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Articles

Effect of Diets Varying in Iron and Saturated Fat on the Gut Microbiota and Intestinal Inflammation: A Crossover Feeding Study among Older Females with Obesity

, , ORCID Icon, , , , , ORCID Icon, , & show all
Pages 876-889 | Received 06 Jul 2022, Accepted 23 Dec 2022, Published online: 10 Jan 2023
 

Abstract

Obesity is considered an independent risk factor for colorectal cancer (CRC). Altered nutrient metabolism, particularly changes to digestion and intestinal absorption, may play an important role in the development of CRC. Iron can promote the formation of tissue-damaging and immune-modulating reactive oxygen species. We conducted a crossover, controlled feeding study to examine the effect of three, 3-week diets varying in iron and saturated fat content on the colonic milieu and systemic markers among older females with obesity. Anthropometrics, fasting venous blood and stool were collected before and after each diet. There was a minimum 3-week washout period between diets. Eighteen participants consumed the three diets (72% Black; mean age 60.4 years; mean body mass index 35.7 kg/m2). Results showed no effect of the diets on intestinal inflammation (fecal calprotectin) or circulating iron, inflammation, and metabolic markers. Pairwise comparisons revealed less community diversity between samples (beta diversity, calculated from 16S rRNA amplicon sequences) among participants when consuming a diet low in iron and high in saturated fat vs. when consuming a diet high in iron and saturated fat. More studies are needed to investigate if dietary iron represents a salient target for CRC prevention among individuals with obesity.

Authors’ Contributions

HRG, MF, and LTH conceptualized the study. AH, AM, SO, and LTH conducted the trial. BPB, BRL, PW, and LTH performed the analysis. MLO, LTH, and PW wrote the manuscript. All authors reviewed and approved the manuscript.

Disclosure Statement

All authors report there are no competing interests to declare.

Additional information

Funding

This work was supported by the American Cancer Society under grant MRSG014-025-01-CNE, LTH; and the National Institutes of Health under grant T32CA057699, PW, AM.

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