Effect of bezafibrate on incidence of type 2 diabetes mellitus in obese patients

被引:67
作者
Tenenbaum, A [1 ]
Motro, M
Fisman, EZ
Adler, Y
Shemesh, J
Tanne, D
Leor, J
Boyko, V
Schwammenthal, E
Behar, S
机构
[1] Chaim Sheba Med Ctr, Cardiac Rehabil Inst, IL-52621 Tel Hashomer, Israel
[2] Chaim Sheba Med Ctr, Neufeld Cardiac Res Inst, Bezafibrate Infarct Prevent Study Coordinating Ct, IL-52621 Tel Hashomer, Israel
关键词
obesity; diabetes mellitus; prevention; bezafibrate;
D O I
10.1093/eurheartj/ehi310
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims To assess the effect of fibric acid derivative bezafibrate on incidence of type 2 diabetes in obese patients over a median 6.3 years follow-up period. Methods and results The study sample comprised 339 non-diabetic obese patients (body mass index >= 30.0 kg/m(2)) aged 42-74. Patients received either bezafibrate retard 400 mg (178 patients) or placebo (161 patients) once daily. Development of new diabetes was recorded in 98 patients: in 56 (37.0%) from the placebo group vs. 42 (27.1%) from the bezafibrate group, (P log-rank=0.01). The median time (interquartile range) until onset of new diabetes was significantly delayed in patients on bezafibrate when compared with those on placebo: 4.0 (2.1-5.0) vs. 2.0 (0.5-3.5) years, P=0.002. Multivariable analysis identified bezafibrate treatment as an independent predictor of reduced risk of new diabetes with hazard ratio (HR) 0.59 [95% confidence interval (CI) 0.39-0.91]. Other significant variables associated with future overt type 2 diabetes in obese patients were triglycerides (50 mg/dL increment) with HR 1.15 (95% CI 1.02-1.28) and fasting glucose (10 mg/dL increment) with HR 2.27 (95% CI 1.83-2.81). Conclusion Bezafibrate, when compared with placebo, reduced the incidence and delayed the onset of type 2 diabetes in obese patients over a long-term follow-up period.
引用
收藏
页码:2032 / 2038
页数:7
相关论文
共 47 条
[1]  
Allison PD., 2010, SURVIVAL ANAL USING
[2]   Clinical significance of pleiotropic effects of statins: Lipid reduction and beyond [J].
Auer, J ;
Berent, R ;
Weber, T ;
Eber, B .
CURRENT MEDICINAL CHEMISTRY, 2002, 9 (20) :1831-1850
[3]   PPARγ, the ultimate thrifty gene [J].
Auwerx, J .
DIABETOLOGIA, 1999, 42 (09) :1033-1049
[4]   The mechanisms of action of PPARs [J].
Berger, J ;
Moller, DE .
ANNUAL REVIEW OF MEDICINE, 2002, 53 :409-435
[5]  
Bonow Robert O., 2004, American Journal of Medicine, V116, p2S
[6]   Acarbose for prevention of type 2 diabetes mellitus: the STOPNIDDM randomised trial [J].
Chiasson, JL ;
Josse, RG ;
Gomis, R ;
Hanefeld, M ;
Karasik, A ;
Laakso, M .
LANCET, 2002, 359 (9323) :2072-2077
[7]  
Collins R, 2002, LANCET, V360, P7, DOI 10.1016/S0140-6736(02)09327-3
[8]   Prevention of Type 2 diabetes mellitus. A review of the evidence and its application in a UK setting [J].
Davies, MJ ;
Tringham, JR ;
Troughton, J ;
Khunti, KK .
DIABETIC MEDICINE, 2004, 21 (05) :403-414
[9]   The prevention of type 2 diabetes mellitus [J].
Davies, MJ .
CLINICAL MEDICINE, 2003, 3 (05) :470-474
[10]   Prevalence of the metabolic syndrome among US adults - Findings from the Third National Health and Nutrition Examination Survey [J].
Ford, ES ;
Giles, WH ;
Dietz, WH .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (03) :356-359