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1.6.5 Studies <strong>of</strong> inflammatory markers in blood and uine<br />

Inflammatory markers have also been studied in blood and urine and I am going to briefly<br />

review what has been found in this area. Blood and urine samples are relatively easy to obtain<br />

when compared to the general anaesthesia or sedation required for bronchoscopy, lavage and<br />

biopsy, are more consistently obtainable than induced sputum and less likely to cause side<br />

effects than these other procedures. However blood testing is still seen as invasive by children<br />

and most adults. Also, these compartments are removed from the direct area <strong>of</strong> interest and<br />

reflect systemic findings, which may or may not be related to the lung.<br />

As with results from sampling the lung, monitoring <strong>of</strong> inflammatory markers in blood have<br />

shown an increase in eosinophils, ECP and EDN levels in children and adults with asthma<br />

compared to control groups. In some studies these correlated with asthma severity or current<br />

symptomatology (Krisdansson, Shimizu et al. 1994; Parra, Prieto et al. 1996; Rao, Frederick<br />

et al. 1996; Remes, Korppi et al. 1998; Yazicioglu, Ones et al. 1999; Stelmach, Gorski et al.<br />

2002), and although other studies also found higher levels, no such correlations were found<br />

(Pizzichini,Pizzichini et al. 1997; Bacci, Cianchetti et al. 1998; Niimi and Matsumoto 1999;<br />

Stelmach, Jerzynska et al. 2001; Stelmach, Jerzynska et al. 2001; Aldridge, Hancox et al.<br />

2002; Reichenbach, Jarisch et al. 2002) or even mixed results were obtained (Currie, Syme_<br />

Grant et al. 2o03). In adults, a large cross sectional study <strong>of</strong> almost 7000 subjects found<br />

physician diagnosed asthma was significantly associated with serum eosinophil count<br />

(Schwartz and Weiss 1993). Serum eosinophil and ECP levels during acute asthma were<br />

corelated with more severe exacerbations and less bronchodilator responsiveness in 48 adults<br />

(Lee, Ire et al. 1997). Plasma total IgE, plasma specific IgE, blood eosinophil percentage and<br />

exhaled NO were thought to account for 55.5Vo <strong>of</strong> the variance seen in bronchial hyper-<br />

reactivity (I-eung, Wong et al. 2005). Urinary levels <strong>of</strong> EDN did increase at time <strong>of</strong> asthma<br />

exacerbation (Cottin, Deviller et al. l99g).<br />

In children, ECP and eosinophilic peroxidase (EPO) in both serum and urine showed reduced<br />

gradation in levels from asthmatics with current symptoms to symptom free asthmatic<br />

children and to healthy children (Lonnkvist, Hellman et al. 2001). Both urinary EDN and<br />

serum ECP were significantly higher in children with atopic asthma than control subjects<br />

(Kristjansson, Strannegard et al. 1996). In both studies levels decreased with IHCS treatment<br />

(Kristjansson, Strannegard et al. 1996;Lonnkvist, Hellman et al. 2001) and in one increased if<br />

treatment was reduced (Lonnkvist, Hellman et al. 2001). Urinary EDN levels were increased<br />

in 80 asthmatic children compared to 24 controls, and were higher in symptomatic than<br />

4l

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