Abstract
Background: Atopic dermatitis (AD) is an inflammatory skin disease with eczematous pruritic lesions. Topical corticosteroids are the most widely used and the mainstay of treatment for AD. There are some studies that percutaneous systemic absorption of topical steroids may occur and lead to suppression of hypothalamic-pituitaryadrenal axis (HPAA). However, almost in all of these studies, “basic” HPAA function (before application of topical steroids) was not evaluated. Aim: The aim of this study was to investigate basal serum cortisol, adrenocorticotropic hormone (ACTH), and IgE levels in patients with AD and their correlation with disease severity. Methods: Levels of basal serum cortisol, ACTH, and IgE were assessed by ELISA in 31 patients with AD and 31 control subjects. Clinical severity of AD was evaluated by the SCORAD (SCORing Atopic Dermatitis) index. Results: Data analysis showed no statistical difference for basal serum cortisol and ACTH levels between two groups. The serum IgE level was significantly higher in AD group (P=0.02). The SCORAD index was correlated with serum IgE level, but not with the basal serum cortisol level and ACTH level. Conclusions: Basal serum cortisol and ACTH levels are normal in AD patients. Serum IgE level is significantly higher in AD patients and correlated with disease severity.
Highlights
Atopic dermatitis (AD) is an inflammatory skin disease with an onset in infancy or early childhood
Data analysis showed no statistical difference for basal serum cortisol and adrenocorticotropic hormone (ACTH) levels between two groups
The SCORAD index was correlated with serum IgE level, but not with the basal serum cortisol level and ACTH level
Summary
Atopic dermatitis (AD) is an inflammatory skin disease with an onset in infancy or early childhood. It is characterized by severe pruritus, chronic and relapsing course, and typical clinical morphology including xerosis and eczematous lesions [1,2]. Unpredictable course, chronic and relapsing nature of the disease and disturbing pruritus can impose extensive psychological and emotional burden to patients with AD and their families [8,9,10,11]. Atopic dermatitis (AD) is an inflammatory skin disease with eczematous pruritic lesions. There are some studies that percutaneous systemic absorption of topical steroids may occur and lead to suppression of hypothalamic-pituitaryadrenal axis (HPAA). Almost in all of these studies, “basic” HPAA function (before application of topical steroids) was not evaluated
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