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Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study

Dysbiosis of gut microbiota (GM) has been involved in the pathophysiology of arterial hypertension (HT), via a putative role of short chain fatty acids (SCFAs). Its role in the circadian regulation of blood pressure (BP), also called “the dipping profile”, has been poorly investigated. Sixteen male...

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Autores principales: Huart, Justine, Cirillo, Arianna, Taminiau, Bernard, Descy, Julie, Saint-Remy, Annie, Daube, Georges, Krzesinski, Jean-Marie, Melin, Pierrette, de Tullio, Pascal, Jouret, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146767/
https://www.ncbi.nlm.nih.gov/pubmed/33946722
http://dx.doi.org/10.3390/metabo11050282
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author Huart, Justine
Cirillo, Arianna
Taminiau, Bernard
Descy, Julie
Saint-Remy, Annie
Daube, Georges
Krzesinski, Jean-Marie
Melin, Pierrette
de Tullio, Pascal
Jouret, François
author_facet Huart, Justine
Cirillo, Arianna
Taminiau, Bernard
Descy, Julie
Saint-Remy, Annie
Daube, Georges
Krzesinski, Jean-Marie
Melin, Pierrette
de Tullio, Pascal
Jouret, François
author_sort Huart, Justine
collection PubMed
description Dysbiosis of gut microbiota (GM) has been involved in the pathophysiology of arterial hypertension (HT), via a putative role of short chain fatty acids (SCFAs). Its role in the circadian regulation of blood pressure (BP), also called “the dipping profile”, has been poorly investigated. Sixteen male volunteers and 10 female partners were subjected to 24 h ambulatory BP monitoring and were categorized in normotensive (NT) versus HT, as well as in dippers versus non-dippers. Nuclear magnetic resonance (NMR)-based metabolomics was performed on stool samples. A 5-year comparative follow-up of BP profiles and stool metabolomes was done in men. Significant correlations between stool metabolome and 24 h mean BP levels were found in both male and female cohorts and in the entire cohort (R(2) = 0.72, R(2) = 0.79, and R(2) = 0.45, respectively). Multivariate analysis discriminated dippers versus non-dippers in both male and female cohorts and in the entire cohort (Q(2) = 0.87, Q(2) = 0.98, and Q(2) = 0.68, respectively). Fecal amounts of acetate, propionate, and butyrate were higher in HT versus NT patients (p = 0.027; p = 0.015 and p = 0.015, respectively), as well as in non-dippers versus dippers (p = 0.027, p = 0.038, and p = 0.036, respectively) in the entire cohort. SCFA levels were significantly different in patients changing of dipping status over the 5-year follow-up. In conclusion, stool metabolome changes upon global and circadian BP profiles in both genders.
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spelling pubmed-81467672021-05-26 Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study Huart, Justine Cirillo, Arianna Taminiau, Bernard Descy, Julie Saint-Remy, Annie Daube, Georges Krzesinski, Jean-Marie Melin, Pierrette de Tullio, Pascal Jouret, François Metabolites Article Dysbiosis of gut microbiota (GM) has been involved in the pathophysiology of arterial hypertension (HT), via a putative role of short chain fatty acids (SCFAs). Its role in the circadian regulation of blood pressure (BP), also called “the dipping profile”, has been poorly investigated. Sixteen male volunteers and 10 female partners were subjected to 24 h ambulatory BP monitoring and were categorized in normotensive (NT) versus HT, as well as in dippers versus non-dippers. Nuclear magnetic resonance (NMR)-based metabolomics was performed on stool samples. A 5-year comparative follow-up of BP profiles and stool metabolomes was done in men. Significant correlations between stool metabolome and 24 h mean BP levels were found in both male and female cohorts and in the entire cohort (R(2) = 0.72, R(2) = 0.79, and R(2) = 0.45, respectively). Multivariate analysis discriminated dippers versus non-dippers in both male and female cohorts and in the entire cohort (Q(2) = 0.87, Q(2) = 0.98, and Q(2) = 0.68, respectively). Fecal amounts of acetate, propionate, and butyrate were higher in HT versus NT patients (p = 0.027; p = 0.015 and p = 0.015, respectively), as well as in non-dippers versus dippers (p = 0.027, p = 0.038, and p = 0.036, respectively) in the entire cohort. SCFA levels were significantly different in patients changing of dipping status over the 5-year follow-up. In conclusion, stool metabolome changes upon global and circadian BP profiles in both genders. MDPI 2021-04-29 /pmc/articles/PMC8146767/ /pubmed/33946722 http://dx.doi.org/10.3390/metabo11050282 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Huart, Justine
Cirillo, Arianna
Taminiau, Bernard
Descy, Julie
Saint-Remy, Annie
Daube, Georges
Krzesinski, Jean-Marie
Melin, Pierrette
de Tullio, Pascal
Jouret, François
Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study
title Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study
title_full Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study
title_fullStr Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study
title_full_unstemmed Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study
title_short Human Stool Metabolome Differs upon 24 h Blood Pressure Levels and Blood Pressure Dipping Status: A Prospective Longitudinal Study
title_sort human stool metabolome differs upon 24 h blood pressure levels and blood pressure dipping status: a prospective longitudinal study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146767/
https://www.ncbi.nlm.nih.gov/pubmed/33946722
http://dx.doi.org/10.3390/metabo11050282
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