Framing the future of antifungals in atopic dermatitis

被引:30
作者
Nikkels, AF [1 ]
Piérard, GE [1 ]
机构
[1] Univ Liege, Med Ctr, Dept Dermatopathol, B-4000 Liege, Belgium
关键词
itraconazole; ketoconazole; fluconazole; atopic dermatitis; Malassezia;
D O I
10.1159/000069968
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic dermatitis (AD) is a frequent chronic inflammatory skin disease. Some fungal colonization or infection of the skin may exacerbate AD severity, particularly the so-called head and neck variant. In addition, excessive intestinal colonization by Candida albicans may represent an additional triggering factor. Hence, there is a rationale to use antifungals in selected AD patients. Early trials with topical ketoconazole in head and neck AD showed a decrease in Malassezia colonization, but no significant improvement was observed in the clinical severity. In contrast, clinical improvement and decreased serum IgE were obtained in patients with positive Malassezia radioallergosorbent tests (RASTs) who were treated by oral ketoconazole. Some preliminary data suggested that oral itraconazole treatment in AD patients reduced the need for topical corticosteroids, provided clinical improvement particularly in head and neck AD, reduced the cutaneous and intestinal fungal colonization that may trigger AD, reduced the percentage of positive Malassezia cultures and demonstrated a decrease in C. albicans and Malassezia FAST values. Furthermore, beside its antifungal action, itraconazole in part relieves pruritus and inflammation. In conclusion, oral itraconazole treatment can alleviate AD severity in selected patients. Fluconazole is also effective. Further research is warranted to identify whether the load in skin surface fungal agents, the fungal FAST values and specific prick testing should be assessed in order to optimize the antifungal management in AD patients.
引用
收藏
页码:398 / 400
页数:3
相关论文
共 41 条
  • [1] Abeck D, 2000, Am J Clin Dermatol, V1, P41
  • [2] ADACHI A, 1998, ALLERGY, V67, P238
  • [3] ADACHI A, 1999, JPN J ALLERGOL, V48, P719
  • [4] Decreased oxidative state in non-lesional skin of atopic dermatitis
    Antille, C
    Sorg, O
    Lübbe, J
    Saurat, JH
    [J]. DERMATOLOGY, 2002, 204 (01) : 69 - 71
  • [5] KETOCONAZOLE IN ATOPIC-DERMATITIS - THERAPEUTIC RESPONSE IS CORRELATED WITH DECREASE IN SERUM IGE
    BACK, O
    SCHEYNIUS, A
    JOHANSSON, SGO
    [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 1995, 287 (05) : 448 - 451
  • [6] Bavbek S., 1997, Journal of Allergy and Clinical Immunology, V99, pS478
  • [7] BROBERG A, 1995, ACTA DERM-VENEREOL, V75, P46
  • [8] BROBERG A, 1992, ACTA DERM-VENEREOL, V72, P187
  • [9] Natural killer and dendritic cell contact in lesional atopic dermatitis skin -: Malassezia-influenced cell interaction
    Buentke, E
    Heffler, LC
    Wilson, JL
    Wallin, RPA
    Löfman, C
    Chambers, BJ
    Ljunggren, HG
    Scheynius, A
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (04) : 850 - 857
  • [10] CLEMMENSEN OJ, 1983, SEMIN DERMATOL, V2, P26