Henderson R C, Lin P P, Greene W B
University of North Carolina at Chapel Hill 27599-7055, USA.
J Bone Joint Surg Am. 1995 Nov;77(11):1671-81. doi: 10.2106/00004623-199511000-00005.
Bone-mineral density was studied in a heterogeneous group of 139 children (mean age, nine years; range, three to fifteen years) who had spastic cerebral palsy. The evaluation included serum analyses and a nutritional assessment based on a dietary history and anthropometric measurements. The bone-mineral density of the proximal parts of the femora and the lumbar spine was measured with dual-energy x-ray absorptiometry and was normalized for age against a series of ninety-five normal children and adolescents who served as controls. Bone-mineral density varied greatly but averaged nearly one standard deviation below the age-matched normal means for both the proximal parts of the femora (-0.92 standard deviation) and the lumbar spine (-0.80 standard deviation). Ambulatory status was the factor that best correlated with bone-mineral density. Nutritional status, assessed on the basis of caloric intake, skinfolds, and body-mass index, was the second most significant variable. The pattern of involvement, durations of immobilization in a cast, and a calcium intake of less than 500 milligrams per day were additional factors of less significance. The age when the child first walked, previous fractures, use of anticonvulsants, and serum vitamin-D levels did not correlate with bone-mineral density after adjustment for covariance with the ambulatory status and the nutritional status. Serum levels of calcium, phosphate, alkaline phosphatase, and osteocalcin were not reliable indicators of low bone-mineral density.
对139名患有痉挛性脑瘫的儿童(平均年龄9岁,范围3至15岁)这一异质性群体进行了骨密度研究。评估包括血清分析以及基于饮食史和人体测量的营养评估。使用双能X线吸收法测量股骨近端和腰椎的骨密度,并针对一系列95名作为对照的正常儿童和青少年按年龄进行标准化。骨密度差异很大,但股骨近端(-0.92标准差)和腰椎(-0.80标准差)的平均水平比年龄匹配的正常均值低近一个标准差。行走状态是与骨密度最相关的因素。基于热量摄入、皮褶厚度和体重指数评估的营养状况是第二显著变量。受累模式、石膏固定的持续时间以及每日钙摄入量低于500毫克是其他不太重要的因素。在对行走状态和营养状况进行协方差调整后,儿童首次行走的年龄、既往骨折史、抗惊厥药的使用以及血清维生素D水平与骨密度均无相关性。血清钙、磷、碱性磷酸酶和骨钙素水平不是低骨密度的可靠指标。