成骨不全症的成像:我们的现状和未来。

IF 1.6 4区 医学 Q3 GENETICS & HEREDITY
S. Gazzotti , R. Sassi , M.P. Aparisi Gómez , A. Moroni , E. Brizola , M. Miceli , A. Bazzocchi
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引用次数: 0

摘要

成骨不全症(OI)是一种罕见的表型和遗传异质性遗传性骨骼发育不良。成骨不全症的特征包括骨质脆弱、易骨折、骨骼畸形、生长发育减慢,以及大量相关的继发性特征(包括骨骼和骨骼外)。目前,骨质疏松症的诊断主要依据临床表现,也可通过基因检测进行确诊。然而,影像学检查仍是评估该疾病的关键。本文旨在回顾目前各种放射技术在产后OI诊断和监测中发挥的作用,并讨论OI影像学的最新进展和未来展望。传统 X 射线照相术和双能 X 射线吸收测定法(DXA)是目前在 OI 中最常用的两种成像模式。骨质疏松症的主要影像学特征包括全身骨质疏松/骨质疏松症、骨畸形和骨折。DXA 是目前评估骨矿密度(BMD),特别是骨矿密度面积(aBMD)最有效的技术。然而,DXA 有很大的局限性,无法根据 aBMD 全面描述 OI 骨质脆弱的特征。新的 DXA 衍生参数(如骨小梁评分 (TBS))可进一步揭示 OI 引起的骨骼变化,但证据仍然有限。计算机断层扫描(CT)和磁共振成像(MRI)等技术可作为解决问题的方法或在特定情况下发挥作用,包括评估颅颈异常。最近的证据支持使用高分辨率外周定量计算机断层扫描(HR-pQCT)作为一种有前途的工具,以改进对 OI 骨脆性的描述。然而,HR-pQCT 目前仍主要是一种研究技术。定量计算机断层扫描(QCT)是测定中心部位 BMD 的 DXA 的替代方法,具有明显的优势,但辐射量要高得多。定量超声(QUS)是一种便携、廉价、无辐射的模式,可作为 DXA 评估的补充,提供有关骨质的信息。然而,QUS 在 OI 中的实用性证据尚不充分。射频超声多谱勒(REMS)是一种新兴的非电离成像方法,有望用于诊断低 BMD 和预测骨折风险,但迄今为止仅有一项已发表的研究对其在 OI 中的作用进行了调查。总之,几种不同的放射学技术已被证明可有效诊断和监测 OI,但每种技术都有其自身的特异性和特殊性。临床医生应了解各种方式在患者治疗过程的不同阶段所发挥的战略作用。在这种情况下,制定国际指南,包括关于成像在诊断和监测 OI 中的作用的建议,同时在该领域开展持续积极的研究,可大大提高患者护理的标准化程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Imaging in osteogenesis imperfecta: Where we are and where we are going

Osteogenesis imperfecta (OI) is a rare phenotypically and genetically heterogeneous group of inherited skeletal dysplasias. The hallmark features of OI include bone fragility and susceptibility to fractures, bone deformity, and diminished growth, along with a plethora of associated secondary features (both skeletal and extraskeletal). The diagnosis of OI is currently made on clinical grounds and may be confirmed by genetic testing. However, imaging remains pivotal in the evaluation of this disease. The aim of this article is to review the current role played by the various radiologic techniques in the diagnosis and monitoring of OI in the postnatal setting as well as to discuss recent advances and future perspectives in OI imaging. Conventional Radiography and Dual-energy X-ray Absorptiometry (DXA) are currently the two most used imaging modalities in OI. The cardinal radiographic features of OI include generalized osteopenia/osteoporosis, bone deformities, and fractures. DXA is currently the most available technique to assess Bone Mineral Density (BMD), specifically areal BMD (aBMD). However, DXA has important limitations and cannot fully characterize bone fragility in OI based on aBMD. Novel DXA-derived parameters, such as Trabecular Bone Score (TBS), may provide further insight into skeletal changes induced by OI, but evidence is still limited. Techniques like Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) can be useful as problem-solvers or in specific settings, including the evaluation of cranio-cervical abnormalities. Recent evidence supports the use of High-Resolution peripheral Quantitative Computed Tomography (HR-pQCT) as a promising tool to improve the characterization of bone fragility in OI. However, HR-pQCT remains a primarily research technique at present. Quantitative Computed Tomography (QCT) is an alternative to DXA for the determination of BMD at central sites, with distinct advantages but considerably higher radiation exposure. Quantitative Ultrasound (QUS) is a portable, inexpensive, and radiation-free modality that may complement DXA evaluation, providing information on bone quality. However, evidence of usefulness of QUS in OI is poor. Radiofrequency Echographic Multi Spectrometry (REMS) is an emerging non-ionizing imaging method that holds promise for the diagnosis of low BMD and for the prediction of fracture risk, but so far only one published study has investigated its role in OI. To conclude, several different radiologic techniques have proven to be effective in the diagnosis and monitoring of OI, each with their own specificities and peculiarities. Clinicians should be aware of the strategic role of the various modalities in the different phases of the patient care process. In this scenario, the development of international guidelines including recommendations on the role of imaging in the diagnosis and monitoring of OI, accompanied by continuous active research in the field, could significantly improve the standardization of patient care.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
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