Impact of Glycemic Treatment Choices on Cardiovascular Complications in Type 2 Diabetes

被引:22
作者
Weiss, Irene A. [1 ]
Valiquette, Guy [1 ]
Schwarcz, Monica D. [1 ]
机构
[1] New York Med Coll, Dept Med, Div Endocrinol, Westchester Med Ctr, Valhalla, NY 10595 USA
关键词
type; 2; diabetes; glycemic control; cardiovascular outcomes; PEPTIDASE-4 INHIBITOR SITAGLIPTIN; SULFONYLUREA DRUGS INCREASE; PIOGLITAZONE CLINICAL-TRIAL; ACUTE MYOCARDIAL-INFARCTION; CORONARY-HEART-DISEASE; BONE-MINERAL DENSITY; RISK-FACTORS; GLUCOSE CONTROL; INSULIN-RESISTANCE; METFORMIN THERAPY;
D O I
10.1097/CRD.0b013e3181a7b34c
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As the diabetic population has significant morbidity and mortality from cardiovascular disease (CVD), much of its medical care focuses oil CVD prevention and treatment. Some medications used to treat hyperglycemia may have beneficial effects on CV outcomes, others may have negative effects, while still others seem to have no direct effect. Although past epidemiological Studies have shown it relationship between glycated hemoglobin levels and CV events in patients with type 2 diabetes, recent large randomized clinical trials (ACCORD, ADVANCE, and VADT) lasting 3.5 to 5.6 years have found that intensive glycemic control either has no impact oil CV outcomes or even worsens them. Results of the 10-year follow-up of the UKPDS Suggest that tight glycemic control of younger, newly diagnosed patients with type 2 diabetes may have CV benefits many years later. Because the pathogenesis of atherosclerosis spans decades, it may be that beneficial effects of tight glycemic control on CV outcomes are mainly in younger patients without established macrovascular disease. There is an emerging notion that tight glycemic control may be beneficial in primary prevention of CVD in younger patients with diabetes, but may become deleterious in older patients with established or subclinical CVD. Thus, while tight control may lessen microvascular disease, it may increase the risk of hypoglycemia and possibly of adverse CV events. In each patient, the goals of glycemic control need to be individualized based on age, overall prognosis, presence of macrovascular disease, and risk of hypoglycemica.
引用
收藏
页码:165 / 175
页数:11
相关论文
共 127 条
[1]   CLONING OF THE BETA-CELL HIGH-AFFINITY SULFONYLUREA RECEPTOR - A REGULATOR OF INSULIN-SECRETION [J].
AGUILARBRYAN, L ;
NICHOLS, CG ;
WECHSLER, SW ;
CLEMENT, JP ;
BOYD, AE ;
GONZALEZ, G ;
HERRERASOSA, H ;
NGUY, K ;
BRYAN, J ;
NELSON, DA .
SCIENCE, 1995, 268 (5209) :423-426
[2]   Rosiglitazone causes bone loss in mice by suppressing osteoblast differentiation and bone formation [J].
Ali, AA ;
Weinstein, RS ;
Stewart, SA ;
Parfitt, AM ;
Manolagas, SC ;
Jilka, RL .
ENDOCRINOLOGY, 2005, 146 (03) :1226-1235
[3]   Standards of Medical Care in Diabetes-2009 [J].
不详 .
DIABETES CARE, 2009, 32 :S13-S61
[4]  
[Anonymous], 2007 national diabetes fact sheet
[5]   Effect of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy on glycemic control in patients with type 2 diabetes [J].
Aschner, Pablo ;
Kipnes, Mark S. ;
Lunceford, Jared K. ;
Sanchez, Matilde ;
Mickel, Carolyn ;
Williams-Herman, Debora E. .
DIABETES CARE, 2006, 29 (12) :2632-2637
[6]   Drug therapy - Metformin [J].
Bailey, CJ ;
Turner, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (09) :574-579
[7]   Pioglitazone reduces hepatic fat content and augments splanchnic glucose uptake in patients with type 2 diabetes [J].
Bajaj, M ;
Suraamornkul, S ;
Pratipanawatr, T ;
Hardies, LJ ;
Pratipanawatr, W ;
Glass, L ;
Cersosimo, E ;
Miyazaki, Y ;
DeFronzo, RA .
DIABETES, 2003, 52 (06) :1364-1370
[8]   Do sulfonylurea drugs increase the risk of cardiac events? [J].
Bell, DSH .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2006, 174 (02) :185-186
[9]   Meglitinide analogues for type 2 diabetes mellitus (Review) [J].
Black, C. ;
Donnelly, P. ;
McIntyre, L. ;
Royle, P. L. ;
Shepard, J. P. ;
Thomas, S. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2007, (02)
[10]   Interim analysis of the effects of exenatide treatment on A1C, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with type 2 diabetes [J].
Blonde, L. ;
Klein, E. J. ;
Han, J. ;
Zhang, B. ;
Mac, S. M. ;
Poon, T. H. ;
Taylor, K. L. ;
Trautmann, M. E. ;
Kim, D. D. ;
Kendall, D. M. .
DIABETES OBESITY & METABOLISM, 2006, 8 (04) :436-447