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Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial

BACKGROUND: The gut microbiota has been suggested to play a significant role in the development of overweight and obesity. However, the effects of calorie restriction on gut microbiota of overweight and obese adults, especially over longer durations, are largely unexplored. METHODS: Here, we longitu...

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Autores principales: Sowah, Solomon A., Milanese, Alessio, Schübel, Ruth, Wirbel, Jakob, Kartal, Ece, Johnson, Theron S., Hirche, Frank, Grafetstätter, Mirja, Nonnenmacher, Tobias, Kirsten, Romy, López-Nogueroles, Marina, Lahoz, Agustín, Schwarz, Kathrin V., Okun, Jürgen G., Ulrich, Cornelia M., Nattenmüller, Johanna, von Eckardstein, Arnold, Müller, Daniel, Stangl, Gabriele I., Kaaks, Rudolf, Kühn, Tilman, Zeller, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919571/
https://www.ncbi.nlm.nih.gov/pubmed/35287713
http://dx.doi.org/10.1186/s13073-022-01030-0
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author Sowah, Solomon A.
Milanese, Alessio
Schübel, Ruth
Wirbel, Jakob
Kartal, Ece
Johnson, Theron S.
Hirche, Frank
Grafetstätter, Mirja
Nonnenmacher, Tobias
Kirsten, Romy
López-Nogueroles, Marina
Lahoz, Agustín
Schwarz, Kathrin V.
Okun, Jürgen G.
Ulrich, Cornelia M.
Nattenmüller, Johanna
von Eckardstein, Arnold
Müller, Daniel
Stangl, Gabriele I.
Kaaks, Rudolf
Kühn, Tilman
Zeller, Georg
author_facet Sowah, Solomon A.
Milanese, Alessio
Schübel, Ruth
Wirbel, Jakob
Kartal, Ece
Johnson, Theron S.
Hirche, Frank
Grafetstätter, Mirja
Nonnenmacher, Tobias
Kirsten, Romy
López-Nogueroles, Marina
Lahoz, Agustín
Schwarz, Kathrin V.
Okun, Jürgen G.
Ulrich, Cornelia M.
Nattenmüller, Johanna
von Eckardstein, Arnold
Müller, Daniel
Stangl, Gabriele I.
Kaaks, Rudolf
Kühn, Tilman
Zeller, Georg
author_sort Sowah, Solomon A.
collection PubMed
description BACKGROUND: The gut microbiota has been suggested to play a significant role in the development of overweight and obesity. However, the effects of calorie restriction on gut microbiota of overweight and obese adults, especially over longer durations, are largely unexplored. METHODS: Here, we longitudinally analyzed the effects of intermittent calorie restriction (ICR) operationalized as the 5:2 diet versus continuous calorie restriction (CCR) on fecal microbiota of 147 overweight or obese adults in a 50-week parallel-arm randomized controlled trial, the HELENA Trial. The primary outcome of the trial was the differential effects of ICR versus CCR on gene expression in subcutaneous adipose tissue. Changes in the gut microbiome, which are the focus of this publication, were defined as exploratory endpoint of the trial. The trial comprised a 12-week intervention period, a 12-week maintenance period, and a final follow-up period of 26 weeks. RESULTS: Both diets resulted in ~5% weight loss. However, except for Lactobacillales being enriched after ICR, post-intervention microbiome composition did not significantly differ between groups. Overall weight loss was associated with significant metabolic improvements, but not with changes in the gut microbiome. Nonetheless, the abundance of the Dorea genus at baseline was moderately predictive of subsequent weight loss (AUROC of 0.74 for distinguishing the highest versus lowest weight loss quartiles). Despite the lack of consistent intervention effects on microbiome composition, significant study group-independent co-variation between gut bacterial families and metabolic biomarkers, anthropometric measures, and dietary composition was detectable. Our analysis in particular revealed associations between insulin sensitivity (HOMA-IR) and Akkermansiaceae, Christensenellaceae, and Tanerellaceae. It also suggests the possibility of a beneficial modulation of the latter two intestinal taxa by a diet high in vegetables and fiber, and low in processed meat. CONCLUSIONS: Overall, our results suggest that the gut microbiome remains stable and highly individual-specific under dietary calorie restriction. TRIAL REGISTRATION: The trial, including the present microbiome component, was prospectively registered at ClinicalTrials.govNCT02449148 on May 20, 2015. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-022-01030-0.
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spelling pubmed-89195712022-03-16 Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial Sowah, Solomon A. Milanese, Alessio Schübel, Ruth Wirbel, Jakob Kartal, Ece Johnson, Theron S. Hirche, Frank Grafetstätter, Mirja Nonnenmacher, Tobias Kirsten, Romy López-Nogueroles, Marina Lahoz, Agustín Schwarz, Kathrin V. Okun, Jürgen G. Ulrich, Cornelia M. Nattenmüller, Johanna von Eckardstein, Arnold Müller, Daniel Stangl, Gabriele I. Kaaks, Rudolf Kühn, Tilman Zeller, Georg Genome Med Research BACKGROUND: The gut microbiota has been suggested to play a significant role in the development of overweight and obesity. However, the effects of calorie restriction on gut microbiota of overweight and obese adults, especially over longer durations, are largely unexplored. METHODS: Here, we longitudinally analyzed the effects of intermittent calorie restriction (ICR) operationalized as the 5:2 diet versus continuous calorie restriction (CCR) on fecal microbiota of 147 overweight or obese adults in a 50-week parallel-arm randomized controlled trial, the HELENA Trial. The primary outcome of the trial was the differential effects of ICR versus CCR on gene expression in subcutaneous adipose tissue. Changes in the gut microbiome, which are the focus of this publication, were defined as exploratory endpoint of the trial. The trial comprised a 12-week intervention period, a 12-week maintenance period, and a final follow-up period of 26 weeks. RESULTS: Both diets resulted in ~5% weight loss. However, except for Lactobacillales being enriched after ICR, post-intervention microbiome composition did not significantly differ between groups. Overall weight loss was associated with significant metabolic improvements, but not with changes in the gut microbiome. Nonetheless, the abundance of the Dorea genus at baseline was moderately predictive of subsequent weight loss (AUROC of 0.74 for distinguishing the highest versus lowest weight loss quartiles). Despite the lack of consistent intervention effects on microbiome composition, significant study group-independent co-variation between gut bacterial families and metabolic biomarkers, anthropometric measures, and dietary composition was detectable. Our analysis in particular revealed associations between insulin sensitivity (HOMA-IR) and Akkermansiaceae, Christensenellaceae, and Tanerellaceae. It also suggests the possibility of a beneficial modulation of the latter two intestinal taxa by a diet high in vegetables and fiber, and low in processed meat. CONCLUSIONS: Overall, our results suggest that the gut microbiome remains stable and highly individual-specific under dietary calorie restriction. TRIAL REGISTRATION: The trial, including the present microbiome component, was prospectively registered at ClinicalTrials.govNCT02449148 on May 20, 2015. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-022-01030-0. BioMed Central 2022-03-14 /pmc/articles/PMC8919571/ /pubmed/35287713 http://dx.doi.org/10.1186/s13073-022-01030-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sowah, Solomon A.
Milanese, Alessio
Schübel, Ruth
Wirbel, Jakob
Kartal, Ece
Johnson, Theron S.
Hirche, Frank
Grafetstätter, Mirja
Nonnenmacher, Tobias
Kirsten, Romy
López-Nogueroles, Marina
Lahoz, Agustín
Schwarz, Kathrin V.
Okun, Jürgen G.
Ulrich, Cornelia M.
Nattenmüller, Johanna
von Eckardstein, Arnold
Müller, Daniel
Stangl, Gabriele I.
Kaaks, Rudolf
Kühn, Tilman
Zeller, Georg
Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial
title Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial
title_full Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial
title_fullStr Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial
title_full_unstemmed Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial
title_short Calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial
title_sort calorie restriction improves metabolic state independently of gut microbiome composition: a randomized dietary intervention trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919571/
https://www.ncbi.nlm.nih.gov/pubmed/35287713
http://dx.doi.org/10.1186/s13073-022-01030-0
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