.437 (0.324~0.589) <0.001 0.442(0.314~0.624) <0.001
    ALT 1.076(1.036~1.119) <0.001 1.009(0.959~1.060) 0.736
    AST 1.132 (1.089~1.177) <0.001 1.096(1.051~1.142) <0.001
    PLT 0.985 (0.98~0.991) <0.001 0.992(0.986~0.998) 0.006
    下载: 导出CSV

    表  3  列线图、APRI、FIB-4诊断显著肝损伤的效能比较

    诊断参数 AUC 95%CI 界值 敏感度(%) 特异度(%) 阳性预测值(%) 阴性预测值(%) Youden指数
    列线图 0.845 0.795 ~ 0.895 141.4 74.4 84.7 57.0 92.4 0.59
    APRI 0.781 0.723 ~ 0.840 0.338 70.7 77.7 46.4 90.7 0.48
    FIB-4 0.802 0.746 ~ 0.859 0.882 78.1 72.3 43.5 92.3 0.50
    下载: 导出CSV
  • [1] Chinese Society of Infectious Diseases, Chinese Medical Association, Chinese Society of Infectious Diseases, 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.

    中华医学会肝病学分会, 中华医学会感染病学分会. 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.
    [2] TERRAULT NA, LOK A, MCMAHON BJ, et al. Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance[J]. Hepatology, 2018, 67(4): 1560-1599. DOI: 10.1002/hep.29800.
    [3] SARIN SK, KUMAR M, LAU GK, et al. Asian-Pacific clinical practice guidelines on the management of hepatitis B: A 2015 update[J]. Hepatol Int, 2016, 10(1): 1-98. DOI: 10.1007/s12072-015-9675-4.
    [4] European Association for the Study of the Liver. EASL 2017 clinical practice guidelines on the management of hepatitis B virus infection[J]. J Hepatol, 2017, 67(2): 370-398. DOI: 10.1016/j.jhep.2017.03.021.
    [5] GAO HY, LIU N, LI CX, et al. Clinical features and liver histopathological analysis of patients in the immune tolerance stage of chronic hepatitis B virus infection[J]. Chin Hepatol, 2018, 23(2): 136-139. DOI: 10.14000/j.cnki.issn.1008-1704.2018.02.012.

    高红艳, 刘娜, 李春霞, 等. 慢性乙型肝炎病毒感染者免疫耐受期的临床特征与肝组织病理学分析[J]. 肝脏, 2018, 23(2): 136-139. DOI: 10.14000/j.cnki.issn.1008-1704.2018.02.012.
    [6] XING YF, ZHOU DQ, HE JS, et al. Clinical and histopathological features of chronic hepatitis B virus infected patients with high HBV DNA viral load and normal alanine aminotransferase level: A multicentre-based study in China[J]. PLoS One, 2018, 13(9): e0203220. DOI: 10.1371/journal.pone.0203220.
    [7] 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.
    [8] 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.
    [9] SETO WK, LAI CL, IP PP, et al. A large population histology study showing the lack of association between ALT elevation and significant fibrosis in chronic hepatitis B[J]. PLoS One, 2012, 7(2): e32622. DOI: 10.1371/journal.pone.0032622.
    [10] KIM HL, KIM GA, PARK JA, et al. Cost-effectiveness of antiviral treatment in adult patients with immune-tolerant phase chronic hepatitis B[J]. Gut, 2020. [Online ahead of print]. DOI: 10.1136/gutjnl-2020-321309.
    [11] KIM GA, LIM YS, HAN S, et al. High risk of hepatocellular carcinoma and death in patients with immune-tolerant-phase chronic hepatitis B[J]. Gut, 2018, 67(5): 945-952. DOI: 10.1136/gutjnl-2017-314904.
    [12] GAO HY, LIU N, LI CX, et al. Research advances in influencing factors for natural prognosis of patients with chronic HBV infection in immune tolerance phase[J]. J Clin Hepatol, 2017, 33(8): 1572-1575. DOI: 10.3969/j.issn.1001-5256.2017.08.035.

    高红艳, 刘娜, 李春霞, 等. 慢性HBV感染者免疫耐受期自然转归相关影响因素的研究进展[J]. 临床肝胆病杂志, 2017, 33(8): 1572-1575. DOI:10. 3969/j.issn.1001-5256.2017.08.035.
    [13] ZHOU LL, LIU N, LI CX, et al. Research advances in the diagnosis and treatment of patients in the immune tolerance stage of chronic hepatitis B virus infection[J]. J Clin Hepatol, 2019, 35(8): 1824-1827. DOI: 10.3969/j.issn.1001-5256.2019.08.039.

    周路路, 刘娜, 李春霞, 等. 慢性HBV感染免疫耐受期诊治进展[J]. 临床肝胆病杂志, 2019, 35(8): 1824-1827. DOI: 10.3969/j.issn.1001-5256.2019.08.039.
    [14] LIU M, ZUO LL, ZHANG RY, et al. Research progress of antiviral therapy in patients with chronic HBV infection in immune tolerance phase[J]. Chin J Infect Dis, 2020, 38(11): 750-752. DOI: 10.3760/cma.j.cn311365-20190422-00138.

    刘敏, 左丽丽, 张茹薏, 等. 乙型肝炎免疫耐受期患者进行抗病毒治疗的研究进展[J]. 中华传染病杂志, 2020, 38(11): 750-752. DOI: 10.3760/cma.j.cn311365-20190422-00138.
    [15] 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.
    [16] LOK AS, MCMAHON BJ, BROWN RS Jr, et al. Antiviral therapy for chronic hepatitis B viral infection in adults: A systematic review and meta-analysis[J]. Hepatology, 2016, 63(1): 284-306. DOI: 10.1002/hep.28280.
    [17] LEE HW, CHON YE, KIM BK, et al. Negligible HCC risk during stringently defined untreated immune-tolerant phase of chronic hepatitis B[J]. Eur J Intern Med, 2021, 84: 68-73. DOI: 10.1016/j.ejim.2020.10.022.
    [18] KLAIR JS, VANCURA J, MURALI AR. PRO: Patients with chronic hepatitis B in immune-tolerant phase should be treated[J]. Clin Liver Dis (Hoboken), 2020, 15(1): 21-24. DOI: 10.1002/cld.892.
    [19] ROCKEY DC, CALDWELL SH, GOODMAN ZD, et al. Liver biopsy[J]. Hepatology, 2009, 49(3): 1017-1044. DOI: 10.1002/hep.22742.
    [20] Chinese Society of Hepatology and Chinese Society of Infectious Diseases, Chinese Medical Association. The guideline of prevention and treatment for chronic hepatitis B(2015 version)[J]. J Clin Hepatol, 2015, 31(12): 1941-1960. DOI: 10.3969/j.issn.1001-5256.2015.12.002.

    中华医学会肝病学分会, 中华医学会感染病学分会. 慢性乙型肝炎防治指南(2015年版)[J]. 临床肝胆病杂志, 2015, 31(12): 1941-1960. DOI: 10. 3969 /j. issn. 1001-5256. 2015. 12. 002.
    [21] 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
    [22] Polaris Observatory Collaborators. Global prevalence, treatment, and prevention of hepatitis B virus infection in 2016: A modelling study[J]. Lancet Gastroenterol Hepatol, 2018, 3(6): 383-403. DOI: 10.1016/S2468-1253(18)30056-6.
    [23] 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.
    [24] LIAW YF, CHU CM. Immune tolerance phase of chronic hepatitis B[J]. Gastroenterology, 2017, 152(5): 1245-1246. DOI: 10.1053/j.gastro.2016.11.057.
    [25] KENNEDY PTF, BERTOLETTI A, MASON WS. Reply to immune tolerance phase of chronic hepatitis B[J]. Gastroenterology, 2017, 152(5): 1246-1247. DOI: 10.1053/j.gastro.2017.03.002.
    [26] WANG H, XUE L, YAN R, et al. Comparison of FIB-4 and APRI in Chinese HBV-infected patients with persistently normal ALT and mildly elevated ALT[J]. J Viral Hepat, 2013, 20(4): e3-e10. DOI: 10.1111/jvh.12010.
    [27] FATTOVICH G, BORTOLOTTI F, DONATO F. Natural history of chronic hepatitis B: Special emphasis on disease progression and prognostic factor[J]. J Hepatol, 2008, 48(2): 335-352. DOI: 10.1016/j.jhep.2007.11.011.
    [28] RAFFETTI E, FATTOVICH G, DONATO F. Incidence of hepatocellular carcinoma in untreated subjects with chronic hepatitis B: A systematic review and meta-analysis[J]. Liver Int, 2016, 36(9): 1239-1251. DOI: 10.1111/liv.13142.
    [29] ILOEJE UH, YANG HI, SU J, et al. Predicting cirrhosis risk based on the level of circulating hepatitis B viral load[J]. Gastroenterology, 2006, 130(3): 678-686. DOI: 10.1053/j.gastro.2005.11.016.
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