Ltaief-Boudrigua Aïcha, Lina-Granade Genevieve, Truy Eric, Hermann Ruben, Chevrel Guillaume
Department of Radiology, Edouard Herriot Hospital, Hospices Civils de Lyon, 69003 Lyon, France.
Department of Oto-Rhino-Laryngology, Head and Neck Surgery, Edouard Herriot Hospital, Hospices Civils de Lyon, 69003 Lyon, France.
J Clin Med. 2022 Apr 13;11(8):2171. doi: 10.3390/jcm11082171.
To determine whether temporal bone computed tomography (CT) features are linked to the presence and type of hearing loss in osteogenesis imperfecta (OI) when considering hearing-impaired OI patients and normally hearing (NH) OI ones. A secondary objective was to assess whether other factors influence CT features in a large sample: age, type of mutation, or bone mineral density (BMD).
A total of 41 adults with OI underwent CTs and pure-tone audiometry in 82 ears. Hearing thresholds were normal in 64 out of 82 ears, and most had not been operated on for stapedectomy or stapedotomy. Ossicle density, footplates, oval and round windows, retrofenestral peri- and endolabyrinths, and temporal pneumatization were analyzed twice by an experienced radiologist. CT features were compared to hearing, age, collagen mutations, and bone mineral density.
Unexpectedly a high prevalence of footplate, ossicle, and otic capsule anomalies was observed, even in NH ears. Footplate hypodensity or thickening was mostly found in ears without conductive hearing loss. There were significantly more retrofenestral anomalies or window obstruction in ears with a sensorineural hearing loss component than in ears without. Age was significantly higher in ears with middle layer hypodensity than in ears without. Patients with mutations were expected to have reduced collagen quantity and had significantly more footplate or retrofenestral anomalies than those with qualitative mutations. BMD was significantly higher in ears without temporal hyperpneumatization.
Temporal bone CT features in OI are present in a large proportion of patients, had they hearing loss or not, and might be determined more by collagen mutation type than by age or BMD.
在考虑听力受损的成骨不全(OI)患者和听力正常(NH)的OI患者时,确定颞骨计算机断层扫描(CT)特征是否与OI患者听力损失的存在及类型相关。第二个目的是在一个大样本中评估其他因素是否影响CT特征:年龄、突变类型或骨矿物质密度(BMD)。
共有41例成年OI患者接受了CT检查和82耳的纯音听力测定。82耳中有64耳听力阈值正常,且大多数未接受过镫骨切除术或镫骨造孔术。一位经验丰富的放射科医生对听小骨密度、镫骨底板、椭圆窗和圆窗、窗后周围及内迷路以及颞骨气化进行了两次分析。将CT特征与听力、年龄、胶原蛋白突变和骨矿物质密度进行比较。
出乎意料的是,即使在听力正常的耳中也观察到镫骨底板、听小骨和耳囊异常的高患病率。镫骨底板低密度或增厚多见于无传导性听力损失的耳中。与无感音神经性听力损失成分的耳相比,有感音神经性听力损失成分的耳中窗后异常或窗阻塞明显更多。中层低密度的耳中年龄显著高于无中层低密度的耳。预期有突变的患者胶原蛋白量减少,与有定性突变的患者相比,其镫骨底板或窗后异常明显更多。无颞骨过度气化的耳中骨矿物质密度显著更高。
OI患者颞骨CT特征在很大比例的患者中存在,无论他们是否有听力损失,并且可能更多地由胶原蛋白突变类型而非年龄或骨矿物质密度决定。