Abstract
Introduction: Serum amyloid A (SAA) and C-reactive protein (CRP) are both acute-phase reactants synthesized by the liver upon stimulation by proinflammatory cytokines reflecting both the acute and chronic inflammatory states. Methods: We have established a one-step, sandwich ELISA on microplate for SAA using commercial antibodies for coating and detection. Results: This in-house ELISA has a sensitivity of 0.12 mg/l. Both within-day and between-day CVs were < 10%. The in-house assay correlated well with the commercial ELISA kit from Anogen (r = 0.95). We also established the reference range for apparently healthy Chinese. Statistically higher SAA values were found in those > 50 years old. No difference was found between genders. We found only slightly increased levels of SAA in early stage of type 2 diabetics, but highly increased levels of SAA were detected in patients with acute myocardial infarction, generally associated with intense inflammation. At the early stage of type 2 diabetes associated with low inflammation, SAA was found to be complementary to CRP in test sensitivity. Conclusions: Based on our data and reports from the literature we believe that SAA responds differently than CRP in inflammatory diseases such as in type 2 diabetes and acute myocardial infarction, and is complementary to CRP in test sensitivity.
| Original language | English |
|---|---|
| Pages (from-to) | 72-76 |
| Number of pages | 5 |
| Journal | Clinica Chimica Acta |
| Volume | 376 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - 01 02 2007 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- CRP
- ELISA
- Inflammation
- Reference range
- SAA
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