European Journal of Internal Medicine
Volume 20 , Pages S329-S339 , July 2009

Clinical Application of Incretin-Based Therapy: Therapeutic Potential, Patient Selection and Clinical Use

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    Postulated role of insulin resistance, β-cell dysfunction, and an impaired incretin effect in the pathogenesis of type 2 diabetes mellitus. (Adapted from J Clin Endocrinol Metab, [23] Diabetes, Eur J

    Postulated role of insulin resistance, β-cell dysfunction, and an impaired incretin effect in the pathogenesis of type 2 diabetes mellitus. (Adapted from J Clin Endocrinol Metab, [23] Diabetes, Eur J Clin Endocrinol, [25] and J Clin Invest [26].)

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    Representative depiction of the natural history of type 2 diabetes mellitus highlighting the role of insulin resistance, insulin deficiency, and impaired incretin effect. Both the time course and rela

    Representative depiction of the natural history of type 2 diabetes mellitus highlighting the role of insulin resistance, insulin deficiency, and impaired incretin effect. Both the time course and relative function are descriptive. These 3 core pathophysiologic defects likely combine to contribute to the progressive nature of the disease, and may account for much of the deterioration in glucose control observed clinical in patients with type 2 diabetes. IFG = impaired fasting glucose; IGT = impaired glucose tolerance. For glucose, 1 mg/dL = 0.5551 mmol/L. (Courtesy of the International Diabetes Center © 2008.)

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    International Diabetes Center (IDC) treatment algorithm for the management of type 2 diabetes. This recommended approach to treatment underscores the central importance of established glycemic targets

    International Diabetes Center (IDC) treatment algorithm for the management of type 2 diabetes. This recommended approach to treatment underscores the central importance of established glycemic targets and the critical role of diabetes self-management education and nutrition and activity counseling. It further underscores the selection of drug therapies based on pathophysiologic characteristics and individual patient characteristics. To convert glucose measurements, 1 mg/dL = 0.5551 mmol/L. CV = cardiovascular; DPP-4 = dipeptidyl peptidase–4; FPG = fasting plasma glucose; GI = gastrointestinal; GLP-1 = glucagonlike peptide–1; OA = oral antidiabetic medication; RPG = random plasma glucose; SMBG = self-monitoring of blood glucose; SU = sulfonylurea; TZD = thiazolidinedione. *Saxagliptin and liraglutide pending US and EU regulatory review at time of this publication. †Limited clinical data for combination therapy with insulin plus either DPP-4 inhibitor or GLP-1 agonist. (Adapted from Diabetes Care, J Fam Pract, [40] J Clin Outcomes Manag, [41] Am J Manag Care, [42] Staged Diabetes Management: a Systematic Approach, [45] Endocr Pract, [46] and Popul Health Manag [47]. Courtesy of the International Diabetes Center © 2009.)

 This article is a copublication with The American Journal of Medicine, 122, S37-S50. For citation purposes please use European Journal of Internal Medicine, 20, S329-S339.

PII: S0953-6205(09)00098-3

doi: 10.1016/j.ejim.2009.05.009

European Journal of Internal Medicine
Volume 20 , Pages S329-S339 , July 2009