TY - JOUR
T1 - Akkermansia muciniphila and improved metabolic health during a dietary intervention in obesity
T2 - Relationship with gut microbiome richness and ecology
AU - MICRO-Obes Consortium
AU - Dao, Maria Carlota
AU - Everard, Amandine
AU - Aron-Wisnewsky, Judith
AU - Sokolovska, Nataliya
AU - Prifti, Edi
AU - Verger, Eric O.
AU - Kayser, Brandon D.
AU - Levenez, Florence
AU - Chilloux, Julien
AU - Hoyles, Lesley
AU - Dumas, Marc Emmanuel
AU - Rizkalla, Salwa W.
AU - Doré, Joel
AU - Cani, Patrice D.
AU - Clément, Karine
AU - Le Mouhaër, Sylvie
AU - Cotillard, Aurélie
AU - Kennedy, Sean P.
AU - Pons, Nicolas
AU - Le Chatelier, Emmanuelle
AU - Almeida, Mathieu
AU - Quinquis, Benoit
AU - Galleron, Nathalie
AU - Batto, Jean Michel
AU - Renault, Pierre
AU - Zucker, Jean Daniel
AU - Ehrlich, Stanislav Dusko
AU - Blottière, Hervé
AU - Leclerc, Marion
AU - Juste, Catherine
AU - De Wouters, Tomas
AU - Lepage, Patricia
N1 - Funding Information:
The authors thank Sophie Gougis who contributed to the dietary counselling, Soraya Fellahi (Department of Biochemistry and Hormonology, Tenon hospital) for analyses of inflammatory markers, Dominique Bonnefont-Rousselot and Randa Bittar (Department of Metabolic Biochemistry, Pitié-Salpểtrière hospital) for help with the analysis of plasma lipid profile. This work was supported by Agence Nationale de la Recherche (ANR MICRO-Obes), KOT-Ceprodi and the association Fondation Coeur et Arteres (clinical investigation) as well as European Union''s Seventh Framework Program under grant agreement MetaHIT HEALTH-F4-2012-305312, and grant agreement HEALTH-F4-2012-305312 (METACARDIS). PDC is a research associate at FRS-FNRS (Fonds de la Recherche Scientifique), Belgium. AE is a postdoctoral researcher at FRS-FNRS, Belgium. PDC is the recipient of grants from FRS-FNRS (convention J.0084.15, convention 3.4579.11) and PDR (Projet de Recherche, convention: T.0138.14) and ERC Starting Grant 2013 (European Research Council, Starting grant 336452-ENIGMO). This work was supported by the Fonds de la Recherche Scientifique-FNRS for the FRFS-WELBIO under Grant n° WELBIO-CR-2012S-02R.
PY - 2016/3
Y1 - 2016/3
N2 - Objective: Individuals with obesity and type 2 diabetes differ from lean and healthy individuals in their abundance of certain gut microbial species and microbial gene richness. Abundance of Akkermansia muciniphila, a mucin-degrading bacterium, has been inversely associated with body fat mass and glucose intolerance in mice, but more evidence is needed in humans. The impact of diet and weight loss on this bacterial species is unknown. Our objective was to evaluate the association between faecal A. muciniphila abundance, faecal microbiome gene richness, diet, host characteristics, and their changes after calorie restriction (CR). Design: The intervention consisted of a 6-week CR period followed by a 6-week weight stabilisation diet in overweight and obese adults (N=49, including 41 women). Faecal A. muciniphila abundance, faecal microbial gene richness, diet and bioclinical parameters were measured at baseline and after CR and weight stabilisation. Results: At baseline A. muciniphila was inversely related to fasting glucose, waist-to-hip ratio and subcutaneous adipocyte diameter. Subjects with higher gene richness and A. muciniphila abundance exhibited the healthiest metabolic status, particularly in fasting plasma glucose, plasma triglycerides and body fat distribution. Individuals with higher baseline A. muciniphila displayed greater improvement in insulin sensitivity markers and other clinical parameters after CR. These participants also experienced a reduction in A. muciniphila abundance, but it remained significantly higher than in individuals with lower baseline abundance. A. muciniphila was associated with microbial species known to be related to health. Conclusions :A. muciniphila is associated with a healthier metabolic status and better clinical outcomes after CR in overweight/obese adults. The interaction between gut microbiota ecology and A. muciniphila warrants further investigation. Trial registration number NCT01314690.
AB - Objective: Individuals with obesity and type 2 diabetes differ from lean and healthy individuals in their abundance of certain gut microbial species and microbial gene richness. Abundance of Akkermansia muciniphila, a mucin-degrading bacterium, has been inversely associated with body fat mass and glucose intolerance in mice, but more evidence is needed in humans. The impact of diet and weight loss on this bacterial species is unknown. Our objective was to evaluate the association between faecal A. muciniphila abundance, faecal microbiome gene richness, diet, host characteristics, and their changes after calorie restriction (CR). Design: The intervention consisted of a 6-week CR period followed by a 6-week weight stabilisation diet in overweight and obese adults (N=49, including 41 women). Faecal A. muciniphila abundance, faecal microbial gene richness, diet and bioclinical parameters were measured at baseline and after CR and weight stabilisation. Results: At baseline A. muciniphila was inversely related to fasting glucose, waist-to-hip ratio and subcutaneous adipocyte diameter. Subjects with higher gene richness and A. muciniphila abundance exhibited the healthiest metabolic status, particularly in fasting plasma glucose, plasma triglycerides and body fat distribution. Individuals with higher baseline A. muciniphila displayed greater improvement in insulin sensitivity markers and other clinical parameters after CR. These participants also experienced a reduction in A. muciniphila abundance, but it remained significantly higher than in individuals with lower baseline abundance. A. muciniphila was associated with microbial species known to be related to health. Conclusions :A. muciniphila is associated with a healthier metabolic status and better clinical outcomes after CR in overweight/obese adults. The interaction between gut microbiota ecology and A. muciniphila warrants further investigation. Trial registration number NCT01314690.
UR - http://www.scopus.com/inward/record.url?scp=84960253261&partnerID=8YFLogxK
U2 - 10.1136/gutjnl-2014-308778
DO - 10.1136/gutjnl-2014-308778
M3 - Article
C2 - 26100928
AN - SCOPUS:84960253261
SN - 0017-5749
VL - 65
SP - 426
EP - 436
JO - Gut
JF - Gut
IS - 3
ER -