Effect of sitagliptin therapy on triglyceride‐rich lipoprotein kinetics in patients with type 2 diabetes. Issue 12 (19th August 2014)
- Record Type:
- Journal Article
- Title:
- Effect of sitagliptin therapy on triglyceride‐rich lipoprotein kinetics in patients with type 2 diabetes. Issue 12 (19th August 2014)
- Main Title:
- Effect of sitagliptin therapy on triglyceride‐rich lipoprotein kinetics in patients with type 2 diabetes
- Authors:
- Tremblay, A. J.
Lamarche, B.
Kelly, I.
Charest, A.
Lépine, M.‐C.
Droit, A.
Couture, P. - Abstract:
- <abstract abstract-type="main" id="dom12359-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="dom12359-sec-0001" sec-type="section"> <title>Aim</title> <p id="dom12359-para-0001">To investigate the effects of sitagliptin therapy on the kinetics of triglyceride‐rich lipoprotein (TRL) apolipoprotein (apo)B‐48, VLDL apoB‐100, apoE and apoC‐III in patients with type 2 diabetes.</p> </sec> <sec id="dom12359-sec-0002" sec-type="section"> <title>Methods</title> <p id="dom12359-para-0002">Twenty‐two subjects with type 2 diabetes were recruited in this double‐blind crossover study, during which the subjects received sitagliptin (100 mg/day) or placebo for a 6‐week period each. At the end of each phase of treatment, the <italic>in vivo</italic> kinetics of the different apolipoproteins were assessed using a primed‐constant infusion of <sc>l</sc>‐[5, 5, 5‐D3]leucine for 12 h, with the participants in a constantly fed state.</p> </sec> <sec id="dom12359-sec-0003" sec-type="section"> <title>Results</title> <p id="dom12359-para-0003">Sitagliptin therapy significantly reduced fasting plasma triglyceride (−15.4%, p = 0.03), apoB‐48 (−16.3%, p = 0.03) and free fatty acid concentrations (−9.5%, p = 0.04), as well as plasma HbA1c (placebo: 7.0% ± 0.8 vs. sitagliptin: 6.6% ± 0.7, p &lt; 0.0001) and plasma glucose levels (−13.5%, p = 0.001), without any significant effect on insulin levels. Kinetic results showed that treatment with sitagliptin significantly reduced the<abstract abstract-type="main" id="dom12359-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="dom12359-sec-0001" sec-type="section"> <title>Aim</title> <p id="dom12359-para-0001">To investigate the effects of sitagliptin therapy on the kinetics of triglyceride‐rich lipoprotein (TRL) apolipoprotein (apo)B‐48, VLDL apoB‐100, apoE and apoC‐III in patients with type 2 diabetes.</p> </sec> <sec id="dom12359-sec-0002" sec-type="section"> <title>Methods</title> <p id="dom12359-para-0002">Twenty‐two subjects with type 2 diabetes were recruited in this double‐blind crossover study, during which the subjects received sitagliptin (100 mg/day) or placebo for a 6‐week period each. At the end of each phase of treatment, the <italic>in vivo</italic> kinetics of the different apolipoproteins were assessed using a primed‐constant infusion of <sc>l</sc>‐[5, 5, 5‐D3]leucine for 12 h, with the participants in a constantly fed state.</p> </sec> <sec id="dom12359-sec-0003" sec-type="section"> <title>Results</title> <p id="dom12359-para-0003">Sitagliptin therapy significantly reduced fasting plasma triglyceride (−15.4%, p = 0.03), apoB‐48 (−16.3%, p = 0.03) and free fatty acid concentrations (−9.5%, p = 0.04), as well as plasma HbA1c (placebo: 7.0% ± 0.8 vs. sitagliptin: 6.6% ± 0.7, p &lt; 0.0001) and plasma glucose levels (−13.5%, p = 0.001), without any significant effect on insulin levels. Kinetic results showed that treatment with sitagliptin significantly reduced the pool size of TRL apoB‐48 by −20.8% (p = 0.03), paralleled by a reduction in the production rate of these particles (−16.0%, p = 0.03). The VLDL apoB‐100 pool size was also significantly decreased by sitagliptin therapy (−9.3%, p = 0.03), mainly because of a reduction in the hepatic secretion of these lipoproteins, although this difference did not reach statistical significance (−9.2%, p = 0.06).</p> </sec> <sec id="dom12359-sec-0004" sec-type="section"> <title>Conclusions</title> <p id="dom12359-para-0004">Treatment with sitagliptin for 6 weeks reduced triglyceride‐rich apoB‐containing lipoprotein levels by reducing the synthesis of these particles.</p> </sec> </abstract> … (more)
- Is Part Of:
- Diabetes, obesity & metabolism. Volume 16:Issue 12(2014:Dec.)
- Journal:
- Diabetes, obesity & metabolism
- Issue:
- Volume 16:Issue 12(2014:Dec.)
- Issue Display:
- Volume 16, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 16
- Issue:
- 12
- Issue Sort Value:
- 2014-0016-0012-0000
- Page Start:
- 1223
- Page End:
- 1229
- Publication Date:
- 2014-08-19
- Subjects:
- Diabetes -- Periodicals
Obesity -- Periodicals
Metabolism -- Disorders -- Periodicals
Clinical pharmacology -- Periodicals
616.462 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=1462-8902&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1463-1326 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/dom.12359 ↗
- Languages:
- English
- ISSNs:
- 1462-8902
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3579.601970
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4018.xml