Pregled bibliografske jedinice broj: 978376
Gastrin - A Potential Predictor of Response to Incretin Therapy in Diabetes Type 2 Patients
Gastrin - A Potential Predictor of Response to Incretin Therapy in Diabetes Type 2 Patients // Endocrine, Metabolic & Immune Disorders - Drug Targets, 17 (2017), 4; 297-302 doi:10.2174/1871530317666171003162104 (međunarodna recenzija, članak, znanstveni)
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Naslov
Gastrin - A Potential Predictor of Response to
Incretin Therapy in Diabetes Type 2 Patients
Autori
Bilić-Čurčić, Ines ; Cigrovski Berković, Maja
Izvornik
Endocrine, Metabolic & Immune Disorders - Drug Targets (1871-5303) 17
(2017), 4;
297-302
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Diabetes mellitus ; GLP-1RA ; gastrin ; incretin therapy ; personalized treatment ; β-cell preservation
Sažetak
Personalized management of diabetes has become an imperative since majority of monotherapy fails within 3 years of its use. Identifying responders from nonresponders for a certain type of therapy would reduce a period of unsuccessful treatment and minimize health care costs. Incretin therapies, mainly glucagon-like peptide (GLP)-1 receptor agonists (GLP- 1RA) are relatively new glucose-lowering agents which increase insulin and lower glucagon response as well as slow down glucose absorption by acting on gastric emptying. However, problem with incretin- based therapy is distinguishing responders from non- responders and currently lack of specific predictors of treatment response. DISCUSSION: Experimental data demonstrated that activation of GLP-1 and gastrin signaling induces beta cell neogenesis, leading to glucose-dependent insulin secretion. Several studies demonstrated better glycemic control in patients with type 2 diabetes (DMT2) co-treated with proton pump inhibitors (PPI) and incretin based therapy agents. CONCLUSION: Higher gastrin levels in patients with diabetes prior to initiation of treatment with incretin mimetics could suggest a better potential for reversible human β-cell reprogramming with concomitant incretin therapy. Therefore, baseline levels of endogenous gastrin could be used as a predictor of response to GLP-1 therapy. In addition, treatment with PPI could also raise gastrin levels and in patients treated with GLP-1RA, lead to better glycemic control by initiating β-cell neogenesis and proliferation of pancreatic β-cells.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti, Kineziologija
POVEZANOST RADA
Ustanove:
Kineziološki fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE