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Research article summary (published 30 Aug 2009):

Type 2 diabetes: where we are today: an overview of disease burden, current treatments, and treatment strategies.

Full Abstract

OBJECTIVE: To provide an overview of the disease burden and current strategies in the treatment of patients with type 2 diabetes. DATA SOURCES: Medline search of all relevant clinical and review articles. STUDY SELECTION: By the author. DATA EXTRACTION: By the author. DATA SYNTHESIS: The prevalence of diabetes in the United States has reached epidemic proportions with the total diagnosed and undiagnosed cases among people aged 20 years or older estimated at 12.9%, and it continues to rise at an alarming rate. This upsurge has been paralleled by an increase in rates of obesity. Type 2 diabetes accounts for up to 95% of diabetes cases and is often comorbid with hypertension and dyslipidemia. CONCLUSION: Tight glycemic control is necessary for the management of type 2 diabetes, but progressive deterioration of beta-cell function can lead to a loss of glycemic control. Oral antidiabetes drugs and insulin are effective but do not always correct the associated metabolic and glucoregulatory dysfunctions, and hypoglycemia and weight gain are common adverse effects of these agents. A clear need exists for aggressive therapeutic options-particularly incretin-based agents-that can be combined with existing agents to preserve beta-cell function and halt the progression of type 2 diabetes.

 

Author information

Author/s: Campbell, R Keith (RK);

Affiliation: Dept. of Pharmacotherapy, College of Pharmacy, Washington State University, Pullman, WA 99164-6510, USA. rkcamp(-atsign-)wsu.edu

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

Journal: Journal of the American Pharmacists Association : JAPhA (J Am Pharm Assoc (2003)), published in United States. (Language: eng)

Reference: -2009 Sep-Oct; vol 49 Suppl 1 (issue ) : pp S3-9

Dates: Created 2009/10/05; Completed 2009/10/29;

PMID: 19801365, status: MEDLINE (last retrieval date: 10/29/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Blood Glucose (0) ; Dipeptidyl-Peptidase IV Inhibitors (0) ; Hemoglobin A, Glycosylated (0) ; Hypoglycemic Agents (0) ; Incretins (0) ; Receptors, Glucagon (0) ; glucagon-like peptide receptor (0) ; hemoglobin A1c protein, human (0) ; Antigens, CD26 (EC 3.4.14.5) ; DPP4 protein, human (EC 3.4.14.5)

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