» Articles » PMID: 38806467

Gut Microbiome Remodeling and Metabolomic Profile Improves in Response to Protein Pacing with Intermittent Fasting Versus Continuous Caloric Restriction

Abstract

The gut microbiome (GM) modulates body weight/composition and gastrointestinal functioning; therefore, approaches targeting resident gut microbes have attracted considerable interest. Intermittent fasting (IF) and protein pacing (P) regimens are effective in facilitating weight loss (WL) and enhancing body composition. However, the interrelationships between IF- and P-induced WL and the GM are unknown. The current randomized controlled study describes distinct fecal microbial and plasma metabolomic signatures between combined IF-P (n = 21) versus a heart-healthy, calorie-restricted (CR, n = 20) diet matched for overall energy intake in free-living human participants (women = 27; men = 14) with overweight/obesity for 8 weeks. Gut symptomatology improves and abundance of Christensenellaceae microbes and circulating cytokines and amino acid metabolites favoring fat oxidation increase with IF-P (p < 0.05), whereas metabolites associated with a longevity-related metabolic pathway increase with CR (p < 0.05). Differences indicate GM and metabolomic factors play a role in WL maintenance and body composition. This novel work provides insight into the GM and metabolomic profile of participants following an IF-P or CR diet and highlights important differences in microbial assembly associated with WL and body composition responsiveness. These data may inform future GM-focused precision nutrition recommendations using larger sample sizes of longer duration. Trial registration, March 6, 2020 (ClinicalTrials.gov as NCT04327141), based on a previous randomized intervention trial.

Citing Articles

The cyclic metabolic switching theory of intermittent fasting.

Mattson M Nat Metab. 2025; .

PMID: 40087409 DOI: 10.1038/s42255-025-01254-5.


Metabolic Reprogramming in Gut Microbiota Exposed to Polystyrene Microplastics.

Chi J, Patterson J, Jin Y, Kim K, Lalime N, Hawley D Biomedicines. 2025; 13(2).

PMID: 40002859 PMC: 11853289. DOI: 10.3390/biomedicines13020446.


The Positive Effects of Training and Time-Restricted Eating in Gut Microbiota Biodiversity in Patients with Multiple Myeloma.

Czerwinska-Ledwig O, Nowak-Zaleska A, Zychowska M, Meyza K, Palka T, Dzidek A Nutrients. 2025; 17(1.

PMID: 39796496 PMC: 11722647. DOI: 10.3390/nu17010061.


Nutritional optimization of fecal microbiota transplantation in humans: a scoping review.

Teigen L, Hoeg A, Zehra H, Shah P, Johnson R, Hutchison K Gut Microbes. 2025; 17(1):2446378.

PMID: 39772953 PMC: 11730610. DOI: 10.1080/19490976.2024.2446378.


The microbiome's influence on obesity: mechanisms and therapeutic potential.

Tadese D, Mwangi J, Luo L, Zhang H, Huang X, Michira B Sci China Life Sci. 2024; 68(3):657-672.

PMID: 39617855 DOI: 10.1007/s11427-024-2759-3.


References
1.
Mirzayi C, Renson A, Zohra F, Elsafoury S, Geistlinger L, Kasselman L . Reporting guidelines for human microbiome research: the STORMS checklist. Nat Med. 2021; 27(11):1885-1892. PMC: 9105086. DOI: 10.1038/s41591-021-01552-x. View

2.
Jasbi P, Shi X, Chu P, Elliott N, Hudson H, Jones D . Metabolic Profiling of Neocortical Tissue Discriminates Alzheimer's Disease from Mild Cognitive Impairment, High Pathology Controls, and Normal Controls. J Proteome Res. 2021; 20(9):4303-4317. PMC: 11060066. DOI: 10.1021/acs.jproteome.1c00290. View

3.
Atarashi K, Tanoue T, Oshima K, Suda W, Nagano Y, Nishikawa H . Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota. Nature. 2013; 500(7461):232-6. DOI: 10.1038/nature12331. View

4.
Bruun J, Pedersen S, Kristensen K, Richelsen B . Opposite regulation of interleukin-8 and tumor necrosis factor-alpha by weight loss. Obes Res. 2002; 10(6):499-506. DOI: 10.1038/oby.2002.68. View

5.
Jasbi P, Mohr A, Shi X, Mahmood T, Zhu Q, Bruening M . Microbiome and metabolome profiles of high screen time in a cohort of healthy college students. Sci Rep. 2022; 12(1):3452. PMC: 8891328. DOI: 10.1038/s41598-022-07381-3. View