Atorvastatin in factorial with omega-3 EE90 risk reduction in diabetes (AFORRD): a randomised controlled trial
Atorvastatin in factorial with omega-3 EE90 risk reduction in diabetes (AFORRD): a randomised controlled trial
Aims/hypothesis: the aim of the study was to examine the impact of statin or omega-3-acid ethyl esters 90 (omega-3 EE90; omega-3-acid ethyl esters 90 refers to a mixture of ethyl esters of n-3 fatty acids) on estimated cardiovascular disease (CVD) risk in community-based people with type 2 diabetes but without known CVD and not taking lipid-lowering therapy.
Methods: a central computer randomised 800 patients in 59 UK general practices to atorvastatin (n∈=∈401, 20 mg/day) or placebo (n∈=∈399) and omega-3 EE90 (n∈=∈397, 2 g/day) or placebo (n∈=∈403) in a concealed factorial manner. Participants with LDL-cholesterol <2.6 mmol/l, triacylglycerol <1.5 mmol/l and estimated 10-year CVD risk <20% were compared at 4 months.
Results: mean (SD) age was 63.5 (11.7) years, HbA 1c 6.9 (1.1) % and known diabetes duration (median [interquartile range]) was 4 (2-8) years. Fifty-seven per cent were men, 90% white and 74% had an estimated 10-year CVD risk ≥20%. Of 732 patients with 4-month data, more allocated atorvastatin (n∈=∈371) compared with placebo (n∈=∈361) achieved LDL-cholesterol <2.6 mmol/l (91% vs 24%, p∈<∈0.001) and had estimated 10-year CVD risks <20% (38% vs 26%, p∈<∈0.001). No differences were seen between those allocated omega-3 EE90 (n∈=∈371) compared with placebo (n∈=∈361) for participants achieving triacylglycerol <1.5 mmol/l (65% vs 60%, p∈=∈0.18) or estimated 10-year CVD risks <20% (34% vs 30%, p∈=∈0.18). There were no side effects of note.
Conclusions/ interpretation: many community-based diabetic patients without known CVD remain at high CVD risk despite statin treatment and require additional risk-reduction strategies. The impact of omega-3 EE90 on CVD risk will remain uncertain until clinical endpoint trial results are available. Trial registration: ISRCT no. 76737502 Funding: The study was funded by Pfizer.
Atorvastatin, Cardiovascular risk, N-3 polyunsaturated fatty acids, Omega-3 EE90, Primary care, Type 2 diabetes
50-59
Holman, R.R.
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Paul, S.
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Farmer, A.
d1e10144-e42a-476a-bb0c-12d188fe70af
Tucker, L.
13223955-60e8-4185-bb64-60fd9ae833ea
Stratton, I.M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Neil, H.A.W.
ded0352b-edc2-499f-a8b9-51f82489f985
January 2009
Holman, R.R.
d03ac9f9-2f1d-40c9-827f-939b8b05b25f
Paul, S.
bcabbbe9-30de-4b66-a26e-929d9cc2a949
Farmer, A.
d1e10144-e42a-476a-bb0c-12d188fe70af
Tucker, L.
13223955-60e8-4185-bb64-60fd9ae833ea
Stratton, I.M.
772f25b9-23c0-4240-a3f6-1e76b03b172f
Neil, H.A.W.
ded0352b-edc2-499f-a8b9-51f82489f985
Holman, R.R., Paul, S., Farmer, A., Tucker, L., Stratton, I.M. and Neil, H.A.W.
(2009)
Atorvastatin in factorial with omega-3 EE90 risk reduction in diabetes (AFORRD): a randomised controlled trial.
Diabetologia, 52 (1), .
(doi:10.1007/s00125-008-1179-5).
Abstract
Aims/hypothesis: the aim of the study was to examine the impact of statin or omega-3-acid ethyl esters 90 (omega-3 EE90; omega-3-acid ethyl esters 90 refers to a mixture of ethyl esters of n-3 fatty acids) on estimated cardiovascular disease (CVD) risk in community-based people with type 2 diabetes but without known CVD and not taking lipid-lowering therapy.
Methods: a central computer randomised 800 patients in 59 UK general practices to atorvastatin (n∈=∈401, 20 mg/day) or placebo (n∈=∈399) and omega-3 EE90 (n∈=∈397, 2 g/day) or placebo (n∈=∈403) in a concealed factorial manner. Participants with LDL-cholesterol <2.6 mmol/l, triacylglycerol <1.5 mmol/l and estimated 10-year CVD risk <20% were compared at 4 months.
Results: mean (SD) age was 63.5 (11.7) years, HbA 1c 6.9 (1.1) % and known diabetes duration (median [interquartile range]) was 4 (2-8) years. Fifty-seven per cent were men, 90% white and 74% had an estimated 10-year CVD risk ≥20%. Of 732 patients with 4-month data, more allocated atorvastatin (n∈=∈371) compared with placebo (n∈=∈361) achieved LDL-cholesterol <2.6 mmol/l (91% vs 24%, p∈<∈0.001) and had estimated 10-year CVD risks <20% (38% vs 26%, p∈<∈0.001). No differences were seen between those allocated omega-3 EE90 (n∈=∈371) compared with placebo (n∈=∈361) for participants achieving triacylglycerol <1.5 mmol/l (65% vs 60%, p∈=∈0.18) or estimated 10-year CVD risks <20% (34% vs 30%, p∈=∈0.18). There were no side effects of note.
Conclusions/ interpretation: many community-based diabetic patients without known CVD remain at high CVD risk despite statin treatment and require additional risk-reduction strategies. The impact of omega-3 EE90 on CVD risk will remain uncertain until clinical endpoint trial results are available. Trial registration: ISRCT no. 76737502 Funding: The study was funded by Pfizer.
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More information
Accepted/In Press date: 22 August 2008
e-pub ahead of print date: 11 November 2008
Published date: January 2009
Additional Information:
Funding Information:
Funding: The study was funded by Pfizer.
Trial registration: ISRCT no. 76737502.
Keywords:
Atorvastatin, Cardiovascular risk, N-3 polyunsaturated fatty acids, Omega-3 EE90, Primary care, Type 2 diabetes
Identifiers
Local EPrints ID: 487052
URI: http://eprints.soton.ac.uk/id/eprint/487052
ISSN: 0012-186X
PURE UUID: 95dd529a-0b24-42f8-8306-0e430c0772dd
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Date deposited: 12 Feb 2024 17:31
Last modified: 18 Mar 2024 04:01
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Contributors
Author:
R.R. Holman
Author:
S. Paul
Author:
A. Farmer
Author:
L. Tucker
Author:
I.M. Stratton
Author:
H.A.W. Neil
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