A novel method to assess the potential role of sweating abnormalities in the pathogenesis of atopic dermatitis. Issue 4 (23rd November 2017)

• Record Type: Journal Article
• Authors: Shimoda‐Komatsu, Yurie; Sato, Yohei; Yamazaki, Yoshimi; Takahashi, Ryo; Shiohara, Tetsuo
• Other Names: Biedermann T. guestEditor.; Kabashima K. guestEditor.
• Is Part Of: Experimental dermatology. Volume 27:Issue 4(2018)
• Page Start: 386
• Page End: 392
• Publication Date: 2017-11-23
• Subjects: atopy -- dermcidin -- hypohidrosis -- sweating responses -- thermal stimulus; Dermatology -- Periodicals; 616.5
• DOI: 10.1111/exd.13448
• Languages: English
• ISSNs: 0906-6705

Abstract

Abstract: Although atopic dry skin is believed to be caused by defects in skin genes important for maintaining skin barrier function, the role of sweat in atopic dermatitis (AD) has been apparently underestimated. Given the great capacity of sweat to maintain and increase skin hydration, defective sweating responses may be a logical place to look for changes that predispose individuals to the disease. We investigated how disease process and sweating defects progress from early asymptomatic stages to the onset of clinically apparent disease by employing the impression mould technique, which allows an accurate quantification of individual sweat gland/duct activity in relation to skin surface topography. Insensible and sensible sweating responses under baseline conditions and after thermal stimulus, respectively, were measured in various stages of AD patients and healthy controls. In controls, under baseline conditions, sweat ducts/glands at the dermal folds secreted basal levels of sweat (insensible sweating), thereby maintaining skin hydration. Not only such insensible sweating but also sensible sweating markedly decreased even in the earliest asymptomatic stage and the decrease was followed by compensatory hyperhidrosis at the ridge: leakage of sweat into the dermis could represent the initial event resulting in the decreased sweating and inflammation. The defects eventually progressed involving all of the ducts/glands to develop systemic dry skin. AD skin is characterized by varying degrees of functional impairment of sweat ducts/glands depending on the stage, and this defect would be among the reasons for the inability of AD patients to maintain skin hydration.