肥胖2型糖尿病患者肠道菌群和炎症标志物的关联:一项综合介入研究的事后分析

IF 3.1 4区 医学 Q2 Agricultural and Biological Sciences Bioscience of Microbiota, Food and Health Pub Date : 2022-01-01 Epub Date: 2022-02-16 DOI:10.12938/bmfh.2021-081
Yukiko Sugawara, Akio Kanazawa, Masanori Aida, Yasuto Yoshida, Yuichiro Yamashiro, Hirotaka Watada
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引用次数: 2

摘要

肠道生态失调引起的慢性炎症与代谢性疾病的病理生理有关。合成制剂有助于改善肠道生态失调;然而,目前尚不清楚哪种类型的细菌作为合成驱动的慢性炎症改善的关键标志物。在这里,我们对一项为期24周的随机对照研究进行了事后分析,该研究使用合生学来研究肠道微生物群和炎症标志物之间的关系。我们对86例肥胖2型糖尿病患者进行了研究,发现他们在服用合成益生菌后,白细胞介素-6 (IL-6)水平降低。在我们的基线分析中,青少年双歧杆菌和onderdonkii的相对丰度与IL-6、脂多糖结合蛋白(LBP)和高敏c反应蛋白(Hs-CRP)水平呈正相关。直肠真杆菌的相对丰度与LBP和Hs-CRP水平呈正相关,拟杆菌的相对丰度与LBP水平呈正相关。根据我们的应答者分析,在基线和24周时,较高的体重指数(平均超过30 kg/m2)、低丰度的卡苗拟杆菌和meracbacteroides的患者,以及与基线相比直肠杆菌和Shannon指数相对丰度变化最小的患者,与基线相比,IL-6水平下降。然而,应答者的血糖控制没有变化。总之,我们在肥胖2型糖尿病患者中确定了四种细菌种类(B. adolescent, A. onderdonkii, E. rectale和B. thetaiotaomicron)与慢性炎症和预测标志物(B. caccae, P. merdae和肥胖严重程度)相关。
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Association of gut microbiota and inflammatory markers in obese patients with type 2 diabetes mellitus: post hoc analysis of a synbiotic interventional study.

Chronic inflammation caused by gut dysbiosis is associated with the pathophysiology of metabolic disease. Synbiotics are useful for ameliorating gut dysbiosis; however, it remains unclear what types of bacteria act as key markers for synbiotic-driven improvement of chronic inflammation. Here, we performed a post hoc analysis of a 24-week randomized controlled study using synbiotics to investigate the association between gut microbiota and inflammatory markers. We characterized the responders who showed lower interleukin-6 (IL-6) levels in response to synbiotic supplementation among 86 obese patients with type 2 diabetes mellitus. In our baseline analysis, the relative abundances of Bifidobacterium adolescentis and Alistipes onderdonkii correlated positively with IL-6, lipopolysaccharide binding protein (LBP), and high-sensitivity C-reactive protein (Hs-CRP) levels. The relative abundance of Eubacterium rectale correlated positively with LBP and Hs-CRP levels, and that of Bacteroides thetaiotaomicron correlated positively with LBP levels. Based on our responder analysis, patients with higher body mass indices (over 30 kg/m2 on average), low abundances of Bacteroides caccae and Parabacteroides merdae at baseline and 24 weeks, and minimal changes in the relative abundance of E. rectale and Shannon index from baseline showed decreased IL-6 levels compared with baseline. However, glycemic control in responders was unchanged. In conclusion, we identified four bacterial species (B. adolescentis, A. onderdonkii, E. rectale, and B. thetaiotaomicron) related to chronic inflammation and predictive markers (B. caccae, P. merdae, and severity of obesity) in responders to synbiotic supplementation among obese patients with type 2 diabetes.

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来源期刊
Bioscience of Microbiota, Food and Health
Bioscience of Microbiota, Food and Health Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
5.50
自引率
3.20%
发文量
24
期刊介绍: Bioscience of Microbiota, Food and Health (BMFH) is a peer-reviewed scientific journal with a specific area of focus: intestinal microbiota of human and animals, lactic acid bacteria (LAB) and food immunology and food function. BMFH contains Full papers, Notes, Reviews and Letters to the editor in all areas dealing with intestinal microbiota, LAB and food immunology and food function. BMFH takes a multidisciplinary approach and focuses on a broad spectrum of issues.
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