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Plant- and marine-derived n-3 polyunsaturated fatty acids have differential effects on fasting and postprandial blood lipid concentrations and on the susceptibility of LDL to oxidative modification in moderately hyperlipidemic subjects

Plant- and marine-derived n-3 polyunsaturated fatty acids have differential effects on fasting and postprandial blood lipid concentrations and on the susceptibility of LDL to oxidative modification in moderately hyperlipidemic subjects
Plant- and marine-derived n-3 polyunsaturated fatty acids have differential effects on fasting and postprandial blood lipid concentrations and on the susceptibility of LDL to oxidative modification in moderately hyperlipidemic subjects
Background: Dietary ?-linolenic acid (ALA) can be converted to long-chain n-3 polyunsaturated fatty acids (PUFAs) in humans and may reproduce some of the beneficial effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on cardiovascular disease risk factors.
Objective: This study aimed to compare the effects of increased dietary intakes of ALA and EPA+DHA on a range of atherogenic risk factors.
Design: This was a placebo-controlled, parallel study involving 150 moderately hyperlipidemic subjects randomly assigned to 1 of 5 interventions: 0.8 or 1.7 g EPA+DHA/d, 4.5 or 9.5 g ALA/d, or an n-6 PUFA control for 6 mo. Fatty acids were incorporated into 25 g of fat spread and 3 capsules to be consumed daily.
Results: The change in fasting or postprandial lipid, glucose, or insulin concentrations or in blood pressure was not significantly different after any of the n-3 PUFA interventions compared with the n-6 PUFA control. The mean (± SEM) change in fasting triacylglycerols after the 1.7-g/d EPA+DHA intervention (-7.7 ± 4.99%) was significantly (P < 0.05) different from the change after the 9.5-g/d ALA intervention (10.9 ± 4.5%). The ex vivo susceptibility of LDL to oxidation was higher after the 1.7-g/d EPA+DHA intervention than after the control and ALA interventions (P < 0.05). There was no significant change in plasma ?-tocopherol concentrations or in whole plasma antioxidant status in any of the groups.
Conclusion: At estimated biologically equivalent intakes, dietary ALA and EPA+DHA have different physiologic effects.
?-Linolenic acid, eicosapentaenoic acid, docosahexaenoic acid, polyunsaturated fatty acids, n-3 fatty acids, lipids, plasma fatty acid, LDL oxidation, moderately hyperlipidemic subjects, triacylglycerol
783-795
Finnegan, Yvonne E.
55946247-9cb4-4562-b11b-30e410669aac
Minihane, Anne M.
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Leigh-Firbank, Elizabeth C.
a67870ab-b4cf-4e48-bfa4-e941ff993976
Kew, Samantha
0388d70a-7691-4660-9896-95a45099a5db
Meijer, Gert W.
eb75ba75-abf1-4878-b6a4-38761350e9a2
Muggli, Reto
f23e2520-28a7-4bbd-a027-472c2a2e0bd5
Calder, Philip C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Williams, Christine M.
4cf5b7be-8973-4ed3-9150-5caf74999670
Finnegan, Yvonne E.
55946247-9cb4-4562-b11b-30e410669aac
Minihane, Anne M.
323fcab6-215c-4c13-b8d4-2ad242a31900
Leigh-Firbank, Elizabeth C.
a67870ab-b4cf-4e48-bfa4-e941ff993976
Kew, Samantha
0388d70a-7691-4660-9896-95a45099a5db
Meijer, Gert W.
eb75ba75-abf1-4878-b6a4-38761350e9a2
Muggli, Reto
f23e2520-28a7-4bbd-a027-472c2a2e0bd5
Calder, Philip C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Williams, Christine M.
4cf5b7be-8973-4ed3-9150-5caf74999670

Finnegan, Yvonne E., Minihane, Anne M., Leigh-Firbank, Elizabeth C., Kew, Samantha, Meijer, Gert W., Muggli, Reto, Calder, Philip C. and Williams, Christine M. (2003) Plant- and marine-derived n-3 polyunsaturated fatty acids have differential effects on fasting and postprandial blood lipid concentrations and on the susceptibility of LDL to oxidative modification in moderately hyperlipidemic subjects. American Journal of Clinical Nutrition, 77 (4), 783-795.

Record type: Article

Abstract

Background: Dietary ?-linolenic acid (ALA) can be converted to long-chain n-3 polyunsaturated fatty acids (PUFAs) in humans and may reproduce some of the beneficial effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on cardiovascular disease risk factors.
Objective: This study aimed to compare the effects of increased dietary intakes of ALA and EPA+DHA on a range of atherogenic risk factors.
Design: This was a placebo-controlled, parallel study involving 150 moderately hyperlipidemic subjects randomly assigned to 1 of 5 interventions: 0.8 or 1.7 g EPA+DHA/d, 4.5 or 9.5 g ALA/d, or an n-6 PUFA control for 6 mo. Fatty acids were incorporated into 25 g of fat spread and 3 capsules to be consumed daily.
Results: The change in fasting or postprandial lipid, glucose, or insulin concentrations or in blood pressure was not significantly different after any of the n-3 PUFA interventions compared with the n-6 PUFA control. The mean (± SEM) change in fasting triacylglycerols after the 1.7-g/d EPA+DHA intervention (-7.7 ± 4.99%) was significantly (P < 0.05) different from the change after the 9.5-g/d ALA intervention (10.9 ± 4.5%). The ex vivo susceptibility of LDL to oxidation was higher after the 1.7-g/d EPA+DHA intervention than after the control and ALA interventions (P < 0.05). There was no significant change in plasma ?-tocopherol concentrations or in whole plasma antioxidant status in any of the groups.
Conclusion: At estimated biologically equivalent intakes, dietary ALA and EPA+DHA have different physiologic effects.

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More information

Published date: 2003
Keywords: ?-Linolenic acid, eicosapentaenoic acid, docosahexaenoic acid, polyunsaturated fatty acids, n-3 fatty acids, lipids, plasma fatty acid, LDL oxidation, moderately hyperlipidemic subjects, triacylglycerol
Organisations: Dev Origins of Health & Disease

Identifiers

Local EPrints ID: 25488
URI: http://eprints.soton.ac.uk/id/eprint/25488
PURE UUID: 1a2d9e8b-86cc-40ce-a9ff-121011c445d3
ORCID for Philip C. Calder: ORCID iD orcid.org/0000-0002-6038-710X

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Date deposited: 19 Apr 2006
Last modified: 23 Jul 2022 01:39

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Contributors

Author: Yvonne E. Finnegan
Author: Anne M. Minihane
Author: Elizabeth C. Leigh-Firbank
Author: Samantha Kew
Author: Gert W. Meijer
Author: Reto Muggli
Author: Christine M. Williams

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