泛素特异性蛋白酶 53 (USP53) 相关遗传性慢性胆汁淤积症患儿的自然病程和预后。

IF 2.4 3区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of Pediatric Gastroenterology and Nutrition Pub Date : 2024-10-23 DOI:10.1002/jpn3.12392
Seema Alam, Bikrant Bihari Lal, Aathira Ravindranath, Ashish Bavdekar, Nirmala Dheivamani, Pandey Snehavardhan, Aashay Shah, Parijat Ram Tripathi, Aabha Nagral, K P Srikanth, Ira Shah, Somashekara Hosaagrahara Ramakrishna, Arya Suchismita, Yogesh Waikar, Vaibhav Shah, Zahabiya Nalwalla, Karunesh Kumar, Arjun Maria, Anupam Sibal, Viswanathan M Sivaramakrishnan, Nishant Wadhwa, A Ashritha, Vikrant Sood, Rajeev Khanna
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引用次数: 0

摘要

泛素特异性蛋白酶 53(USP53)对细胞紧密连接的形成至关重要,该基因的变异会破坏紧密连接,导致胆汁淤积。我们描述了来自印度进行性家族性肝内胆汁淤积症登记处的 USP53 基因突变患者的临床表现和预后。我们纳入了所有 29 例携带 USP53 基因突变的患者,这些患者或为同卵、或为复合杂合子、或为杂合子,并伴有胆汁淤积症。与胆汁淤积症相关的USP53基因变异患者的预后良好,82.7%的患者可以存活,而17.3%的患者需要进行肝移植。93%的患者在出生后3个月内出现黄疸,48.8%的患者在出生后3个月内出现黄疸。21例(72.4%)黄疸消退。76%的患者在中位年龄为7个月时出现瘙痒症状(10/22,45%的患者病情严重,4人(18.1%)药物治疗无效)。他们中的大多数(82.7%)有双拷贝突变。20例(69%)存在蛋白质截断突变,9例(31%)存在错义突变。基因型与结果之间没有相关性。
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Natural course and outcomes of children with ubiquitin-specific protease 53 (USP53)-related genetic chronic cholestasis.

Ubiquitin-specific protease 53 (USP53) is essential for formation of cellular tight junctions and variations in this gene disrupt the tight junctions, resulting in cholestasis. We describe the clinical manifestations and outcomes of patients with USP53 mutations from the Indian progressive familial intrahepatic cholestasis registry. All 29 patients who harbored mutations in the USP53 gene either in the homozygous, compound heterozygous, or heterozygous state and presented with cholestasis were included. USP53 variants related to cholestasis had good outcomes, with native liver survival in 82.7%, whereas 17.3% required liver transplantation. Jaundice developed in 93% and within 3 months of age in 48.8%. Jaundice resolved in 21 (72.4%). Pruritus 76% at a median age of 7 months (severe in 10/22, 45% and refractory to medical therapy in 4, 18.1%). Majority of them (82.7%) had biallelic mutations. Protein-truncating mutations were present in 20 (69%) and missense mutations in 9 (31%). No correlation was found between the genotype and the outcome.

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来源期刊
CiteScore
5.30
自引率
13.80%
发文量
467
审稿时长
3-6 weeks
期刊介绍: ​The Journal of Pediatric Gastroenterology and Nutrition (JPGN) provides a forum for original papers and reviews dealing with pediatric gastroenterology and nutrition, including normal and abnormal functions of the alimentary tract and its associated organs, including the salivary glands, pancreas, gallbladder, and liver. Particular emphasis is on development and its relation to infant and childhood nutrition.
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