TY - JOUR
T1 - Prominent mediatory role of gut microbiome in the effect of lifestyle on host metabolic phenotypes
AU - Adriouch, Solia
AU - Belda, Eugeni
AU - Swartz, Timothy D
AU - Forslund, Sofia
AU - Prifti, Edi
AU - Aron-Wisnewsky, Judith
AU - Chakaroun, Rima
AU - Nielsen, Trine
AU - Poitou, Christine
AU - Bel-Lassen, Pierre
AU - Rouault, Christine
AU - Le Roy, Tiphaine
AU - Andrikopoulos, Petros
AU - Chechi, Kanta
AU - Puig-Castellví, Francesc
AU - Dionicio, Inés Castro
AU - Froguel, Philippe
AU - Holmes, Bridget
AU - Alili, Rohia
AU - Andreelli, Fabrizio
AU - Soula, Hedi
AU - Salem, Joe-Elie
AU - Falony, Gwen
AU - Vieira-Silva, Sara
AU - Raes, Jeroen
AU - Bork, Peer
AU - Stumvoll, Michael
AU - Pedersen, Oluf
AU - Ehrlich, S Dusko
AU - Dumas, Marc-Emmanuel
AU - Oppert, Jean-Michel
AU - Dao, Maria Carlota
AU - Zucker, Jean-Daniel
AU - Clément, Karine
PY - 2025/12/31
Y1 - 2025/12/31
N2 - Lifestyle factors influence both gut microbiome composition and host metabolism, yet their combined and mediating effects on host phenotypes remain poorly characterized in cardiometabolic populations. In 1,643 participants from the MetaCardis study, we developed a composite lifestyle score (QASD: dietary quality, physical activity, smoking, and diet diversity) that outperformed individual lifestyle variables in explaining microbial gene richness and exhibited a significant impact on the gut microbiome composition. While bidirectional pathways linking the QASD score, host phenotypes, and microbiome composition were assessed, causal inference-based mediation analyses indicated stronger effects when the microbiome was modeled as the mediator variable, particularly in relation to the insulin resistance-associated profile. Microbiome gene richness emerged as a key mediator explaining 27.8% of QASD score's effect on the insulin resistance marker (HOMA-IR), while no significant mediation was observed on BMI. Extended mediation analyses on microbial species and serum metabolomics deconfounded for drug use and clinical profiles identified 47 mediations where microbial taxa mediated more than 20% of the effect of the QASD score on serum metabolites associated with insulin resistance. Notably, several Faecalibacterium lineages enriched in individuals with high QASD score played a significant mediatory role in increasing the serum biomarkers of microbiome diversity (as cinnamoylglycine or 3-phenylpropionate). Conversely, elevated levels of secondary bile acids in individuals with low QASD scores were strongly mediated by high levels of Clostridium bolteae. These findings highlight distinct and clinically relevant microbiome pathways linking lifestyle behaviors to cardiometabolic risks.One sentence summary:The gut microbiome mediates the impact of diet quality and diversity, physical activity and smoking status - combined in a composite lifestyle score - on cardiometabolic phenotypes.
AB - Lifestyle factors influence both gut microbiome composition and host metabolism, yet their combined and mediating effects on host phenotypes remain poorly characterized in cardiometabolic populations. In 1,643 participants from the MetaCardis study, we developed a composite lifestyle score (QASD: dietary quality, physical activity, smoking, and diet diversity) that outperformed individual lifestyle variables in explaining microbial gene richness and exhibited a significant impact on the gut microbiome composition. While bidirectional pathways linking the QASD score, host phenotypes, and microbiome composition were assessed, causal inference-based mediation analyses indicated stronger effects when the microbiome was modeled as the mediator variable, particularly in relation to the insulin resistance-associated profile. Microbiome gene richness emerged as a key mediator explaining 27.8% of QASD score's effect on the insulin resistance marker (HOMA-IR), while no significant mediation was observed on BMI. Extended mediation analyses on microbial species and serum metabolomics deconfounded for drug use and clinical profiles identified 47 mediations where microbial taxa mediated more than 20% of the effect of the QASD score on serum metabolites associated with insulin resistance. Notably, several Faecalibacterium lineages enriched in individuals with high QASD score played a significant mediatory role in increasing the serum biomarkers of microbiome diversity (as cinnamoylglycine or 3-phenylpropionate). Conversely, elevated levels of secondary bile acids in individuals with low QASD scores were strongly mediated by high levels of Clostridium bolteae. These findings highlight distinct and clinically relevant microbiome pathways linking lifestyle behaviors to cardiometabolic risks.One sentence summary:The gut microbiome mediates the impact of diet quality and diversity, physical activity and smoking status - combined in a composite lifestyle score - on cardiometabolic phenotypes.
KW - Humans
KW - Gastrointestinal Microbiome/physiology
KW - Life Style
KW - Male
KW - Female
KW - Middle Aged
KW - Insulin Resistance
KW - Phenotype
KW - Bacteria/classification
KW - Diet
KW - Adult
KW - Exercise
KW - lifestyle
KW - nutrition
KW - mediation
KW - Gut microbiome
UR - https://www.scopus.com/pages/publications/105025172112
U2 - 10.1080/19490976.2025.2599565
DO - 10.1080/19490976.2025.2599565
M3 - Journal article
C2 - 41408736
SN - 1949-0976
VL - 17
SP - 2599565
JO - Gut Microbes
JF - Gut Microbes
IS - 1
ER -