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Chronic Kidney Disease and Gut Microbiota: What Is Their Connection in Early Life?

期刊

出版社

MDPI
DOI: 10.3390/ijms23073954

关键词

chronic kidney disease; hypertension; children; short-chain fatty acids; developmental origins of health and disease (DOHaD); gut microbiota; probiotics; prebiotics; trimethylamine-N-oxide

资金

  1. Ministry of Science and Technology, Taiwan [MOST 110-2314-B-182-020-MY3, MOST 110-2314-B-182A-029]
  2. Chang Gung Memorial Hospital, Kaohsiung, Taiwan [CORPG8M0081, CORPG8M0151]

向作者/读者索取更多资源

The gut-kidney interaction and gut microbiota-targeted therapies have gained increasing attention in the research of chronic kidney disease (CKD). Understanding the impact of early-life gut microbiome on CKD and the development of early interventions are crucial for reducing CKD.
The gut-kidney interaction implicating chronic kidney disease (CKD) has been the focus of increasing interest in recent years. Gut microbiota-targeted therapies could prevent CKD and its comorbidities. Considering that CKD can originate in early life, its treatment and prevention should start in childhood or even earlier in fetal life. Therefore, a better understanding of how the early-life gut microbiome impacts CKD in later life and how to develop ideal early interventions are unmet needs to reduce CKD. The purpose of the current review is to summarize (1) the current evidence on the gut microbiota dysbiosis implicated in pediatric CKD; (2) current knowledge supporting the impact of the gut-kidney axis in CKD, including inflammation, immune response, alterations of microbiota compositions, short-chain fatty acids, and uremic toxins; and (3) an overview of the studies documenting early gut microbiota-targeted interventions in animal models of CKD of developmental origins. Treatment options include prebiotics, probiotics, postbiotics, etc. To accelerate the transition of gut microbiota-based therapies for early prevention of CKD, an extended comprehension of gut microbiota dysbiosis implicated in renal programming is needed, as well as a greater focus on pediatric CKD for further clinical translation.

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