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成骨不全症患者的骨密度与听力损失的相关性研究。

Association between bone mineral density and hearing loss in osteogenesis imperfecta.

机构信息

Department of Otorhinolaryngology, Unit for Osteoporosis, Ghent University Hospital, Ghent, Belgium.

出版信息

Laryngoscope. 2012 Feb;122(2):401-8. doi: 10.1002/lary.22408. Epub 2012 Jan 17.

Abstract

OBJECTIVES/HYPOTHESIS: Osteogenesis imperfecta (OI) is a heritable connective tissue disorder, predominantly characterized by bone fragility. In half of the patients, progressive hearing loss develops, which is associated with abnormal bony changes involving the middle ear ossicles and stapes footplate. In the present study, we investigated whether the development of hearing loss in OI may be related to the overall aberrant bone quality.

STUDY DESIGN

Observational study.

METHODS

Following audiologic evaluation, 56 adult OI patients were classified as presenting normal hearing or conductive/mixed or pure sensorineural hearing loss. Areal bone mineral density (BMD) (aBMD) was measured using lumbar spine (LS) and whole body (WB) dual X-ray absorptiometry. By means of peripheral computed tomography, volumetric BMD (vBMD) and morphometric bone parameters were determined at distal and proximal radius, providing separate results for trabecular and cortical bone. The obtained bone parameters were compared between normal-hearing OI patients and those with either conductive/mixed or pure sensorineural hearing loss.

RESULTS

Z scores demonstrated decreased LS aBMD, WB aBMD, and trabecular vBMD in OI adults compared to the healthy population. Patients with conductive/mixed hearing loss had lower trabecular vBMD compared to those with normal hearing or pure sensorineural loss at both whole-group and between-relatives comparisons.

CONCLUSIONS

It is hypothesized that OI patients with lower BMD might be more susceptible to accumulating microfractures, which may interfere with the bone remodeling inhibition pathways in the temporal bone and, therefore, contribute to stapes footplate fixation and a conductive hearing loss component.

摘要

目的/假设:成骨不全症(OI)是一种遗传性结缔组织疾病,主要表现为骨骼脆弱。在一半的患者中,会出现进行性听力损失,这与中耳听小骨和镫骨底板的异常骨改变有关。在本研究中,我们研究了 OI 患者听力损失的发展是否与整体异常骨质量有关。

研究设计

观察性研究。

方法

在进行听力评估后,将 56 名成年 OI 患者分为听力正常、传导性/混合性或纯感音神经性听力损失。使用腰椎(LS)和全身(WB)双能 X 线吸收仪测量面积骨矿物质密度(aBMD)。通过外周计算机断层扫描,在桡骨远端和近端测量体积骨矿物质密度(vBMD)和形态学骨参数,为骨小梁和皮质骨分别提供结果。将正常听力 OI 患者与传导性/混合性或纯感音神经性听力损失患者的骨参数进行比较。

结果

与健康人群相比,OI 成人的 LS aBMD、WB aBMD 和骨小梁 vBMD 的 Z 分数降低。在整体组和亲属间比较中,传导性/混合性听力损失患者的骨小梁 vBMD 均低于正常听力或纯感音神经性听力损失患者。

结论

我们假设 BMD 较低的 OI 患者可能更容易出现微骨折,这可能会干扰颞骨中的骨重塑抑制途径,从而导致镫骨底板固定和传导性听力损失成分。

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