Batterham Marijka J, Van Loo Christel, Charlton Karen E, Cliff Dylan P, Okely Anthony D
1National Institute for Applied Statistics Research Australia,University of Wollongong,Northfields Avenue,Wollongong,NSW 2522,Australia.
2Faculty of Social Sciences,University of Wollongong,Wollongong,NSW 2522,Australia.
Br J Nutr. 2016 Apr 14;115(7):1273-80. doi: 10.1017/S0007114516000040. Epub 2016 Feb 16.
The aim of this study was to demonstrate the use of testing for equivalence in combination with the Bland and Altman method when assessing agreement between two dietary methods. A sample data set, with eighty subjects simulated from previously published studies, was used to compare a FFQ with three 24 h recalls (24HR) for assessing dietary I intake. The mean I intake using the FFQ was 126·51 (sd 54·06) µg and using the three 24HR was 124·23 (sd 48·62) µg. The bias was -2·28 (sd 43·93) µg with a 90% CI 10·46, 5·89 µg. The limits of agreement (LOA) were -88·38, 83·82 µg. Four equivalence regions were compared. Using the conventional 10 % equivalence range, the methods are shown to be equivalent both by using the CI (-12·4, 12·4 µg) and the two one-sided tests approach (lower t=-2·99 (79 df), P=0·002; upper t=2·06 (79 df), P=0·021). However, we make a case that clinical decision making should be used to set the equivalence limits, and for nutrients where there are potential issues with deficiency or toxicity stricter criteria may be needed. If the equivalence region is lowered to ±5 µg, or ± 10 µg, these methods are no longer equivalent, and if a wider limit of ±15 µg is accepted they are again equivalent. Using equivalence testing, acceptable agreement must be assessed a priori and justified; this makes the process of defining agreement more transparent and results easier to interpret than relying on the LOA alone.
本研究的目的是证明在评估两种膳食方法之间的一致性时,等效性检验与布兰德-奥特曼方法联合使用的情况。使用一个样本数据集(由先前发表的研究模拟出的80名受试者)来比较一份食物频率问卷(FFQ)与三次24小时膳食回顾法(24HR),以评估膳食碘摄入量。使用FFQ测得的碘摄入量均值为126.51(标准差54.06)μg,使用三次24HR测得的碘摄入量均值为124.23(标准差48.62)μg。偏差为-2.28(标准差43.93)μg,90%置信区间为-10.46,5.89μg。一致性界限(LOA)为-88.38,83.82μg。比较了四个等效区间。使用传统的10%等效范围,通过置信区间(-12.4,12.4μg)和双侧单侧检验方法(下限t=-2.99(79自由度),P=0.002;上限t=2.06(79自由度),P=0.021)均表明两种方法等效。然而,我们认为临床决策应被用于设定等效界限,对于存在缺乏或毒性潜在问题的营养素,可能需要更严格的标准。如果等效区间降至±5μg或±10μg,这些方法不再等效,如果接受更宽的±15μg界限,它们又再次等效。使用等效性检验时,必须事先评估并证明可接受的一致性;这使得定义一致性的过程比仅依赖一致性界限更透明,结果也更易于解释