Bromocriptine Mesylate for Glycemic Management in Type 2 Diabetes Mellitus

被引:37
作者
Kerr, Jessica L. [1 ]
Timpe, Erin M. [1 ]
Petkewicz, Katherine A. [1 ]
机构
[1] So Illinois Univ, Edwardsville Sch Pharm, Edwardsville, IL 62026 USA
关键词
bromocriptine; circadian rhythm; diabetes; QUICK-RELEASE BROMOCRIPTINE; DOPAMINE;
D O I
10.1345/aph.1P271
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To review the pharmacologic characteristics, safety, and efficacy of bromocriptine mesylate for glycemic control in patients with type 2 diabetes mellitus. DATA SOURCES: A Scopus and MEDLINE search (1950 June 2010) was conducted using the key words bromocriptine, diabetes, and circadian rhythm. Data were also received from the manufacturer. STUDY SELECTION AND DATA EXTRACTION: Available abstracts, studies, and review articles published in English with human data discussing bromocriptine treatment for type 2 diabetes mellitus were reviewed. DATA SYNTHESIS: Bromocriptine is an ergot derivative available for treatment of type 2 diabetes. The mechanism of action of this agent is unclear; however, activity as a dopamine D-2 receptor agonist seems to provide the primary mechanism for utility in resetting the circadian rhythm in patients with type 2 diabetes. Other mechanisms, including alpha-1 antagonist, (alpha-2 agonist, and serotonin and prolactin modulator, may also help to explain bromocriptine's glucose-lowering effects. Studies with bromocriptine have included 4328 patients with type 2 diabetes. The majority of available trials conducted enrolled patients for a study duration of 6-24 weeks. One trial evaluating the safety and efficacy of bromocriptine concluded after 52 weeks of follow-up. Endpoints of hemoglobin A(1c) (A1C) reduction and plasma glucose concentrations were the primary focus of all studies, with statistically significant differences found. Bromocriptine use resulted in a mean A1C reduction of 0.27% (range 0.1-0.6), while placebo resulted in a mean A1C increase of 0.48% (range 0.3-1.1). Incidence of adverse effects of nausea, vomiting, headache, and rhinitis was greater than that of placebo in clinical trials. Cardiovascular endpoints did not differ from those of placebo. CONCLUSIONS: Bromocriptine has demonstrated efficacy as an adjunctive agent in the management of type 2 diabetes. Caution may be warranted in the elderly population or patients at risk for suspected drug- drug interactions. Further studies of longer duration may help to define the role of bromocriptine in the management of diabetes.
引用
收藏
页码:1777 / 1785
页数:9
相关论文
共 18 条
[1]   Does bromocriptine improve glycemic control of obese type-2 diabetics? [J].
Aminorroaya, A ;
Janghorbani, M ;
Ramezani, M ;
Haghighi, S ;
Amini, M .
HORMONE RESEARCH, 2004, 62 (02) :55-59
[2]  
[Anonymous], DRUGS FDA
[3]   D2 dopamine receptor Taq1A polymorphism, body weight, and dietary intake in type 2 diabetes [J].
Barnard, Neal D. ;
Noble, Ernest P. ;
Ritchie, Terty ;
Cohen, Joshua ;
Jenkins, David J. A. ;
Tumer-McGrievy, Gabrielle ;
Gloede, Lise ;
Green, Amber A. ;
Ferdowsian, Hope .
NUTRITION, 2009, 25 (01) :58-65
[4]   EFFECT OF BROMOCRIPTINE ON MATURITY ONSET DIABETES [J].
BARNETT, AH ;
GAILER, K ;
CHAPMAN, C ;
HAYTER, CJ .
POSTGRADUATE MEDICAL JOURNAL, 1980, 56 (651) :11-14
[5]  
Cincotta AH, 2008, DIABETOLOGIA, V51, pS22
[6]  
Cincotta A H, 1999, Expert Opin Investig Drugs, V8, P1683, DOI 10.1517/13543784.8.10.1683
[7]   THE THRIFTY GENOTYPE IN NON-INSULIN-DEPENDENT DIABETES [J].
DOWSE, G ;
ZIMMET, P .
BRITISH MEDICAL JOURNAL, 1993, 306 (6877) :532-533
[8]   Randomized Clinical Trial of Quick-Release Bromocriptine Among Patients With Type 2 Diabetes on Overall Safety and Cardiovascular Outcomes [J].
Gaziano, J. Michael ;
Cincotta, Anthony H. ;
O'Connor, Christopher M. ;
Ezrokhi, Michael ;
Rutty, Dean ;
Ma, Z. J. ;
Scranton, Richard E. .
DIABETES CARE, 2010, 33 (07) :1503-1508
[9]  
GAZIANO JM, 2007, DIABETES S1A, V56, P50
[10]   Association of the antidiabetic effects of bromocriptine with a shift in the daily rhythm of monoamine metabolism within the suprachiasmatic nuclei of the Syrian hamster [J].
Luo, SQ ;
Luo, J ;
Cincotta, AH .
CHRONOBIOLOGY INTERNATIONAL, 2000, 17 (02) :155-172