Menu
Currency
GWAS Study

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

Kanoni S, Kumar S, Amerikanou C et al.

34025683 PubMed ID
GWAS Study Type
87 Participants
28 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KS
Kanoni S
KS
Kumar S
AC
Amerikanou C
KM
Kurth MJ
SM
Stathopoulou MG
BS
Bourgeois S
MC
Masson C
KA
Kannt A
CL
Cesarini L
KM
Kontoe MS
MM
Milanović M
RF
Roig FJ
BM
Beribaka M
CJ
Campolo J
JN
Jiménez-Hernández N
MN
Milošević N
LC
Llorens C
SI
Smyrnioudis I
FM
Francino MP
MN
Milić N
KA
Kaliora AC
TM
Trivella MG
RM
Ruddock MW
MM
Medić-Stojanoska M
GA
Gastaldelli A
LJ
Lamont J
DP
Deloukas P
DG
Dedoussis GV
VS
Visvikis-Siest S
Chapter II

Abstract

Summary of the research findings

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.

35 European or unknown ancestry mastiha exposed individuals, 52 European or unknown ancestry unexposed individuals

Chapter III

Study Statistics

Key metrics and study information

87
Total Participants
GWAS
Study Type
No
Replicated
European, NR
Ancestry
Greece, Italy, Serbia
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.