Bone mass and density in preadolescent boys with and without Down syndrome

被引:22
作者
Wu, J. [1 ]
机构
[1] Georgia State Univ, Dept Kinesiol & Hlth, Atlanta, GA 30302 USA
关键词
Bone mass; Bone mineral density; Down syndrome; DXA; Lumbar spine; Whole body; X-RAY ABSORPTIOMETRY; MINERAL DENSITY; VOLUMETRIC DENSITY; MENTAL-RETARDATION; GROWTH CHARTS; YOUNG MEN; CHILDREN; DENSITOMETRY; PROGRAM; ADOLESCENTS;
D O I
10.1007/s00198-013-2393-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Preadolescent boys with Down syndrome at 7-10 years of age have lower bone mass and density in the pelvis than age-matched children without Down syndrome. However, bone mass and density of total body less head and lumbar spine are not different between these two groups. This study aimed to assess bone mineral content (BMC) and density (BMD) in preadolescent boys with and without Down syndrome (DS) at 7-10 years of age. Eleven preadolescent boys with DS and eleven age-matched children without DS participated in this study. Dual-energy X-ray absorptiometry was used to measure BMC and BMD in whole body and lumbar spine. Both BMC and BMD of total body less head (TBLH) and lumbar spine (vertebrae L2-L4) were compared between the two groups, with and without adjusting for physical characteristics such as bone area, body height, and total lean mass. Two bone mineral apparent density (BMAD) variables were calculated to estimate volumetric BMD in the lumbar spine. Both BMC and BMD in the pelvis were lower in the DS group, after adjusting for physical characteristics. However, with and without adjusting for physical characteristics, the two groups were not different in BMC and BMD of the arms, legs, and TBLH from the whole body scan and in BMC, BMD, and BMAD of the lumbar spine from the lumbar spine scan. These findings indicate that the pelvis may be the first site to show the significant difference in BMC and BMD between preadolescent boys with and without DS. It also suggests that significantly lower BMC and BMD in whole body and lumbar spine, which is usually observed in young adults with DS, may not occur before adolescence.
引用
收藏
页码:2847 / 2854
页数:8
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