银屑病关节炎患者肠道微生物组研究

IF 1.3 Q4 RHEUMATOLOGY
Gustavo Moreira Amorim, Gláucio Ricardo Werner Castro, Sueli Carneiro
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引用次数: 0

摘要

背景:肠道菌群失调可能在银屑病等免疫介导疾病中发挥作用。人们对了解微生物组的影响越来越感兴趣,并推测肠道微生物组的改变与银屑病进展为银屑病关节炎有关。本研究的目的是研究伴有或不伴有银屑病关节炎的严重银屑病患者的肠道微生物组:从 30 名银屑病患者的粪便样本中提取的总 DNA 进行了 V3/V4 16S rRNA 基因测序和生物信息学分析:我们发现银屑病关节炎患者的肠道微生物组组成存在相对丰度差异,尤其是差异丰度。在差异丰度上,银屑病关节炎患者的类杆菌科(P=0.02)、类杆菌属(P=0.02)和均匀类杆菌(P=0.03)的数量更多。然而,本研究并未显示α或β多样性存在显著差异:本研究显示,银屑病关节炎患者的肠道微生物组组成模式不同,其中乳杆菌属的表达量明显过高。这加强了微生物组在银屑病中的重要性。不过,需要注意的是,可能由于患者人数较少,一些之前描述的与较低的多样性和组间不同聚类有关的发现未能得到证实。此外,肠道微生物组的影响程度仍然难以理解。菌群失调是疾病的原因还是结果?然而,微生物组值得我们关注,尤其是因为它带来了通过饮食、益生元和益生菌、预处理分析、预后分析,甚至微生物组调节和移植进行干预的不同机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of the Gut Microbiome in Patients with Psoriatic Arthritis.

Background: Gut dysbiosis may play a role in immune-mediated diseases, such as psoriasis. There is a growing interest in understanding microbiome influence, with speculations around the importance of an altered gut microbiome linked to the progression to psoriatic arthritis in psoriasis. The objective of this study is to study the gut microbiome in patients with severe psoriatic disease with or without psoriatic arthritis.

Methods: V3/V4 16S rRNA gene sequencing and bioinformatics analyses were performed with the total DNA extracted from the stool samples of 30 patients with psoriatic disease, 15 of whom had documented psoriatic arthritis.

Results: We found differences in gut microbiome composition in psoriatic arthritis patients when looking for relative and especially differential abundances. Bacteroidaceae family (P = .02), Bacteroides genus (P=.02), and Bacteroides uniformis (P=.03) were more abundant in psoriatic arthritis patients on differential abundance, adjusted for each taxonomic level. However, the present study did not show significant differences in alpha or beta diversity.

Conclusion: This study shows different patterns of gut microbiome composition in patients with psoriatic arthritis, with significant overexpression of the Bacteroides genus. This reinforces the microbiome as a field of interest in psoriasis. Nevertheless, it should be noted that some previously described findings related to lower diversity and different clustering between groups could not be demonstrated, probably due to the small number of patients. Additionally, it remains difficult to understand the magnitude of the gut microbiome influence. Is dysbiosis a cause or consequence of the disease? However, the microbiome deserves our attention, especially since it brings different opportunities for intervention through diet, prebiotics and probiotics, pretreatment analysis, prognosis, and even microbiome modulation and transplantation.

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