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螺内酯的抗雄激素治疗用于治疗化脓性汗腺炎。

Antiandrogen therapy with spironolactone for the treatment of hidradenitis suppurativa.

机构信息

Stony Brook University School of Medicine, Stony Brook, New York.

Harvard Medical School and Clinical Laboratory for Epidemiology and Applied Research in Skin, Department of Dermatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.

出版信息

J Am Acad Dermatol. 2019 Jan;80(1):114-119. doi: 10.1016/j.jaad.2018.06.063. Epub 2018 Jul 10.

Abstract

BACKGROUND

Hormonal therapy is a potential treatment for hidradenitis suppurativa (HS). However, few data exist describing the efficacy of spironolactone in treatment of HS.

OBJECTIVE

To assess whether spironolactone treatment improves HS disease severity and patient-reported pain.

METHODS

We performed a single-center chart review of female patients with HS who were treated with spironolactone between 2000 and 2017. Primary outcome measurements included the HS Physician's Global Assessment (HS-PGA), Hurley staging, inflammatory lesion count, fistula count, and a numeric rating scale for pain.

RESULTS

On average, subjects were exposed to 75 mg of spironolactone daily over a 7.1-month follow-up period. Patients achieved significant disease improvement with regard to pain (Δ-1.5 [P = .01]), inflammatory lesions (Δ-1.3 [P = .02]), and HS-PGA score (Δ-0.6 [P < .001]). As expected, no change was found for Hurley stage (Δ0 [P = .32]) or fistulas (Δ0 [P = .73]). There was no difference in improvement between subjects who received less than 75 mg of spironolactone daily (n = 25; average dose, 45 mg/d) and those who received more than 100 mg daily (n = 21; average dose, 112 mg/d).

LIMITATIONS

Retrospective nature, limited sample size, and variations in severity measures documented were limiting factors.

CONCLUSIONS

Management of HS with spironolactone reduces lesion count, HS-PGA score, and pain. Lower doses appear to be effective and may be an appropriate option for patients with tolerability concerns.

摘要

背景

激素治疗是治疗化脓性汗腺炎(HS)的一种潜在方法。然而,目前很少有数据描述螺内酯治疗 HS 的疗效。

目的

评估螺内酯治疗是否能改善 HS 的严重程度和患者报告的疼痛。

方法

我们对 2000 年至 2017 年间接受螺内酯治疗的 HS 女性患者进行了单中心病历回顾。主要结局测量包括 HS 医师整体评估(HS-PGA)、Hurley 分期、炎症病变计数、瘘管计数和疼痛数字评分量表。

结果

平均而言,患者接受了 75mg 螺内酯治疗,随访时间为 7.1 个月。患者的疼痛(Δ-1.5,P =.01)、炎症病变(Δ-1.3,P =.02)和 HS-PGA 评分(Δ-0.6,P <.001)均有显著改善。如预期的那样,Hurley 分期(Δ0,P =.32)或瘘管(Δ0,P =.73)无变化。接受少于 75mg 螺内酯/天(n=25;平均剂量为 45mg/d)和接受多于 100mg 螺内酯/天(n=21;平均剂量为 112mg/d)的患者之间的改善无差异。

局限性

回顾性研究、样本量有限以及记录的严重程度测量的变化是限制因素。

结论

螺内酯治疗 HS 可减少病变计数、HS-PGA 评分和疼痛。较低剂量似乎有效,对于有耐受性问题的患者可能是一种合适的选择。

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