نتایج جستجو برای: dipeptidyl peptidase 4

تعداد نتایج: 1310834  

2016
Sevin Demir Sule Temizkan Mehmet Sargin

Background. Our aim was to define the conditions that affect therapeutic success when dipeptidyl peptidase-4 (DPP-4) inhibitor is added to metformin monotherapy. Materials and Methods. We reviewed the medical records of 56 patients who had received DPP-4 inhibitor as an add-on to metformin monotherapy and evaluated their response in the first year of therapy. Fasting blood glucose (FBG), HbA1c,...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2015
Mitsutoshi Asakura Hideaki Fujii Koichiro Atsuda Tomoo Itoh Ryoichi Fujiwara

The major metabolic pathway of vildagliptin in mice, rats, dogs, and humans is hydrolysis at the cyano group to produce a carboxylic acid metabolite M20.7 (LAY151), whereas the major metabolic enzyme of vildagliptin has not been identified. In the present study, we determined the contribution rate of dipeptidyl peptidase-4 (DPP-4) to the hydrolysis of vildagliptin in the liver. We performed hyd...

2016
Seung-Hyun Ko Dae-Jung Kim Jong-Heon Park Cheol-Young Park Chang Hee Jung Hyuk-Sang Kwon Joong-Yeol Park Kee-Ho Song Kyungdo Han Ki-Up Lee Kyung-Soo Ko

This study investigated trends in the prescription of antidiabetic medications for patients with type 2 diabetes, focusing on changing patterns of prescriptions and the cost of drugs during the last 10 years. Retrospective data on patients with type 2 diabetes aged 30 years or older were analyzed using information from the National Health Information Database collected by the National Health In...

2016
Rajesh Krishna Carol Addy Daniel Tatosian Xiaoli S. Glasgow Isaias Noel Gendrano III Martine Robberechts Wouter Haazen J.N. de Hoon Marleen Depré Ashley Martucci Joanna Z. Peng Amy O. Johnson‐Levonas John A. Wagner S. Aubrey Stoch

The pharmacokinetics (PK) and pharmacodynamics (PD) of omarigliptin, a novel once-weekly DPP-4 inhibitor, were assessed following single and multiple doses in healthy subjects. Absorption was rapid, and food did not influence single-dose PK. Accumulation was minimal, and steady state was reached after 2 to 3 weeks. Weekly (area under the curve) AUC and Cmax displayed dose proportionality within...

2017
Shimin Chen Enfa Zhao Wenfei Li Jiehong Wang

BACKGROUND Previous studies have reported conflicting results for the relationship between dipeptidyl peptidase-4 (DPP-4) inhibitor drugs and acute pancreatitis. The aim of this study was to investigate the association between DPP-4 inhibitors and an increased risk of acute pancreatitis using meta-analysis. METHODS We conducted a comprehensive search in PubMed, Embase, Web of Science, and Coc...

2011
Dror Dicker

The first dipeptidyl peptidase 4 (DPP4) inhibitor sitagliptin was approved in 2006 as treatment for diabetes concurrently with lifestyle changes. A combined product of sitagliptin and glucophage was approved by the U.S. Food and Drug Administration in 2007. The second DPP-4 inhibitor, saxagliptin, was approved in theU.S. It was approved both as monotherapy as well as in combination with metform...

2014
Mariko Oishi Katsuya Yamazaki Fuminobu Okuguchi Hidekatsu Sugimoto Azuma Kanatsuka Atsunori Kashiwagi

AIMS/INTRODUCTION Six kinds of oral antidiabetic drugs (OADs), including the new dipeptidyl peptidase 4 (DPP-4) inhibitors, are available. The present study aimed to define trends within the prescribing patterns of OADs, as well as changes in glycemic control in Japan over a 10-year period from 2002 to 2011. MATERIALS AND METHODS We carried out a cross-sectional study using data of type 2 dia...

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