首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree
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Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree

机译:家族性佩吉特氏骨性疾病中发生的巨细胞瘤:大家族谱系的临床特征和连锁分析报告

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Neoplastic degeneration represents a rare but serious complication of Paget's disease of bone (PDB). Although osteosarcomas have been described in up to 1% of PDB cases, giant cell tumors are less frequent and mainly occur in patients with polyostotic disease. We recently characterized a large pedigree with 14 affected members of whom four developed giant cell tumors at pagetic sites. The high number of affected subjects across multiple generations allowed us to better characterize the clinical phenotype and look for possible susceptibility loci. Of interest, all the affected members had polyostotic PDB, but subjects developing giant cell tumors showed an increased disease severity with a reduced clinical response to bisphosphonate treatment and an increased prevalence of bone pain, deformities, and fractures. Together with an increased occurrence of common pagetic complications, affected patients of this pedigree also evidenced a fivefold higher prevalence of coronary artery disease with respect to either the unaffected family members or a comparative cohort of 150 unrelated PDB cases from the same geographical area. This association was further enhanced in the four cases with PDB and giant cell tumors, all of them developing coronary artery disease before 60 years of age. Despite the early onset and the severe phenotype, PDB patients from this pedigree were negative for the presence of SQSTM1 or TNFRSF11A mutations, previously associated with enhanced disease severity. Genome-wide linkage analysis identified six possible candidate regions on chromosomes 1, 5, 6, 8, 10, and 20. Because the chromosome 8 and 10 loci were next to the TNFRSF11B and OPTN genes, we extended the genetic screening to these two genes, but we failed to identify any causative mutation at both the genomic and transcription level, suggesting that a different genetic defect is associated with PDB and potentially giant cell tumor of bone in this pedigree.
机译:赘生性变性代表了Paget骨病(PDB)的罕见但严重的并发症。尽管在多达1%的PDB病例中已经描述了骨肉瘤,但巨细胞瘤的发生率较低,主要发生在多骨症患者中。我们最近对一个大谱系进行了特征分析,其中有14个受影响的成员,其中有4个在分页部位出现了巨细胞瘤。多代患者的患病人数众多,使我们能够更好地表征临床表型并寻找可能的易感基因座。有趣的是,所有受影响的成员均患有多骨性PDB,但发展为巨细胞瘤的受试者表现出疾病严重程度增加,对双膦酸盐治疗的临床反应减少,以及骨痛,畸形和骨折的患病率增加。再加上常见的寻呼并发症的发生率增加,该血统的受累患者也证明相对于未受影响的家庭成员或来自同一地理区域的150个无关PDB病例的比较队列,冠状动脉疾病的患病率高出五倍。在4例PDB和巨细胞瘤病例中,这种关联性进一步增强,它们均在60岁之前发展为冠状动脉疾病。尽管有早期发作和严重的表型,但该谱系的PDB患者对SQSTM1或TNFRSF11A突变的存在阴性,以前与疾病严重程度增加相关。全基因组连锁分析确定了1、5、6、8、10和20号染色体上的六个可能候选区域。由于8和10号染色体位点紧邻TNFRSF11B和OPTN基因,我们将遗传筛选扩展到了这两个基因,但我们未能在基因组和转录水平上鉴定出任何致病突变,这表明该谱系中PDB和潜在的骨巨细胞瘤与其他遗传缺陷有关。

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