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Clinical utility and validity of minoxidil response testing in androgenetic alopecia.

Andy Goren, Jerry Shapiro, Janet Roberts, John McCoy, Nisha Desai et al.
Meta-Analysis Dermatologic therapy 2015 72 citazioni
PubMed DOI
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Study Design

Tipo di studio
Meta-Analysis
Popolazione
androgenetic alopecia patients
Intervento
Clinical utility and validity of minoxidil response testing in androgenetic alopecia. None
Comparatore
None
Esito primario
None
Direzione dell'effetto
Mixed
Rischio di bias
Low

Abstract

Clinical response to 5% topical minoxidil for the treatment of androgenetic alopecia (AGA) is typically observed after 3-6 months. Approximately 40% of patients will regrow hair. Given the prolonged treatment time required to elicit a response, a diagnostic test for ruling out nonresponders would have significant clinical utility. Two studies have previously reported that sulfotransferase enzyme activity in plucked hair follicles predicts a patient's response to topical minoxidil therapy. The aim of this study was to assess the clinical utility and validity of minoxidil response testing. In this communication, the present authors conducted an analysis of completed and ongoing studies of minoxidil response testing. The analysis confirmed the clinical utility of a sulfotransferase enzyme test in successfully ruling out 95.9% of nonresponders to topical minoxidil for the treatment of AGA.

TL;DR

The analysis confirmed the clinical utility of a sulfotransferase enzyme test in successfully ruling out 95.9% of nonresponders to topical minoxidil for the treatment of AGA.

Used In Evidence Reviews

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