Doxycycline and minocycline for the management of acne: a review of efficacy and safety with emphasis on clinical implications

A significant number of patients with moderate-to-severe inflammatory acne are candidates for oral antibiotic therapy. Use of tetracycline for acne has yielded to second-generation molecules doxycycline and minocycline, which are associated with numerous benefits over their predecessor, especially l...

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Published in:Journal of drugs in dermatology Vol. 9; no. 11; p. 1407
Main Author: Kircik, Leon H
Format: Journal Article
Language:English
Published: United States 01-11-2010
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Abstract A significant number of patients with moderate-to-severe inflammatory acne are candidates for oral antibiotic therapy. Use of tetracycline for acne has yielded to second-generation molecules doxycycline and minocycline, which are associated with numerous benefits over their predecessor, especially less frequent dosing and improved safety. Nonetheless, these agents are associated with certain potential side effects, including gastrointestinal (GI) concerns, staining of developing teeth in children, candidiasis, vestibular concerns and, somewhat more controversially, photosensitivity. Additionally, minocycline may be associated with the development of autoantibodies, including anti-nuclear antibody (ANA), anti-neutrophil cytoplasmic antibody (ANCA) and anti-phospholipid antibodies with or without associated clinical symptoms. Given their similar efficacy for the management of moderate-to-severe acne vulgaris, the choice of doxycycline or minocycline may depend on specific clinical considerations, including patient satisfaction with therapy, compliance and convenience. Data and clinical experience suggest that enteric-coated doxycycline, with its low rate of GI symptoms, may represent a more tolerable treatment option for many acne patients and therefore be associated with better likelihood of compliance.
AbstractList A significant number of patients with moderate-to-severe inflammatory acne are candidates for oral antibiotic therapy. Use of tetracycline for acne has yielded to second-generation molecules doxycycline and minocycline, which are associated with numerous benefits over their predecessor, especially less frequent dosing and improved safety. Nonetheless, these agents are associated with certain potential side effects, including gastrointestinal (GI) concerns, staining of developing teeth in children, candidiasis, vestibular concerns and, somewhat more controversially, photosensitivity. Additionally, minocycline may be associated with the development of autoantibodies, including anti-nuclear antibody (ANA), anti-neutrophil cytoplasmic antibody (ANCA) and anti-phospholipid antibodies with or without associated clinical symptoms. Given their similar efficacy for the management of moderate-to-severe acne vulgaris, the choice of doxycycline or minocycline may depend on specific clinical considerations, including patient satisfaction with therapy, compliance and convenience. Data and clinical experience suggest that enteric-coated doxycycline, with its low rate of GI symptoms, may represent a more tolerable treatment option for many acne patients and therefore be associated with better likelihood of compliance.
Author Kircik, Leon H
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  givenname: Leon H
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  email: wedoderm@bellsouth.net
  organization: Mount Sinai Medical Center, New York, NY, USA. wedoderm@bellsouth.net
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References 22052262 - J Drugs Dermatol. 2011 Sep;10(9):965-6; author reply 966
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Snippet A significant number of patients with moderate-to-severe inflammatory acne are candidates for oral antibiotic therapy. Use of tetracycline for acne has yielded...
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StartPage 1407
SubjectTerms Acne Vulgaris - drug therapy
Anti-Bacterial Agents - adverse effects
Anti-Bacterial Agents - therapeutic use
Doxycycline - adverse effects
Doxycycline - therapeutic use
Humans
Minocycline - adverse effects
Minocycline - therapeutic use
Title Doxycycline and minocycline for the management of acne: a review of efficacy and safety with emphasis on clinical implications
URI https://www.ncbi.nlm.nih.gov/pubmed/21061764
Volume 9
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