Journal Article10.1016/J.JACI.2003.09.033
Atopic dermatitis and the atopic march.
TL;DR: Preliminary prevention studies with oral antihistamines provide evidence that early intervention might slow the atopic march, which has a tremendously negative effect on the quality of life of patients as well as family.
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Abstract: Atopic dermatitis (AD), one of the most common skin disorders seen in infants and children, usually has its onset during the first 6 months of life. The prevalence of AD is similar in the United States, Europe, and Japan and is increasing, similar to that of other atopic disorders, particularly asthma. AD has been classified into 3 sequential phases: infantile, childhood, and adult, each with characteristic physical findings. AD has a tremendously negative effect on the quality of life of patients as well as family, most commonly disturbing sleep. The condition also creates a great financial burden for both the family and society. The cutaneous manifestations of atopy often represent the beginning of the atopic march. On the basis of several longitudinal studies, approximately half of AD patients will develop asthma, particularly with severe AD, and two thirds will develop allergic rhinitis. Epicutaneous sensitization has been thought to be responsible, with subsequent migration of sensitized T cells into the nose and airways, causing upper and lower airway disease. Animal models and human observation concur with this theory. Preliminary prevention studies with oral antihistamines provide evidence that early intervention might slow the atopic march.
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Citations
ΔNp63 Controls a TLR3-Mediated Mechanism That Abundantly Provides Thymic Stromal Lymphopoietin in Atopic Dermatitis
Terufumi Kubo,Ryuta Kamekura,Ayako Kumagai,Koji Kawata,Keiji Yamashita,Yukari Mitsuhashi,Takashi Kojima,Kotaro Sugimoto,Akihiro Yoneta,Yasuyuki Sumikawa,Toshiharu Yamashita,Noriyuki Sato,Tetsuo Himi,Shingo Ichimiya +13 more
TL;DR: The results indicate that ΔNp63lo/- keratinocytes generate TSLP through a putative autocrine and/or paracrine pathway upon TLR3 stimulation within AD lesions, since moieties of damaged cells and pathogens stimulateTLR3.
Feline allergic diseases: introduction and proposed nomenclature.
Richard E.W Halliwell,Cherie M. Pucheu-Haston,Thierry Olivry,Christine Prost,Hilary A. Jackson,Frane Banovic,Tim Nuttall,Domenico Santoro,Petra Bizikova,Ralf S. Mueller +9 more
TL;DR: In this article, the authors reviewed the literature, assessed the status of knowledge of the topic and the extent to which these diseases could be categorized as atopic in nature, and made recommendations concerning nomenclature.
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CSACI position statement: safety of topical calcineurin inhibitors in the management of atopic dermatitis in children and adults
TL;DR: The Canadian Society of Allergy and Clinical Immunology (CSACI) recognizes that the benefits of TCIs should be carefully weighed with the theoretical risks in advising patients, and acknowledges that long-term studies remain in progress.
Homeopathy in paediatric atopic diseases: long-term results in children with atopic dermatitis.
TL;DR: Pupils treated with homeopathy seem to show a reduced tendency to maintain AD and develop asthma (and allergic rhinitis) in adult age, according to the data from the literature.
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20-O-β-D-glucopyranosyl-20(S)-protopanaxadiol-fortified ginseng extract attenuates the development of atopic dermatitis-like symptoms in NC/Nga mice.
Jong Rhan Kim,Jinhwan Choi,Jiyoung Kim,Heejeung Kim,Heerim Kang,Eun-Hye Kim,Jeong-Hwa Chang,Yeong-Eun Kim,Young Jin Choi,Ki Won Lee,Hyong Joo Lee +10 more
TL;DR: Oral administration of GFGE significantly attenuated DFE-induced increases in dermatitis score, ear thickness, scratching time, and severity of skin lesions in NC/Nga mice, suggesting that GFGE might be an alternative therapeutic agent for the prevention of AD.
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