Dia Spectr
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by John, L. E.
Right arrow Articles by Hamilton, R. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by John, L. E.
Right arrow Articles by Hamilton, R. A.
Social Bookmarking
 Add to CiteULike   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Diabetes Spectrum 20:59-63, 2007
© American Diabetes Association ®, Inc., 2007


Pharmacy Update

Expanded Use of Exenatide in the Management of Type 2 Diabetes

Linda E. John, PharmD, Michael P. Kane, PharmD, FCCP, BCPS, Robert S. Busch, MD, FACE and Robert A. Hamilton, PharmD

The first 300 words of the full text of this article appear below.


    Introduction
 
Exenatide is an incretin mimetic agent that possesses multiple mechanisms of glucose lowering. It enhances glucose-dependent insulin secretion by the pancreatic ß-cell, leading to insulin release in the presence of elevated glucose concentrations. It also moderates glucagon secretion and lowers serum glucagon concentrations during periods of hyperglycemia. Lower glucagon concentrations lead to decreased hepatic glucose output and decreased insulin demand. Exenatide also slows gastric emptying, thereby reducing the rate at which meal-derived glucose appears in the circulation, thereby further decreasing postprandial blood glucose levels. Finally, administration of exenatide has been shown to reduce subsequent food intake by increasing satiety, often resulting in weight loss.1

Exenatide is indicated as an adjunctive therapy to improve glycemic control in patients with type 2 diabetes who are taking metformin and/or a sulfonylurea but have not achieved adequate glycemic control.1 To decrease gastrointestinal intolerance, exenatide is initiated at 5 µg subcutaneously twice daily and increased after 1 month to a target maintenance dose of 10 µg twice daily. Three 30-week studies as add-on therapy to sulfonylurea, metformin, and sufonylurea/metformin have demonstrated hemoglobin A1c (A1C) reductions of ~ 1% with an average weight loss of 1.4–1.8 kg.24 Therapy was generally well tolerated with the most frequent adverse events classified as mild or moderate and gastrointestinal in nature. Severe hypoglycemia was not observed during these studies.24

The concurrent use of exenatide with insulin, meglitinides, or {alpha}-glucosidase inhibitors has not been reported. Published information regarding the use of exenatide with thiazolidinediones (TZDs) is limited to two abstracts.5,6 The objective of this study was to determine the effectiveness and safety of off-label exenatide use in patients with type 2 diabetes.


    Methods
 
A retrospective review of the electronic medical records of one private-practice endocrinologist was conducted. The study was approved by the Albany College of Pharmacy investigational review board. The study population . . . [Full Text of this Article]


    Results
 

    Discussion
 

    Conclusions
 

Add to CiteULike CiteULike   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Diabetes Diabetes Care Clinical Diabetes Diabetes Spectrum
Copyright © 2007 by the American Diabetes Association.