Abstract

ObjectivesA multicenter study to compare results of BRAHMS Kryptor PCT with those obtained using four BRAHMS-partnered procalcitonin (PCT) automated immunoassays (DiaSorin Liaison, BioMérieux Vidas, Roche Cobas E601 and Siemens Advia Centaur) and the Diazyme immunotubidimetric assay implemented on four clinical chemistry platforms (Abbott Architect c16000, Siemens Advia 2400, Roche Cobas C501 and Beckman Coulter AU5800). Design and methodsOne hundred serum samples from in-patients with PCT values between 0.10 and 58.7ng/mL were divided into aliquots and tested with the nine different reagents and analyzers. BRAHMS PCT Kryptor results were used as reference. ResultsCompared to BRAHMS PCT Kryptor, significant differences in results were observed on Vidas, Advia Centaur, Architect, Cobas C501 and AU5800. However, the correlation coeffiecients (r) with BRAHMS PCT Kryptor were between 0.899 and 0.988. The mean bias was less than ±1.02ng/mL, except for Vidas (2.70ng/mL). The agreement at three clinically relevant cut-offs was optimal: between 83–98% at 0.50ng/mL, 90–97% at 2.0ng/mL, and 98% at 10ng/mL. The comparison of Diazyme PCT across the four clinical chemistry analyzers yielded high correlation coefficients (r between 0.952 and 0.976), a mean bias less than ±0.9ng/mL, acceptable agreement at 0.5ng/mL (>82%), and high concordance at the 2.0ng/mL (>97%) and 10ng/mL (>98%) cut-offs. ConclusionsThe methods and applications evaluated in this multicenter study are aligned with BRAHMS PCT Kryptor and can be used for predicting the risk of progression to systemic inflammation in patients with bacterial infections using the conventional PCT diagnostic thresholds.

Highlights

  • Procalcitonin (PCT), a 116 amino acid peptide with molecular weight 14.5 kDa, belongs to the calcitonin superfamily of peptides

  • No significant decay of PCT immunoreactivity was observed after one week of storage at À70 °C, as attested by the negligible bias observed between fresh and frozen serum analyzed with BRAHMS PCT Kryptor

  • Significant differences compared to BRAHMS PCT Kryptor were observed for two BRAHMS-partnered PCT automated immunoassays (Vidas BRAHMS PCT and Advia Centaur BRAHMS PCT) and for three Diazyme PCT applications on Architect, Cobas C501 and AU5800 (Table 2)

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Summary

Introduction

Procalcitonin (PCT), a 116 amino acid peptide with molecular weight 14.5 kDa, belongs to the calcitonin superfamily of peptides. The original product of this gene, a 141 amino acid peptide known as pre-PCT, undergoes a proteolytic cleavage of the 25 amino acid signal peptide to produce the PCT molecule, which is further processed to generate the mature, 32 amino acid-long calcitonin. The transcription of CALC-1 gene is suppressed in non-neuroendocrine tissues, so that the C cells of the thyroid gland are responsible for the entire synthesis of PCT and calcitonin [1].

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