Reliability and Validity of Contemporary Bioelectrical Impedance Analysis Devices for Body Composition Assessment

J. Merrigan, Nina L Stute, J. Eckerle, Nick S. Mackowski, J. Walters, Maegan L. O'Connor, Kristyn N. Barrett, Robert Robert, A. Strang, Joshua A. Hagen
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引用次数: 2

Abstract

Introduction: The aim was to determine reliability and validity of bioelectrical impedance analysis (BIA) compared to dual energy x-ray absorptiometry (DEXA). Methods:  Participants (n=93) were fasted and euhydrated (confirmed with urine specific gravity, USG) and underwent anthropometrics, DEXA scan (GE Prodigy), and three repeated trials on each BIA device (i.e., InBody 770, SECA mBCA 514, and FitTrack). A subset of participants (n=36) re-tested 12-weeks later to investigate longitudinal changes. Results: All BIA devices had acceptable within-session reliability (coefficient of variation < 2%). Agreement with DEXA was unacceptable, poor, and moderate for FitTrack (Lin’s Concordance Correlation Coefficient, CCC=0.61), InBody (CCC=0.88), and SECA (CCC=0.91). FitTrack did not demonstrate systematic bias but had wide limits of agreement and larger underestimations occurring at higher BF%. InBody showed systematic underestimations with proportionate bias demonstrating more error at lower BF%. SECA demonstrated no bias but tended to underestimate BF% according to Bland-Altman Plots. Errors in BIA BF% estimates were not related with USG but were associated with DEXA measured BF%. The subtle 12-week changes in BF% did not agree between BIA and DEXA. Conclusions: Caution should be taken when using BIA devices to assess BF% as devices demonstrated unacceptable agreement compared to DEXA.
当代生物阻抗分析设备用于身体成分评估的可靠性和有效性
前言:目的是确定生物电阻抗分析(BIA)与双能x射线吸收仪(DEXA)的可靠性和有效性。方法:参与者(n=93)禁食和脱水(用尿比重USG确认),并进行人体测量、DEXA扫描(GE Prodigy),以及在每个BIA设备(即InBody 770、SECA mBCA 514和FitTrack)上进行三次重复试验。一部分参与者(n=36)在12周后重新测试以调查纵向变化。结果:所有BIA器械具有可接受的会话内信度(变异系数< 2%)。FitTrack (Lin’s一致性相关系数,CCC=0.61)、InBody (CCC=0.88)和SECA (CCC=0.91)与DEXA的一致性是不可接受的、差的和中等的。FitTrack没有显示出系统偏差,但有广泛的一致性限制,并且在较高的BF%时出现较大的低估。InBody显示出系统的低估与比例偏差,在较低的BF%时显示出更大的误差。根据Bland-Altman图,SECA没有表现出偏见,但倾向于低估BF%。BIA BF%估计的误差与USG无关,但与DEXA测量的BF%相关。BIA和DEXA在12周内BF%的细微变化并不一致。结论:使用BIA装置评估BF%时应谨慎,因为与DEXA相比,BIA装置显示出不可接受的一致性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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