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Host-diet-gut microbiome interactions influence human energy balance: a randomized clinical trial.
Corbin, Karen D; Carnero, Elvis A; Dirks, Blake; Igudesman, Daria; Yi, Fanchao; Marcus, Andrew; Davis, Taylor L; Pratley, Richard E; Rittmann, Bruce E; Krajmalnik-Brown, Rosa; Smith, Steven R.
Afiliação
  • Corbin KD; AdventHealth Translational Research Institute, Orlando, FL, USA.
  • Carnero EA; AdventHealth Translational Research Institute, Orlando, FL, USA.
  • Dirks B; Biodesign Center for Health through Microbiomes, Arizona State University, Tempe, AZ, USA.
  • Igudesman D; Biodesign Swette Center for Environmental Biotechnology, Arizona State University, Tempe, AZ, USA.
  • Yi F; AdventHealth Translational Research Institute, Orlando, FL, USA.
  • Marcus A; AdventHealth Translational Research Institute, Orlando, FL, USA.
  • Davis TL; Biodesign Center for Health through Microbiomes, Arizona State University, Tempe, AZ, USA.
  • Pratley RE; Skyology Inc, San Francisco, CA, USA.
  • Rittmann BE; Biodesign Center for Health through Microbiomes, Arizona State University, Tempe, AZ, USA.
  • Krajmalnik-Brown R; Biodesign Swette Center for Environmental Biotechnology, Arizona State University, Tempe, AZ, USA.
  • Smith SR; AdventHealth Translational Research Institute, Orlando, FL, USA.
Nat Commun ; 14(1): 3161, 2023 05 31.
Article em En | MEDLINE | ID: mdl-37258525
ABSTRACT
The gut microbiome is emerging as a key modulator of human energy balance. Prior studies in humans lacked the environmental and dietary controls and precision required to quantitatively evaluate the contributions of the gut microbiome. Using a Microbiome Enhancer Diet (MBD) designed to deliver more dietary substrates to the colon and therefore modulate the gut microbiome, we quantified microbial and host contributions to human energy balance in a controlled feeding study with a randomized crossover design in young, healthy, weight stable males and females (NCT02939703). In a metabolic ward where the environment was strictly controlled, we measured energy intake, energy expenditure, and energy output (fecal and urinary). The primary endpoint was the within-participant difference in host metabolizable energy between experimental conditions [Control, Western Diet (WD) vs. MBD]. The secondary endpoints were enteroendocrine hormones, hunger/satiety, and food intake. Here we show that, compared to the WD, the MBD leads to an additional 116 ± 56 kcals (P < 0.0001) lost in feces daily and thus, lower metabolizable energy for the host (89.5 ± 0.73%; range 84.2-96.1% on the MBD vs. 95.4 ± 0.21%; range 94.1-97.0% on the WD; P < 0.0001) without changes in energy expenditure, hunger/satiety or food intake (P > 0.05). Microbial 16S rRNA gene copy number (a surrogate of biomass) increases (P < 0.0001), beta-diversity changes (whole genome shotgun sequencing; P = 0.02), and fermentation products increase (P < 0.01) on an MBD as compared to a WD along with significant changes in the host enteroendocrine system (P < 0.0001). The substantial interindividual variability in metabolizable energy on the MBD is explained in part by fecal SCFAs and biomass. Our results reveal the complex host-diet-microbiome interplay that modulates energy balance.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Microbioma Gastrointestinal Tipo de estudo: Clinical_trials Limite: Female / Humans / Male Idioma: En Revista: Nat Commun Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Microbioma Gastrointestinal Tipo de estudo: Clinical_trials Limite: Female / Humans / Male Idioma: En Revista: Nat Commun Ano de publicação: 2023 Tipo de documento: Article