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J Am Coll Cardiol, 2008; 51:59-67, doi:10.1016/j.jacc.2007.08.050 © 2008 by the American College of Cardiology Foundation |

* Commonwealth Scientific and Industrial Research Organisation–Human Nutrition, Adelaide, Australia
Department of Nutrition and Dietetics, Flinders University, Adelaide, Australia.
Manuscript received April 11, 2007; revised manuscript received July 27, 2007, accepted July 30, 2007.
* Reprint requests and correspondence: Dr. Grant D. Brinkworth, CSIRO-Human Nutrition, P.O. Box 10041 BC, Adelaide, South Australia 5000, Australia. (Email: grant.brinkworth{at}csiro.au).
Objectives: This study was designed to compare the effects of an energy-reduced, isocaloric very-low-carbohydrate, high-fat (VLCHF) diet and a high-carbohydrate, low-fat (HCLF) diet on weight loss and cardiovascular disease (CVD) risk outcomes.
Background: Despite the popularity of the VLCHF diet, no studies have compared the chronic effects of weight loss and metabolic change to a conventional HCLF diet under isocaloric conditions.
Methods: A total of 88 abdominally obese adults were randomly assigned to either an energy-restricted (
6 to 7 MJ, 30% deficit), planned isocaloric VLCHF or HCLF diet for 24 weeks in an outpatient clinical trial. Body weight, blood pressure, fasting glucose, lipids, insulin, apolipoprotein B (apoB), and C-reactive protein (CRP) were measured at weeks 0 and 24.
Results: Weight loss was similar in both groups (VLCHF –11.9 ± 6.3 kg, HCLF –10.1 ± 5.7 kg; p = 0.17). Blood pressure, CRP, fasting glucose, and insulin reduced similarly with weight loss in both diets. The VLCHF diet produced greater decreases in triacylglycerols (VLCHF –0.64 ± 0.62 mmol/l, HCLF –0.35 ± 0.49 mmol/l; p = 0.01) and increases in high-density lipoprotein cholesterol (HDL-C) (VLCHF 0.25 ± 0.28 mmol/l, HCLF 0.08 ± 0.17 mmol/l; p = 0.002). Low-density lipoprotein cholesterol (LDL-C) decreased in the HCLF diet but remained unchanged in the VLCHF diet (VLCHF 0.06 ± 0.58 mmol/l, HCLF –0.46 ± 0.71 mmol/l; p < 0.001). However, a high degree of individual variability for the LDL response in the VLCHF diet was observed, with 24% of individuals reporting an increase of at least 10%. The apoB levels remained unchanged in both diet groups.
Conclusions: Under isocaloric conditions, VLCHF and HCLF diets result in similar weight loss. Overall, although both diets had similar improvements for a number of metabolic risk markers, an HCLF diet had more favorable effects on the blood lipid profile. This suggests that the potential long-term effects of the VLCHF diet for CVD risk remain a concern and that blood lipid levels should be monitored. (Long-term health effects of high and low carbohydrate, weight loss diets in obese subjects with the metabolic syndrome; http://www.anzctr.org.au; ACTR No. 12606000203550).
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