P1219 接受生物疗法的炎症性肠病患者肠道微生物群的变化

W. C. Tai, C. C. Yao, Y. -. Tsai
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引用次数: 0

摘要

炎症性肠病(IBD)主要包括克罗恩病(CD)和溃疡性结肠炎(UC),与肠道菌群失调的组成和代谢变化有关。这是一项前瞻性研究,共招募了 14 名接受生物疗法的 IBD 患者和 13 名接受常规治疗的 IBD 对照组患者。通过对粪便样本进行 16S 核糖体 RNA 基因测序,确定了肠道微生物群的分类组成。我们对基线、生物疗法开始后第 6 周和第 48 周的粪便样本进行了评估。我们还通过 BD 活动评分评估了炎症水平和对生物制剂的治疗反应(CD 患者通过克罗恩病活动指数 [CDAI] 评估,UC 患者通过梅奥评分评估)。 在 CD 组中,我们招募了 7 名接受生物制剂治疗(抗肿瘤坏死因子 4 和抗整合素 3)的 CD 患者和 6 名对照组;在 UC 组中,我们招募了 7 名接受生物制剂治疗(抗肿瘤坏死因子 2 和抗整合素 5)的 UC 患者和 7 名对照组。与对照组相比,生物制剂组患者在基线期的群落α多样性明显较低,但在第6周和第48周达到缓解后,群落α多样性和丰富度分别呈上升趋势。在前 10 个分类群的细菌分布中,固有菌的丰度逐渐增加(生物制剂 W0、W6、W48 和对照组的相对丰度分别为 46.3%、51.7%、62.0% 和 66.4%)。相反,类杆菌的丰度则有所下降(W0、W6、W48 和对照组的相对丰度分别为 18.3%、18.8%、10.2% 和 6.4%)。我们的研究还发现,生物制剂治疗后,F/B 比值明显增加。(F/B比值分别为9.4、12.5、64.0和84.3)。相比之下,在 W0 期,生物制剂组患者的肠杆菌科和类杆菌科细菌数量明显较多。 生物制剂治疗改善了 IBD 患者的群落多样性,提高了 F/B 比率,这似乎与临床炎症程度有关。肠杆菌科等代表菌群失调的细菌可诱发结肠炎症,在 IBD 活动度较高的患者中数量更多。还需要进一步开展更大规模的前瞻性研究,以确定生物疗法是否会引起肠道微生物组的长期变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P1219 Changes in gut microbiota of patients with inflammatory bowel disease receiving biologic therapy
Inflammatory bowel disease (IBD), comprising the predominant forms Crohn’s disease (CD) and ulcerative colitis (UC), is associated with compositional and metabolic changes in the intestinal dysbiosis. The aim of this study is to evaluate the composition in the microbiota of IBD patients who received biologic therapy This is a prospective study recruited 14 patients with IBD received biologic therapy and 13 IBD controls who received conventional treatment . The taxonomic composition of the gut microbiota was determined by 16S ribosomal RNA gene sequencing of stool samples. The stool samples at baseline, weeks 6 and 48 after biologic therapy initiation were assessed. We also evaluated the level of inflammation and treatment response of biologics by BD activity score (CD patient by Crohn’s disease activity index [CDAI] and in UC patient by Mayo score). In CD group, we recruited 7 CD patients receiving biologic therapy (Anti-tumor Necrosis Factor for 4 and anti-integrin for 3) and 6 controls.In UC group, we recruited 7 UC patient receiving biological therapy (Anti-tumor Necrosis Factor for 2 and anti-integrin for 5) and 7 controls. Community α-diversity was lower in patients at baseline of biologics group compare to controls significantly but increase abundance and richness after achieving remission in trend at week 6 and week 48, respectively. In Top 10 taxon bacterial distribution, the Firmicutes were increase its abundances gradually ( relative abundance in biologics W0,W6,W48 and controls were 46.3%, 51.7%,62.0%, and 66.4%, respectively). Conversely, the Bacteroidetes were decrease its abundances ( relative abundance in biologics W0,W6,W48 and controls were18.3%, 18.8%, 10.2% and 6.4%, respectively). Increased F/B ratio significantly after biologics therapy also found in our study. (F/B ratio were 9.4, 12.5,64.0,and 84.3,respectively). Patients in control group had higher abundance of Firmicutes of the phylum.By contrast, Enterobacteriaceae and Bacteroidaceae were significantly more abundant in patients of biologics group at W0 . Treatment with biologic therapy induced improvement of community diversity and increased F/B ratio in IBD patients which seemed correlate the level of clinical inflammation. The dysbiosis-representative bacteria, such as Enterobacteriaceae, could induce colonic inflammation,were more abundant in patients who had higher activity of IBD. Further larger prospective studies are needed to determine whether the biologic therapy could induce long-term changes of intestinal microbiome.
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