Panacea Index Logo

Command Palette

Search for a command to run...

Mediterranean diet consumption affects the endocannabinoid system in overweight and obese subjects: possible links with gut microbiome, insulin resistance and inflammation.

European journal of nutrition
October 1, 2021
Silvia Tagliamonte et al. (9 authors)
Journal ArticleRandomized Controlled TrialHuman StudyClinical
Study Details

Study Goal

The researchers investigated whether a Mediterranean diet (MD) increased fecal Akkermansia muciniphila abundance and its relationship with metabolic health markers.

Results Summary

The MD intervention increased fecal Akkermansia muciniphila abundance independently of body weight changes. Higher baseline endocannabinoid tone and microbiome functionality influenced individualized improvements in insulin sensitivity and inflammation.

Population

Overweight and obese subjects (mean age 43 ± 1.4 years, BMI 31.1 ± 0.5 kg/m²) with lifestyle risk factors for metabolic diseases.

Effective Dosage

Not specified

Duration

8 weeks

Interactions

None mentioned

Extracted Claims (6)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Mediterranean diet (MD)
decrease
plasma arachidonoylethanolamide (AEA)
overweight and obese subjects with lifestyle risk factors for metabolic diseases
p = 0.02
lowered
#1
Mediterranean diet (MD)
increase
plasma oleoylethanolamide/palmitoylethanolamide (OEA/PEA)
overweight and obese subjects with lifestyle risk factors for metabolic diseases
p = 0.009
increased
#2
Mediterranean diet (MD)
increase
plasma OEA/AEA
overweight and obese subjects with lifestyle risk factors for metabolic diseases
p = 0.006
increased
#3
Mediterranean diet (MD)
increase
faecal Akkermansia muciniphila
overweight and obese subjects with lifestyle risk factors for metabolic diseases
p = 0.026
increased
#4
Mediterranean diet (MD)
decrease
homeostatic model assessment of insulin resistance index
individuals with low-plasma OEA/PEA at baseline
p = 0.01
decreased
#5
Mediterranean diet (MD)
decrease
serum high-sensitive C-reactive protein
individuals with high-plasma OEA/PEA at baseline
p = 0.02
decreased
#6
Abstract

PURPOSE: To investigate whether a Mediterranean diet (MD) affected the plasma concentrations of endocannabinoids (ECs), N-acylethanolamines (NAEs) and their specific ratios in subjects with lifestyle risk factors for metabolic diseases. To identify the relationship between circulating levels of these compounds and gut microbiome, insulin resistance and systemic inflammation. METHODS: A parallel 8-week randomised controlled trial was performed involving 82 overweight and obese subjects aged (mean ± SEM) 43 ± 1.4 years with a BMI of 31.1 ± 0.5 kg/m RESULTS: The MD intervention lowered plasma arachidonoylethanolamide (AEA, p = 0.02), increased plasma oleoylethanolamide/palmitoylethanolamide (OEA/PEA, p = 0.009) and OEA/AEA (p = 0.006) and increased faecal Akkermansia muciniphila (p = 0.026) independent of body weight changes. OEA/PEA positively correlated with abundance of key microbial players in diet-gut-health interplay and MD adherence. Following an MD, individuals with low-plasma OEA/PEA at baseline decreased homeostatic model assessment of insulin resistance index (p = 0.01), while individuals with high-plasma OEA/PEA decreased serum high-sensitive C-reactive protein (p = 0.02). CONCLUSIONS: We demonstrated that a switch from a CT to an isocaloric MD affects the endocannabinoid system and increases A. muciniphila abundance in the gut independently of body weight changes. Endocannabinoid tone and microbiome functionality at baseline drives an individualised response to an MD in ameliorating insulin sensitivity and inflammation. Clinical Trial Registry number and website NCT03071718; www.clinicaltrials.gov.

Medical Subject Headings (MeSH)
Diet, MediterraneanEndocannabinoidsGastrointestinal MicrobiomeHumansInflammationInsulin ResistanceObesityOverweight
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations47
Citations/Year11.8
Relative Citation Ratio3.90
NIH Percentile89.8%
Research Impact Scores
APT Score0.75
Weight Score2.87
Normalized Score0.67
Related Supplements