Microbiome–metabolome reveals the contribution of gut–kidney axis on kidney disease

代谢组 肾脏疾病 微生物群 疾病 肠道微生物群 生物信息学 医学 代谢组学 生物 计算生物学 病理 内科学
作者
Yuanyuan Chen,Dan‐Qian Chen,Lin Chen,Jingru Liu,Nosratola D. Vaziri,Yan Guo,Ying‐Yong Zhao
出处
期刊:Journal of Translational Medicine [BioMed Central]
卷期号:17 (1): 5-5 被引量:419
标识
DOI:10.1186/s12967-018-1756-4
摘要

Dysbiosis represents changes in composition and structure of the gut microbiome community (microbiome), which may dictate the physiological phenotype (health or disease). Recent technological advances and efforts in metagenomic and metabolomic analyses have led to a dramatical growth in our understanding of microbiome, but still, the mechanisms underlying gut microbiome-host interactions in healthy or diseased state remain elusive and their elucidation is in infancy. Disruption of the normal gut microbiota may lead to intestinal dysbiosis, intestinal barrier dysfunction, and bacterial translocation. Excessive uremic toxins are produced as a result of gut microbiota alteration, including indoxyl sulphate, p-cresyl sulphate, and trimethylamine-N-oxide, all implicated in the variant processes of kidney diseases development. This review focuses on the pathogenic association between gut microbiota and kidney diseases (the gut-kidney axis), covering CKD, IgA nephropathy, nephrolithiasis, hypertension, acute kidney injury, hemodialysis and peritoneal dialysis in clinic. Targeted interventions including probiotic, prebiotic and symbiotic measures are discussed for their potential of re-establishing symbiosis, and more effective strategies for the treatment of kidney diseases patients are suggested. The novel insights into the dysbiosis of the gut microbiota in kidney diseases are helpful to develop novel therapeutic strategies for preventing or attenuating kidney diseases and complications.

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