Center for Natural Sciences and Humanities, Federal University of ABC, Santo André-SP, Brazil.
J Am Nutr Assoc. 2024 Feb;43(2):139-146. doi: 10.1080/27697061.2023.2232021. Epub 2023 Jul 17.
Atopic dermatitis (AD) is a prevalent chronic skin disease affecting all age groups. The connection with the gut microbiome led to oral probiotics as a therapeutic strategy. However, being viable microorganisms, probiotics might present risks. Thus, non-viable postbiotics have been considered as an alternative. We aimed to evaluate the efficacy of oral postbiotics for managing symptoms of AD in pediatric and adult patients. A systematic review was conducted following PRISMA guidelines. Nine randomized controlled trials assessing the effects of non-viable spp. administered orally to patients diagnosed with AD were included in the review, in which 512 subjects were evaluated after the intervention. Most studies allowed the concomitant usage of corticosteroids. Three studies focused on adults and indicated symptom improvement. In contrast, three out of six trials evaluating pediatric patients did not report postbiotics-favoring results. The dosage seems to be relevant for outcome determination. Two trials compared postbiotics with their viable analogs, and only one reported positive results in both groups. Postbiotics-associated shifts in gut microbial communities were reported in one trial. Mild adverse effects were detected by a single study. The overall results suggested that postbiotics might be successfully used as adjuvant AD therapy in adults. Thus far, data do not indicate efficacy in pediatric patients. Standardizing nomenclatures and experimental procedures, as well as expanding the studies to more geographic locations and assessing comprehensively the effects on the gut microbiome would provide better perspectives of postbiotics as a therapeutic option for AD.
特应性皮炎(AD)是一种普遍存在的慢性皮肤病,影响所有年龄段。与肠道微生物组的联系导致口服益生菌成为一种治疗策略。然而,作为有活力的微生物,益生菌可能存在风险。因此,非活性后生元已被认为是一种替代方法。我们旨在评估口服后生元在管理儿科和成年患者 AD 症状方面的疗效。按照 PRISMA 指南进行了系统评价。纳入了 9 项评估非活性 spp.经口给予 AD 患者的影响的随机对照试验,干预后对 512 名受试者进行了评估。大多数研究允许同时使用皮质类固醇。三项研究针对成年人,并表明症状改善。相比之下,评估儿科患者的 6 项试验中有 3 项没有报告后生元有利的结果。剂量似乎对结果的确定很重要。两项试验比较了后生元和它们的活菌类似物,只有一项报告了两组的阳性结果。一项试验报告了后生元相关的肠道微生物群落的变化。一项研究检测到轻微的不良反应。总体结果表明,后生元可能成功地用作成人 AD 的辅助治疗。迄今为止,数据并未表明在后生元在儿科患者中有效。标准化命名法和实验程序,以及扩大研究范围到更多地理位置,并全面评估对肠道微生物组的影响,将为后生元作为 AD 的治疗选择提供更好的前景。