Generalized Joint Hypermobility Is Associated with Type-A Hip Dysplasia in Patients Undergoing Periacetabular Osteotomy.

IF 4.4 1区 医学 Q1 ORTHOPEDICS
Hangyu Ping, Xiangpeng Kong, Hong Zhang, Dianzhong Luo, Qing Jiang, Wei Chai
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引用次数: 0

Abstract

Background: Joint hypermobility may be associated with developmental dysplasia of the hip (DDH), but no definite conclusion has been reached. On the basis of long-term clinical observations, we hypothesized that joint hypermobility was associated with the occurrence, imaging findings, and clinical symptoms of DDH.

Methods: We conducted a case-control study that included 175 Chinese Han patients between 13 and 45 years of age with Hartofilakidis type-A hip dysplasia. All of these patients underwent periacetabular osteotomy (PAO) between November 2021 and February 2023. An additional 76 individuals of comparable age and sex but without hip dysplasia were selected from the general population to serve as healthy controls. The Beighton 9-point scoring system was used to evaluate joint hypermobility, and a score of ≥4 was defined as generalized joint hypermobility. Standing anteroposterior pelvic radiographs were reviewed. For patients with DDH, the lateral center-edge angle, Tönnis angle, Sharp angle, lateralization of the femoral head, and patient-reported outcomes (iHOT-12, HHS, and WOMAC) were also collected to determine the radiographic severity or clinical symptoms of DDH.

Results: Patients with DDH had an elevated prevalence of generalized joint hypermobility compared with that in the healthy population (27% versus 12%; p = 0.009). Among patients with DDH, those with concomitant generalized joint hypermobility had lower lateral center-edge angles (3.55° versus 9.36°; p = 0.012), greater lateralization of the femoral head (13.78 versus 12.17 mm; p = 0.020), greater standardized lateralization of the femoral head (0.64 versus 0.54; p = 0.009), and lower iHOT-12 scores (35.22 versus 40.96; p = 0.009) than did those without concomitant generalized joint hypermobility. Further multivariable linear regression analysis revealed that higher Beighton scores and younger age were predictive of more severe hip dysplasia. However, the Beighton score was not found to be independently associated with patient-reported outcomes according to multivariable linear regression analysis.

Conclusions: The prevalence of generalized joint hypermobility was greater in patients with DDH than in healthy controls. A higher degree of joint hypermobility was also correlated with more severe hip dysplasia. These results suggest that joint laxity, in addition to bone or cartilage factors, is an important factor related to DDH.

Level of evidence: Prognostic Level III . See Instructions for Authors for a complete description of levels of evidence.

接受髋关节周围截骨术的患者全身关节过度活动与 A 型髋关节发育不良有关。
背景:关节过度活动可能与髋关节发育不良(DDH)有关,但尚未得出明确结论。根据长期的临床观察,我们假设关节活动度过大与 DDH 的发生、影像学检查结果和临床症状有关:我们进行了一项病例对照研究,纳入了 175 名年龄在 13 至 45 岁之间、患有 Hartofilakidis A 型髋关节发育不良的中国汉族患者。所有这些患者都在 2021 年 11 月至 2023 年 2 月期间接受了髋臼周围截骨术(PAO)。另外还从普通人群中挑选了76名年龄和性别相当但没有髋关节发育不良的患者作为健康对照组。采用Beighton 9点评分法评估关节活动度过大,得分≥4分为全身关节活动度过大。对站立位前正位骨盆X光片进行复查。对于DDH患者,还收集了外侧中心边缘角、Tönnis角、Sharp角、股骨头外侧化和患者报告结果(iHOT-12、HHS和WOMAC),以确定DDH的影像学严重程度或临床症状:结果:与健康人群相比,DDH患者的全身关节活动度增高(27%对12%;P = 0.009)。在DDH患者中,伴有全身关节活动过度的患者外侧中心-边缘角度较低(3.55°对9.36°;p = 0.012),股骨头外侧化程度较高(13.78 mm对12.17 mm;p = 0.020)、更大的股骨头标准化外侧化(0.64 对 0.54;p = 0.009)以及更低的 iHOT-12 评分(35.22 对 40.96;p = 0.009)。进一步的多变量线性回归分析表明,Beighton评分越高、年龄越小,髋关节发育不良的程度越严重。然而,根据多变量线性回归分析,Beighton评分与患者报告的结果并无独立关联:结论:与健康对照组相比,DDH患者全身关节过度活动的发生率更高。结论:与健康对照组相比,DDH患者全身关节活动度过大的比例更高,关节活动度过大还与更严重的髋关节发育不良相关。这些结果表明,除了骨或软骨因素外,关节松弛也是与DDH相关的一个重要因素:预后III级。有关证据级别的完整描述,请参阅《作者须知》。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.90
自引率
7.50%
发文量
660
审稿时长
1 months
期刊介绍: The Journal of Bone & Joint Surgery (JBJS) has been the most valued source of information for orthopaedic surgeons and researchers for over 125 years and is the gold standard in peer-reviewed scientific information in the field. A core journal and essential reading for general as well as specialist orthopaedic surgeons worldwide, The Journal publishes evidence-based research to enhance the quality of care for orthopaedic patients. Standards of excellence and high quality are maintained in everything we do, from the science of the content published to the customer service we provide. JBJS is an independent, non-profit journal.
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