Han Na Oh, Seung Yong Shin, Jong-Hwa Kim, Jihye Baek, Hyo Jong Kim, Kang-Moon Lee, Soo Jung Park, Seok-Young Kim, Hyung-Kyoon Choi, Wonyong Kim, Woo Jun Sul, Chang Hwan Choi
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Regardless of clinical remission status at each time point, patients with UC exhibited microbial community distinctions from healthy controls. Distinct amplicon sequence variants (ASVs) differences were identified throughout the course of Adalimumab (ADA) treatment at each time point. A notable reduction in gut microbiome dissimilarity was observed only in remitters. Remitters demonstrated a decrease in the relative abundances of Burkholderia-Caballeronia-Paraburkholderia and Staphylococcus as the treatment progressed. Additionally, there was an observed increase in the relative abundances of Bifidobacterium and Dorea. Given the distribution of the 48 ASVs with high or low relative abundances in the pre-treatment samples according to clinical remission at week 8, a clinical remission at week 8 with a sensitivity and specificity of 72.4% and 84.3%, respectively, was predicted on the receiver operating characteristic curve (area under the curve, 0.851).</p><p><strong>Conclusions: </strong>The gut microbiota undergoes diverse changes according to the treatment response during ADA treatment. 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引用次数: 0
摘要
背景:尽管对溃疡性结肠炎患者接受抗肿瘤坏死因子α(抗 TNF-α)治疗后肠道微生物群的变化已有大量研究,但对与抗 TNF-α 作用相关的纵向变化却知之甚少。本研究旨在探讨溃疡性结肠炎(UC)患者在接受抗TNF-α(阿达木单抗)治疗期间肠道微生物群的动态变化:结果:UC患者的微生物群组成受疾病严重程度和范围的影响。无论每个时间点的临床缓解状况如何,UC 患者的微生物群落都与健康对照组有所不同。在阿达木单抗(ADA)治疗的整个过程中,每个时间点都发现了明显的扩增子序列变异(ASVs)差异。仅在缓解者中观察到肠道微生物群落差异性的显著降低。随着治疗的进展,缓解者的伯克霍尔德菌-卡巴拉氏菌-帕拉伯克霍尔德菌和葡萄球菌的相对丰度有所下降。此外,还观察到双歧杆菌和多雷氏菌的相对丰度有所增加。根据治疗前样本中相对丰度较高或较低的 48 种 ASV 在第 8 周临床缓解期的分布情况,根据接收者操作特征曲线(曲线下面积为 0.851)预测第 8 周临床缓解期的敏感性和特异性分别为 72.4% 和 84.3%:结论:在 ADA 治疗期间,肠道微生物群会根据治疗反应发生不同的变化。这些变化为预测 ADA 治疗反应提供了见解,并为 UC 提供了新的治疗目标。
Dynamic changes in the gut microbiota composition during adalimumab therapy in patients with ulcerative colitis: implications for treatment response prediction and therapeutic targets.
Background: While significant research exists on gut microbiota changes after anti-tumor necrosis factor-alpha (anti TNF-α) therapy for ulcerative colitis, little is known about the longitudinal changes related to the effects of anti TNF-α. This study aimed to investigate the dynamics of gut microbiome changes during anti TNF-α (adalimumab) therapy in patients with ulcerative colitis (UC).
Results: The microbiota composition was affected by the disease severity and extent in patients with UC. Regardless of clinical remission status at each time point, patients with UC exhibited microbial community distinctions from healthy controls. Distinct amplicon sequence variants (ASVs) differences were identified throughout the course of Adalimumab (ADA) treatment at each time point. A notable reduction in gut microbiome dissimilarity was observed only in remitters. Remitters demonstrated a decrease in the relative abundances of Burkholderia-Caballeronia-Paraburkholderia and Staphylococcus as the treatment progressed. Additionally, there was an observed increase in the relative abundances of Bifidobacterium and Dorea. Given the distribution of the 48 ASVs with high or low relative abundances in the pre-treatment samples according to clinical remission at week 8, a clinical remission at week 8 with a sensitivity and specificity of 72.4% and 84.3%, respectively, was predicted on the receiver operating characteristic curve (area under the curve, 0.851).
Conclusions: The gut microbiota undergoes diverse changes according to the treatment response during ADA treatment. These changes provide insights into predicting treatment responses to ADA and offer new therapeutic targets for UC.
Gut PathogensGASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍:
Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology.
Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).