Abstract

Progress improving zinc nutrition globally is slowed by limited understanding of population zinc status. This challenge is compounded when small differences in measurement can bias the determination of zinc deficiency rates. Our objective was to evaluate zinc analytical accuracy and precision among different instrument types and sample matrices using a standardized method. Participating laboratories analyzed zinc content of plasma, serum, liver samples, and controls, using a standardized method based on current practice. Instrument calibration and drift were evaluated using a zinc standard. Accuracy was evaluated by percent error vs. reference, and precision by coefficient of variation (CV). Seven laboratories in 4 countries running 9 instruments completed the exercise: 4 atomic absorbance spectrometers (AAS), 1 inductively coupled plasma optical emission spectrometer (ICP-OES), and 4 ICP mass spectrometers (ICP-MS). Calibration differed between individual instruments up to 18.9% (p < 0.001). Geometric mean (95% CI) percent error was 3.5% (2.3%, 5.2%) and CV was 2.1% (1.7%, 2.5%) overall. There were no significant differences in percent error or CV among instrument types (p = 0.91, p = 0.15, respectively). Among sample matrices, serum and plasma zinc measures had the highest CV: 4.8% (3.0%, 7.7%) and 3.9% (2.9%, 5.4%), respectively (p < 0.05). When using standardized materials and methods, similar zinc concentration values, accuracy, and precision were achieved using AAS, ICP-OES, or ICP-MS. However, method development is needed for improvement in serum and plasma zinc measurement precision. Differences in calibration among instruments demonstrate a need for harmonization among laboratories.

Highlights

  • 20% of the global population is at risk of inadequate zinc intake [1]

  • We developed a standardized method based on a review of recent human studies, and instructed participating laboratories to implement the method for the analysis of a standardized set of samples and controls

  • Zinc concentration was most frequently determined in serum (n = 69), plasma (n = 48), and food composites (n = 12)

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Summary

Introduction

Zinc is an essential micronutrient with unique roles in protein structure and as a cofactor in substrate binding and enzymatic activity. Due to these molecular roles, zinc contributes to broad range of functions including DNA transcription and repair, cell signaling, energy metabolism, immune and central nervous system function, and growth [2,3,4]. The distribution of plasma or serum zinc concentration within a population does, allow the determination of population zinc status [6]. Plasma or serum zinc concentration is one of three recommended biomarkers for assessment of zinc status at the population level along with dietary zinc intake and the prevalence of stunting among children under 5 [2]

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