Why the study?
Does a new conventional CRP assay (Tina-quant) provide comparable analytical precision and concordance to hs-CRP assays for cardiovascular risk assessment?
Does a new conventional CRP assay (Tina-quant) provide comparable analytical precision and concordance to hs-CRP assays for cardiovascular risk assessment?
A new conventional CRP assay demonstrates satisfactory concordance and precision compared to hs-CRP assays, suggesting it can be used for cardiovascular risk assessment with potential operational and financial advantages.
May enable conventional CRP use for CV risk assessment; leaves open outcome validation vs hs-CRP.
BACKGROUND: Subclinical inflammation was shown to play a role in the context of cardiovascular disorder processes. American College of Cardiology/American Heart Association guidelines on cardiovascular risk assessment in specific clinical contexts recommend the use of C-reactive protein (CRP) measurement with high sensitive (hs)-CRP assays that meet the precision requirements for values <2 mg/L. Until now, only hs-CRP assays reached the required limit of quantification. However, new regular CRP assays allow measuring CRP down to 0.6 mg/L. METHODS: A multisite comparative study between hs-CRP and a new conventional CRP assay (Tina-quant) was performed to evaluate the possibility of using regular CRP assays for cardiovascular risk assessment. RESULTS: A satisfactory concordance was observed between regular CRP assays and the hs-CRP assay. Both assays met the analytical precision requirements at the different cutpoints tested (1.00, 2.00, and 3.00 mg/L). CONCLUSION: These results suggest that this new regular CRP assay can be used for cardiovascular risk assessment, which is expected to provide substantial operational and financial advantages when compared with hs-CRP assays.
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Graça et al. (2018) studied this question.
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