Bridging the Gap from Enterotypes to Personalized Dietary Recommendations: A Metabolomics Perspective on Microbiome Research

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dc.identifier.uri http://dx.doi.org/10.15488/16667
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/16794
dc.contributor.author Bartsch, Madeline
dc.contributor.author Hahn, Andreas
dc.contributor.author Berkemeyer, Shoma
dc.date.accessioned 2024-03-20T07:11:00Z
dc.date.available 2024-03-20T07:11:00Z
dc.date.issued 2023
dc.identifier.citation Bartsch, M.; Hahn, A.; Berkemeyer, S.: Bridging the Gap from Enterotypes to Personalized Dietary Recommendations: A Metabolomics Perspective on Microbiome Research. In: Metabolites 13 (2023), Nr. 12, 1182. DOI: https://doi.org/10.3390/metabo13121182
dc.description.abstract Advances in high-throughput DNA sequencing have propelled research into the human microbiome and its link to metabolic health. We explore microbiome analysis methods, specifically emphasizing metabolomics, how dietary choices impact the production of microbial metabolites, providing an overview of studies examining the connection between enterotypes and diet, and thus, improvement of personalized dietary recommendations. Acetate, propionate, and butyrate constitute more than 95% of the collective pool of short-chain fatty acids. Conflicting data on acetate’s effects may result from its dynamic signaling, which can vary depending on physiological conditions and metabolic phenotypes. Human studies suggest that propionate has overall anti-obesity effects due to its well-documented chemistry, cellular signaling mechanisms, and various clinical benefits. Butyrate, similar to propionate, has the ability to reduce obesity by stimulating the release of appetite-suppressing hormones and promoting the synthesis of leptin. Tryptophan affects systemic hormone secretion, with indole stimulating the release of GLP-1, which impacts insulin secretion, appetite suppression, and gastric emptying. Bile acids, synthesized from cholesterol in the liver and subsequently modified by gut bacteria, play an essential role in the digestion and absorption of dietary fats and fat-soluble vitamins, but they also interact directly with intestinal microbiota and their metabolites. One study using statistical methods identified primarily two groupings of enterotypes Bacteroides and Ruminococcus. The Prevotella-dominated enterotype, P-type, in humans correlates with vegetarians, high-fiber and carbohydrate-rich diets, and traditional diets. Conversely, individuals who consume diets rich in animal fats and proteins, typical in Western-style diets, often exhibit the Bacteroides-dominated, B-type, enterotype. The P-type showcases efficient hydrolytic enzymes for plant fiber degradation but has limited lipid and protein fermentation capacity. Conversely, the B-type features specialized enzymes tailored for the degradation of animal-derived carbohydrates and proteins, showcasing an enhanced saccharolytic and proteolytic potential. Generally, models excel at predictions but often struggle to fully elucidate why certain substances yield varied responses. These studies provide valuable insights into the potential for personalized dietary recommendations based on enterotypes. eng
dc.language.iso eng
dc.publisher Basel : MDPI
dc.relation.ispartofseries Metabolites 13 (2023), Nr. 12
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0
dc.subject acetate eng
dc.subject bile acids eng
dc.subject butyrate eng
dc.subject enterotypes eng
dc.subject metabolomics eng
dc.subject personalized dietary recommendations eng
dc.subject propionate eng
dc.subject tryptophan eng
dc.subject.ddc 570 | Biowissenschaften, Biologie
dc.subject.ddc 540 | Chemie
dc.title Bridging the Gap from Enterotypes to Personalized Dietary Recommendations: A Metabolomics Perspective on Microbiome Research eng
dc.type Article
dc.type Text
dc.relation.essn 2218-1989
dc.relation.doi https://doi.org/10.3390/metabo13121182
dc.bibliographicCitation.issue 12
dc.bibliographicCitation.volume 13
dc.bibliographicCitation.firstPage 1182
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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