Short-Term Effect of Hypergastrinemia Following Esomeprazole Treatment On Well-Controlled Type 2 Diabetes Mellitus: A Prospective Study

dc.contributor.authorBozkus, Yusuf
dc.contributor.authorMousa, Umut
dc.contributor.authorIyidir, Ozlem T.
dc.contributor.authorKirnap, Nazli
dc.contributor.authorDemir, Canan C.
dc.contributor.authorNar, Asli
dc.contributor.authorTutuncu, Neslihan B.
dc.contributor.orcID0000-0002-1816-3903en_US
dc.contributor.orcID0000-0002-6976-6659en_US
dc.contributor.orcID0000-0002-8078-9376en_US
dc.contributor.orcID0000-0001-5305-6807en_US
dc.contributor.orcID0000-0003-0998-8388en_US
dc.contributor.pubmedID31995024en_US
dc.contributor.researcherIDABG-5027-2020en_US
dc.contributor.researcherIDAAA-5419-2021en_US
dc.contributor.researcherIDAAK-4857-2021en_US
dc.contributor.researcherIDI-1735-2018en_US
dc.contributor.researcherIDK-7904-2019en_US
dc.contributor.researcherIDAAA-2743-2021en_US
dc.date.accessioned2021-05-16T16:26:57Z
dc.date.available2021-05-16T16:26:57Z
dc.date.issued2020
dc.description.abstractObjective: Proton pump inhibitor (PPI) drugs reduce gastric acid secretion and lead to an increase in serum gastrin levels. Many preclinical and some clinical researches have established some positive effects of gastrin or PPI therapy on glucose regulation. The aim of this study was to prospectively investigate the short term effects of esomeprazole on glycaemic control in patients with type 2 diabetes mellitus. In addition, the presence of an association between this effect and gastrin levels was evaluated. Methods: Thirty-two subjects with type 2 diabetes mellitus were enrolled and grouped as intervention (n=16) and control (n=16). The participants in the intervention group were prescribed 40 mg of esomeprazole treatment for three months. At the beginning of the study and at the 3rd month, HbA1c level (%) and gastrin levels (pmol/L) of participants were assessed. Then, the groups were compared in terms of their baseline and 3rd month values. Results: In the intervention group, the mean gastrin level increased significantly from 34.3 +/- 14.4 pmol/L to 87.4 +/- 43.6 pmol/L (p<0.001). The mean HbA1c level was similar to the pre-treatment level (6.3 +/- 0.7% vs. 6.4 +/- 0.9%, p=0.441). There were no statistically significant differences in all parameters of the control group. The majority of individuals were on metformin monotherapy (65.6 %). The subgroup analysis of metformin monotherapy revealed that, in intervention group, there was a significant increase in gastrin levels (39.9 +/- 12.6 vs. 95.5 +/- 52.5, p=0.026), but the HbA1c levels did not change (6.0 +/- 0.4 % vs. 5.9 +/- 0.6 %, p=0.288); and in control group, gastrin levels did not change (37.5 +/- 26.7 vs. 36.1 +/- 23.3, p=0.367), but there was an increase in HbA1c levels (6.1 +/- 0.50 vs. 6.4 +/- 0.60, p=0.01). Conclusion: Our study demonstrates that esomeprazole has no extra benefit for the controlled diabetic patient in three months. However, in only the metformin-treated subgroup, esomeprazole may prevent the rise in HbA1c level.en_US
dc.identifier.endpage1096en_US
dc.identifier.issn1871-5303en_US
dc.identifier.issue7en_US
dc.identifier.scopus2-s2.0-85090616705en_US
dc.identifier.startpage1090en_US
dc.identifier.urihttp://hdl.handle.net/11727/5858
dc.identifier.volume20en_US
dc.identifier.wos000567647700014en_US
dc.language.isoengen_US
dc.relation.isversionof10.2174/1871530320666200129124555en_US
dc.relation.journalENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETSen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEsomeprazoleen_US
dc.subjectgastrinen_US
dc.subjectHbA1cen_US
dc.subjecttype 2 diabetesen_US
dc.subjectdiabetes treatmenten_US
dc.subjectincretinen_US
dc.titleShort-Term Effect of Hypergastrinemia Following Esomeprazole Treatment On Well-Controlled Type 2 Diabetes Mellitus: A Prospective Studyen_US
dc.typearticleen_US

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: