Long-term fasting: Multi-system adaptations in humans (GENESIS) study–A single-arm interventional trial
Fasting provokes fundamental changes in the activation of metabolic and signaling pathways leading to longer and healthier lifespans in animal models. Although the involvement of different metabolites in fueling human fasting metabolism is well known, the contribution of tissues and organs to their...
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Published in | Frontiers in nutrition (Lausanne) Vol. 9; p. 951000 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
17.11.2022
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Abstract | Fasting provokes fundamental changes in the activation of metabolic and signaling pathways leading to longer and healthier lifespans in animal models. Although the involvement of different metabolites in fueling human fasting metabolism is well known, the contribution of tissues and organs to their supply remains partly unclear. Also, changes in organ volume and composition remain relatively unexplored. Thus, processes involved in remodeling tissues during fasting and food reintroduction need to be better understood. Therefore, this study will apply state-of-the-art techniques to investigate the effects of long-term fasting (LF) and food reintroduction in humans by a multi-systemic approach focusing on changes in body composition, organ and tissue volume, lipid transport and storage, sources of protein utilization, blood metabolites, and gut microbiome profiles in a single cohort. This is a prospective, single-arm, monocentric trial. One hundred subjects will be recruited and undergo 9 ± 3 day-long fasting periods (250 kcal/day). We will assess changes in the composition of organs, bones and blood lipid profiles before and after fasting, as well as high-density lipoprotein (HDL) transport and storage, untargeted metabolomics of peripheral blood mononuclear cells (PBMCs), protein persulfidation and shotgun metagenomics of the gut microbiome. The first 32 subjects, fasting for 12 days, will be examined in more detail by magnetic resonance imaging (MRI) and spectroscopy to provide quantitative information on changes in organ volume and function, followed by an additional follow-up examination after 1 and 4 months. The study protocol was approved by the ethics board of the State Medical Chamber of Baden-Württemberg on 26.07.2021 and registered at
ClinicalTrials.gov
(NCT05031598). The results will be disseminated through peer-reviewed publications, international conferences and social media. |
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AbstractList | Fasting provokes fundamental changes in the activation of metabolic and signaling pathways leading to longer and healthier lifespans in animal models. Although the involvement of different metabolites in fueling human fasting metabolism is well known, the contribution of tissues and organs to their supply remains partly unclear. Also, changes in organ volume and composition remain relatively unexplored. Thus, processes involved in remodeling tissues during fasting and food reintroduction need to be better understood. Therefore, this study will apply state-of-the-art techniques to investigate the effects of long-term fasting (LF) and food reintroduction in humans by a multi-systemic approach focusing on changes in body composition, organ and tissue volume, lipid transport and storage, sources of protein utilization, blood metabolites, and gut microbiome profiles in a single cohort. This is a prospective, single-arm, monocentric trial. One hundred subjects will be recruited and undergo 9 ± 3 day-long fasting periods (250 kcal/day). We will assess changes in the composition of organs, bones and blood lipid profiles before and after fasting, as well as high-density lipoprotein (HDL) transport and storage, untargeted metabolomics of peripheral blood mononuclear cells (PBMCs), protein persulfidation and shotgun metagenomics of the gut microbiome. The first 32 subjects, fasting for 12 days, will be examined in more detail by magnetic resonance imaging (MRI) and spectroscopy to provide quantitative information on changes in organ volume and function, followed by an additional follow-up examination after 1 and 4 months. The study protocol was approved by the ethics board of the State Medical Chamber of Baden-Württemberg on 26.07.2021 and registered at
ClinicalTrials.gov
(NCT05031598). The results will be disseminated through peer-reviewed publications, international conferences and social media. Fasting provokes fundamental changes in the activation of metabolic and signaling pathways leading to longer and healthier lifespans in animal models. Although the involvement of different metabolites in fueling human fasting metabolism is well known, the contribution of tissues and organs to their supply remains partly unclear. Also, changes in organ volume and composition remain relatively unexplored. Thus, processes involved in remodeling tissues during fasting and food reintroduction need to be better understood. Therefore, this study will apply state-of-the-art techniques to investigate the effects of long-term fasting (LF) and food reintroduction in humans by a multi-systemic approach focusing on changes in body composition, organ and tissue volume, lipid transport and storage, sources of protein utilization, blood metabolites, and gut microbiome profiles in a single cohort. This is a prospective, single-arm, monocentric trial. One hundred subjects will be recruited and undergo 9 ± 3 day-long fasting periods (250 kcal/day). We will assess changes in the composition of organs, bones and blood lipid profiles before and after fasting, as well as high-density lipoprotein (HDL) transport and storage, untargeted metabolomics of peripheral blood mononuclear cells (PBMCs), protein persulfidation and shotgun metagenomics of the gut microbiome. The first 32 subjects, fasting for 12 days, will be examined in more detail by magnetic resonance imaging (MRI) and spectroscopy to provide quantitative information on changes in organ volume and function, followed by an additional follow-up examination after 1 and 4 months. The study protocol was approved by the ethics board of the State Medical Chamber of Baden-Württemberg on 26.07.2021 and registered at ClinicalTrials.gov (NCT05031598). The results will be disseminated through peer-reviewed publications, international conferences and social media. [ClinicalTrials.gov], identifier [NCT05031598]. Fasting provokes fundamental changes in the activation of metabolic and signaling pathways leading to longer and healthier lifespans in animal models. Although the involvement of different metabolites in fueling human fasting metabolism is well known, the contribution of tissues and organs to their supply remains partly unclear. Also, changes in organ volume and composition remain relatively unexplored. Thus, processes involved in remodeling tissues during fasting and food reintroduction need to be better understood. Therefore, this study will apply state-of-the-art techniques to investigate the effects of long-term fasting (LF) and food reintroduction in humans by a multi-systemic approach focusing on changes in body composition, organ and tissue volume, lipid transport and storage, sources of protein utilization, blood metabolites, and gut microbiome profiles in a single cohort. This is a prospective, single-arm, monocentric trial. One hundred subjects will be recruited and undergo 9 ± 3 day-long fasting periods (250 kcal/day). We will assess changes in the composition of organs, bones and blood lipid profiles before and after fasting, as well as high-density lipoprotein (HDL) transport and storage, untargeted metabolomics of peripheral blood mononuclear cells (PBMCs), protein persulfidation and shotgun metagenomics of the gut microbiome. The first 32 subjects, fasting for 12 days, will be examined in more detail by magnetic resonance imaging (MRI) and spectroscopy to provide quantitative information on changes in organ volume and function, followed by an additional follow-up examination after 1 and 4 months. The study protocol was approved by the ethics board of the State Medical Chamber of Baden-Württemberg on 26.07.2021 and registered at ClinicalTrials.gov (NCT05031598). The results will be disseminated through peer-reviewed publications, international conferences and social media.Fasting provokes fundamental changes in the activation of metabolic and signaling pathways leading to longer and healthier lifespans in animal models. Although the involvement of different metabolites in fueling human fasting metabolism is well known, the contribution of tissues and organs to their supply remains partly unclear. Also, changes in organ volume and composition remain relatively unexplored. Thus, processes involved in remodeling tissues during fasting and food reintroduction need to be better understood. Therefore, this study will apply state-of-the-art techniques to investigate the effects of long-term fasting (LF) and food reintroduction in humans by a multi-systemic approach focusing on changes in body composition, organ and tissue volume, lipid transport and storage, sources of protein utilization, blood metabolites, and gut microbiome profiles in a single cohort. This is a prospective, single-arm, monocentric trial. One hundred subjects will be recruited and undergo 9 ± 3 day-long fasting periods (250 kcal/day). We will assess changes in the composition of organs, bones and blood lipid profiles before and after fasting, as well as high-density lipoprotein (HDL) transport and storage, untargeted metabolomics of peripheral blood mononuclear cells (PBMCs), protein persulfidation and shotgun metagenomics of the gut microbiome. The first 32 subjects, fasting for 12 days, will be examined in more detail by magnetic resonance imaging (MRI) and spectroscopy to provide quantitative information on changes in organ volume and function, followed by an additional follow-up examination after 1 and 4 months. The study protocol was approved by the ethics board of the State Medical Chamber of Baden-Württemberg on 26.07.2021 and registered at ClinicalTrials.gov (NCT05031598). The results will be disseminated through peer-reviewed publications, international conferences and social media.[ClinicalTrials.gov], identifier [NCT05031598].Clinical trial registration[ClinicalTrials.gov], identifier [NCT05031598]. Fasting provokes fundamental changes in the activation of metabolic and signaling pathways leading to longer and healthier lifespans in animal models. Although the involvement of different metabolites in fueling human fasting metabolism is well known, the contribution of tissues and organs to their supply remains partly unclear. Also, changes in organ volume and composition remain relatively unexplored. Thus, processes involved in remodeling tissues during fasting and food reintroduction need to be better understood. Therefore, this study will apply state-of-the-art techniques to investigate the effects of long-term fasting (LF) and food reintroduction in humans by a multi-systemic approach focusing on changes in body composition, organ and tissue volume, lipid transport and storage, sources of protein utilization, blood metabolites, and gut microbiome profiles in a single cohort. This is a prospective, single-arm, monocentric trial. One hundred subjects will be recruited and undergo 9 ± 3 day-long fasting periods (250 kcal/day). We will assess changes in the composition of organs, bones and blood lipid profiles before and after fasting, as well as high-density lipoprotein (HDL) transport and storage, untargeted metabolomics of peripheral blood mononuclear cells (PBMCs), protein persulfidation and shotgun metagenomics of the gut microbiome. The first 32 subjects, fasting for 12 days, will be examined in more detail by magnetic resonance imaging (MRI) and spectroscopy to provide quantitative information on changes in organ volume and function, followed by an additional follow-up examination after 1 and 4 months. The study protocol was approved by the ethics board of the State Medical Chamber of Baden-Württemberg on 26.07.2021 and registered at ClinicalTrials.gov (NCT05031598). The results will be disseminated through peer-reviewed publications, international conferences and social media.Clinical trial registration[ClinicalTrials.gov], identifier [NCT05031598]. |
Author | Madeo, Frank Wilhelmi de Toledo, Françoise Mitchell, Sarah J. von Schacky, Clemens Viallon, Magalie Croisille, Pierre Grundler, Franziska Ruscica, Massimiliano Mesnage, Robin Hofer, Sebastian J. |
AuthorAffiliation | 2 UJM-Saint-Etienne, INSA, CNRS UMR 5520, INSERM U1206, CREATIS, F-42023, Université de Lyon , Saint-Étienne , France 10 Department of Health Sciences and Technology, ETH Zürich , Schwerzenbach , Switzerland 7 Institute of Molecular Biosciences, NAWI Graz, University of Graz , Graz , Austria 1 Buchinger Wilhelmi Clinic , Überlingen , Germany 6 Omegametrix , Martinsried , Germany 8 BioHealth Graz , Graz , Austria 4 Department of Medical and Molecular Genetics, Faculty of Life Sciences and Medicine, King’s College London , London , United Kingdom 5 Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano , Milan , Italy 3 Department of Radiology, University Hospital Saint-Étienne , Saint-Étienne , France 9 BioTechMed Graz , Graz , Austria |
AuthorAffiliation_xml | – name: 3 Department of Radiology, University Hospital Saint-Étienne , Saint-Étienne , France – name: 8 BioHealth Graz , Graz , Austria – name: 2 UJM-Saint-Etienne, INSA, CNRS UMR 5520, INSERM U1206, CREATIS, F-42023, Université de Lyon , Saint-Étienne , France – name: 10 Department of Health Sciences and Technology, ETH Zürich , Schwerzenbach , Switzerland – name: 4 Department of Medical and Molecular Genetics, Faculty of Life Sciences and Medicine, King’s College London , London , United Kingdom – name: 5 Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano , Milan , Italy – name: 9 BioTechMed Graz , Graz , Austria – name: 7 Institute of Molecular Biosciences, NAWI Graz, University of Graz , Graz , Austria – name: 1 Buchinger Wilhelmi Clinic , Überlingen , Germany – name: 6 Omegametrix , Martinsried , Germany |
Author_xml | – sequence: 1 givenname: Franziska surname: Grundler fullname: Grundler, Franziska – sequence: 2 givenname: Magalie surname: Viallon fullname: Viallon, Magalie – sequence: 3 givenname: Robin surname: Mesnage fullname: Mesnage, Robin – sequence: 4 givenname: Massimiliano surname: Ruscica fullname: Ruscica, Massimiliano – sequence: 5 givenname: Clemens surname: von Schacky fullname: von Schacky, Clemens – sequence: 6 givenname: Frank surname: Madeo fullname: Madeo, Frank – sequence: 7 givenname: Sebastian J. surname: Hofer fullname: Hofer, Sebastian J. – sequence: 8 givenname: Sarah J. surname: Mitchell fullname: Mitchell, Sarah J. – sequence: 9 givenname: Pierre surname: Croisille fullname: Croisille, Pierre – sequence: 10 givenname: Françoise surname: Wilhelmi de Toledo fullname: Wilhelmi de Toledo, Françoise |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36466423$$D View this record in MEDLINE/PubMed |
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Copyright | Copyright © 2022 Grundler, Viallon, Mesnage, Ruscica, von Schacky, Madeo, Hofer, Mitchell, Croisille and Wilhelmi de Toledo. Copyright © 2022 Grundler, Viallon, Mesnage, Ruscica, von Schacky, Madeo, Hofer, Mitchell, Croisille and Wilhelmi de Toledo. 2022 Grundler, Viallon, Mesnage, Ruscica, von Schacky, Madeo, Hofer, Mitchell, Croisille and Wilhelmi de Toledo |
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Keywords | magnetic resonance imaging (MRI) organ size metabolomics lipoprotein metabolism long-term fasting microbiome protein utilisation |
Language | English |
License | Copyright © 2022 Grundler, Viallon, Mesnage, Ruscica, von Schacky, Madeo, Hofer, Mitchell, Croisille and Wilhelmi de Toledo. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Nutrition and Metabolism, a section of the journal Frontiers in Nutrition These authors have contributed equally to this work and share first authorship Edited by: Ellen E. Blaak, Maastricht University, Netherlands These authors have contributed equally to this work and share last authorship Reviewed by: Benjamin D. Horne, Intermountain Healthcare, United States; Ana Luísa De Sousa-Coelho, Algarve Biomedical Center Research Institute (ABC-RI), Portugal |
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