Collins A L, Saunders S, McCarthy H D, Williams J E, Fuller N J
Department of Health Human Sciences, London Metropolitan University, London, UK.
Int J Obes Relat Metab Disord. 2004 Jan;28(1):80-90. doi: 10.1038/sj.ijo.0802466.
To determine and compare the extent of within- and between-laboratory precision in body volume (BV) measurements using air displacement plethysmography (ADP), the BOD POD body composition system, and to interpret any such variability in terms of body composition estimates.
Repeated test procedures of BV assessment using the BOD POD ADP were reproduced at two laboratories for the estimation of precision, both within and between laboratories.
In total, 30 healthy adult volunteers, 14 men (age, 19-48 y; body mass index (BMI), 19.7-30.3 kg/m2) and 16 women (age, 19-40 y; BMI, 16.3-35.7 kg/m2), were each subjected to two test procedures at both laboratories. Two additional volunteers were independently subjected to 10 repeated test procedures at both laboratories.
Repeated measurements of BV, uncorrected for the effects of isothermal air in the lungs and the surface area artifact, were obtained using the BOD POD ADP, with the identical protocol being faithfully applied at both laboratories. Uncorrected BV measurements were adjusted to give estimates of actual BV that were used to calculate body density (body weight (BWt)/actual BV) from which estimates of body composition were derived. The differences between repeated BV measurements or body composition estimates were used to assess within-laboratory precision (repeatability), as standard deviation (SD) and coefficient of variation; the differences between measurements reproduced at each laboratory were used to determine between-laboratory precision (reproducibility), as bias and 95% limits of agreement (from SD of the differences between laboratories).
The extent of within-laboratory methodological precision for BV (uncorrected and actual) was variable according to subject, sample group and laboratory conditions (range of SD, 0.04-0.13 l), and was mostly due to within-individual biological variability (typically 78-99%) rather than to technical imprecision. There was a significant (P<0.05) bias between laboratories for the 10 repeats on the two independent subjects (up to 0.29 l). Although no significant bias (P=0.077) was evident for the sample group of 30 volunteers (-0.05 l), the 95% limits of agreement were considerable (-0.68 to 0.58 l). The effects of this variability in BV on body composition were relatively greater: for example, within-laboratory precision (SD) for body fat as % BWt was between 0.56 and 1.34% depending on the subject and laboratory; the bias (-0.59%) was not significant between laboratories, but there were large 95% limits of agreement (-3.67 to 2.50%).
Within-laboratory precision for each BOD POD instrument was reasonably good, but was variable according to the prevailing conditions. Although the bias between the two instruments was not significant for the BV measurements, implying that they can be used interchangeably for groups of similar subjects, the relatively large 95% limits of agreement indicate that greater consideration may be needed for assessing individuals with different ADP instruments. Therefore, use of a single ADP instrument is apparently preferable when assessing individuals on a longitudinal basis.
使用空气置换体积描记法(ADP)、BOD POD人体成分分析系统测定并比较实验室内部和实验室之间在身体体积(BV)测量方面的精密度,并根据身体成分估计值解释任何此类变异性。
在两个实验室重复进行使用BOD POD ADP评估BV的测试程序,以估计实验室内部和实验室之间的精密度。
共有30名健康成年志愿者,其中14名男性(年龄19 - 48岁;体重指数(BMI)19.7 - 30.3 kg/m²)和16名女性(年龄19 - 40岁;BMI 16.3 - 35.7 kg/m²),在两个实验室均接受了两次测试程序。另外两名志愿者在两个实验室独立接受了10次重复测试程序。
使用BOD POD ADP对BV进行重复测量,未校正肺部等温空气和表面积伪影的影响,两个实验室均忠实地应用相同方案。对未校正的BV测量值进行调整,以给出实际BV的估计值,用于计算身体密度(体重(BWt)/实际BV),并由此得出身体成分的估计值。重复BV测量值或身体成分估计值之间的差异用于评估实验室内部精密度(重复性),以标准差(SD)和变异系数表示;每个实验室重复测量值之间的差异用于确定实验室之间的精密度(再现性),以偏差和95%一致性界限(根据实验室之间差异的SD)表示。
BV(未校正和实际)的实验室内部方法精密度程度因受试者、样本组和实验室条件而异(SD范围为0.04 - 0.13升),主要归因于个体内部的生物学变异性(通常为78 - 99%),而非技术不精确性。对于两名独立受试者的10次重复测量,实验室之间存在显著(P<0.05)偏差(高达0.29升)。虽然30名志愿者样本组未显示出显著偏差(P = 0.077)(-0.05升),但95%一致性界限相当大(-0.68至0.58升)。BV这种变异性对身体成分的影响相对更大:例如,根据受试者和实验室不同,身体脂肪占体重百分比的实验室内部精密度(SD)在0.56%至1.34%之间;实验室之间的偏差(-0.59%)不显著,但95%一致性界限较大(-3.67至2.50%)。
每个BOD POD仪器的实验室内部精密度相当不错,但因当前条件而异。虽然两种仪器在BV测量方面的偏差不显著,这意味着它们可用于类似受试者群体的互换使用,但相对较大的95%一致性界限表明,在评估使用不同ADP仪器的个体时可能需要更多考虑。因此,在纵向评估个体时,显然最好使用单一的ADP仪器。