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Acute phase reactants in allergic airway disease
Suna Büyüköztürk1, Asli Akkor Gelincik, Sema Genç
1Department of Allergy, Istanbul University Faculty of Medicine, Turkey. sbuyuk@gediknet.com
The Tohoku Journal of Experimental Medicine
|October 27, 2004
Summary
Serum amyloid A (SAA) levels are elevated in patients with allergic rhinitis and asthma, suggesting a role in airway inflammation. Other acute phase reactants like CRP and fibrinogen showed no significant changes.
Area of Science:
- Immunology
- Respiratory Medicine
- Biochemistry
Background:
- Acute phase reactants are known pro-inflammatory molecules.
- Their specific role in allergic airway diseases remains largely unexplored.
- This study investigates three key acute phase proteins in allergic rhinitis and asthma.
Purpose of the Study:
- To examine blood concentrations of C-reactive protein (CRP), serum amyloid A (SAA), and fibrinogen.
- To compare these levels in patients with allergic rhinitis and asthma against healthy controls.
- To explore potential correlations between these markers and lung function (FEV1).
Main Methods:
- Blood samples were collected from non-smoker patients with allergic rhinitis (n=50), asthma (n=20), and healthy controls (n=20).
- Exclusion criteria included recent infections, trauma, rheumatological illnesses, malignancy, or obesity.
- Serum CRP and SAA, and plasma fibrinogen levels were analyzed.
Main Results:
- Mean CRP and fibrinogen levels did not significantly differ between patient groups and controls.
- Mean SAA levels were significantly higher in both allergic rhinitis and asthma groups compared to controls (p=0.002 and p=0.02, respectively).
- No significant correlation was found between FEV1 values and serum marker levels.
Conclusions:
- Serum amyloid A (SAA) is elevated in patients suffering from allergic rhinitis and asthma.
- SAA may play a significant role in the inflammatory processes underlying these allergic airway diseases.
- Further research is warranted to elucidate the precise mechanisms of SAA in allergic airway inflammation.