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Carmen and Ann Adams Department of Pediatrics, Obstetrics and Gynecology, Wayne State University, Detroit, Michigan (W.W.K.K., M.H.)
Childrens Nutrition Research Center, Baylor College of Medicine, Houston, Texas (R.J.S., K.J.E.)
Address correspondence to: Dr. Winston Koo, Hutzel Hospital, Department of Pediatrics, 4707 St. Antoine Blvd, Detroit MI 48201. E-mail wkoo{at}wayne.edu
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ABSTRACT |
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Methods: Forty-one piglets (6190 +/ 5856g, mean +/ SD) were scanned in duplicate with a fan-beam densitometer (Hologic QDR4500A, Hologic Inc, Bedford, MA) in the infant whole body scan mode. The same scans were analyzed with two software versions: vKH6 (validated with carcass chemical measurement) and v11.2 (commercial software from the same densitometer manufacturer).
Results: All analysis values were highly correlated (r = 0.90 to 1.00) and DXA values for total weights were almost identical. However, v11.2 results consistently overestimated bone mineral content (49.3 +/ 23.4%, mean +/ SD), bone area (21.1 +/ 8.2%), bone mineral density (24.1 +/ 22.2%), and fat mass (160.9 +/ 71.7%) but underestimated lean mass (14.3 +/ 5.5%) when compared to the values from vKH6. Differences between software versions increased with heavier piglets.
Conclusion: The commercial software for fan-beam DXA measurement of piglets, matched for the size of human infants and young children, has major inaccuracies for bone mineral and body composition that become further exaggerated with increasing weight of the subject.
Key words: one, body composition, pig, infant, dual energy X-ray absorptiometry
Abbreviations: DXA = dual energy X-ray absorptiometry
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INTRODUCTION |
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With the older pencil beam DXA technique, different versions of software used for the study of infants and small animals of similar body mass provided different results [5,6]. The development and release of the newer fan beam DXA densitometer also has led to the availability of multiple software versions since the initial prototype (v8.26, Hologic Inc., Bedford, MA), but there are no data to document the validity of the recent software versions for the measurement of infants and small animals of similar body mass.
This study aims to determine the relationship between an independent software version that was validated with carcass chemical analysis with a recent commercial software released by the manufacturer of the same fan beam DXA densitometer. Comparisons were obtained for the measurements of bone mineral mass and soft tissue composition.
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METHODS |
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One investigator (MH) supervised all aspects of scan acquisition and analysis using vKH6, and determined that all scans were free from movement artifacts [7,8]. Analysis of the same scans using v11.2 was independently performed by one investigator (RS) without knowledge of the previous scan results. Of the 82 scans performed for this study, one scan was inadvertently deleted before analysis. For each DXA parameter (total weight, bone mineral content, bone area, bone mineral density, lean mass and fat mass), the values from duplicate total body scans were highly significantly correlated (r = 0.98 to 1.00, p < 0.001 for all comparisons) regardless of the software used for scan analysis. The precision of DXA measurements calculated with the method of Gluer et al [9] for total weight, bone mineral content, bone area, bone mineral density, lean mass and fat mass using the infant whole body vKH6 software were 0.2, 1.9, 1.4, 1.7, 1.0 and 13.1% respectively. The precision results for the corresponding parameters using the scanners infant whole body software v11.2 were 0.2, 2.3, 1.1, 1.5, 1.3 and 6.9% respectively.
Data analysis employed paired t test, and the limits of agreement between the commercial and validated softwares were determined with the Bland and Altman technique [10]. Except for the piglet with a single scan, all analyses were based on the average of the duplicate measurements.
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RESULTS |
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DISCUSSION |
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Similar to the observations with pencil beam DXA measurements in small subjects [5,6], this study demonstrated that the commercial software used with the newer generation fan-beam DXA technique to examine piglets of a size comparable with human infants and young children results in grossly discrepant bone mineral mass and body composition measurements. In an earlier study, we demonstrated that the prototype commercial software version v8.26 could not provide results comparable to the chemical carcass measurements [14]. Thus taken together with the findings in this study, inaccuracies continue to exist in commercial software versions for fan beam DXA measurements of small subjects, although the relative differences among the various upgrades from the prototype v8.26 to the recent v11.2 are not known. Since the physics of the DXA technique is not a priori based on knowing the species being examined, the concerns for bone and soft tissue results are applicable to both animals and humans. Furthermore, the DXA data in the present study were generated under optimal conditions with sedated piglets thereby eliminating any spurious data from movement artifacts [7,8].
Our data also demonstrated that inaccuracies of the v11.2 software version for the fan beam DXA tend to worsen with increasing body weight, thus raising concerns for longitudinal growth studies. The trend towards similar bone mineral density values at larger weights may indicate the improved ability to more accurately detect the bone edge and therefore delineation of bone area. Alternately, a difference in the threshold value for bone detection may result in less noticeable difference as bone mineralization increased in larger piglets. In any case, any improvement in bone mineral density measurements is of minor clinical importance since this measurement in growing subjects is of questionable value [15,16].
With the older but most widely used pencil beam DXA technique in the study of small subjects, the uncritical acceptance by some investigators of the earlier unvalidated versions of the infant software continues to contribute to the conflicting data in the literature [3,7,8]. Unfortunately, subsequent improvements in the software may not be re-applied to the earlier scans because of differences in scan acquisition technique and non-compatibility of software. For the newer fan-beam DXA technique, an examination of our data show that despite the multiple upgrades in software versions from the prototype v8.26 to the v11. 2, there has been no apparent improvement in the analysis algorithm for the infant mode. It is therefore critical that the validity of the various softwares used with the newer generation of fan-beam DXA instruments must be adequately tested before extensive publications of research and clinical data for bone or soft tissue body composition. Furthermore, if updated versions of the software are automatically loaded onto instruments during routine maintenance or repairs, then adequate documentation of the impact of the changes on bone or body composition must be included.
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CONCLUSION |
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ADDENDUM |
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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Received April 14, 2004. Accepted June 11, 2004.
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REFERENCES |
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