Risk of mortality and adverse cardiovascular outcomes in type 2 diabetes: a comparison of patients treated with sulfonylureas and metformin

被引:238
作者
Evans, JMM [1 ]
Ogston, SA
Emslie-Smith, A
Morris, AD
机构
[1] Univ Dundee, Sch Med, Sect Publ Hlth, Div Community Hlth Sci, Dundee, Scotland
[2] Mill Practice, Dundee, Scotland
[3] Univ Dundee, Sch Med, Div Med & Therapeut, Dundee, Scotland
关键词
cardiovascular risk; metformin; sulfonylureas;
D O I
10.1007/s00125-006-0176-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to evaluate the risk of adverse cardiovascular outcomes in patients with type 2 diabetes newly treated with sulfonylureas and metformin. The Diabetes Audit and Research in Tayside Scotland (DARTS) diabetes information system and the Medicines Monitoring Unit (MEMO) dispensed prescribing database for the population of Tayside, Scotland (400,000 people) were employed. Patients newly prescribed with oral hypoglycaemic agents between 1994 and 2001 were classified into five study cohorts according to the treatment received: metformin only, sulfonylureas only, sulfonylureas added to metformin, metformin added to sulfonylureas, and both drugs simultaneously. In Cox regression analyses, we estimated relative risks for all-cause mortality, cardiovascular mortality and cardiovascular hospital admission for patients in the five study cohorts, with metformin monotherapy as the reference group. Of the 5,730 study patients, 1,000 died during a maximum of 8 years follow-up. Patients in the sulfonylureas only cohort had increased risks of mortality and cardiovascular mortality, with unadjusted relative risks of 3.12 (95% CI 2.54-3.84) and 3.71 (95% CI 2.64-5.22), respectively. After adjusting for differences between groups (age, sex, duration of diabetes, blood pressure, cholesterol, HbA(1c), smoking, previous hospital admission, treatment with cardiovascular medication), these relative risks were 1.43 (95% CI 1.15-1.77) and 1.70 (95% CI 1.18-2.45), respectively. Patients in the combination cohorts had significantly increased risks of cardiovascular hospital admission, as well as increased risks of mortality and cardiovascular mortality. In this cohort study of patients newly treated with oral hypoglycaemic agents, those treated with sulfonylureas only, or combinations of sulfonylureas and metformin, were at higher risk of adverse cardiovascular outcomes than those treated with metformin alone.
引用
收藏
页码:930 / 936
页数:7
相关论文
共 16 条
[1]  
[Anonymous], 1994, INT STAT CLASS DIS R, V10th
[2]  
CARSTAIRS V R M, 1990, Health Bulletin (Edinburgh), V48, P162
[3]  
Evans J. M. M., 1995, Pharmaceutical Medicine (London), V9, P177
[4]   Oral antidiabetic treatment in patients with coronary disease: Time-related increased mortality on combined glyburide/metformin therapy over a 7.7-year follow-up [J].
Fisman, EZ ;
Tenenbaum, A ;
Boyko, V ;
Benderly, M ;
Adler, Y ;
Friedensohn, A ;
Kohanovski, M ;
Rotzak, R ;
Schneider, H ;
Behar, S ;
Motro, MT .
CLINICAL CARDIOLOGY, 2001, 24 (02) :151-158
[5]   Mortality in type 2 diabetic subjects prescribed metformin and sulphonylurea drugs in combination: cohort study [J].
Gulliford, M ;
Latinovic, R .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2004, 20 (03) :239-245
[6]   Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction [J].
Haffner, SM ;
Lehto, S ;
Rönnemaa, T ;
Pyörälä, K ;
Laakso, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (04) :229-234
[7]   Decreased mortality associated with the use of metformin compared with sulfonylurea monotherapy in type 2 diabetes [J].
Johnson, JA ;
Majumdar, SR ;
Simpson, SH ;
Toth, EL .
DIABETES CARE, 2002, 25 (12) :2244-2248
[8]   Sulphonylurea treatment of NIDDM patients with cardiovascular disease: A mixed blessing? [J].
Leibowitz, G ;
Cerasi, E .
DIABETOLOGIA, 1996, 39 (05) :503-514
[9]   The diabetes audit and research in Tayside Scotland (DARTS) study: electronic record linkage to create a diabetes register [J].
Morris, AD ;
Boyle, DIR ;
MacAlpine, R ;
EmslieSmith, A ;
Jung, RT ;
Newton, RW ;
MacDonald, TM .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7107) :524-528
[10]   Some answers, more controversy, from UKPDS [J].
Nathan, DM .
LANCET, 1998, 352 (9131) :832-833