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Cited 26 time in webofscience Cited 28 time in scopus
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Differential effects of typical Korean versus american-style diets on gut microbial composition and metabolic profile in healthy overweight koreans: A randomized crossover trialopen access

Authors
Shin, J.-H.[Shin, J.-H.]Jung, S.[Jung, S.]Kim, S.-A.[Kim, S.-A.]Kang, M.-S.[Kang, M.-S.]Kim, M.-S.[Kim, M.-S.]Joung, H.[Joung, H.]Hwang, G.-S.[Hwang, G.-S.]Shin, D.-M.[Shin, D.-M.]
Issue Date
Oct-2019
Publisher
MDPI AG
Keywords
American diet; Enterotype; Gut microbiota; Korean diet; Metabolomics; Randomized crossover trial
Citation
Nutrients, v.11, no.10
Indexed
SCIE
SCOPUS
Journal Title
Nutrients
Volume
11
Number
10
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/13973
DOI
10.3390/nu11102450
ISSN
2072-6643
Abstract
The Westernized diet has been associated with the pathogenesis of metabolic diseases, whereas a Korean diet has been reported to exert beneficial effects on health in several studies. However, the effects of Western and Korean diets on the gut microbiome and host metabolome are unclear. To examine the diet-specific effects on microbiome and metabolome, we conducted a randomized crossover clinical trial of typical Korean diet (TKD), typical American diet (TAD), and recommended American diet (RAD). The trial involved a 4-week consumption of an experimental diet followed by a 2-week interval before diet crossover. 16S rRNA sequencing analysis identified 16, 10, and 14 differential bacteria genera specific to TKD, RAD, and TAD, respectively. The Firmucutes-Bacteroidetes ratio was increased by TKD. Nuclear magnetic resonance metabolome profiling revealed that TKD enriched branched chain amino acid metabolism, whereas ketone body metabolism was evident in RAD and TAD. Microbiome and metabolome responses to the experimental diets varied with individual enterotypes. These findings provide evidence that the gut microbiome and host metabolome rapidly respond to different cultural diets. The findings will inform clarification of the diet-related communication networks of the gut microbiome and host metabolome in humans. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.
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