Park Kwang-Won, Kim Jung-Hyun, Sung Sam, Lee Min Young, Song Hae-Ryong
*Institute for Rare Diseases and Department of Orthopaedic Surgery, Korea University Medical Center, Guro Hospital, Seoul †Pohang St.Mary's Hospital, Pohang, Korea.
J Pediatr Orthop. 2014 Oct-Nov;34(7):738-42. doi: 10.1097/BPO.0000000000000172.
Determining the skeletal age in patients with multiple epiphyseal dysplasia (MED) is essential for predicting the adult height and guiding the timing of limb lengthening, epiphysiodesis, and other surgical procedures. In the present study, we examined the patterns of skeletal age delay using 3 different methods, the Greulich-Pyle (GP) atlas method, the Tanner-Whitehouse 3 (TW3) method using radius-ulna-short bones (RUS) scoring system, and the TW3 method using the carpal bone maturity scoring system.
Left hand radiographs from 23 patients (age range, 3 to 14 y) with MED were examined to determine the skeletal age. We examined the reliability of the 3 different methods and evaluated the difference between the chronological age and the skeletal age.
The interobserver and intraobserver reliabilities were higher with the GP atlas method and the TW3 RUS method compared with the TW3 carpal bone maturity scoring system. There was significant skeletal age delay irrespective of the method used (P<0.01). When we used the TW3 carpal method, the pattern of skeletal age delay was significantly distinct from the other 2 methods. According to the measurement method, there was no statistically significant difference in the developmental skeletal age pattern among the COMP gene group, the MATN3 gene group, and other gene groups.
Our findings indicate that there is a distinct skeletal maturation pattern in patients with MED. The skeletal age is relatively delayed compared with the chronological age irrespective of the measuring method utilized. However, use of either the GP atlas or the TW3 RUS method provided more accurate information on the skeletal development in the patients with MED than that provided by the TW3 carpal bone maturity scoring system.
Level I. Diagnostic study.
确定多发性骨骺发育不良(MED)患者的骨骼年龄对于预测成人身高以及指导肢体延长、骨骺阻滞和其他外科手术的时机至关重要。在本研究中,我们使用3种不同方法检查了骨骼年龄延迟的模式,即格鲁利希-派尔(GP)图谱法、使用桡骨-尺骨-短骨(RUS)评分系统的坦纳-怀特豪斯3(TW3)法以及使用腕骨成熟度评分系统的TW3法。
对23例年龄在3至14岁之间的MED患者的左手X线片进行检查以确定骨骼年龄。我们检查了这3种不同方法的可靠性,并评估了实际年龄与骨骼年龄之间的差异。
与TW3腕骨成熟度评分系统相比,GP图谱法和TW3 RUS法的观察者间和观察者内可靠性更高。无论使用何种方法,骨骼年龄均有显著延迟(P<0.01)。当我们使用TW3腕骨法时,骨骼年龄延迟模式与其他2种方法显著不同。根据测量方法,COMP基因组、MATN3基因组和其他基因组之间的发育骨骼年龄模式无统计学显著差异。
我们的研究结果表明,MED患者存在独特的骨骼成熟模式。无论采用何种测量方法,骨骼年龄相对于实际年龄均相对延迟。然而,与TW3腕骨成熟度评分系统相比,使用GP图谱法或TW3 RUS法能提供关于MED患者骨骼发育更准确的信息。
I级。诊断性研究。