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成骨不全症患者上肢的临床、影像学和生物力学评估

Clinical, Radiographic, and Biomechanical Evaluation of the Upper Extremity in Patients with Osteogenesis Imperfecta.

作者信息

Oder Katharina, Unglaube Fabian, Farr Sebastian, Kranzl Andreas, Stauffer Alexandra, Ganger Rudolf, Raimann Adalbert, Mindler Gabriel T

机构信息

Department of Pediatric Orthopaedics, Orthopaedic Hospital Speising, Speisinger Strasse 109, 1130 Vienna, Austria.

Laboratory for Gait and Movement Analysis, Orthopaedic Hospital Speising, Speisinger Strasse 109, 1130 Vienna, Austria.

出版信息

J Clin Med. 2024 Aug 31;13(17):5174. doi: 10.3390/jcm13175174.

Abstract

Osteogenesis imperfecta (OI) is a hereditary disorder primarily caused by mutations in type I collagen genes, resulting in bone fragility, deformities, and functional limitations. Studies on upper extremity deformities and associated functional impairments in OI are limited. This cross-sectional study aimed to evaluate upper extremity deformities and functional outcomes in OI. We included patients regardless of their OI subtypes with a minimum age of 7 years. Radiographic analysis of radial head dislocation, ossification of the interosseous membrane, and/or radioulnar synostosis of the forearm were performed, and deformity was categorized as mild, moderate, or severe. Clinical evaluation was performed using the Quick Disabilities of Arm, Shoulder, and Hand (qDASH) questionnaire and shoulder-elbow-wrist range of motion (ROM). Three-dimensional motion analysis of the upper limb was conducted using the Southampton Hand Assessment Procedure (SHAP). The SHAP quantifies execution time through the Linear Index of Function (LIF) and assesses the underlying joint kinematics using the Arm Profile Score (APS). Additionally, the maximum active Range of Motion (aRoM) was measured. Fourteen patients aged 8 to 73 were included. Radiographic findings revealed diverse deformities, including radial head dislocation, interosseous membrane ossification, and radioulnar synostosis. Six patients had mild, six moderate, and two severe deformities of the upper extremity. Severe deformities and radial head dislocation correlated with compromised ROM and worse qDASH scores. The qDASH score ranged from 0 to 37.5 (mean 11.7). APS was increased, and LIF was reduced in OI-affected persons compared with non-affected peers. APS and LIF also varied depending on the severity of bony deformities. aRoM was remarkably reduced for pro-supination. Patients with OI showed variable functional impairment from almost none to severe during daily life activities, mainly depending on the magnitude of deformity in the upper extremity. Larger multicenter studies are needed to confirm the results of this heterogeneous cohort. Retrospective clinical study; Level IV.

摘要

成骨不全症(OI)是一种遗传性疾病,主要由I型胶原蛋白基因突变引起,导致骨骼脆弱、畸形和功能受限。关于OI患者上肢畸形及相关功能障碍的研究有限。这项横断面研究旨在评估OI患者的上肢畸形和功能结局。我们纳入了年龄最小7岁、不考虑OI亚型的患者。对桡骨头脱位、骨间膜骨化和/或前臂桡尺骨融合进行了影像学分析,并将畸形分为轻度、中度或重度。使用手臂、肩部和手部快速残疾问卷(qDASH)和肩肘腕关节活动范围(ROM)进行临床评估。使用南安普敦手部评估程序(SHAP)对上肢进行三维运动分析。SHAP通过功能线性指数(LIF)量化执行时间,并使用手臂轮廓评分(APS)评估潜在的关节运动学。此外还测量了最大主动活动范围(aRoM)。纳入了14名年龄在8至73岁之间的患者。影像学检查结果显示存在多种畸形,包括桡骨头脱位、骨间膜骨化和桡尺骨融合。6例患者上肢畸形为轻度,6例为中度,2例为重度。严重畸形和桡骨头脱位与ROM受损及更差的qDASH评分相关。qDASH评分范围为0至37.5(平均11.7)。与未受影响的同龄人相比,OI患者的APS升高而LIF降低。APS和LIF也因骨畸形的严重程度而异。旋前-旋后aRoM显著降低。OI患者在日常生活活动中表现出从几乎无到严重程度不等的功能障碍,主要取决于上肢畸形的程度。需要更大规模的多中心研究来证实这个异质性队列的结果。回顾性临床研究;IV级。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/252f/11396301/1472ce1bbde8/jcm-13-05174-g001.jpg

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