AI Article Synopsis

  • - The study aimed to compare the effects of a typical Food Distribution Program on Indian Reservations (FDPIR) diet with a DGA-compliant FDPIR diet on inflammation, appetite, and energy intake among American Indian and non-AI individuals.
  • - Using a randomized crossover design, participants (n=13) tried both dietary conditions, revealing no notable differences in inflammation and appetite, but statistically significant higher energy intake (14% more kcal) on the typical FDPIR diet.
  • - The findings suggest that a higher calorie intake from the typical FDPIR diet could elevate the risk of obesity and related diseases like type 2 diabetes, highlighting the importance of adhering to dietary guidelines.

Article Abstract

Objective: To compare the effects of a typical Food Distribution Program on Indian Reservations (FDPIR) diet with an FDPIR diet that meets Dietary Guidelines for Americans (DGA) on inflammation response, appetite and energy intake on a combination of American Indian (AI) and non-AI individuals.

Design: A within-subjects, randomised, crossover design was used to compare two dietary conditions: (1) a FDPIR diet that met DGA and (2) a FDPIR diet that did not meet DGA. Each participant served as their own control and was exposed to both dietary conditions. Repeated-measures ANOVA and t tests assessed significance between the two dietary conditions.

Setting: This took place in the Montana State University Nutrition Research Laboratory in the USA.

Participants: Female and male participants (n 13) aged 18-55 years from the university and local community.

Results: There were no significant differences in inflammatory response and appetite sensations between the two dietary conditions. Findings indicated that participants ate 14 % more (P < 0·01) kcal on a typical FDPIR diet compared with a FDPIR diet that met DGA.

Conclusions: Higher energy intake during a typical FDPIR diet compared with a FDPIR diet that meets DGA may increase risk for obesity and nutrition-related diseases, including type 2 diabetes and other chronic inflammatory conditions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884777PMC
http://dx.doi.org/10.1017/S1368980020002852DOI Listing

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