Medicina Fluminensis, Vol. 55 No. 3, 2019.
Review article
https://doi.org/10.21860/medflum2019_221600
Diabetes mellitus and DPP IV/CD26 Inhibitors
Lara Batičić
orcid.org/0000-0002-2837-4157
; Zavod za medicinsku kemiju, biokemiju i kliničku kemiju, Medicinski fakultet Sveučilišta u Rijeci, Rijeka, Hrvatska
Lara Ivanović
; Studentica Medicinskog fakulteta Sveučilišta u Rijeci, Rijeka, Hrvatska
Antonijo Grčić
; Student Medicinskog fakulteta Sveučilišta u Rijeci, Rijeka, Hrvatska
Ester Pernjak Pugel
; Zavod za histologiju i embriologiju, Medicinski fakultet, Sveučilište u Rijeci, Rijeka, Hrvatska
Jadranka Varljen
; Zavod za medicinsku kemiju, biokemiju i kliničku kemiju, Medicinski fakultet Sveučilišta u Rijeci, Rijeka, Hrvatska
Dijana Detel
orcid.org/0000-0001-8986-0880
; Zavod za medicinsku kemiju, biokemiju i kliničku kemiju, Medicinski fakultet Sveučilišta u Rijeci, Rijeka, Hrvatska
Abstract
Diabetes (lat. Diabetes mellitus) is a chronic metabolic disease characterized by persistent hyperglycaemia and carbohydrate, fat and protein metabolism disorders. Diabetes could be classified as type 1 or 2, gestational diabetes, and other, less common forms. Due to a prominent increase in the incidence and prevalence of the disease, it represents a significant public-health problem, being between the ten leading causes of mortality in the world. Dipeptidyl peptidase IV, or molecule CD26 (DPP IV / CD26, EC 3.4.14.5), is an ubiquitous multifunctional transmembrane and soluble glycoprotein and serine peptidase, recognized as a crucial factor in maintaining glucose homeostasis, primarily due to the ability to hydrolize incretins. Scientific and clinical studies have shown a high therapeutic potential of DPP IV/CD26 inhibitors in diabetic patients. This review focuses on various aspects of type 1 and 2 diabetes and newer treatment approaches for these diseases, with a special focus on DPP IV/CD26 inhibitors as effective therapeutic options.
Keywords
CD26; Diabetes mellitus; dipeptidyl peptidase IV; DPP IV/CD26 inhibitors
Hrčak ID:
221600
URI
Publication date:
1.9.2019.
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