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匈牙利骨Paget病队列中SQSTM1基因变异模式

Pattern of SQSTM1 Gene Variants in a Hungarian Cohort of Paget's Disease of Bone.

作者信息

Donáth Judit, Balla Bernadett, Pálinkás Márton, Rásonyi Rita, Vastag Gyula, Alonso Nerea, Prieto Beatriz Larraz, Vallet Mahéva, Ralston Stuart H, Poór Gyula

机构信息

National Institute of Rheumatology and Physiotherapy, Budapest, Hungary.

PentaCore Laboratories, Budapest, Hungary.

出版信息

Calcif Tissue Int. 2021 Feb;108(2):159-164. doi: 10.1007/s00223-020-00758-4. Epub 2020 Sep 25.

Abstract

Paget's disease of bone (PDB) is characterized by focal or multifocal increase in bone turnover. One of the most well-established candidate genes for susceptibility to PDB is Sequestosome 1 (SQSTM1). Mutations in SQSTM1 have been documented among Western-European, British and American patients with PDB. However, there is no information on SQSTM1 mutation status in PDB patients from the Central- and Eastern-European regions. In this study, we conducted a mutation screening for SQSTM1 gene variants in 82 PDB patients and 100 control participants in Hungary. Mutations of SQSTM1 were detected in 18 PDB patients (21.95%); associations between genotype and clinical characteristics were also analyzed. Altogether, six different exonic alterations, including two types of UTR variants in the SQSTM1 gene, were observed in our PDB patients. Similarly, to previous genetic studies on Paget's disease, our most commonly detected variant was the c.1175C > T (p.Pro392Leu) in nine cases (four in monostotic and five in polyostotic form). We have surveyed the germline SQSTM1 variant distribution among Hungarian patients with PDB. We also highlighted that the pattern of the analyzed disease-associated pathophysiological parameters could partially discriminate PDB patients with normal or mutant SQSTM1 genotype. However, our findings also underline and strengthen that not solely SQSTM1 stands in the background of the complex PDB etiology.

摘要

骨佩吉特病(PDB)的特征是骨转换呈局灶性或多灶性增加。骨佩吉特病易感性最确定的候选基因之一是聚集体蛋白1(SQSTM1)。在西欧、英国和美国的骨佩吉特病患者中已记录到SQSTM1突变。然而,关于中东欧地区骨佩吉特病患者的SQSTM1突变状态尚无相关信息。在本研究中,我们对匈牙利的82例骨佩吉特病患者和100名对照参与者进行了SQSTM1基因变异的突变筛查。在18例骨佩吉特病患者(21.95%)中检测到了SQSTM1突变;还分析了基因型与临床特征之间的关联。在我们的骨佩吉特病患者中总共观察到六种不同的外显子改变,包括SQSTM1基因中的两种UTR变异类型。同样,与先前关于佩吉特病的基因研究一样,我们最常检测到的变异是c.1175C>T(p.Pro392Leu),共9例(单骨型4例,多骨型5例)。我们调查了匈牙利骨佩吉特病患者中种系SQSTM1变异的分布情况。我们还强调,所分析的疾病相关病理生理参数模式可以部分区分具有正常或突变SQSTM1基因型的骨佩吉特病患者。然而,我们的研究结果也强调并强化了,复杂的骨佩吉特病病因背后不仅仅是SQSTM1。

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