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COVID-19 virus next to N Latex SAA Assay bottle

N Latex SAA Assay Add sensitivity in diagnosis and monitoring of inflammatory processes

Available on Atellica NEPH 630 System
Available on Atellica NEPH 630 System

The Serum Amyloid A (SAA) Assay* for use on Atellica® NEPH 630,* BN™ II, and BN ProSpec® Systems is designed to enhance diagnostic sensitivity for infections.

Parallel determination of CRP and SAA is useful in diagnosing inflammatory processes, especially viral infections, due to a strong rise in its blood concentration within a few hours.1,2

Recent studies show that SAA can be a prognostic marker for decline and death in COVID-19 patients. 3,4,5

Features & Benefits

The Serum Amyloid A (SAA) Assay* from Siemens Healthineers provides:

  • High specificity based on monoclonal antibodies
  • Fully automated testing for improved workflow
  • A broad initial measuring range (3–200 mg/L) that helps reduce the need for redilutions and supports economical reagent use
  • A complete kit, including reagent, calibrator, controls, and supplementary reagent (SCS Cleaner reagent available separately)
  • The ability to perform parallel determination of SAA and CRP, which can enhance diagnostic sensitivity for infections 2

Clinical Use

High sensitivity in diagnosis and monitoring of inflammatory processes.

Serum amyloid A (SAA) represents a protein family and is an acute-phase protein mainly produced by the liver in response to proinflammatory cytokines secreted by the activated monocytes/macrophage lineages.

Like C-reactive protein (CRP), SAA determination can be used in the diagnosis and monitoring of inflammatory and infectious processes. In contrast to CRP, SAA levels show a stronger response to viral infections, while CRP responds more strongly to systemic bacterial infections.2

SAA plasma levels can increase up to 1000-fold, for instance, due to the effect of IL-6 in the course of a cytokine storm. First elevations are seen 3–6 hours after an inflammatory stimulus, reaching a peak concentration in 2–3 days.2,6

Mo et al. studied 118 patients with COVIDâ€19 (102 mild, 16 severe) for the prognostic value of the inflammation markers SAA, CRP, and PCT applying receiver operating characteristic (ROC) curve analysis, a mathematical procedure to determine the predictive value of the cutoff for a test.3

SAA clearly had the highest predictive value for disease progression of the three inflammation markers (AUC = 0.968).

Figure 1. The diagnostic value of inflammatory indicators in predicting acute aggravation of COVIDâ€19 (orange: SAA, grey: CRP, teal: PCT).3

SAA, as currently understood, is one of the strongest indicators of SARS-CoV-2 inflammation compared to other acute-phase proteins.

Technical Specifications

Assay principle

Latex-enhanced immunonephelometry

Sample type

Human serum, heparinized plasma

Reference range

<6.4 mg/L

Initial measuring ranges

3.0–200 mg/L

Detection limit

0.8 mg/L

Measuring time

6 minutes

Onboard reagent stability

4 weeks (Atellica NEPH 630* and BN ProSpec Systems)
5 days on BN II System

Calibration frequency

1 week (lot-dependent)

Precision

Intra-assay CV ≤6.2%
Inter-assay CV ≤4.7%
Total CV ≤6.4%

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