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©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Diabetes. Jun 10, 2016; 7(11): 230-238
Published online Jun 10, 2016. doi: 10.4239/wjd.v7.i11.230
Published online Jun 10, 2016. doi: 10.4239/wjd.v7.i11.230
Prediction of the effect on antihyperglycaemic action of sitagliptin by plasma active form glucagon-like peptide-1
Akifumi Kushiyama, Takako Kikuchi, Kentaro Tanaka, Tazu Tahara, Toshiko Takao, Yukiko Onishi, Yoko Yoshida, Shoji Kawazu, Yasuhiko Iwamoto, Division of Diabetes and Metabolism, Institute for Adult Diseases, Asahi Life Foundation, Tokyo 103-0002, Japan
Kentaro Tanaka, Department of Nephrology, School of Medicine, Faculty of Medicine, Toho University, Tokyo 103-0002, Japan
Author contributions: Kushiyama A designed research; Kikuchi T, Tahara T, Takao T, Onishi Y and Yoshida Y performed research; Kushiyama A and Tanaka K analyzed data; Kushiyama A, Kawazu S and Iwamoto Y wrote paper.
Institutional review board statement: The protocol was approved by the Institutional Review Board (IRB) of the Institute for Adult Diseases, Asahi Life Foundation.
Clinical trial registration statement: The study is a prospective, single-arm study and was registered at UMIN-CTR (Registration NO: UMIN000010645).
Informed consent statement: All of the subjects gave written informed consent to be included in this study.
Conflict-of-interest statement: Not declared.
Data sharing statement: The authors declare no conflicts of interest regarding this manuscript.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Akifumi Kushiyama, MD, PhD, Division of Diabetes and Metabolism, Institute for Adult Diseases, Asahi Life Foundation, 2-2-6 Nihonbashi, Bakurocho, Chuo-ku, Tokyo 103-0002, Japan. kusiyaa-tky@umin.ac.jp
Telephone: +81-3-3639-5501 Fax: +81-3-36395520
Received: January 22, 2016
Peer-review started: January 22, 2016
First decision: March 1, 2016
Revised: March 22, 2016
Accepted: April 21, 2016
Article in press: April 22, 2016
Published online: June 10, 2016
Processing time: 132 Days and 23.2 Hours
Peer-review started: January 22, 2016
First decision: March 1, 2016
Revised: March 22, 2016
Accepted: April 21, 2016
Article in press: April 22, 2016
Published online: June 10, 2016
Processing time: 132 Days and 23.2 Hours
Core Tip
Core tip: This clinical trials study revealed novel non-responders for the sitagliptin treatment of patients with type 2 diabetes. The fasting active form of glucagon-like peptide-1 (GLP-1) is related to Hemoglobin A1c (HbA1c) lowering and is independent of the previously reported factors associated with non-responders, such as high body mass index or low baseline HbA1c. These non-responders did not show fasting active GLP-1 elevation after sitagliptin administration, nor following ameliorated beta cell function and insulin secretion. The mechanism of poor responsiveness is still not unveiled, however, measuring active GLP-1 might be a good marker for prognosis, and may help clarifying one aspect of response variation against sitagliptin.