Rosiglitazone evaluated for cardiovascular outcomes in oral agent combination therapy for type 2 diabetes (RECORD): a multicentre, randomised, open-label trial

被引:1062
作者
Home, Philip D. [1 ,2 ]
Pocock, Stuart J. [3 ]
Beck-Nielsen, Henning [4 ]
Curtis, Paula S. [5 ]
Gomis, Ramon [6 ]
Hanefeld, Markolf [7 ]
Jones, Nigel P. [8 ]
Komajda, Michel [9 ,10 ]
McMurray, John J. V. [11 ]
机构
[1] Newcastle Diabet Ctr, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Newcastle, Newcastle Upon Tyne, Tyne & Wear, England
[3] London Sch Hyg & Trop Med, Med Stat Unit, London WC1, England
[4] Dept Endocrinol & Metab, Odense, Denmark
[5] GlaxoSmithKline Res & Dev Ltd, Greenford, Middx, England
[6] Univ Barcelona, Hosp Clin, Barcelona, Spain
[7] Forsch Bereich Endokrinol & Stoffwechsel, Zentrum Klin Studien, Dresden, Germany
[8] GlaxoSmithKline Res & Dev Ltd, Harlow, Essex, England
[9] Univ Paris 06, Paris, France
[10] Hop La Pitie Salpetriere, Dept Cardiol, Paris, France
[11] Univ Glasgow, British Heart Fdn, Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
关键词
BLOOD-GLUCOSE CONTROL; MYOCARDIAL-INFARCTION; HEART-ASSOCIATION; CARDIAC OUTCOMES; METFORMIN; RISK; SULFONYLUREAS; COMPLICATIONS; MONOTHERAPY; FAILURE;
D O I
10.1016/S0140-6736(09)60953-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Rosiglitazone is an insulin sensitiser used in combination with metformin, a sulfonylurea, or both, for lowering blood glucose in people with type 2 diabetes. We assessed cardiovascular outcomes after addition of rosiglitazone to either metformin or sulfonylurea compared with the combination of the two over 5-7 years of follow-up. We also assessed comparative safety. Methods In a multicentre, open-label trial, 4447 patients with type 2 diabetes on metformin or sulfonylurea monotherapy with mean haemoglobin A(1c) (HbA(1c)) of 7.9% were randomly assigned to addition of rosiglitazone (n=2220) or to a combination of metformin and sulfonylurea (active control group, n=2227). The primary endpoint was cardiovascular hospitalisation or cardiovascular death, with a hazard ratio (HR) non-inferiority margin of 1.20. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00379769. Findings 321 people in the rosiglitazone group and 323 in the active control group experienced the primary outcome during a mean 5.5-year follow-up, meeting the criterion of non-inferiority (HR 0.99, 95% CI 0.85-1.16). HR was 0.84 (0.59-1.18) for cardiovascular death, 1.14 (0.80-1.63) for myocardial infarction, and 0.72 (0.49-1.06) for stroke. Heart failure causing admission to hospital or death occurred in 61 people in the rosiglitazone group and 29 in the active control group (HR 2.10, 1.35-3.27, risk difference per 1000 person-years 2.6, 1.1-4.1). Upper and distal lower limb fracture rates were increased mainly in women randomly assigned to rosiglitazone. Mean HbA(1c) was lower in the rosiglitazone group than in the control group at 5 years. Interpretation Addition of rosiglitazone to glucose-lowering therapy in people with type 2 diabetes is confirmed to increase the risk of heart failure and of some fractures, mainly in women. Although the data are inconclusive about any possible effect on myocardial infarction, rosiglitazone does not increase the risk of overall cardiovascular morbidity or mortality compared with standard glucose-lowering drugs. Funding GlaxoSmithKline plc, UK.
引用
收藏
页码:2125 / 2135
页数:11
相关论文
共 27 条
  • [1] [Anonymous], 2005, Global guideline for Type 2 diabetes
  • [2] Pleiotropic actions of peroxisome proliferator-activated receptors in lipid metabolism and atherosclerosis
    Barbier, O
    Torra, IP
    Duguay, Y
    Blanquart, C
    Fruchart, JC
    Glineur, C
    Staels, B
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (05) : 717 - 726
  • [3] Practical considerations and guidelines for dosing sulfonylureas as monotherapy or combination therapy
    Bell, DSH
    [J]. CLINICAL THERAPEUTICS, 2004, 26 (11) : 1714 - 1727
  • [4] A randomized, placebo-controlled trial assessing the effects of rosiglitazone on echocardiographic function and cardiac status in type 2 diabetic patients with New York Heart Association functional class I or II heart failure
    Dargie, Henry J.
    Hildebrandt, Per R.
    Riegger, Guenter A. J.
    McMurray, John J. V.
    McMorn, Stephen O.
    Roberts, Jeremy N.
    Zambanini, Andrew
    Wilding, John P. H.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 49 (16) : 1696 - 1704
  • [5] Uncertain effects of rosiglitazone on the risk for myocardial infarction and cardiovascular death
    Diamond, George A.
    Bax, Leon
    Kaul, Sanjay
    [J]. ANNALS OF INTERNAL MEDICINE, 2007, 147 (08) : 578 - 581
  • [6] Secondary prevention of macrovascular events in patients with type 2 diabetes in the PROactive Study (PROspective pioglitAzone Clinical Trial In macroVascular Events):: a randomised controlled trial
    Dormandy, JA
    Charbonnel, B
    Eckland, DJA
    Erdmann, E
    Massi-Benedetti, M
    Kmoules, IK
    Skene, AM
    Tan, MH
    Lefébvre, PJ
    Murray, GD
    Standl, E
    Wilcox, RG
    Wlhelmsen, L
    Betteridge, J
    Birkeland, K
    Golay, A
    Heine, RJ
    Korányi, L
    Laakso, M
    Mokán, M
    Norkus, A
    Pirags, V
    Podar, T
    Scheen, A
    Scherbaum, W
    Schernthaner, G
    Schmitz, O
    Skrha, J
    Smith, U
    Taton, J
    [J]. LANCET, 2005, 366 (9493) : 1279 - 1289
  • [7] *EUR MED AG, EUR PUBL ASS REP ACT
  • [8] European Medicines Agency, EUR PUBL ASS REP AV
  • [9] Effects of rosiglitazone alone and in combination with atorvastatin on the metabolic abnormalities in type 2, diabetes mellitus
    Freed, MI
    Ratner, R
    Marcovina, SM
    Kreider, MM
    Biswas, N
    Cohen, BR
    Brunzell, JD
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2002, 90 (09) : 947 - 952
  • [10] *GLAXOSMITHKLINE, FDA ADV COMM BRIEF D