Comprehensive Agreement Analysis of Colorimetric and Turbidimetric Total Protein Assays in Cerebrospinal Fluid

Background/Objectives: Accurate measurement of total protein (TP) in cerebrospinal fluid (CSF) is crucial for diagnosing various neurological conditions. This study aims to evaluate the concordance between a routine colorimetric method and a recently introduced turbidimetric method for measuring CSF TP. Methods: We measured 161 CSF samples using both methods, analyzing the whole population and two subgroups: normal (≤500 mg/L) and pathological (>500 mg/L). Agreement was assessed using Lin’s Concordance Correlation Coefficient (CCC), Bland–Altman, and Deming regression, while clinical concordance was determined with Cohen’s Kappa. Results: The concentrations obtained from the two methods did not differ significantly and were well-correlated across the population and subgroups. The CCC for the entire dataset was 0.9881 (substantial agreement), while the Bland–Altman analysis showed a mean bias of 4.467 mg/L. For the “normal” subgroup (n = 97), the CCC was 0.8722 (poor agreement), with a mean bias of 7.668 mg/L. In the “pathological” subgroup (n = 64), the CCC was 0.9858 (substantial agreement) with a mean bias of −3.838 mg/L. Demin regression did not show statistically significant proportional or constant bias in the whole population. However, a stratified analysis revealed a significant negative constant bias in the “normal” subgroup in absence of significant bias in the “pathological” subgroup. Cohen’s kappa was 0.804, indicating substantial agreement. Conclusions: Both methods showed substantial agreement for quantifying CSF TP and clinical classification, supporting their potential interchangeability for diagnostic purposes. Nonetheless, laboratories should note the presence of bias, particularly for samples near the clinical cut-off value.

• Publication year

  2025

• Venue

  Diagnostics

• Publication date

  2025-12-29

• Fields of study

  Medicine

• Identifiers
  DOI 10.3390/diagnostics16010112PMID 41515607PMCID 12785942
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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