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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Main Authors: Stavroula Kanoni, Satish Kumar, Charalampia Amerikanou, Mary Jo Kurth, Maria G. Stathopoulou, Stephane Bourgeois, Christine Masson, Aimo Kannt, Lucia Cesarini, Maria-Spyridoula Kontoe, Maja Milanović, Francisco J. Roig, Mirjana Beribaka, Jonica Campolo, Nuria Jiménez-Hernández, Nataša Milošević, Carlos Llorens, Ilias Smyrnioudis, M. Pilar Francino, Nataša Milić, Andriana C. Kaliora, Maria Giovanna Trivella, Mark W. Ruddock, Milica Medić-Stojanoska, Amalia Gastaldelli, John Lamont, Panos Deloukas, George V. Dedoussis, Sophie Visvikis-Siest
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2021.683028/full
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author Stavroula Kanoni
Satish Kumar
Charalampia Amerikanou
Mary Jo Kurth
Maria G. Stathopoulou
Stephane Bourgeois
Christine Masson
Aimo Kannt
Lucia Cesarini
Maria-Spyridoula Kontoe
Maja Milanović
Francisco J. Roig
Francisco J. Roig
Mirjana Beribaka
Jonica Campolo
Jonica Campolo
Nuria Jiménez-Hernández
Nuria Jiménez-Hernández
Nataša Milošević
Carlos Llorens
Ilias Smyrnioudis
M. Pilar Francino
M. Pilar Francino
Nataša Milić
Andriana C. Kaliora
Maria Giovanna Trivella
Maria Giovanna Trivella
Mark W. Ruddock
Milica Medić-Stojanoska
Milica Medić-Stojanoska
Amalia Gastaldelli
John Lamont
Panos Deloukas
Panos Deloukas
George V. Dedoussis
Sophie Visvikis-Siest
spellingShingle Stavroula Kanoni
Satish Kumar
Charalampia Amerikanou
Mary Jo Kurth
Maria G. Stathopoulou
Stephane Bourgeois
Christine Masson
Aimo Kannt
Lucia Cesarini
Maria-Spyridoula Kontoe
Maja Milanović
Francisco J. Roig
Francisco J. Roig
Mirjana Beribaka
Jonica Campolo
Jonica Campolo
Nuria Jiménez-Hernández
Nuria Jiménez-Hernández
Nataša Milošević
Carlos Llorens
Ilias Smyrnioudis
M. Pilar Francino
M. Pilar Francino
Nataša Milić
Andriana C. Kaliora
Maria Giovanna Trivella
Maria Giovanna Trivella
Mark W. Ruddock
Milica Medić-Stojanoska
Milica Medić-Stojanoska
Amalia Gastaldelli
John Lamont
Panos Deloukas
Panos Deloukas
George V. Dedoussis
Sophie Visvikis-Siest
Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD
Frontiers in Immunology
non-alcoholic fatty liver disease
inflammation
oxidative stress
Mastiha
nutrigenetics
randomized clinical trial
author_facet Stavroula Kanoni
Satish Kumar
Charalampia Amerikanou
Mary Jo Kurth
Maria G. Stathopoulou
Stephane Bourgeois
Christine Masson
Aimo Kannt
Lucia Cesarini
Maria-Spyridoula Kontoe
Maja Milanović
Francisco J. Roig
Francisco J. Roig
Mirjana Beribaka
Jonica Campolo
Jonica Campolo
Nuria Jiménez-Hernández
Nuria Jiménez-Hernández
Nataša Milošević
Carlos Llorens
Ilias Smyrnioudis
M. Pilar Francino
M. Pilar Francino
Nataša Milić
Andriana C. Kaliora
Maria Giovanna Trivella
Maria Giovanna Trivella
Mark W. Ruddock
Milica Medić-Stojanoska
Milica Medić-Stojanoska
Amalia Gastaldelli
John Lamont
Panos Deloukas
Panos Deloukas
George V. Dedoussis
Sophie Visvikis-Siest
author_sort Stavroula Kanoni
title 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_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_sort nutrigenetic interactions might modulate the antioxidant and anti-inflammatory status in mastiha-supplemented patients with nafld
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2021-05-01
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/m2) 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/m2) 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 RegistrationClinicalTrials.gov, identifier NCT03135873.
topic non-alcoholic fatty liver disease
inflammation
oxidative stress
Mastiha
nutrigenetics
randomized clinical trial
url https://www.frontiersin.org/articles/10.3389/fimmu.2021.683028/full
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spelling doaj-01cf24ceb3e947749ca21d7d2aed1f4f2021-05-07T09:14:20ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-05-011210.3389/fimmu.2021.683028683028Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLDStavroula Kanoni0Satish Kumar1Charalampia Amerikanou2Mary Jo Kurth3Maria G. Stathopoulou4Stephane Bourgeois5Christine Masson6Aimo Kannt7Lucia Cesarini8Maria-Spyridoula Kontoe9Maja Milanović10Francisco J. Roig11Francisco J. Roig12Mirjana Beribaka13Jonica Campolo14Jonica Campolo15Nuria Jiménez-Hernández16Nuria Jiménez-Hernández17Nataša Milošević18Carlos Llorens19Ilias Smyrnioudis20M. Pilar Francino21M. Pilar Francino22Nataša Milić23Andriana C. Kaliora24Maria Giovanna Trivella25Maria Giovanna Trivella26Mark W. Ruddock27Milica Medić-Stojanoska28Milica Medić-Stojanoska29Amalia Gastaldelli30John Lamont31Panos Deloukas32Panos Deloukas33George V. Dedoussis34Sophie Visvikis-Siest35William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United KingdomEA_1122, IGE-PCV, Université de Loraine, Nancy, FranceDepartment of Nutrition and Dietetics, School of Health Science and Education, Harokopio University, Athens, GreeceRandox Laboratories Ltd (RANDOX), Crumlin, United KingdomEA_1122, IGE-PCV, Université de Loraine, Nancy, FranceWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United KingdomEA_1122, IGE-PCV, Université de Loraine, Nancy, FranceFraunhofer Institute of Translational Medicine and Pharmacology, Frankfurt, GermanyASST Grande Ospedale Metropolitano Niguarda, Milan, ItalyEA_1122, IGE-PCV, Université de Loraine, Nancy, FranceFaculty of Medicine, University of Novi Sad, Novi Sad, SerbiaBiotechvana, Parc Científic, Universitat de València, Valencia, SpainFacultad de Ciencias de la Salud, Universidad San Jorge, Zaragoza, Spain0Department of Biology, Faculty of Technology Zvornik, University of East Sarajevo, Zvornik, Bosnia and HerzegovinaASST Grande Ospedale Metropolitano Niguarda, Milan, Italy1Institute of Clinical Physiology National Research Council, Pisa, Italy2Area de Genòmica i Salut, Fundació per al Foment de la Investigació Sanitária i Biomèdica de la Comunitat Valenciana (FISABIO-Salut Pública), Valencia, Spain3CIBER en Epidemiología y Salud Pública, Madrid, SpainFaculty of Medicine, University of Novi Sad, Novi Sad, SerbiaBiotechvana, Parc Científic, Universitat de València, Valencia, Spain4Chios Mastic Gum Growers Association, Chios, Greece2Area de Genòmica i Salut, Fundació per al Foment de la Investigació Sanitária i Biomèdica de la Comunitat Valenciana (FISABIO-Salut Pública), Valencia, Spain3CIBER en Epidemiología y Salud Pública, Madrid, SpainFaculty of Medicine, University of Novi Sad, Novi Sad, SerbiaDepartment of Nutrition and Dietetics, School of Health Science and Education, Harokopio University, Athens, GreeceASST Grande Ospedale Metropolitano Niguarda, Milan, Italy1Institute of Clinical Physiology National Research Council, Pisa, ItalyRandox Laboratories Ltd (RANDOX), Crumlin, United KingdomFaculty of Medicine, University of Novi Sad, Novi Sad, Serbia5Clinic for Endocrinology, Diabetes and Metabolic Diseases, Clinical Centre of Vojvodina, Novi Sad, Serbia1Institute of Clinical Physiology National Research Council, Pisa, ItalyRandox Laboratories Ltd (RANDOX), Crumlin, United KingdomWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom6Centre for Genomic Health, Life Sciences, Queen Mary University of London, London, United KingdomDepartment of Nutrition and Dietetics, School of Health Science and Education, Harokopio University, Athens, GreeceEA_1122, IGE-PCV, Université de Loraine, Nancy, FranceNon-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/m2) 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/m2) 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 RegistrationClinicalTrials.gov, identifier NCT03135873.https://www.frontiersin.org/articles/10.3389/fimmu.2021.683028/fullnon-alcoholic fatty liver diseaseinflammationoxidative stressMastihanutrigeneticsrandomized clinical trial