Ifeanyi Onyema Oshim, N. Agbakoba, K. Anukam, A. A. Obroh, C. M. Obi, Amaechi Chukwudi Ofodile
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引用次数: 0
摘要
背景:代谢疾病如2型糖尿病(T2DM)和肥胖已成为世界范围内重要的公共卫生问题。大量证据表明,肠道变形菌门和细菌门与这些合并症有关。因此,肠道微生物群作为代谢紊乱预后的一个有希望的靶点。本研究的目的是评估肠道变形菌群和拟杆菌群在肥胖相关的2型糖尿病中的作用。采用针对V3-V4高变区16S rRNA测序对10例成人的肠道菌群特征进行研究,并使用SPSS version 26对数据进行分析。结果:Pearson相关分析显示,拟杆菌门与体重指数(BMI)相关性显著(r = 0.666, p = 0.002*),其次是变形菌门(r = 0.464, p = 0.045*)、厚壁菌门与BMI (p>0.05)、放线菌门与BMI (p>0.05)、厚壁菌门与糖化血红蛋白(HbA1c) (p>0.05)、拟杆菌门与HbA1c (p>0.05)、变形菌门与HbA1c (p>0.05)、放线菌门与HbA1c (p>0.05)。结论:变形菌门和拟杆菌门的丰度与肥胖相关的2型糖尿病有显著相关性。然而,这些门/分类群与肥胖相关的2型糖尿病的Hb1Ac无显著相关性。
Association of Proteobacteria and Bacteriodetes with Obese Related Type-2 Diabetes Mellitus
Background: Metabolic conditions such as Type2 diabetes mellitus (T2DM) and obesity have become worldwide public health important. Numerous evidences indicate that gut Proteobacteria and Bacteriodetes are associated with these co-morbidities. Thus, the gut microbiota serves as a promising target for prognosis of metabolic disorders. The aim of this study is to evaluate the role of gut Proteobacteria and Bacteriodetes on obese related Type 2 diabetes mellitus. The gut microbiota signature of 10 adults was studied using 16S rRNA sequencing targeting V3–V4 hypervariable regions and obtained data was analyzed using Statistical Package for the Social Science (SPSS version 26). Result: The Pearson correlation analysis showed that phyla Bacteriodetes was significant positive when correlated with Body mass index (BMI) (r = 0.666, p = 0.002*), followed by phyla proteobacteria (r = 0.464, p = 0.045*), Firmicutes versus BMI (p>0.05), Actinobacteria versus BMI (p>0.05), while Firmicutes versus Glycated hemoglobin(HbA1c) (p>0.05), Bacteriodetes versus HbA1c (p>0.05), Proteobacteria versus HbA1c (p>0.05), Actinobacteria versus HbA1c (p> 0.05). Conclusion: The study revealed the abundance of phyla Proteobacteria and phyla Bacteriodetes were significantly associated with obese related type 2 diabetes mellitus. Although, these Phyla/ taxa showed no significant correlation with Hb1Ac in obese related type 2 diabetes mellitus.