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dc.contributor.authorKeech, Aen_US
dc.contributor.authorSimes, Ren_US
dc.contributor.authorBarter, Pen_US
dc.contributor.authorBest, Jen_US
dc.contributor.authorScott, Ren_US
dc.contributor.authorTaskinen, Men_US
dc.contributor.authorForder, Pen_US
dc.contributor.authorPillai, Aen_US
dc.contributor.authorDavis, Ten_US
dc.contributor.authorGlasziou, Pen_US
dc.contributor.authorDrury, Pen_US
dc.contributor.authorKesäniemi, Yen_US
dc.contributor.authorSullivan, Den_US
dc.contributor.authorHunt, Den_US
dc.contributor.authorColman, Pen_US
dc.contributor.authord⿿Emden, Men_US
dc.contributor.authorWhiting, Men_US
dc.contributor.authorEhnholm, Cen_US
dc.contributor.authorLaakso, Men_US
dc.contributor.authorAnsquer, J-Cen_US
dc.contributor.authorFraitag, Ben_US
dc.contributor.authorAnderson, Nen_US
dc.contributor.authorHankey, Gen_US
dc.contributor.authorLehto, Sen_US
dc.contributor.authorMann, Sen_US
dc.contributor.authorRomo, Men_US
dc.contributor.authorLi, Len_US
dc.contributor.authorHennekens, Cen_US
dc.contributor.authorMacMahon, Sen_US
dc.contributor.authorPocock, Sen_US
dc.contributor.authorTonkin, Aen_US
dc.contributor.authorWilhelmsen, Len_US
dc.contributor.authorForder, Pen_US
dc.contributor.authorAkauola, Hen_US
dc.contributor.authorAlford, Fen_US
dc.contributor.authorBeinart, Ien_US
dc.contributor.authorBohra, Sen_US
dc.contributor.authorBoyages, Sen_US
dc.contributor.authorConnor, Hen_US
dc.contributor.authorDarnell, Den_US
dc.contributor.authorDavis, Ten_US
dc.contributor.authorDavoren, Pen_US
dc.contributor.authorLepre, Fen_US
dc.contributor.authorLooze, Fen_US
dc.contributor.authorDuffield, Aen_US
dc.contributor.authorFassett, Ren_US
dc.contributor.authorFlack, Jen_US
dc.contributor.authorFulcher, Gen_US
dc.contributor.authorHamwood, Sen_US
dc.contributor.authorHarmelin, Den_US
dc.contributor.authorJackson, R.en_US
dc.contributor.authoral, eten_US
dc.description.abstractBackground Patients with type 2 diabetes mellitus are at increased risk of cardiovascular disease, partly owing to dyslipidaemia, which can be amenable to fibrate therapy. We designed the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study to assess the effect of fenofibrate on cardiovascular disease events in these patients. Methods We did a multinational, randomised controlled trial with 9795 participants aged 50-75 years, with type 2 diabetes mellitus, and not taking statin therapy at study entry. After a placebo and a fenofibrate run-in phase, we randomly assigned patients (2131 with previous cardiovascular disease and 7664 without) with a total-cholesterol concentration of 3簭6絠mmol/L and a total-cholesterol/HDL-cholesterol ratio of 4簠or more or plasma triglyceride of 1簭5簠mmol/L to micronised fenofibrate 200 mg daily (n=4895) or matching placebo (n=4900). Our primary outcome was coronary events (coronary heart disease death or non-fatal myocardial infarction); the outcome for prespecified subgroup analyses was total cardiovascular events (the composite of cardiovascular death, myocardial infarction, stroke, and coronary and carotid revascularisation). Analysis was by intention to treat. The study was prospectively registered (number ISRCTN 64783481). Findings Vital status was confirmed on all but 22 patients. Averaged over the 5 years' study duration, similar proportions in each group discontinued study medication (10% placebo vs 11% fenofibrate) and more patients allocated placebo (17%) than fenofibrate (8%; p<0簰01) commenced other lipid treatments, predominantly statins. 5繥 (n=288) of patients on placebo and 5粥 (n=256) of those on fenofibrate had a coronary event (relative reduction of 11%; hazard ratio [HR] 0縹, 95% CI 0緵-1簵; p=0籶). This finding corresponds to a significant 24% reduction in non-fatal myocardial infarction (0緶, 0網-0繴; p=0簱0) and a non-significant increase in coronary heart disease mortality (1籹, 0繰-1絷; p=0粲). Total cardiovascular disease events were significantly reduced from 13繥 to 12絥 (0縹, 0縰-0繹; p=0簳5). This finding included a 21% reduction in coronary revascularisation (0緹, 0綸-0繳; p=0簰3). Total mortality was 6綥 in the placebo group and 7糥 in the fenofibrate group (p=0籸). Fenofibrate was associated with less albuminuria progression (p=0簰2), and less retinopathy needing laser treatment (5粥 vs 3綥, p=0簰03). There was a slight increase in pancreatitis (0絥 vs 0縥, p=0簳1) and pulmonary embolism (0緥 vs 1籥, p=0簲2), but no other significant adverse effects. Interpretation Fenofibrate did not significantly reduce the risk of the primary outcome of coronary events. It did reduce total cardiovascular events, mainly due to fewer non-fatal myocardial infarctions and revascularisations. The higher rate of starting statin therapy in patients allocated placebo might have masked a moderately larger treatment benefit.en_US
dc.publisherLancet Publishing Groupen_US
dc.publisher.placeUnited Kingdomen_US
dc.relation.ispartofjournalThe Lanceten_US
dc.titleEffects of long-term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD study): randomised controlled trialen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.hasfulltextNo Full Text

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