Ćesić Diana, Lugović Mihić Liborija, Ozretić Petar, Lojkić Ivana, Buljan Marija, Šitum Mirna, Zovak Mario, Vidović Dinko, Mijić August, Galić Nada, Tambić Andrašević Arjana
Department of Dermatology and Venereology, Medikol Clinic, 10000 Zagreb, Croatia.
School of Dental Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Life (Basel). 2023 May 30;13(6):1280. doi: 10.3390/life13061280.
(1) Background: Chronic spontaneous urticaria (CSU) has been linked to the dysbiosis of the gut microbiota. Furthermore, various studies have highlighted the anti-inflammatory properties of short-chain fatty acids (SCFAs), whose production is primarily regulated by the gut microbiota. However, only a few studies have investigated the role of major SCFA producers, such as , in skin inflammatory diseases. (2) Goal: This study aimed to compare the abundance of between CSU patients and healthy controls (HCs). (3) Material and methods: In this case-control study, 16S rRNA sequencing was performed to compare the composition of the gut microbiome between 22 CSU patients and 23 HCs. (4) Results: Beta-diversity revealed significant clustering ( < 0.05) between the CSU patients and HCs. Alpha diversity in the CSU group was significantly decreased according to the Evenness index ( < 0.05). The linear discriminant analysis effect size (LEfSe) identified the significant depletion of the family in CSU patients. (5) Conclusion: Our study revealed the dysbiosis of the gut microbiota in CSU patients, including decreased levels of members, responsible for SCFA production, suggesting that SCFAs may contribute to immune dysfunction in the pathogenesis of CSU. We speculate that the modulation of SCFAs could serve as a prospective additional option in CSU treatment.
(1) 背景:慢性自发性荨麻疹(CSU)与肠道微生物群失调有关。此外,各种研究强调了短链脂肪酸(SCFAs)的抗炎特性,其产生主要由肠道微生物群调节。然而,只有少数研究调查了主要短链脂肪酸产生菌,如 ,在皮肤炎症性疾病中的作用。(2) 目的:本研究旨在比较CSU患者和健康对照(HCs)之间 的丰度。(3) 材料和方法:在这项病例对照研究中,进行了16S rRNA测序,以比较22例CSU患者和23例HCs之间的肠道微生物组组成。(4) 结果:β多样性显示CSU患者和HCs之间存在显著聚类(<0.05)。根据均匀度指数,CSU组的α多样性显著降低(<0.05)。线性判别分析效应大小(LEfSe)确定CSU患者中 科显著减少。(5) 结论:我们的研究揭示了CSU患者肠道微生物群失调,包括负责产生短链脂肪酸的 成员水平降低,这表明短链脂肪酸可能在CSU发病机制中导致免疫功能障碍。我们推测,调节短链脂肪酸可能是CSU治疗中一种潜在的额外选择。