膳食纤维,肠道菌群失调和2型糖尿病

O. Ojo, Qianqian Feng, Osarhumwese Osaretin Ojo, Xiaohua Wang
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引用次数: 0

摘要

背景:全球糖尿病患病率呈上升趋势,其对急性和慢性并发症患者的影响可能是深远的。2型糖尿病患者占大多数,其风险因素包括肥胖、生活方式和肠道菌群失调。据报道,不良的饮食摄入会影响肠道微生物群落。因此,较高的膳食纤维摄入量可能会改变肠道环境,促进微生物的生长和增殖。目的:这是一项系统综述和荟萃分析,研究了膳食纤维对2型糖尿病患者肠道微生物群的影响。方法:本综述按照PRISMA框架进行。检索数据库,根据纳入和排除标准筛选相关文章。结果:9篇符合纳入标准的文章被纳入系统评价和meta分析。高膳食纤维摄入量显著提高了双歧杆菌、总短链脂肪酸(SCFAs)和HbA1c丰度(p < 0.05)。讨论:在膳食纤维的多样性和丰富性方面,促进SCFA生产者可能导致糖化血红蛋白的改善,部分原因是GLP-1的产生增加。结论:高膳食纤维摄入对双歧杆菌、总SCFAs和HbA1c有显著影响(p < 0.05),对丙酸、丁酸和乙酸、空腹血糖和胰岛素抵抗homa - ir稳态模型评估无显著影响(p > 0.05)。
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Dietary fibre, gut microbiota dysbiosis and type 2 diabetes
: Background: Diabetes prevalence is on the increase globally and its impact on those with the condition in terms of acute and chronic complications can be profound. People with type 2 diabetes constitute the majority of those with the condition and the risk factors include obesity, lifestyle and gut microbiota dysbiosis. Poor dietary intake has been reported to influence the community of the gut microbiome. Therefore, a higher intake of dietary fibre may alter the environment in the gut and promote microbial growth and proliferation. Aim: This is a systematic review and meta-analysis which examined the effect of dietary fibre on gut microbiota in patients with type 2 diabetes. Method: This review was conducted in line with the PRISMA framework. Databases were searched for relevant articles which were screened based on inclusion and exclusion criteria. Results: Nine articles which met the inclusion criteria were selected for the systematic review and meta-analysis. High dietary fibre intake significantly improved ( p < 0.05) the abundance of Bifidobacterium, total short-chain fatty acids (SCFAs) and HbA1c. Discussion: The promotion of SCFA producers in terms of greater diversity and abundance by dietary fibre may have resulted in improvement in glycated haemoglobin, partly due to increased GLP–1 production. Conclusion: High consumption of dietary fibre has a significant ( p < 0.05) effect on Bifidobacterium, total SCFAs and HbA1c, but not ( p > 0.05) on propionic, butyric and acetic acid, fasting blood glucose and the homeostatic model assessment of insulin resistance HOMAR–IR.
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