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Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD

Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease with no therapeutic consensus. Oxidation and inflammation are hallmarks in the progression of this complex disease, which also involves interactions between the genetic background and the environment. Mastiha is a natural nut...

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Autores principales: Kanoni, Stavroula, Kumar, Satish, Amerikanou, Charalampia, Kurth, Mary Jo, Stathopoulou, Maria G., Bourgeois, Stephane, Masson, Christine, Kannt, Aimo, Cesarini, Lucia, Kontoe, Maria-Spyridoula, Milanović, Maja, Roig, Francisco J., Beribaka, Mirjana, Campolo, Jonica, Jiménez-Hernández, Nuria, Milošević, Nataša, Llorens, Carlos, Smyrnioudis, Ilias, Francino, M. Pilar, Milić, Nataša, Kaliora, Andriana C., Trivella, Maria Giovanna, Ruddock, Mark W., Medić-Stojanoska, Milica, Gastaldelli, Amalia, Lamont, John, Deloukas, Panos, Dedoussis, George V., Visvikis-Siest, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138178/
https://www.ncbi.nlm.nih.gov/pubmed/34025683
http://dx.doi.org/10.3389/fimmu.2021.683028
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author Kanoni, Stavroula
Kumar, Satish
Amerikanou, Charalampia
Kurth, Mary Jo
Stathopoulou, Maria G.
Bourgeois, Stephane
Masson, Christine
Kannt, Aimo
Cesarini, Lucia
Kontoe, Maria-Spyridoula
Milanović, Maja
Roig, Francisco J.
Beribaka, Mirjana
Campolo, Jonica
Jiménez-Hernández, Nuria
Milošević, Nataša
Llorens, Carlos
Smyrnioudis, Ilias
Francino, M. Pilar
Milić, Nataša
Kaliora, Andriana C.
Trivella, Maria Giovanna
Ruddock, Mark W.
Medić-Stojanoska, Milica
Gastaldelli, Amalia
Lamont, John
Deloukas, Panos
Dedoussis, George V.
Visvikis-Siest, Sophie
author_facet Kanoni, Stavroula
Kumar, Satish
Amerikanou, Charalampia
Kurth, Mary Jo
Stathopoulou, Maria G.
Bourgeois, Stephane
Masson, Christine
Kannt, Aimo
Cesarini, Lucia
Kontoe, Maria-Spyridoula
Milanović, Maja
Roig, Francisco J.
Beribaka, Mirjana
Campolo, Jonica
Jiménez-Hernández, Nuria
Milošević, Nataša
Llorens, Carlos
Smyrnioudis, Ilias
Francino, M. Pilar
Milić, Nataša
Kaliora, Andriana C.
Trivella, Maria Giovanna
Ruddock, Mark W.
Medić-Stojanoska, Milica
Gastaldelli, Amalia
Lamont, John
Deloukas, Panos
Dedoussis, George V.
Visvikis-Siest, Sophie
author_sort Kanoni, Stavroula
collection PubMed
description Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease with no therapeutic consensus. Oxidation and inflammation are hallmarks in the progression of this complex disease, which also involves interactions between the genetic background and the environment. Mastiha is a natural nutritional supplement known to possess antioxidant and anti-inflammatory properties. This study investigated how a 6-month Mastiha supplementation (2.1 g/day) could impact the antioxidant and inflammatory status of patients with NAFLD, and whether genetic variants significantly mediate these effects. We recruited 98 patients with obesity (BMI ≥ 30 kg/m(2)) and NAFLD and randomly allocated them to either the Mastiha or the placebo group for 6 months. The anti-oxidative and inflammatory status was assessed at baseline and post-treatment. Genome-wide genetic data was also obtained from all participants, to investigate gene-by-Mastiha interactions. NAFLD patients with severe obesity (BMI > 35kg/m(2)) taking the Mastiha had significantly higher total antioxidant status (TAS) compared to the corresponding placebo group (P value=0.008). We did not observe any other significant change in the investigated biomarkers as a result of Mastiha supplementation alone. We identified several novel gene-by-Mastiha interaction associations with levels of cytokines and antioxidant biomarkers. Some of the identified genetic loci are implicated in the pathological pathways of NAFLD, including the lanosterol synthase gene (LSS) associated with glutathione peroxidase activity (Gpx) levels, the mitochondrial pyruvate carrier-1 gene (MPC1) and the sphingolipid transporter-1 gene (SPNS1) associated with hemoglobin levels, the transforming growth factor‐beta‐induced gene (TGFBI) and the micro-RNA 129-1 (MIR129-1) associated with IL-6 and the granzyme B gene (GZMB) associated with IL-10 levels. Within the MAST4HEALTH randomized clinical trial (NCT03135873, www.clinicaltrials.gov) Mastiha supplementation improved the TAS levels among NAFLD patients with severe obesity. We identified several novel genome-wide significant nutrigenetic interactions, influencing the antioxidant and inflammatory status in NAFLD. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, identifier NCT03135873.
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spelling pubmed-81381782021-05-22 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD Kanoni, Stavroula Kumar, Satish Amerikanou, Charalampia Kurth, Mary Jo Stathopoulou, Maria G. Bourgeois, Stephane Masson, Christine Kannt, Aimo Cesarini, Lucia Kontoe, Maria-Spyridoula Milanović, Maja Roig, Francisco J. Beribaka, Mirjana Campolo, Jonica Jiménez-Hernández, Nuria Milošević, Nataša Llorens, Carlos Smyrnioudis, Ilias Francino, M. Pilar Milić, Nataša Kaliora, Andriana C. Trivella, Maria Giovanna Ruddock, Mark W. Medić-Stojanoska, Milica Gastaldelli, Amalia Lamont, John Deloukas, Panos Dedoussis, George V. Visvikis-Siest, Sophie Front Immunol Immunology Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease with no therapeutic consensus. Oxidation and inflammation are hallmarks in the progression of this complex disease, which also involves interactions between the genetic background and the environment. Mastiha is a natural nutritional supplement known to possess antioxidant and anti-inflammatory properties. This study investigated how a 6-month Mastiha supplementation (2.1 g/day) could impact the antioxidant and inflammatory status of patients with NAFLD, and whether genetic variants significantly mediate these effects. We recruited 98 patients with obesity (BMI ≥ 30 kg/m(2)) and NAFLD and randomly allocated them to either the Mastiha or the placebo group for 6 months. The anti-oxidative and inflammatory status was assessed at baseline and post-treatment. Genome-wide genetic data was also obtained from all participants, to investigate gene-by-Mastiha interactions. NAFLD patients with severe obesity (BMI > 35kg/m(2)) taking the Mastiha had significantly higher total antioxidant status (TAS) compared to the corresponding placebo group (P value=0.008). We did not observe any other significant change in the investigated biomarkers as a result of Mastiha supplementation alone. We identified several novel gene-by-Mastiha interaction associations with levels of cytokines and antioxidant biomarkers. Some of the identified genetic loci are implicated in the pathological pathways of NAFLD, including the lanosterol synthase gene (LSS) associated with glutathione peroxidase activity (Gpx) levels, the mitochondrial pyruvate carrier-1 gene (MPC1) and the sphingolipid transporter-1 gene (SPNS1) associated with hemoglobin levels, the transforming growth factor‐beta‐induced gene (TGFBI) and the micro-RNA 129-1 (MIR129-1) associated with IL-6 and the granzyme B gene (GZMB) associated with IL-10 levels. Within the MAST4HEALTH randomized clinical trial (NCT03135873, www.clinicaltrials.gov) Mastiha supplementation improved the TAS levels among NAFLD patients with severe obesity. We identified several novel genome-wide significant nutrigenetic interactions, influencing the antioxidant and inflammatory status in NAFLD. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, identifier NCT03135873. Frontiers Media S.A. 2021-05-07 /pmc/articles/PMC8138178/ /pubmed/34025683 http://dx.doi.org/10.3389/fimmu.2021.683028 Text en Copyright © 2021 Kanoni, Kumar, Amerikanou, Kurth, Stathopoulou, Bourgeois, Masson, Kannt, Cesarini, Kontoe, Milanović, Roig, Beribaka, Campolo, Jiménez-Hernández, Milošević, Llorens, Smyrnioudis, Francino, Milić, Kaliora, Trivella, Ruddock, Medić-Stojanoska, Gastaldelli, Lamont, Deloukas, Dedoussis and Visvikis-Siest https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Immunology
Kanoni, Stavroula
Kumar, Satish
Amerikanou, Charalampia
Kurth, Mary Jo
Stathopoulou, Maria G.
Bourgeois, Stephane
Masson, Christine
Kannt, Aimo
Cesarini, Lucia
Kontoe, Maria-Spyridoula
Milanović, Maja
Roig, Francisco J.
Beribaka, Mirjana
Campolo, Jonica
Jiménez-Hernández, Nuria
Milošević, Nataša
Llorens, Carlos
Smyrnioudis, Ilias
Francino, M. Pilar
Milić, Nataša
Kaliora, Andriana C.
Trivella, Maria Giovanna
Ruddock, Mark W.
Medić-Stojanoska, Milica
Gastaldelli, Amalia
Lamont, John
Deloukas, Panos
Dedoussis, George V.
Visvikis-Siest, Sophie
Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD
title Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD
title_full Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD
title_fullStr Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD
title_full_unstemmed Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD
title_short Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD
title_sort nutrigenetic interactions might modulate the antioxidant and anti-inflammatory status in mastiha-supplemented patients with nafld
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138178/
https://www.ncbi.nlm.nih.gov/pubmed/34025683
http://dx.doi.org/10.3389/fimmu.2021.683028
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