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[ATP8B1基因新变异致常染色体隐性遗传I型家族性肝内胆汁淤积症一家系的临床及遗传学分析]

[Clinical and genetic analysis of a Chinese pedigree with autosomal recessive familial intrahepatic cholestasis type I due to a novel variant of ATP8B1 gene].

作者信息

Wang Zhimin, Qi Haili, Wei Xiaojuan, Duan Hualing, Li Xiaohuan, Qi Hongyang

机构信息

Department of Gastroenterology, Xinxiang Central Hospital, Xinxiang, Henan 653001, China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025 May 10;42(5):608-612. doi: 10.3760/cma.j.cn511374-20241224-00680.

Abstract

OBJECTIVE

To investigate the clinical and genetic features of a Chinese pedigree with Progressive familial intrahepatic cholestasis (PFIC) and explore its genotype-phenotype correlation.

METHODS

A patient with PFIC diagnosed at Xinxiang Central Hospital in 2023 was selected as the study subject. The patient was subjected to abdominal magnetic resonance imaging (MRI) and painless gastroscopy. Peripheral blood samples were collected from the patient and his parents for the extraction of genomic DNA and trio-whole exome sequencing (trio-WES). Candidate variants were verified by Sanger sequencing. This study has been approved by the Medical Ethics Committee of Xinxiang Hospital (Ethics No. 2023-241).

RESULTS

MRI scan showed that the patient had significantly enlarged liver and spleen. WES revealed that he has harbored compound heterozygous variants of the ATP8B1 gene, including a c.1710_1711insCCTC (p.A571Pfs*12) frameshifting variant in exon 16 and a c.2989G>A (p.V997M) missense variant in exon 24, which were respectively inherited from his father and mother, and rated as pathogenic (PVS1+PM2_Supporting+PM3+PP1) and likely pathogenic (PM2_Supporting+PM3+PP1) based on the guidelines from the American College of Medical Genetics and Genomics (ACMG).

CONCLUSION

WES can clarify the genetic etiology of patients with speed and accuracy, and facilitate clinical decision-making. The detection of pathogenic variants has provided a basis for clinical diagnosis and enriched the mutational spectrum of the ATP8B1 gene.

摘要

目的

研究一个中国进行性家族性肝内胆汁淤积症(PFIC)家系的临床和遗传特征,并探讨其基因型与表型的相关性。

方法

选取2023年在新乡市中心医院诊断为PFIC的1例患者作为研究对象。对该患者进行腹部磁共振成像(MRI)和无痛胃镜检查。采集患者及其父母的外周血样本,提取基因组DNA并进行三联体全外显子测序(trio-WES)。通过Sanger测序验证候选变异。本研究已获得新乡医院医学伦理委员会批准(伦理编号:2023-241)。

结果

MRI扫描显示患者肝脏和脾脏明显肿大。全外显子测序结果显示,该患者携带ATP8B1基因的复合杂合变异,包括外显子16上的c.1710_1711insCCTC(p.A571Pfs*12)移码变异和外显子24上的c.2989G>A(p.V997M)错义变异,分别遗传自其父亲和母亲,根据美国医学遗传学与基因组学学会(ACMG)的指南,分别被评为致病(PVS1+PM2_Supporting+PM3+PP1)和可能致病(PM2_Supporting+PM3+PP1)。

结论

全外显子测序能够快速、准确地明确患者的遗传病因,有助于临床决策。致病变异的检测为临床诊断提供了依据,丰富了ATP8B1基因的突变谱。

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