ICCBH2013 Oral Communications Diagnostics (6 abstracts)
1Childrens Hospital of Philadelphia, Philadelphia, Pennsylvania, USA; 2University of Pennsylvania, Philadelphia, Pennsylvania, USA; 3Cincinnati Childrens Hospital Medical Center, Cincinnati, Ohio, USA; 4Childrens Hospital, Los Angeles, California, USA; 5Creighton University, Omaha, Nebraska, USA; 6Columbia University Medical Center, New York, New York, USA; 7University of California, San Francisco, California, USA; 8National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
Objective: Total body less head (TBLH) and spine are the recommended DXA sites for bone health assessment in children and adolescents. However, inter-machine differences will affect use and interpretation of results in clinical care and research applications. We examined BMC and areal-BMD (aBMD) at 4 skeletal sites among healthy children to identify the magnitude of inter-machine differences in Z-scores.
Methods: BMDCS evaluated healthy participants, ages 520 years, as previously described. All five centers used Hologic devices and scans were analyzed centrally. Data from the first study visit for subjects with complete data for the distal 1/3 radius, hip, spine and and TBLH, and covariates (demographic information, height and BMI Z-score, race, puberty stage, calcium intake and physical activity) were included in the analysis. BMDCS Z-scores for BMC and areal-BMD were calculated, and differences among study centers assessed by ANCOVA adjusting for covariates. Logistic regression assessed the probability of having a BMC or aBMD Z-score ≤−1.5 among centers after adjusting for covariates.
Results: 1889 subjects (48% females, 24% African American, 17% Hispanic, 47% non-Hispanic white, 12% other) were evaluated. There were significant differences in Z-scores adjusted for covariates among study centers for all measures except total hip aBMD Z-score. Differences from the group mean in adjusted Z-scores were lowest for spine and hip measures (−0.14 to 0.14 SDS), and highest for TBLH aBMD (−0.19 to 0.53 SDS). After adjusting for covariates, the probability of having a Z-score ≤−1.5 (expected probability .067) was not significantly different between centers for most skeletal sites, except for TBLH aBMD (probabilities ranged from 0.02 (95% CI: 0.10.04) to 0.09 (95% CI: 0.070.15)).
Conclusions: Spine aBMD and hip measurements showed relatively good agreement between centers. There was wide variation in DXA whole body scan results obtained on healthy children measured on comparable Hologic DXA devices. This can potentially result in misdiagnosis of children with low bone status in clinical care and research. The recommendation of whole body scans as an optimal measurement site in children should be reconsidered.
Support: R01 HD058886, U54 RR024134, N01-HD-1-3331.