Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.
Clinical Department of Human Genetics, KU Leuven-University of Leuven, University Hospitals Leuven, Leuven, Belgium.
Hum Mutat. 2019 Oct;40(10):1760-1767. doi: 10.1002/humu.23783. Epub 2019 Jun 18.
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximately 1 in 2,000 newborns. Up to 5% of NF1 patients suffer from pseudarthrosis of a long bone (NF1-PA). Current treatments are often unsatisfactory, potentially leading to amputation. To gain more insight into the pathogenesis we cultured cells from PA tissue and normal-appearing periosteum of the affected bone for NF1 mutation analysis. PA cells were available from 13 individuals with NF1. Biallelic NF1 inactivation was identified in all investigated PA cells obtained during the first surgery. Three of five cases sampled during a later intervention showed biallelic NF1 inactivation. Also, in three individuals, we examined periosteum-derived cells from normal-appearing periosteum proximal and distal to the PA. We identified the same biallelic NF1 inactivation in the periosteal cells outside the PA region. These results indicate that NF1 inactivation is required but not sufficient for the development of NF1-PA. We observed that late-onset NF1-PA occurs and is not always preceded by congenital bowing. Furthermore, the failure to identify biallelic inactivation in two of five later interventions and one reintervention with a known somatic mutation indicates that NF1-PA can persist after the removal of most NF1 negative cells.
神经纤维瘤病 1 型(NF1)是一种常染色体显性遗传病,影响大约每 2000 名新生儿中有 1 名。多达 5%的 NF1 患者患有长骨假关节(NF1-PA)。目前的治疗方法往往不尽如人意,可能导致截肢。为了更深入地了解发病机制,我们从 PA 组织和受累骨正常外观的骨膜中培养细胞,进行 NF1 突变分析。PA 细胞可从 13 名 NF1 患者中获得。在第一次手术中获得的所有研究 PA 细胞中均发现了 NF1 的双等位基因失活。在随后的干预中,有 5 例中的 3 例在再次采样时显示出 NF1 的双等位基因失活。此外,在 3 名个体中,我们检查了来自 PA 区域近端和远端正常外观的骨膜来源细胞。我们在 PA 区域外的骨膜细胞中鉴定出相同的 NF1 双等位基因失活。这些结果表明 NF1 失活是 NF1-PA 发生所必需的,但不是充分条件。我们观察到迟发性 NF1-PA 的发生,且并非总是先于先天性弯曲。此外,在五个后续干预中的两个和一个已知存在体细胞突变的再次干预中未检测到 NF1 双等位基因失活表明,在去除大多数 NF1 阴性细胞后,NF1-PA 仍可能持续存在。