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荷兰非典型股骨骨折患者队列中单基因骨病的患病率。

Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients.

机构信息

Department of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.

Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.

出版信息

J Bone Miner Res. 2023 Jun;38(6):896-906. doi: 10.1002/jbmr.4801. Epub 2023 Apr 19.

Abstract

Atypical femur fractures (AFFs), considered rare associations of bisphosphonates, have also been reported in patients with monogenic bone disorders without bisphosphonate use. The exact association between AFFs and monogenic bone disorders remains unknown. Our aim was to determine the prevalence of monogenic bone disorders in a Dutch AFF cohort. AFF patients were recruited from two specialist bone centers in the Netherlands. Medical records of the AFF patients were reviewed for clinical features of monogenic bone disorders. Genetic variants identified by whole-exome sequencing in 37 candidate genes involved in monogenic bone disorders were classified based on the American College of Medical Genetics and Genomics (ACMG) classification guidelines. Copy number variations overlapping the candidate genes were also evaluated using DNA array genotyping data. The cohort comprises 60 AFF patients (including a pair of siblings), with 95% having received bisphosphonates. Fifteen AFF patients (25%) had clinical features of monogenic bone disorders. Eight of them (54%), including the pair of siblings, had a (likely) pathogenic variant in either PLS3, COL1A2, LRP5, or ALPL. One patient carried a likely pathogenic variant in TCIRG1 among patients not suspected of monogenic bone disorders (2%). In total, nine patients in this AFF cohort (15%) had a (likely) pathogenic variant. In one patient, we identified a 12.7 Mb deletion in chromosome 6, encompassing TENT5A. The findings indicate a strong relationship between AFFs and monogenic bone disorders, particularly osteogenesis imperfecta and hypophosphatasia, but mainly in individuals with symptoms of these disorders. The high yield of (likely) pathogenic variants in AFF patients with a clinical suspicion of these disorders stresses the importance of careful clinical evaluation of AFF patients. Although the relevance of bisphosphonate use in this relationship is currently unclear, clinicians should consider these findings in medical management of these patients. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

摘要

非典型股骨骨折(AFFs)被认为是双膦酸盐的罕见相关疾病,也有报道称在未使用双膦酸盐的单基因骨疾病患者中发生。AFFs 与单基因骨疾病的确切关联尚不清楚。我们的目的是确定荷兰 AFF 队列中单基因骨疾病的患病率。AFF 患者从荷兰的两个专科骨科中心招募。对 AFF 患者的病历进行回顾,以评估单基因骨疾病的临床特征。通过全外显子组测序鉴定的 37 个候选基因中的遗传变异,根据美国医学遗传学与基因组学学院(ACMG)分类指南进行分类。还使用 DNA 芯片基因分型数据评估候选基因重叠的拷贝数变异。该队列包括 60 名 AFF 患者(包括一对兄弟姐妹),其中 95%接受了双膦酸盐治疗。15 名 AFF 患者(25%)具有单基因骨疾病的临床特征。其中 8 名(54%),包括这对兄弟姐妹,在 PLS3、COL1A2、LRP5 或 ALPL 中存在(可能)致病性变异。一名未怀疑单基因骨疾病的患者(2%)在 TCIRG1 中携带可能的致病性变异。在这个 AFF 队列中,共有 9 名患者(15%)携带(可能)致病性变异。在一名患者中,我们在 6 号染色体上发现了一个 12.7Mb 的缺失,包含 TENT5A。这些发现表明 AFFs 与单基因骨疾病之间存在很强的关系,特别是成骨不全症和低磷酸酶血症,但主要发生在有这些疾病症状的个体中。在有这些疾病临床怀疑的 AFF 患者中,(可能)致病性变异的高检出率强调了仔细临床评估 AFF 患者的重要性。虽然目前尚不清楚双膦酸盐使用在这种关系中的作用,但临床医生在管理这些患者时应考虑到这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67cf/10946469/c46f1b11071a/JBMR-38-896-g001.jpg

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