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Clinical characteristics and HLA genotypes in Chinese patients with anti-SLA/LP-positive autoimmune hepatitis
Zhang, Hai-Ping1,2; Liu, Yan-Min3; Li, Zhao4; Ma, Yin-Xue1,2; Li, Li-Juan1,2; Zhao, Dan-Tong1,2; Lou, Jin-Li1,2; Gao, Zu-Hua5; Yan, Hui-Ping1,2
第一作者Zhang, Hai-Ping
通讯作者邮箱bjyhp503@ccmu.edu.cn (hui-ping yan) ; bjyhp503@ccmu.edu.cn (zu-hua gao)
心理所单位排序4
摘要

Background: Anti- soluble liver antigen/liver pancreas ( anti-SLA/LP) is a highly specific serological marker for the diagnosis of autoimmune hepatitis (AIH). The aim of the present study was to define the clinical characteristics and human leucocyte antigen (HLA) genotypes of Chinese patients with anti-SLA/LP positive AIH. Methods: Ninety-one AIH patients who were anti-SLA/LP positive were enrolled in this case control study. Clinical information was obtained through reviewing patients' clinical notes. High-resolution genotyping of HLA-A, B, C, DRB1, and DQB1 alleles was performed by sequence-based typing polymerase chain reaction on 62 of the 91 patients. Data from 500 healthy patients were used as baseline controls. Results: Anti-SLA/LP-positive AIH patients were characterized as follows: adults (age 20-80 years), female (88%), and frequent anti-nuclear antibody positivity (91%). Genetically, compared with the controls, HLA-B*35:01 and C*08:01 were significantly more frequent in patients. The frequencies of HLA-B*08:01, B*40:02, DRB1*04: 01, DRB1*04:05, DRB1* 14: 01, and DRB1*16:02 increased, and the frequency in DRB1*15:01 decreased in patients, but did not reach significance after Bonferroni's correction. Patients with other autoimmune diseases had a higher DRB1*04:05 and DQB1*04: 01 allele carrier frequency than those without. DRB1* 04:05 and DQB1*04:01 alleles were found at increased frequency in patients with decompensated liver disease than those with compensated liver disease. Conclusions: Chinese anti-SLA/LP-positive AIH patients have some distinct clinical characteristics than other populations reported in the literature. The presence of certain specific HLA alleles could potentially increase the risk of developing anti-SLA/LP-positive AIH or other autoimmune disease and decompensated liver disease in the Chinese population.

关键词Autoimmune hepatitis (AIH) anti-soluble liver antigen/liver pancreas human leucocyte antigen (HLA)
2021
语种英语
DOI10.21037/atm-20-8036
发表期刊ANNALS OF TRANSLATIONAL MEDICINE
ISSN2305-5839
卷号9期号:2页码:12
期刊论文类型实证研究
收录类别SCI
资助项目Development Center for Medical Science and Technology, National Health, and Family Planning Commission of the People's Republic of China[28-5-5]
出版者AME PUBL CO
WOS关键词LIVER ANTIGEN/LIVER PANCREAS ; ANTIBODIES ; DIAGNOSIS ; AUTOANTIBODIES ; ASSOCIATIONS ; MANAGEMENT ; CRITERIA ; ALLELES ; GENES
WOS研究方向Oncology ; Research & Experimental Medicine
WOS类目Oncology ; Medicine, Research & Experimental
WOS记录号WOS:000636046800031
引用统计
被引频次:4[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://ir.psych.ac.cn/handle/311026/38910
专题中国科学院心理健康重点实验室
通讯作者Gao, Zu-Hua; Yan, Hui-Ping
作者单位1.Capital Med Univ, Beijing Youan Hosp, Clin Lab Ctr, Beijing 100069, Peoples R China
2.Capital Med Univ, Beijing Youan Hosp, Clin Res Ctr Autoimmune Liver Dis, Beijing 100069, Peoples R China
3.Capital Med Univ, Beijing Youan Hosp, Dept Liver Dis Immunol, Beijing, Peoples R China
4.Chinese Acad Sci, Inst Psychol, CAS Key Lab Mental Hlth, Beijing, Peoples R China
5.McGill Univ, Dept Pathol, Montreal, PQ, Canada
推荐引用方式
GB/T 7714
Zhang, Hai-Ping,Liu, Yan-Min,Li, Zhao,et al. Clinical characteristics and HLA genotypes in Chinese patients with anti-SLA/LP-positive autoimmune hepatitis[J]. ANNALS OF TRANSLATIONAL MEDICINE,2021,9(2):12.
APA Zhang, Hai-Ping.,Liu, Yan-Min.,Li, Zhao.,Ma, Yin-Xue.,Li, Li-Juan.,...&Yan, Hui-Ping.(2021).Clinical characteristics and HLA genotypes in Chinese patients with anti-SLA/LP-positive autoimmune hepatitis.ANNALS OF TRANSLATIONAL MEDICINE,9(2),12.
MLA Zhang, Hai-Ping,et al."Clinical characteristics and HLA genotypes in Chinese patients with anti-SLA/LP-positive autoimmune hepatitis".ANNALS OF TRANSLATIONAL MEDICINE 9.2(2021):12.
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