Journal List > Pediatr Allergy Respir Dis > v.22(3) > 1033188

Shin, Kim, Jung, Jin, Han, Park, Oh, and Kim: Association of SCORAD Index and Aeroallergen Sensitization on Urinary Leukotriene E4 in Children with Atopic Dermatitis

Abstract

Purpose

Atopic dermatitis (AD) is a genetically determined, chronic relapsing skin disease. The pathogenesis of AD is complex and the course is unpredictable. Atopy is an important risk factor for the development of AD. Cysteinyl leukotrienes (Cys-LTs) were implicated in the pathophysiology of allergic diseases, and are being targeted for their diagnosis and treatments. Early detection of tissue inflammation of target organ is important to enable early prevention and management of allergic diseases. The aim of our study is to evaluate the differences in urinary leukotrienes E4 (LTE4) levels, according to AD symptom score and aeroallergen sensitization in children with AD by using noninvasive techniques.

Methods

We recruited 46 children with AD, using predetermined criteria. Clinical features of AD were evaluated by a physician, using scoring atopic dermatitis (SCORAD) index. Aeroallergen sensitization was measured by using a skin prick test and UniCap. Urine samples were also collected on day of the 1st and 2nd visits, and were analyzed for LTE4 with an enzyme-linked immunoassay kit.

Results

SCORAD indeces of children with AD were correlated with urinary LTE4 levels. Total immunoglobulin E (IgE) and eosinophil counts also had significant correlation with urinary LTE4 levels. Especially, aeroallergen sensitization of atopic AD significantly correlated with urinary LTE4 of these patients.

Conclusion

Urinary LTE4 levels significantly correlated with serum total IgE and number of sensitized aeroallergen in children with AD. Clinical features of AD evaluated with SCORAD index related with urinary LTE4 level. Urinary LTE4 might be a valuable, noninvasive marker for different pathogenesis of AD.

Figures and Tables

Fig. 1
Relationship between urine log-leukotrienes E4 (LTE4) concentration in pg/mg Cr and overall scoring of atopic dermatitis (SCORAD). The correlation of log-LTE4 concentration to the total SCORAD was detected.(γ=0.340, P = 0.021) (Pearson's correlation coefficient)
pard-22-302-g001
Fig. 2
Relationship between urine leukotrienes E4 (LTE4) concentration in pg/mg Cr and blood total eosinophil counts (A : γ=0.347, P=0.018), serum total immunoglobulin E (IgE) (B : γ=0.390, P=0.007) and number of sensitized allergen (C : γ=0.340, P=0.021; D : γ=0.414, P=0.004). (Pearson's correlation coefficient)
pard-22-302-g002
Table 1
Clinical Characteristics of Study Subjects (n=46)
pard-22-302-i001

*Values are presented as mean±SD. Values are presented as mean (standard error).

SCORAD, scoring of atopic dermatitis; ECP, eosinophil cationic protein; IgE, immunoglobulin E; LTE4, leukotrienes E4.

Table 2
Relationship between Urine Leukotrienes E4 Concentration in pg/mg Cr (mean±SE) and History of Other Allergic Diseases
pard-22-302-i002

SE, standard error.

*Mann-Whitney U test.

Table 3
Relationship between Urine Leukotrienes E4 Concentration in pg/mg Cr and Overall and Objective SCORAD
pard-22-302-i003

SCORAD, scoring of atopic dermatitis.

*Pearson correlation method.

Table 4
Relationship between Changes of Urine Leukotrienes E4 Concentration in pg/mg Cr and changes of SCORAD during 6 months
pard-22-302-i004

SCORAD, scoring of atopic dermatitis.

Spearman's rank correlation coefficient.

References

1. Leung DY, Bieber T. Atopic dermatitis. Lancet. 2003. 361:151–160.
crossref
2. Pelclova D, Navratil T, Fenclova Z, Vlckova S, Kupka K, Urban P, et al. Increased oxidative/nitrosative stress markers measured non-invasively in patients with high 2,3,7,8-tetrachloro-dibenzo-p-dioxin plasma level. Neuro Endocrinol Lett. 2011. 32:Suppl 1. 71–76.
3. Taylor DR, Pavord ID. Biomarkers in the assessment and management of airways diseases. Postgrad Med J. 2008. 84:628–634.
crossref
4. Charman C, Williams H. Outcome measures of disease severity in atopic eczema. Arch Dermatol. 2000. 136:763–769.
crossref
5. Severity scoring of atopic dermatitis: the SCORAD index. Consensus Report of the European Task Force on Atopic Dermatitis. Dermatology. 1993. 186:23–31.
6. Hon KL, Leung TF, Ma KC, Li AM, Wong Y, Li CY, et al. Urinary leukotriene E4 correlates with severity of atopic dermatitis in children. Clin Exp Dermatol. 2004. 29:277–281.
crossref
7. Adamek-Guzik T, Guzik TJ, Czerniawska-Mysik G, Korpanty G, Mastalerz L, Radwan J, et al. Urinary leukotriene levels are increased during exacerbation of atopic eczema/dermatitis syndrome. Relation to clinical status. Allergy. 2002. 57:732–736.
crossref
8. Oymar K, Aksnes L. Increased levels of urinary leukotriene E4 in children with severe atopic eczema/dermatitis syndrome. Allergy. 2005. 60:86–89.
crossref
9. Leung TF, Ma KC, Hon KL, Lam CW, Wan H, Li CY, et al. Serum concentration of macrophage-derived chemokine may be a useful inflammatory marker for assessing severity of atopic dermatitis in infants and young children. Pediatr Allergy Immunol. 2003. 14:296–301.
crossref
10. Austen KF, Maekawa A, Kanaoka Y, Boyce JA. The leukotriene E4 puzzle: finding the missing pieces and revealing the pathobiologic implications. J Allergy Clin Immunol. 2009. 124:406–414.
crossref
11. Kwon SJ, Koo BS, Lee HB, Oh JW. Study of urinary leukotriene E4 and eosinophil cationic protein in nasopharyngeal aspiration from wheezing infants. Pediatr Allergy Respir Dis. 2004. 14:46–52. (Korea).
12. Hanifin JM, Rajka G. Diagnostic features of atopic dermatitis. Acta Derm Venereol (Stockh). 1979. 59:Suppl 92. 44–47.
13. Kumlin M, Stensvad F, Larsson L, Dahlen B, Dahlen SE. Validation and application of a new simple strategy for measurements of urinary leukotriene E4 in humans. Clin Exp Allergy. 1995. 25:467–479.
crossref
14. Sansom JE, Taylor GW, Dollery CT, Archer CB. Urinary leukotriene E4 levels in patients with atopic dermatitis. Br J Dermatol. 1997. 136:790–791.
crossref
15. Hishinuma T, Suzuki N, Aiba S, Tagami H, Mizugaki M. Increased urinary leukotriene E4 excretion in patients with atopic dermatitis. Br J Dermatol. 2001. 144:19–23.
crossref
16. Cho J, Lee JH, Suh J, Yu JS, Lee H, Park E, et al. Change in quality of life according to the change in atopic dermatitis severity. Pediatr Allergy Respir Dis. 2012. 22:86–99. (Korea).
crossref
17. Kunz B, Oranje AP, Labreze L, Stalder JF, Ring J, Taieb A. Clinical validation and guidelines for the SCORAD index: consensus report of the European Task Force on Atopic Dermatitis. Dermatology. 1997. 195:10–19.
crossref
18. Koro O, Furutani K, Hide M, Yamada S, Yamamoto S. Chemical mediators in atopic dermatitis: involvement of leukotriene B4 released by a type I allergic reaction in the pathogenesis of atopic dermatitis. J Allergy Clin Immunol. 1999. 103:663–670.
crossref
19. Maekawa A, Kanaoka Y, Xing W, Austen KF. Functional recognition of a distinct receptor preferential for leukotriene E4 in mice lacking the cysteinyl leukotriene 1 and 2 receptors. Proc Natl Acad Sci U S A. 2008. 105:16695–16700.
crossref
20. Soter NA, Lewis RA, Corey EJ, Austen KF. Local effects of synthetic leukotrienes (LTC4, LTD4, LTE4, and LTB4) in human skin. J Invest Dermatol. 1983. 80:115–119.
crossref
21. Hua Z, Fei H, Mingming X. Evaluation and interference of serum and skin lesion levels of leukotrienes in patients with eczema. Prostaglandins Leukot Essent Fatty Acids. 2006. 75:51–55.
crossref
22. Oyoshi MK, He R, Kanaoka Y, ElKhal A, Kawamoto S, Lewis CN, et al. Eosinophil-derived leukotriene C4 signals via type 2 cysteinyl leukotriene receptor to promote skin fibrosis in a mouse model of atopic dermatitis. Proc Natl Acad Sci U S A. 2012. 109:4992–4997.
crossref
23. Kagi MK. Leukotriene receptor antagonists: a novel therapeutic approach in atopic dermatitis? Dermatology. 2001. 203:280–283.
crossref
24. Nettis E, Pannofino A, Fanelli M, Ferrannini A, Tursi A. Efficacy and tolerability of montelukast as a therapeutic agent for severe atopic dermatitis in adults. Acta Derm Venereol. 2002. 82:297–298.
crossref
25. Yanase DJ, David-Bajar K. The leukotriene antagonist montelukast as a therapeutic agent for atopic dermatitis. J Am Acad Dermatol. 2001. 44:89–93.
crossref
26. Carucci JA, Washenik K, Weinstein A, Shupack J, Cohen DE. The leukotriene antagonist zafirlukast as a therapeutic agent for atopic dermatitis. Arch Dermatol. 1998. 134:785–786.
crossref
27. Ehlayel MS, Bener A, Sabbah A. Montelukast treatment in children with moderately severe atopic dermatitis. Eur Ann Allergy Clin Immunol. 2007. 39:232–236.
28. Broshtilova V, Gantcheva M. Therapeutic hotline: cysteinyl leukotriene receptor antagonist montelukast in the treatment of atopic dermatitis. Dermatol Ther. 2010. 23:90–93.
crossref
29. Veien NK, Busch-Sorensen M, Stausbol-Gron B. Montelukast treatment of moderate to severe atopic dermatitis in adults: a randomized, double-blind, placebo-controlled trial. J Am Acad Dermatol. 2005. 53:147–149.
crossref
30. Friedmann PS, Palmer R, Tan E, Ogboli M, Barclay G, Hotchkiss K, et al. A double-blind, placebo-controlled trial of montelukast in adult atopic eczema. Clin Exp Allergy. 2007. 37:1536–1540.
crossref
31. Fujisawa T, Fujisawa R, Kato Y, Nakayama T, Morita A, Katsumata H, et al. Presence of high contents of thymus and activation-regulated chemokine in platelets and elevated plasma levels of thymus and activation-regulated chemokine and macrophage-derived chemokine in patients with atopic dermatitis. J Allergy Clin Immunol. 2002. 110:139–146.
crossref
32. Gutgesell C, Heise S, Seubert A, Stichtenoth DO, Frolich JC, Neumann C. Comparison of different activity parameters in atopic dermatitis: correlation with clinical scores. Br J Dermatol. 2002. 147:914–919.
crossref
TOOLS
Similar articles