Bone mineral density in children and adolescents with neurofibromatosis type 1

被引:99
作者
Stevenson, David A.
Moyer-Mileur, Laurie J.
Murray, Mary
Slater, Hillarie
Sheng, Xiaoming
Carey, John C.
Dube, Bukhosi
Viskochil, David H.
机构
[1] Univ Utah, Dept Pediat, Div Med Genet, Salt Lake City, UT 84132 USA
[2] Univ Utah, Dept Family & Prevent Med, Salt Lake City, UT 84132 USA
关键词
GENE POLYMORPHISMS; DESCRIPTIVE ANALYSIS; YOUNG; GEOMETRY; SIZE; NF1;
D O I
10.1016/j.jpeds.2006.10.048
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective To assess whether children and adolescents with neurofibromatosis type I (NF1) have decreased bone mineral density (BNID). Study design Bone densitometry of the whole body, flip, and lumbar spine was used in a case-to-control design (84 individuals with NF1:293 healthy individuals without NF1). Subjects were 5 to 18 years old. Subjects with NF1 were compared with control subjects by using an analysis-of-covariance with a fixed set of covariates (age, weight, height, Tanner stage, and sex). Results Subjects with NF1 had decreased areal BMD (aBMD) of the hip (P < .0001), femoral neck (P < .0001), lumbar spine (P = .0025). and whole body subtotal (P < .0001). When subjects with NF1 were separated in groups with and without a skeletal abnormality. those who did not have a skeletal abnormality still had statistically significant decreases in aBMD compared with control subjects (P < .0001 for whole body subtotal aBMD), although they were less pronounced than in those with osseous abnormalities. Conclusions These data suggest that individuals with NF1 have a unique generalized skeletal dysplasia, predisposing them to localized osseous defects. Dual energy x-ray absorptiometry may prove useful in identifying individuals with NF1 who are at risk for clinical osseous complications and monitoring therapeutic trials.
引用
收藏
页码:83 / 88
页数:6
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