Division of Neurosurgery, Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA.
J Neurosurg Spine. 2012 Jul;17(1):57-60. doi: 10.3171/2012.3.SPINE11735. Epub 2012 Apr 27.
Spinopelvic parameters in children with achondroplasia have not been described. Because they observed a unique sagittal spinopelvic phenotype in some achondroplastic children with very horizontal sacrums, the authors sought to quantify the spinopelvic parameters in a pediatric patient population.
A retrospective review was performed to identify all children (age range 1 month-10 years) with a diagnosis of achondroplasia between 2004 and 2009. Clinical and radiographic data were analyzed for age, sex, lumbar lordosis (LL), thoracic kyphosis (TK), thoracolumbar kyphosis (TLK), sacral slope (SS), pelvic tilt (PT), and pelvic incidence (PI). Differences among these variables were analyzed using a 2-tailed, unpaired Student t-test.
Forty children, 23 males and 17 females, with achondroplasia were identified during the study period. The mean age was 2.6 years. Two groups of patients were identified based on PT (that is, negative or positive tilt and horizontal or not horizontal sacrum). A negative PT was identified in all children with an extremely horizontal sacrum. Seventeen children had a negative PT (mean -16.6°), and the mean parameters in this group were 65.4° for LL, 31.7° for TLK, 18.5° for TK, 43.3° for SS, and 26.4° for PI. Twenty-three children had a positive PT (mean 17.9°), and the mean parameters in this group were 53.4° for LL, 41.5° for TLK, 9.6° for TK, 30.8° for SS, and 43.8° for PI. A statistically significant difference was observed for LL (p = 0.01), TLK (p = 0.05), SS (p = 0.006), PT (p = 0.006), and PI (0.0002).
Spinopelvic parameters in achondroplasia are potentially dichotomous. The future implications of this observation are not known and will need to be explored in future long-term studies that follow pediatric patients with achondroplasia through adulthood.
软骨发育不全患儿的脊柱骨盆参数尚未描述。由于作者观察到一些软骨发育不全患儿的骶骨非常水平,存在独特的矢状位脊柱骨盆表型,因此作者试图对儿科患者人群的脊柱骨盆参数进行量化。
回顾性分析 2004 年至 2009 年间诊断为软骨发育不全的所有儿童(年龄 1 个月至 10 岁)。分析临床和影像学数据,包括年龄、性别、腰椎前凸角(lordosis,LL)、胸椎后凸角(kyphosis,TK)、胸腰椎后凸角(thoracolumbar kyphosis,TLK)、骶骨倾斜角(sacral slope,SS)、骨盆倾斜角(pelvic tilt,PT)和骨盆入射角(pelvic incidence,PI)。使用双侧、非配对学生 t 检验分析这些变量之间的差异。
在研究期间,共确定了 40 名软骨发育不全患儿,其中男 23 名,女 17 名。平均年龄为 2.6 岁。根据 PT(即负倾斜或正倾斜和水平或非水平骶骨)将患者分为两组。所有骶骨极度水平的患儿均存在负 PT。17 名患儿存在负 PT(平均-16.6°),该组的平均参数为 65.4°的 LL、31.7°的 TLK、18.5°的 TK、43.3°的 SS 和 26.4°的 PI。23 名患儿存在正 PT(平均 17.9°),该组的平均参数为 53.4°的 LL、41.5°的 TLK、9.6°的 TK、30.8°的 SS 和 43.8°的 PI。在 LL(p=0.01)、TLK(p=0.05)、SS(p=0.006)、PT(p=0.006)和 PI(0.0002)方面,差异有统计学意义。
软骨发育不全患儿的脊柱骨盆参数可能是二分的。这种观察结果的未来意义尚不清楚,需要在未来的长期研究中进一步探索,该研究将通过成年期跟踪软骨发育不全患儿来随访儿科患者。