The Effect of an Oral Probiotic Mixture on Clinical Evolution and the Gut and Skin Microbiome in Patients with Alopecia Areata: A Randomized Clinical Trial

IF 3.4 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Cosmetics Pub Date : 2024-07-13 DOI:10.3390/cosmetics11040119
M. Navarro‐Belmonte, Ángel Aguado-García, Pedro Sánchez-Pellicer, Eva Núñez-Delegido, Laura Navarro-Moratalla, María Martínez-Villaescusa, Alejandro García-Navarro, V. Navarro-López
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Abstract

(1) Background: Given the autoimmune nature of Alopecia Areata (AA) and the immunomodulatory properties of probiotics, this trial was conducted to evaluate the efficacy of a probiotic mixture, consisting of Lactobacillus rhamnosus and Bifidobacterium longum strains, as an adjuvant treatment in a group of AA patients. (2) Method: This study was a 24-week, randomized, double-blind, placebo-controlled clinical trial. Twenty-six patients with AA were included in this study, and their clinical progression, along with changes in gut and skin microbiota, were analyzed. (3) Results: A higher proportion of AA patients treated with the probiotic formula showed improvement compared to the placebo group, based on both the reduction in the number of AA plaques (56% vs. 30%) and the affected scalp surface area (45% vs. 20%). For “activity”, “inactivity”, and “regrowth”, an improvement in 55%, 67%, and 55% of patients was, respectively, observed in the probiotic group, compared to 50%, 40%, and 30% in the placebo group. No changes were observed in the gut microbiota during the intervention period. Regarding skin microbiota, changes were detected in the probiotic group, with reductions in characteristic genera during the study. (4) Conclusions: To our knowledge, this is the first clinical trial assessing the efficacy of a probiotic product in patients with AA. This probiotic mixture in a routine clinical practice setting appears to improve the course of patients. In addition, the skin microbiota of scalp lesions was modified using the probiotic treatment.
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口服益生菌混合物对脱发患者的临床变化以及肠道和皮肤微生物组的影响:随机临床试验
(1) 背景:鉴于脱发症(AA)的自身免疫性质和益生菌的免疫调节特性,本试验旨在评估由鼠李糖乳杆菌和长双歧杆菌菌株组成的益生菌混合物作为辅助治疗手段对一组脱发症患者的疗效。(2)方法:该研究是一项为期 24 周的随机、双盲、安慰剂对照临床试验。研究纳入了 26 名 AA 患者,分析了他们的临床进展以及肠道和皮肤微生物群的变化。(3)结果:与安慰剂组相比,接受益生菌配方治疗的 AA 患者有更高比例的病情得到了改善,这主要基于 AA 斑块数量的减少(56% 对 30%)和受影响头皮表面积的减少(45% 对 20%)。在 "活性"、"非活性 "和 "再生 "方面,益生菌组分别有 55%、67% 和 55% 的患者有所改善,而安慰剂组分别为 50%、40% 和 30%。在干预期间,未观察到肠道微生物群发生变化。在皮肤微生物群方面,益生菌组发现了变化,研究期间特征菌属有所减少。(4)结论:据我们所知,这是首次评估益生菌产品对 AA 患者疗效的临床试验。在常规临床实践中,这种益生菌混合物似乎能改善患者的病情。此外,使用益生菌治疗后,头皮皮损处的皮肤微生物群也发生了改变。
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来源期刊
Cosmetics
Cosmetics Medicine-Surgery
CiteScore
5.20
自引率
12.10%
发文量
108
审稿时长
8 weeks
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