{"title":"Osteogenesis imperfecta.","authors":"Antonella Forlino, Joan C Marini","doi":"10.1016/S0140-6736(15)00728-X","DOIUrl":null,"url":null,"abstract":"<p><p>Osteogenesis imperfecta is a phenotypically and molecularly heterogeneous group of inherited connective tissue disorders that share similar skeletal abnormalities causing bone fragility and deformity. Previously, the disorder was thought to be an autosomal dominant bone dysplasia caused by defects in type I collagen, but in the past 10 years discoveries of novel (mainly recessive) causative genes have lent support to a predominantly collagen-related pathophysiology and have contributed to an improved understanding of normal bone development. Defects in proteins with very different functions, ranging from structural to enzymatic and from intracellular transport to chaperones, have been described in patients with osteogenesis imperfecta. Knowledge of the specific molecular basis of each form of the disorder will advance clinical diagnosis and potentially stimulate targeted therapeutic approaches. In this Seminar, together with diagnosis, management, and treatment, we describe the defects causing osteogenesis imperfecta and their mechanism and interrelations, and classify them into five groups on the basis of the metabolic pathway compromised, specifically those related to collagen synthesis, structure, and processing; post-translational modification; folding and cross-linking; mineralisation; and osteoblast differentiation. </p>","PeriodicalId":15225,"journal":{"name":"Journal of Central South University of Technology","volume":"11 1","pages":"1657-71"},"PeriodicalIF":0.0000,"publicationDate":"2016-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384887/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Central South University of Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/S0140-6736(15)00728-X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/11/3 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
成骨不全症是一组表型和分子异质性的遗传性结缔组织疾病,它们都有类似的骨骼异常,导致骨脆性和畸形。以前,这种疾病被认为是由 I 型胶原缺陷引起的常染色体显性骨发育不良,但在过去 10 年中,新致病基因(主要是隐性致病基因)的发现为主要与胶原相关的病理生理学提供了支持,并有助于加深对正常骨骼发育的理解。成骨不全症患者体内的蛋白质功能缺陷各不相同,有的具有结构性功能,有的具有酶性功能,有的具有细胞内转运功能,有的具有伴侣功能。了解每种形式的成骨不全症的具体分子基础将有助于临床诊断,并有可能激发有针对性的治疗方法。在本讲座中,我们结合诊断、管理和治疗,描述了导致成骨不全症的缺陷及其机制和相互关系,并根据受损的代谢途径将其分为五组,具体涉及胶原合成、结构和加工;翻译后修饰;折叠和交联;矿化;以及成骨细胞分化。
Osteogenesis imperfecta is a phenotypically and molecularly heterogeneous group of inherited connective tissue disorders that share similar skeletal abnormalities causing bone fragility and deformity. Previously, the disorder was thought to be an autosomal dominant bone dysplasia caused by defects in type I collagen, but in the past 10 years discoveries of novel (mainly recessive) causative genes have lent support to a predominantly collagen-related pathophysiology and have contributed to an improved understanding of normal bone development. Defects in proteins with very different functions, ranging from structural to enzymatic and from intracellular transport to chaperones, have been described in patients with osteogenesis imperfecta. Knowledge of the specific molecular basis of each form of the disorder will advance clinical diagnosis and potentially stimulate targeted therapeutic approaches. In this Seminar, together with diagnosis, management, and treatment, we describe the defects causing osteogenesis imperfecta and their mechanism and interrelations, and classify them into five groups on the basis of the metabolic pathway compromised, specifically those related to collagen synthesis, structure, and processing; post-translational modification; folding and cross-linking; mineralisation; and osteoblast differentiation.