Intermittent fasting modulates human gut microbiota diversity in a phenotype-dependent manner: a systematic review

• Published in: Bioscience of Microbiota, Food and Health Vol. 43; no. 3; pp. 170 - 182
• Main Authors: PRAMONO, Adriyan, ARDIARIA, Martha, LIMIJADI, Edward Kurnia Setiawan, NOER, Etika Ratna, LESTARI, Endang Sri, SISWANTO, Ferbian Milas
• Format: Journal Article
• Language: English
• Published: Japan BMFH Press 2024; Japan Science and Technology Agency
• Subjects: diversity; Fasting; gut microbiota; human; Impact analysis; intermittent fasting; Intestinal microflora; Meta-analysis; Metabolic disorders; Metabolic syndrome; Metabolism; Metabolites; Microbiota; Microorganisms; Phenotypes; Phenotypic variations; Qualitative analysis; Quality assessment; Quality control; Review; Reviews; Systematic review; Taxonomy; diversity; intermittent fasting; systematic review; human; gut microbiota
• ISSN: 2186-6953; 2186-3342; 2186-3342
• DOI: 10.12938/bmfh.2023-111

Cumulative evidence suggests that intermittent fasting (IF) has beneficial effects on human metabolic health. It has been indicated that its impact on the gut microbiota may mediate these beneficial effects. As a result, we hypothesized that IF may impact the human gut microbiota. A systematic review was carried out according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) protocol using the PubMed, Scopus, and CINAHL databases. We registered our systematic review protocol in PROSPERO under registration number CRD42021270050. Human intervention studies published until April 30, 2023, were included. The quality of the included studies was assessed using National Institutes of Health (NIH) quality assessment study tools for intervention studies. The search in the database returned 166 studies, of which 13 matched all criteria for the final qualitative analysis. The body of evidence suggests that IF modulates human gut microbiota alpha and beta diversity in lean (relatively healthy) and relatively healthy overweight/obese individuals but not in individuals with metabolic syndrome. Furthermore, IF also alters human gut microbiota composition in all phenotypes. Of interest, the gut microbiota taxa or microbial metabolites after an IF intervention are associated with metabolic markers. According to this review, IF influences the diversity and taxonomic levels of the human gut microbiota. Individual metabolic phenotypes may alter the effect of IF on the diversity and taxonomic levels of the gut microbiota.