Novel therapeutic strategies for the treatment of type 2 diabetes

被引:0
|
作者
Perfetti, R
Barnett, PS
Mathur, R
Egan, JM
机构
[1] Cedars Sinai Med Ctr, Dept Med, Div Endocrinol & Metab, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Los Angeles, CA 90024 USA
[3] NIA, Diabet Sect, Ctr Gerontol Res, Baltimore, MD 21224 USA
来源
DIABETES-METABOLISM REVIEWS | 1998年 / 14卷 / 03期
关键词
insulin resistance; Type; 2; diabetes; novel therapies;
D O I
10.1002/(SICI)1099-0895(1998090)14:3<207::AID-DMR214>3.0.CO;2-J
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes mellitus is the most common endocrine disease, accounting for over 200 million people affected worldwide. It is characterized by a lack of insulin secretion and/or increased cellular resistance to insulin, resulting in hyperglycemia and other metabolic disturbances. People with diabetes suffer from increased morbidity and premature mortality related to cardiovascular, microvascular and neuropathic complications. The Diabetes Control and Complication Trial (DCCT) has convincingly demonstrated the relationship of hyperglycemia to the development and progression of complications and showed that improved glycemic control reduced these complications. Although the DCCT exclusively studied patients with Type 1 diabetes, there is ample evidence to support the belief that the same relationship between metabolic control and clinical outcome exists in patients with Type 2 diabetes. Therefore, a major effort should be made to develop and implement more effective treatment regimes. This article reviews those novel drugs that have been recently introduced for the management of Type 2 diabetes, or that have reached an advanced level of study and will soon be proposed for preliminary clinical trials. They include: (i) compounds that promote the synthesis/secretion of insulin by the P-cell; (ii) inhibitors of the a-glucosidase activity of the small intestine; (iii) substances that enhance the action of insulin at the level of the target tissues; and (iv) inhibitors of free fatty acid oxidation. (C) 1998 John Wiley & Sons, Ltd.
引用
收藏
页码:207 / 225
页数:19
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