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拔取的毛囊中的磺基转移酶活性可预测局部用米诺地尔治疗女性雄激素性脱发的疗效。

Sulfotransferase activity in plucked hair follicles predicts response to topical minoxidil in the treatment of female androgenetic alopecia.

作者信息

Roberts Janet, Desai Nisha, McCoy John, Goren Andy

机构信息

Northwest Dermatology and Research Center, LLC, Portland, Oregon.

出版信息

Dermatol Ther. 2014 Jul-Aug;27(4):252-4. doi: 10.1111/dth.12130. Epub 2014 Apr 28.

Abstract

Two percent topical minoxidil is the only US Food and Drug Administration-approved drug for the treatment of female androgenetic alopecia (AGA). Its success has been limited by the low percentage of responders. Meta-analysis of several studies reporting the number of responders to 2% minoxidil monotherapy indicates moderate hair regrowth in only 13-20% of female patients. Five percent minoxidil solution, when used off-label, may increase the percentage of responders to as much as 40%. As such, a biomarker for predicting treatment response would have significant clinical utility. In a previous study, Goren et al. reported an association between sulfotransferase activity in plucked hair follicles and minoxidil response in a mixed cohort of male and female patients. The aim of this study was to replicate these findings in a well-defined cohort of female patients with AGA treated with 5% minoxidil daily for a period of 6 months. Consistent with the prior study, we found that sulfotransferase activity in plucked hair follicles predicts treatment response with 93% sensitivity and 83% specificity. Our study further supports the importance of minoxidil sulfation in eliciting a therapeutic response and provides further insight into novel targets for increasing minoxidil efficacy.

摘要

2%的局部用米诺地尔是美国食品药品监督管理局批准的唯一用于治疗女性雄激素性脱发(AGA)的药物。其疗效因反应者比例较低而受限。对多项报告2%米诺地尔单一疗法反应者数量的研究进行的荟萃分析表明,只有13% - 20%的女性患者有中度的头发生长。5%的米诺地尔溶液在非标签使用时,反应者比例可能会增加到40%。因此,一种预测治疗反应的生物标志物将具有显著的临床应用价值。在之前的一项研究中,戈伦等人报告了在一组男女混合患者中,拔下的毛囊中的磺基转移酶活性与米诺地尔反应之间的关联。本研究的目的是在一组明确的接受5%米诺地尔每日治疗6个月的女性AGA患者队列中重复这些发现。与先前的研究一致,我们发现拔下的毛囊中的磺基转移酶活性预测治疗反应的敏感性为93%,特异性为83%。我们的研究进一步支持了米诺地尔硫酸化在引发治疗反应中的重要性,并为提高米诺地尔疗效的新靶点提供了进一步的见解。

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