A comparison between sitagliptin or glibenclamide in addition to metformin + pioglitazone on glycaemic control and β‐cell function: the triple oral therapy. Issue 7 (29th March 2013)
- Record Type:
- Journal Article
- Title:
- A comparison between sitagliptin or glibenclamide in addition to metformin + pioglitazone on glycaemic control and β‐cell function: the triple oral therapy. Issue 7 (29th March 2013)
- Main Title:
- A comparison between sitagliptin or glibenclamide in addition to metformin + pioglitazone on glycaemic control and β‐cell function: the triple oral therapy
- Authors:
- Derosa, G.
Cicero, A. F. G.
Franzetti, I. G.
Querci, F.
Carbone, A.
Piccinni, M. N.
D'Angelo, A.
Fogari, E.
Maffioli, P. - Abstract:
- <abstract abstract-type="main" id="dme12158-abs-0001"> <title>Abstract</title> <sec id="dme12158-sec-0001" sec-type="section"> <title>Aims</title> <p>To evaluate which triple oral therapy between metformin + pioglitazone + sitagliptin and metformin + pioglitazone + glibenclamide can be more useful in improving glycaemic control and should be preferred in clinical practice.</p> </sec> <sec id="dme12158-sec-0002" sec-type="section"> <title>Methods</title> <p>During the 2‐year run‐in period, patients were instructed to take metformin monotherapy for the first year, then a combination of metformin and pioglitazone for the second year, then patients were randomized to add glibenclamide or sitagliptin to the dual combination of metformin and pioglitazone for another year.</p> </sec> <sec id="dme12158-sec-0003" sec-type="section"> <title>Results</title> <p>Body weight reached with sitagliptin at 36 months was lower than that reached with glibenclamide. Fasting plasma insulin and homeostasis model assessment of insulin resistance were significantly increased by triple therapy with glibenclamide and decreased by that with sitagliptin. While sitagliptin did not change homeostasis model assessment of β‐cell function, this value was significantly increased by glibenclamide. Fasting plasma proinsulin was not influenced by triple oral therapy including glibenclamide, while it was decreased by the therapy including sitagliptin compared to glibenclamide. Triple oral therapy with sitagliptin<abstract abstract-type="main" id="dme12158-abs-0001"> <title>Abstract</title> <sec id="dme12158-sec-0001" sec-type="section"> <title>Aims</title> <p>To evaluate which triple oral therapy between metformin + pioglitazone + sitagliptin and metformin + pioglitazone + glibenclamide can be more useful in improving glycaemic control and should be preferred in clinical practice.</p> </sec> <sec id="dme12158-sec-0002" sec-type="section"> <title>Methods</title> <p>During the 2‐year run‐in period, patients were instructed to take metformin monotherapy for the first year, then a combination of metformin and pioglitazone for the second year, then patients were randomized to add glibenclamide or sitagliptin to the dual combination of metformin and pioglitazone for another year.</p> </sec> <sec id="dme12158-sec-0003" sec-type="section"> <title>Results</title> <p>Body weight reached with sitagliptin at 36 months was lower than that reached with glibenclamide. Fasting plasma insulin and homeostasis model assessment of insulin resistance were significantly increased by triple therapy with glibenclamide and decreased by that with sitagliptin. While sitagliptin did not change homeostasis model assessment of β‐cell function, this value was significantly increased by glibenclamide. Fasting plasma proinsulin was not influenced by triple oral therapy including glibenclamide, while it was decreased by the therapy including sitagliptin compared to glibenclamide. Triple oral therapy with sitagliptin better improved β‐cell function measures compared with the glibenclamide therapy.</p> </sec> <sec id="dme12158-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Sitagliptin should be preferred to glibenclamide as an addition to the metformin + pioglitazone combination for its better protection of β‐cell secretion and its neutral effect on body weight.</p> </sec> </abstract> … (more)
- Is Part Of:
- Diabetic medicine. Volume 30:Issue 7(2013:Jul.)
- Journal:
- Diabetic medicine
- Issue:
- Volume 30:Issue 7(2013:Jul.)
- Issue Display:
- Volume 30, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 30
- Issue:
- 7
- Issue Sort Value:
- 2013-0030-0007-0000
- Page Start:
- 846
- Page End:
- 854
- Publication Date:
- 2013-03-29
- Subjects:
- Diabetes -- Periodicals
616.462 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=dme ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/dme.12158 ↗
- Languages:
- English
- ISSNs:
- 0742-3071
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3579.606000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3708.xml