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Effect of a plant-based, low-fat diet versus an animal-based, ketogenic diet on ad libitum energy intake.

Authors :
Hall KD
Guo J
Courville AB
Boring J
Brychta R
Chen KY
Darcey V
Forde CG
Gharib AM
Gallagher I
Howard R
Joseph PV
Milley L
Ouwerkerk R
Raisinger K
Rozga I
Schick A
Stagliano M
Torres S
Walter M
Walter P
Yang S
Chung ST
Source :
Nature medicine [Nat Med] 2021 Feb; Vol. 27 (2), pp. 344-353. Date of Electronic Publication: 2021 Jan 21.
Publication Year :
2021

Abstract

The carbohydrate-insulin model of obesity posits that high-carbohydrate diets lead to excess insulin secretion, thereby promoting fat accumulation and increasing energy intake. Thus, low-carbohydrate diets are predicted to reduce ad libitum energy intake as compared to low-fat, high-carbohydrate diets. To test this hypothesis, 20 adults aged 29.9 ± 1.4 (mean ± s.e.m.) years with body mass index of 27.8 ± 1.3 kg m <superscript>-2</superscript> were admitted as inpatients to the National Institutes of Health Clinical Center and randomized to consume ad libitum either a minimally processed, plant-based, low-fat diet (10.3% fat, 75.2% carbohydrate) with high glycemic load (85 g 1,000 kcal <superscript>-1</superscript> ) or a minimally processed, animal-based, ketogenic, low-carbohydrate diet (75.8% fat, 10.0% carbohydrate) with low glycemic load (6 g 1,000 kcal <superscript>-1</superscript> ) for 2 weeks followed immediately by the alternate diet for 2 weeks. One participant withdrew due to hypoglycemia during the low-carbohydrate diet. The primary outcomes compared mean daily ad libitum energy intake between each 2-week diet period as well as between the final week of each diet. We found that the low-fat diet led to 689 ± 73 kcal d <superscript>-1</superscript> less energy intake than the low-carbohydrate diet over 2 weeks (P < 0.0001) and 544 ± 68 kcal d <superscript>-1</superscript> less over the final week (P < 0.0001). Therefore, the predictions of the carbohydrate-insulin model were inconsistent with our observations. This study was registered on ClinicalTrials.gov as NCT03878108 .

Details

Language :
English
ISSN :
1546-170X
Volume :
27
Issue :
2
Database :
MEDLINE
Journal :
Nature medicine
Publication Type :
Academic Journal
Accession number :
33479499
Full Text :
https://doi.org/10.1038/s41591-020-01209-1