4.6 Article

Dietary α-linolenic acid decreases C-reactive protein, serum amyloid A and interleukin-6 in dyslipidaemic patients

Journal

ATHEROSCLEROSIS
Volume 167, Issue 2, Pages 237-242

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/S0021-9150(02)00427-6

Keywords

a-linotenic acid; C-reactive protein; dyslipidaemia; interleukin-6; linoleic acid; serum amyloid A

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Background: Inflammation plays an important role in the pathogenesis of coronary artery disease. We examined whether dietary supplementation with alpha-linolenic acid (ALA, 18:3n-3) affects the levels of inflammatory markers in dyslipidaemic patients. Methods: We recruited 76 male dyslipidaemic patients (mean age = 51 +/- 8 years) following a typical Greek diet. They were randomly assigned either to 15 ml of linseed oil (rich in ALA) per day (n = 50) or to 15 ml of safflower oil (rich in linoleic acid (LA, 18:2n-6)) per day (n = 26). The ratio of n-6:n-3 in linseed oil supplemented group was 1.3:1 and in safflower oil supplemented group 13.2:1. Dietary intervention lasted for 3 months. Blood lipids and C-reactive protein (CRP), serum amyloid A (SAA), and interleukin-6 (IL-6) levels were determined prior and after intervention. CRP and SAA were measured by nephelometry and IL-6 by immunoassay. Results: Dietary supplementation with ALA decreased significantly CRP, SAA and IL-6 levels. The median decrease of CRP was 38% (1.24 vs. 0.93 mg/l, P = 0.0008), of SAA 23.1% (3.24 vs. 2.39 mg/l, P = 0.0001) and of IL-6 10.5% (2.18 vs. 1.7 pg/ml, P = 0.01). The decrease of inflammatory markers was independent of lipid changes. Dietary supplementation with LA did not affect significantly CRP, SAA and IL-6 concentrations but decreased cholesterol levels. Conclusions: Dietary supplementation with ALA for 3 months decreases significantly CRP, SAA and IL-6 levels in dyslipidaemic patients. This anti-inflammatory effect may provide a possible additional mechanism for the beneficial effect of plant n-3 polyunsaturated fatty acids in primary and secondary prevention of coronary artery disease. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.

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