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Volume 58, Issue 12, Pages 1769-1777 (December 2009)


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Effects of dietary carbohydrate restriction versus low-fat diet on flow-mediated dilation

Jeff S. VolekCorresponding Author Informationemail address, Kevin D. Ballard, Ricardo Silvestre, Daniel A. Judelson, Erin E. Quann, Cassandra E. Forsythe, Maria Luz Fernandez, William J. Kraemer

Received 21 February 2009; accepted 16 June 2009. published online 27 July 2009.

Abstract 

We previously reported that a carbohydrate-restricted diet (CRD) ameliorated many of the traditional markers associated with metabolic syndrome and cardiovascular risk compared with a low-fat diet (LFD). There remains concern how CRD affects vascular function because acute meals high in fat have been shown to impair endothelial function. Here, we extend our work and address these concerns by measuring fasting and postprandial vascular function in 40 overweight men and women with moderate hypertriacylglycerolemia who were randomly assigned to consume hypocaloric diets (∼1500 kcal) restricted in carbohydrate (percentage of carbohydrate-fat-protein = 12:59:28) or LFD (56:24:20). Flow-mediated dilation of the brachial artery was assessed before and after ingestion of a high-fat meal (908 kcal, 84% fat) at baseline and after 12 weeks. Compared with the LFD, the CRD resulted in a greater decrease in postprandial triacylglycerol (−47% vs −15%, P = .007), insulin (−51% vs −6%, P = .009), and lymphocyte (−12% vs −1%, P = .050) responses. Postprandial fatty acids were significantly increased by the CRD compared with the LFD (P = .033). Serum interleukin-6 increased significantly over the postprandial period; and the response was augmented in the CRD (46%) compared with the LFD (−13%) group (P = .038). After 12 weeks, peak flow-mediated dilation at 3 hours increased from 5.1% to 6.5% in the CRD group and decreased from 7.9% to 5.2% in the LFD group (P = .004). These findings show that a 12-week low-carbohydrate diet improves postprandial vascular function more than a LFD in individuals with atherogenic dyslipidemia.

Department of Kinesiology and the Department of Nutritional Sciences, University of Connecticut, Storrs, CT 06269-1110, USA

Corresponding Author InformationCorresponding author. Tel.: +1 860 486 6712; fax: +1 860 486 1123.

 JSV, WJK, and MLF had overall responsibility of the study and contributed to experimental design, data analysis and interpretation, and manuscript preparation. KDB, RS, and DAJ performed vascular measurements and analysis as well as biochemical assays. EEQ and CEF were responsible for the dietetic aspects of the study and overseeing the data collection protocols. All authors agreed on the final version of the manuscript, and none had any conflict of interest.

PII: S0026-0495(09)00250-9

doi:10.1016/j.metabol.2009.06.005


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