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Reproducibility of DXA measurements of bone mineral density and body composition in children

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Abstract

Background

The technique of X-ray-based dual photon absorptiometry (DXA) is frequently used in children for the detection of changes in bone mass or body composition. Such changes can only be considered real if the uncertainties arising from the measurement technique are exceeded.

Objective

Our objectives were twofold: (1) to determine the reproducibility of bone mineral density (BMD) measurements in children at the spine and the hip and from the whole body, as well as of whole-body measurements of mineral mass, lean body mass and fat mass in children; and (2) to estimate, from the measured precision, the time interval that needs to elapse before a statistically significant change in a DXA variable can be detected.

Materials and methods

The reproducibility of techniques for the measurement of BMD and body composition using DXA was measured in 15 young children (9 girls and 6 boys) and 17 older children (9 girls and 8 boys).

Results

Reproducibility was derived from the standard deviation of three repeated measurements of spine BMD, total hip BMD, whole-body BMD (WBBMD), whole-body bone mineral content (WBBMC), lean mass and fat mass. Technique precision was better than 0.01 g cm−2 for spine BMD and for WBBMD. Hip BMD measurements were slightly less precise, particularly in younger children (0.013 g cm−2). For body composition variables, technique precision was 13 g for WBBMC, 201 g for lean body mass and 172 g for fat mass in younger children. Technique precision for older children was 18 g, 251 g and 189 g for the corresponding variables. Predictions showed that the absence of a normal increase in WBBMC in a small-for-age girl could be established after 12 months. For spine BMD, a significant increase should be observable after 6 months for boys over the age of 11 years. For younger boys, more than 12 months has to elapse before anticipated changes can be detected with confidence.

Conclusion

The time intervals required to elapse before decisions can be made concerning the significance of observed differences between successive measurements of BMD or body composition in children depend upon the age of the child.

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Correspondence to Colin E. Webber.

Appendix: derivation of DXA reproducibility

Appendix: derivation of DXA reproducibility

Recommended procedures for the evaluation of reproducibility with DXA require repeated measurements on phantoms or human volunteers; reproducibility or precision is given by the standard deviation of the series of measurements. When a phantom is used as the test object, the standard deviation will not include any contribution from subject positioning. Short-term precision is the reproducibility calculated from measurements repeated immediately after repositioning a subject rather than a phantom. Inevitably, short-term precision will be worse than the precision determined from a phantom. Long-term precision is the reproducibility calculated from subject measurements repeated after intervals approaching or exceeding 1 year. The relevant parameter for clinical application of DXA techniques is the long-term precision. However, because measurement of long-term precision is challenging, common practice is to measure in vivo short-term reproducibility and to evaluate long-term stability of DXA equipment from phantom measurements.

Frequently, the standard deviation is expressed as a percentage of the mean value; that is, the CV. Values of CV for lumbar spine BMD measured in phantoms are typically 0.5%. Short-term precision in adults is normally about 1% while long-term in vivo precision is closer to 2% [11]. In children and in adults with osteoporosis, CV has the disadvantage that reproducibility may appear to be worse simply because BMD is smaller and not because the measurements are less reproducible [12]. For example, if the standard deviation of repeated measurements is 0.01 g cm−2, the short-term precision in adults would be about 1% when expressed as a CV whereas in a 3-year-old child, the same standard deviation would yield a CV of about 2.5%. Precision is also frequently expressed as the ICC, which is the proportion of the variance that can be attributed to the subjects expressed as a fraction of the total variance arising from the technique plus that from the subjects. Consequently, the closer the ICC is to unity, the smaller the technique variance.

In this study, short-term precision for each subject was expressed as the standard deviation of the three measurements for each variable. That is, subject precision is given by:

$$\sqrt {\frac{{\Sigma \left( {x_i - \bar x} \right)^2 }}{{\left( {n - 1} \right)}}} $$

where x i is each of the three measurements for a given variable and \(\bar x\) is the mean of the three measurements. The denominator includes the number of measurements (n=3) and expresses the number of degrees of freedom for each subject. Technique precision (TP) is given by an appropriate combination of the precision determined for each subject. Since it is the subject variances that should be averaged, the technique precision is obtained from:

$$TP = \sqrt {\frac{{\sum {\left( {{\text{subject precision}}} \right)^2 } }}{{\text{N}}}} $$

where N is the number of subjects. In this study, TP was determined for groups of both younger and older children. Confidence intervals for TP were evaluated from the expression:

$$\left[ {\frac{{df \times TP^2 }}{{\chi ^2 }}} \right]^{{\raise0.7ex\hbox{$1$} \!\mathord{\left/{\vphantom {1 2}}\right.\kern-\nulldelimiterspace}\!\lower0.7ex\hbox{$2$}}} $$

where df is the total number of degrees of freedom (=2×N) and χ2 is the critical value corresponding to either the probability of exceeding 97.5% or the critical value for falling below 2.5% of the chi-squared distribution.

Establishment of the technique precision allows the derivation of the smallest difference between successive measurements that can be considered statistically significant at the 95% confidence level [13]. This difference is given by 1.96×(TP2 + TP2)½ and is known as the smallest detectable difference (SDD) or the least significant change (LSC). When applied to BMD, the units of the SDD and the LSC are both grams per centimeter squared.

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Leonard, C.M., Roza, M.A., Barr, R.D. et al. Reproducibility of DXA measurements of bone mineral density and body composition in children. Pediatr Radiol 39, 148–154 (2009). https://doi.org/10.1007/s00247-008-1067-7

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  • DOI: https://doi.org/10.1007/s00247-008-1067-7

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