使用阿西霉素和多霉素治疗粉红素

U. Pleyer
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引用次数: 0

摘要

目的:探讨阿奇霉素或多西环素治疗活动性红斑痤疮患者前后泪液中IL-1α和MMP-9浓度的变化。方法:应用阿奇霉素(500 mg/d,每周3天)或强力霉素(200 mg/d)治疗4周后,采用酶联免疫吸附法对泪液样品进行分析。结果:与对照组(IL-1α 0.001 pg/mL, MMP-9 0.2 ng/mL)相比,酒渣鼻眼中IL-1α (37.9 pg/mL)和MMP-9 (26.7 ng/mL)的基线水平有显著差异(p < 0.001)。IL-1α由阿奇霉素治疗前的47.0 pg/mL降至治疗后的23.5 pg/mL (p = 0.024),而多西环素治疗后无明显下降。相反,多西环素治疗后(8.36 pg/mL)基线MMP-9泪液水平(10.28 ng/mL)下降(p = 0.054),而阿奇霉素治疗后则没有下降(p = 0.054)。在多西环素治疗有效和无效的患者中,基线IL-1α泪液水平升高有很强的临床相关性(p = 0.043)。阿奇霉素无反应患者的MMP-9基线水平显著高于多西环素组(p = 0.040)。结论:阿奇霉素治疗后IL-1α水平下降,强力霉素治疗后MMP-9水平下降。在抗生素治疗失败的患者中,基线细胞因子撕裂水平往往显著升高,这表明它们可能作为该疾病的治疗性生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Behandlung okulärer Rosazea mit Azithromycin und Doxycyclin
Aims: The purpose of this paper was to determine the lacrimal concentration of IL-1α and MMP-9 in patients with active ocular rosacea before and after systemic treatment with azithromycin or doxycycline. Methods: After 4 weeks of therapy with azithromycin (500 mg/day, 3 days a week PO) or doxycycline (200 mg/day PO), lacrimal samples were analyzed using an enzyme-linked immunosorbent assay multiplex. Results: There was a significant difference between baseline IL-1α (37.9 pg/mL) and MMP-9 (26.7 ng/mL) in rosacea eyes compared to controls (0.001 pg/mL for IL-1α and 0.2 ng/mL for MMP-9) (p < 0.001). IL-1α decreased from 47.0 pg/mL before azithromycin to 23.5 pg/mL after treatment (p = 0.024), but not after doxycycline therapy. On the contrary, baseline MMP-9 tear levels (10.28 ng/mL) decreased after treatment (8.36 pg/mL) with doxycycline (p = 0.054) but not with azithromycin. There was a strong clinical correlation of higher baseline IL-1α tear levels between patients who responded to doxycycline therapy and those who failed (p = 0.043). Patients unresponsive to azithromycin had significantly higher baseline MMP-9 levels than those with doxycycline (p = 0.040). Conclusions: While IL-1α levels decreased after azithromycin therapy, MMP-9 did so after doxycycline treatment. Baseline cytokine tear levels tend to be markedly elevated in patients with antibiotic failure, suggesting their potential role as therapeutic biomarkers for the disease.
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