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Am J Med Genet A. 2019 Dec;179(12):2393-2419. doi: 10.1002/ajmg.a.61366. Epub 2019 Oct 21.
2
Osteogenesis Imperfecta: New Perspectives From Clinical and Translational Research.成骨不全症:临床与转化研究的新视角
JBMR Plus. 2019 Feb 20;3(8):e10174. doi: 10.1002/jbm4.10174. eCollection 2019 Aug.
3
Mendelian bone fragility disorders.孟德尔遗传性骨脆弱症。
Bone. 2019 Sep;126:11-17. doi: 10.1016/j.bone.2019.04.021. Epub 2019 Apr 27.
4
Endoplasmic reticulum stress is induced in growth plate hypertrophic chondrocytes in G610C mouse model of osteogenesis imperfecta.成骨不全症 G610C 小鼠模型中生长板肥大软骨细胞内质网应激的诱导。
Biochem Biophys Res Commun. 2019 Jan 29;509(1):235-240. doi: 10.1016/j.bbrc.2018.12.111. Epub 2018 Dec 20.
5
Growth characteristics in individuals with osteogenesis imperfecta in North America: results from a multicenter study.北美成骨不全症患者的生长特征:一项多中心研究的结果。
Genet Med. 2019 Feb;21(2):275-283. doi: 10.1038/s41436-018-0045-1. Epub 2018 Jul 4.
6
Bone robusticity in two distinct skeletal dysplasias diverges from established patterns.两种不同骨骼发育不良中的骨强度偏离了既定模式。
J Orthop Res. 2017 Nov;35(11):2392-2396. doi: 10.1002/jor.23543. Epub 2017 May 4.
7
DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum.对598例临床诊断为成骨不全症患者的DNA序列分析:诊断率及突变谱
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8
Osteogenesis imperfecta in children and adolescents-new developments in diagnosis and treatment.儿童和青少年成骨不全症——诊断与治疗的新进展
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10
Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.由COL1A1/COL1A2突变引起的成骨不全症中的脊柱侧弯——基因型-表型相关性及双膦酸盐治疗的效果
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使用掌指骨模式轮廓评估成骨不全症患者的纵向骨生长情况。

Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profiles.

作者信息

Rauch Damian, Robinson Marie-Eve, Seiltgens Cristian, Sutton V Reid, Lee Brendan, Glorieux Francis, Rauch Frank

机构信息

Shriners Hospital for Children and McGill University, Montreal, Quebec, Canada.

Shriners Hospital for Children and McGill University, Montreal, Quebec, Canada; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.

出版信息

Bone. 2020 Nov;140:115547. doi: 10.1016/j.bone.2020.115547. Epub 2020 Jul 27.

DOI:10.1016/j.bone.2020.115547
PMID:32730936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7502481/
Abstract

OBJECTIVE

Osteogenesis imperfecta (OI) is commonly associated with short stature, but it is unclear whether this is exclusively secondary to fractures and bone deformities or whether there is a primary defect in longitudinal bone growth. As metacarpal and phalangeal bones are rarely affected by fractures and deformities, any length deficits in these bones should reflect a direct disease effect on longitudinal growth. This study therefore assessed the relationship of hand bone length with clinical OI type and genotype.

STUDY DESIGN

Prospective study.

RESULTS

The length of all 19 tubular hand bones were measured in 144 individuals (age 6 to 57 years; 68 female) who had OI caused by COL1A1 or COL1A2 variants. Measurements of bone length were converted to z-scores using published reference data. Bone length was mostly normal in OI type I but was significantly decreased in OI types III and IV. Mean hand bone length z-score (i.e., the average length z-score of all 19 bones of a hand) was -0.2 for OI type I, -2.9 for OI type III and -1.2 for OI type IV. Mean hand bone length z-score was positively associated with height z-score (r = 0.65, P < 0.001). Regarding genotype-phenotype correlations, mean hand bone length z-score was close to 0 in individuals with COL1A1 mutations leading to haploinsufficiency but were significantly lower in the presence of mutations leading to triple-helical glycine substitutions in either the alpha 1 or alpha 2 chain of collagen type I.

CONCLUSION

COL1A1 and COL1A2 mutations affect bone growth not only by inducing fractures and bone deformities, but also through longitudinal growth deficits in bones that do not fracture or deform.

摘要

目的

成骨不全(OI)通常与身材矮小有关,但尚不清楚这是否完全继发于骨折和骨畸形,还是纵向骨生长存在原发性缺陷。由于掌骨和指骨很少受到骨折和畸形的影响,这些骨骼的任何长度不足都应反映疾病对纵向生长的直接影响。因此,本研究评估了手部骨骼长度与临床OI类型和基因型的关系。

研究设计

前瞻性研究。

结果

对144例由COL1A1或COL1A2变异导致OI的个体(年龄6至57岁;68名女性)的全部19块手部管状骨长度进行了测量。使用已发表的参考数据将骨长度测量值转换为z分数。I型OI患者的骨长度大多正常,但III型和IV型OI患者的骨长度显著降低。I型OI患者的平均手部骨长度z分数(即一只手所有19块骨头的平均长度z分数)为-0.2,III型OI患者为-2.9,IV型OI患者为-1.2。平均手部骨长度z分数与身高z分数呈正相关(r = 0.65,P < 0.001)。关于基因型-表型相关性,在导致单倍体不足的COL1A1突变个体中,平均手部骨长度z分数接近0,但在导致I型胶原α1或α2链三螺旋甘氨酸替代的突变个体中,该分数显著更低。

结论

COL1A1和COL1A2突变不仅通过引发骨折和骨畸形影响骨生长,还通过未发生骨折或畸形的骨骼的纵向生长不足来影响骨生长。