中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

母女同患原发性胆汁性胆管炎报告并基因分析

秦玉洁 周文秀 周兴念 程明亮 李宏

引用本文:
Citation:

母女同患原发性胆汁性胆管炎报告并基因分析

DOI: 10.3969/j.issn.1001-5256.2023.02.021
基金项目: 

国家自然科学基金 (82060123);

贵州省卫健委科技基金项目 (gzwjk2019-1-082)

伦理学声明:本例报告已获得患者知情同意。
利益冲突声明:所有作者均声明不存在利益冲突。
作者贡献声明:秦玉洁负责文章撰写;周文秀负责临床资料收集整理;周兴念负责研究数据的获取分析解释过程;程明亮、李宏负责拟定写作思路,指导撰写文章并最后定稿。
详细信息
    通信作者:

    李宏, 625062102@qq.com (ORCID: 0000-0003-0601-3198)

Report and genetic analysis of autoimmune liver diseases between mother and daughter

Research funding: 

National Natural Science Foundation of China (82060123);

Project of Guizhou Province Health Commission Science and Technology (gzwjk2019-1-082)

More Information
  • 图  1  患者肝脏病理结果

    注:a,HE染色,×100;b,Masson染色,×100;c,IgG染色,×100;d,IgG4染色,×100;e,CK7染色,×100;f,CK19染色,×100。

    Figure  1.  The pathology of patient's liver specimen

    图  2  患者女儿肝脏病理结果

    注:a,HE染色,×100;b,Masson染色,×100;c,IgG染色,×100;d,IgG4染色,×100;e,CK7染色,×100;f,CK19染色,×100。

    Figure  2.  The pathology of patient daughter's liver specimen

    表  1  患者基因变异功能注释

    Table  1.   Functional annotation of genetic variants of patients

    突变类型 女儿 母亲
    所有突变 通过QC过滤 所有突变 通过QC过滤
    移码突变 236 205 236 210
    剪接突变 165 150 168 151
    停止突变 98 91 92 88
    止损突变 15 13 14 11
    错义突变 11089 10601 11073 10585
    总突变 11603 11060 11583 11045
    下载: 导出CSV

    表  2  患者候选基因变异功能注释

    Table  2.   Functional annotation of candidate genetic variants of patients

    突变类型 女儿 母亲
    剪接突变 6 4
    停止突变 7 11
    止损突变 1 1
    错义突变 284 277
    总突变 298 293
    下载: 导出CSV

    表  3  患者共有变异基因的SNP位点及相应氨基酸变化

    Table  3.   SNP sites and corresponding amino acid changes of patients' shared variant genes

    基因符号 SNP注释 染色体位置 外显子位置 碱基突变 氨基酸突变
    GPSM2 rs141562079 chr1 Exon11 C1216T R406W
    CACNA1S rs1465455126 chr1 Exon18 G2449T A817S
    CRYBA2 rs375552220 chr2 Exon4 T457C Y153H
    SLC7A14 rs2276717 chr3 Exon6 G988A G330R
    CA13 rs755805228 chr8 Exon7 G740A R247H
    NOTCH1 rs1396528813 chr9 Exon15 C2361G N787K
    PNPLA7 rs553960639 chr9 Exon29 G3248A R1083H
    IFT140 rs566450108 chr16 Exon21 G2758T A920S
    BEST2 rs773939596 chr19 Exon4 T320C M107T
    下载: 导出CSV
  • [1] WANG TT, LU CL, FAN XL, et al. Clinical and pathological features of autoimmune hepatitis-primary biliary cholangitis overlap syndrome versus autoimmune hepatitis[J]. J Clin Hepatol, 2017, 33(11): 2179-2185. DOI: 10.3969/j.issn.1001-5256.2017.11.026.

    王婷婷, 鲁昌立, 凡小丽, 等. 自身免疫性肝炎-原发性胆汁性胆管炎重叠综合征的临床及病理学特征分析[J]. 临床肝胆病杂志, 2017, 33(11): 2179-2185. DOI: 10.3969/j.issn.1001-5256.2017.11.026.
    [2] TRIVEDI PJ, HIRSCHFIELD GM. Recent advances in clinical practice: epidemiology of autoimmune liver diseases[J]. Gut, 2021, 70(10): 1989-2003. DOI: 10.1136/gutjnl-2020-322362.
    [3] CORDELL HJ, FRYETT JJ, UENO K, et al. Corrigendum to An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs[J]. J Hepatol, 2022, 76(2): 489. DOI: 10.1016/j.jhep.2021.11.015.
    [4] GONZALEZ RS, WASHINGTON K. Primary biliary cholangitis and autoimmune hepatitis[J]. Surg Pathol Clin, 2018, 11(2): 329-349. DOI: 10.1016/j.path.2018.02.010.
    [5] GULAMHUSEIN AF, JURAN BD, ATKINSON EJ, et al. Low incidence of primary biliary cirrhosis (PBC) in the first-degree relatives of PBC probands after 8 years of follow-up[J]. Liver Int, 2016, 36(9): 1378-1382. DOI: 10.1111/liv.13143.
    [6] ZOGRAFOS TA, GATSELIS N, ZACHOU K, et al. Primary biliary cirrhosis-specific autoantibodies in first degree relatives of Greek primary biliary cirrhosis patients[J]. World J Gastroenterol, 2012, 18(34): 4721-4728. DOI: 10.3748/wjg.v18.i34.4721.
    [7] ÖRNOLFSSON KT, OLAFSSON S, BERGMANN OM, et al. Using the Icelandic genealogical database to define the familial risk of primary biliary cholangitis[J]. Hepatology, 2018, 68(1): 166-171. DOI: 10.1002/hep.29675.
    [8] SELMI C, MAYO MJ, BACH N, et al. Primary biliary cirrhosis in monozygotic and dizygotic twins: genetics, epigenetics, and environment[J]. Gastroenterology, 2004, 127(2): 485-492. DOI: 10.1053/j.gastro.2004.05.005.
    [9] SELMI C, BALKWILL DL, INVERNIZZI P, et al. Patients with primary biliary cirrhosis react against a ubiquitous xenobiotic-metabolizing bacterium[J]. Hepatology, 2003, 38(5): 1250-1257. DOI: 10.1053/jhep.2003.50446.
    [10] LIU HY, DENG AM, ZHOU Y, et al. Analysis of HLA alleles polymorphism in Chinese patients with primary biliary cirrhosis[J]. Hepatobiliary Pancreat Dis Int, 2006, 5(1): 129-132.
    [11] XU H, ZHANG S, HUANG L, et al. Identification of novel variants in the FZD4 gene associated with familial exudative vitreoretinopathy in Chinese families[J]. Clin Exp Ophthalmol, 2020, 48(3): 356-365. DOI: 10.1111/ceo.13690.
    [12] HW XQ, ZHANG YF, YU JJ, et al. High expression of G-protein signaling modulator 2 in hepatocellular carcinoma facilitates tumor growth and metastasis by activating the PI3K/AKT signaling pathway[J]. Tumour Biol, 2017, 39(3): 1-10. DOI: 10.1177/1010428317695971.
    [13] SCHWABE RF, TABAS I, PAJVANI UB. Mechanisms of fibrosis development in nonalcoholic steatohepatitis[J]. Gastroenterology, 2020, 158(7): 1913-1928. DOI: 10.1053/j.gastro.2019.11.311.
    [14] ESMAIL MM, SAEED NM, MICHEL HE, et al. The ameliorative effect of niclosamide on bile duct ligation induced liver fibrosis via suppression of NOTCH and Wnt pathways[J]. Toxicol Lett, 2021, 347: 23-35. DOI: 10.1016/j.toxlet.2021.04.018.
    [15] CROQUELOIS A, BLINDENBACHER A, TERRACCIANO L, et al. Inducible inactivation of Notch1 causes nodular regenerative hyperplasia in mice[J]. Hepatology, 2005, 41(3): 487-496. DOI: 10.1002/hep.20571.
    [16] ZHANG X, DU G, XU Y, et al. Inhibition of notch signaling pathway prevents cholestatic liver fibrosis by decreasing the differentiation of hepatic progenitor cells into cholangiocytes[J]. Lab Invest, 2016, 96(3): 350-360.
  • 加载中
图(2) / 表(3)
计量
  • 文章访问数:  972
  • HTML全文浏览量:  467
  • PDF下载量:  75
  • 被引次数: 0
出版历程
  • 收稿日期:  2022-06-10
  • 录用日期:  2022-07-28
  • 出版日期:  2023-02-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回