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Gut-derived Appetite Hormones Do Not Explain Energy Intake Differences in Humans Following Low-carbohydrate Versus Low-fat Diets

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Abstract

Objective: The objective of this study was to explore how dietary macronutrient composition influences postprandial appetite hormone responses and subsequent energy intake.

Methods: A total of 20 adults (mean [SEM], age 30 [1] years, BMI 27.8 [1.3] kg/m, n = 8 with normal weight, n = 6 with overweight, n = 6 with obesity) consumed a low-fat (LF) diet (10% fat, 75% carbohydrate) and a low-carbohydrate (LC) diet (10% carbohydrate, 75% fat) for 2 weeks each in an inpatient randomized crossover design. At the end of each diet, participants consumed isocaloric macronutrient-representative breakfast test meals, and 6-h postprandial responses were measured. Ad libitum energy intake was measured for the rest of the day.

Results: The LC meal resulted in greater mean postprandial plasma active glucagon-like peptide-1 (GLP-1; LC: 6.44 [0.78] pg/mL, LF: 2.46 [0.26] pg/mL; p < 0.0001), total glucose-dependent insulinotropic polypeptide (GIP; LC: 578 [60] pg/mL, LF: 319 [37] pg/mL; p = 0.0004), and peptide YY (PYY; LC: 65.6 [5.6] pg/mL, LF: 50.7 [3.8] pg/mL; p = 0.02), whereas total ghrelin (LC: 184 [25] pg/mL, LF: 261 [47] pg/mL; p = 0.0009), active ghrelin (LC: 91 [9] pg/mL, LF: 232 [28] pg/mL; p < 0.0001), and leptin (LC: 26.9 [6.5] ng/mL, LF: 35.2 [7.5] ng/mL; p = 0.01) were lower compared with LF. Participants ate more during LC at lunch (244 [85] kcal; p = 0.01) and dinner (193 [86] kcal; p = 0.04), increasing total subsequent energy intake for the day compared with LF (551 [103] kcal; p < 0.0001).

Conclusions: In the short term, endogenous gut-derived appetite hormones do not necessarily determine ad libitum energy intake.

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References
1.
Watkins J, Koumanov F, Gonzalez J . Protein- and Calcium-Mediated GLP-1 Secretion: A Narrative Review. Adv Nutr. 2021; 12(6):2540-2552. PMC: 8634310. DOI: 10.1093/advances/nmab078. View

2.
Demeke S, Rohde K, Chollet-Hinton L, Sutton C, Kong K, Fazzino T . Change in hyper-palatable food availability in the US food system over 30 years: 1988-2018. Public Health Nutr. 2022; 26(1):182-189. PMC: 9672140. DOI: 10.1017/S1368980022001227. View

3.
Williams D, Baskin D, Schwartz M . Evidence that intestinal glucagon-like peptide-1 plays a physiological role in satiety. Endocrinology. 2008; 150(4):1680-7. PMC: 2659282. DOI: 10.1210/en.2008-1045. View

4.
Lewis H, Ahern A, Solis-Trapala I, Walker C, Reimann F, Gribble F . Effect of reducing portion size at a compulsory meal on later energy intake, gut hormones, and appetite in overweight adults. Obesity (Silver Spring). 2015; 23(7):1362-70. PMC: 7212075. DOI: 10.1002/oby.21105. View

5.
Jastreboff A, Aronne L, Ahmad N, Wharton S, Connery L, Alves B . Tirzepatide Once Weekly for the Treatment of Obesity. N Engl J Med. 2022; 387(3):205-216. DOI: 10.1056/NEJMoa2206038. View