Glimepiride: Role of a new sulfonylurea in the treatment of type 2 diabetes mellitus

被引:68
作者
Campbell, RK [1 ]
机构
[1] Washington State Univ, Coll Pharm, Pullman, WA 99164 USA
关键词
glimepiride; diabetes mellitus;
D O I
10.1345/aph.17360
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To review the clinical pharmacology data regarding the sulfonylurea glimepiride, and to summarize the clinical trials of glimepiride efficacy and safety alone and in combination with insulin for the treatment of type 2 diabetes mellitus. DATA SOURCES: A MEDLINE database search (English language, January 1985-April 1997) was performed to identify relevant published articles, including reviews and abstracts; the manufacturer (Hoechst Marion Roussel, Kansas City, MO) provided unpublished data. STUDY SELECTION: Pharmacology information was taken from representative original research articles. Eight clinical studies were selected for analysis on the basis of large enrollment, appropriate study design, and publication of results. DATA EXTRACTION: All clinical trials, published and unpublished, were reviewed. DATA SYNTHESIS: Glimepiride is a sulfonylurea that is pharmacologically distinct from other sulfonylureas because of differences in receptor-binding properties and potentially selective effects on ATP-sensitive K+ channels. The pharmacokinetic and pharmacodynamic profile of glimepiride makes it suitable for once daily dosing. The safety and efficacy of glimepiride have been confirmed in studies involving more than 5000 patients with type 2 diabetes. In one study, once-daily doses of 1-8 mg reduced fasting plasma glucose from baseline by 43-74 mg/dL more than did placebo (p < 0.001), and hemoglobin (Hb) A(1C) values decreased by 1.2-1.9% more than with placebo (p < 0.001). Two-thirds of patients achieved tight control (i.e., HbA(1C) less than or equal to 7.2%). Glimepiride was as effective as second-generation sulfonylureas. The most common adverse events were dizziness and headache, but no single adverse event occurred in more than 2% of patients. CONCLUSIONS: Glimepiride appears to be a useful option for patients with type 2 diabetes not controlled by diet and exercise and who want to achieve tight glucose control. Glimepiride can be used alone, in combination with other antihyperglycemic agents, or in patients with secondary sulfonylurea failure, as an adjunct to insulin therapy.
引用
收藏
页码:1044 / 1052
页数:9
相关论文
共 40 条
[11]   Cardiovascular effects of conventional sulfonylureas and glimepiride [J].
Geisen, K ;
Vegh, A ;
Krause, E ;
Popp, JG .
HORMONE AND METABOLIC RESEARCH, 1996, 28 (09) :496-507
[12]  
GOLDBERG RB, 1996, DIABETES CARE, V19, P847
[13]  
Goldberg RB, 1997, POSTGRADUATE MED SPE, P45
[14]   THERAPEUTIC COMPARISON OF METFORMIN AND SULFONYLUREA, ALONE AND IN VARIOUS COMBINATIONS - A DOUBLE-BLIND CONTROLLED-STUDY [J].
HERMANN, LS ;
SCHERSTEN, B ;
BITZEN, PO ;
KJELLSTROM, T ;
LINDGARDE, F ;
MELANDER, A .
DIABETES CARE, 1994, 17 (10) :1100-1109
[15]  
*HOECHST ROUSS PHA, 1995, PRESCR INF AM GLIM
[16]   ACHILLES HEEL OF THE UNIVERSITY-GROUP-DIABETES-PROGRAM [J].
KILO, C ;
MILLER, JP ;
WILLIAMSON, JR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1980, 243 (05) :450-457
[17]  
KLIMT CR, 1970, DIABETES, V19, P747
[18]   THE MOLECULAR INTERACTION OF SULFONYLUREAS WITH BETA-CELL ATP-SENSITIVE K+-CHANNELS [J].
KRAMER, W ;
MULLER, G ;
GIRBIG, F ;
GUTJAHR, U ;
KOWALEWSKI, S ;
HARTZ, D ;
SUMM, HD .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1995, 28 :S67-S80
[19]   DIFFERENTIAL INTERACTION OF GLIMEPIRIDE AND GLIBENCLAMIDE WITH THE BETA-CELL SULFONYLUREA RECEPTOR .2. PHOTOAFFINITY-LABELING OF A 65 KDA PROTEIN BY [H-3] GLIMEPIRIDE [J].
KRAMER, W ;
MULLER, G ;
GIRBIG, F ;
GUTJAHR, U ;
KOWALEWSKI, S ;
HARTZ, D ;
SUMM, HD .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1191 (02) :278-290
[20]   ADENOSINE TRIPHOSPHATE-DEPENDENT K-CURRENTS ACTIVATED BY METABOLIC INHIBITION IN RAT VENTRICULAR MYOCYTES DIFFER FROM THOSE ELICITED BY THE CHANNEL OPENER RILMAKALIM [J].
KRAUSE, E ;
ENGLERT, H ;
GOGELEIN, H .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1995, 429 (05) :625-635