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Review
. 2024 Jan 4;16(1):176.
doi: 10.3390/nu16010176.

Nutrition and Disorders of Gut-Brain Interaction

Affiliations
Review

Nutrition and Disorders of Gut-Brain Interaction

Emidio Scarpellini et al. Nutrients. .

Abstract

Background: Disorders of gut-brain interaction (DGBIs) have a complex pathophysiology that is often characterized by a relationship between food ingestion and triggering of symptoms. Understanding of the underlying mechanisms and the role of nutrients as a therapeutic target are rapidly evolving.

Aims and methods: We performed a narrative review of the literature using the following keywords, their acronyms, and their associations: nutrients, disorders of gut-brain interaction; functional dyspepsia; malabsorption; irritable bowel syndrome; diarrhea; constipation.

Results: Functional dyspepsia displayed a significant correlation between volume, fat and/or wheat abundance, chemical composition of ingested food and symptoms of early satiety, fullness and weight loss. Carbohydrate malabsorption is related to enzyme deficiency throughout the GI tract. Food composition and richness in soluble vs. non-soluble fibers is related to constipation and diarrhea. The elimination of fermentable oligo-, di-, monosaccharides and polyols (FODMAPs) has a significant and non-unidirectional impact on irritable bowel syndrome (IBS) symptoms.

Conclusions: Food volume, nutritive and chemical composition, and its malabsorption are associated with symptom generation in DGBIs. Further multicenter, randomized-controlled clinical trials are needed to clarify the underlying pathophysiology.

Keywords: constipation; diarrhea; disturbances of gut–brain axis; functional dyspepsia; irritable bowel syndrome; malabsorption; nutrients.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Physiopathological mechanisms at the basis of food role in DGBI symptom generation. In light grey box, the least evidence-based pathophysiological food-symptoms association mechanism; in dark grey box the most evidence-based pathophysiological one.

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