Diabetes therapy : research, treatment and education of diabetes and related disorders

Tirzepatide’s real-world effects in Japanese people with type 2 diabetes

Updated

Abstract

In a study of 324 Japanese patients with type 2 diabetes mellitus, tirzepatide treatment for 24 weeks resulted in a median HbA1c reduction from 7.9% to 6.8% and a body weight decrease from 82.5 kg to 80.0 kg.

  • Tirzepatide administration was associated with a significant reduction in glycated hemoglobin (HbA1c) levels, with a median change of -0.9%.
  • Patients experienced an average decrease in body weight of -2.0 kg after 24 weeks of treatment.
  • Greater HbA1c reductions were observed in patients who had not previously used GLP-1 receptor agonists.
  • Changes in HbA1c levels were significantly correlated with baseline HbA1c levels, but not with body mass index (BMI).

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Full Text

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Funding

Competing interests

Declarations. Conflict of interest: Makoto Ohara has received lecture fees from Eli Lilly Japan K.K. Munenori Hiromura has received lecture fees from Eli Lilly Japan K.K. Yusaku Mori holds an endowed chair funded by Nippon Boehringer Ingelheim Co., Ltd. Sho-ichi Yamagishi has received lecture fees from Bayer Yakuhin, Ltd., Kowa Company, Ltd., and Novo Nordisk Pharma, Ltd. Noriyuki Takahashi, Hiroki Yokoyama, Hiroaki Seino, Shutaro Ozawa, Takemasa Omachi, Nobuaki Takehana, Tomoki Fujikawa, Ayako Ohara, Shunichiro Irie, Naoya Osaka, Michishige Terasaki, Aya Yoshihara, and Tomoyasu Fukui have nothing to disclose. Ethical Approval: The study protocol was approved by the Institutional Review Board (Ethics Committee) of Showa Medical University (approval No. 2024-200-B). Informed consent was waived due to the retrospective, non-interventional design. An opt-out approach was used: study information was publicly disclosed (institutional website and/or notice boards at each participating site), and patients could decline participation by requesting that their clinical information (existing medical record data) not be used for research. Upon such request, the patient’s data were excluded from the analysis. Opting out did not affect clinical care. The study was conducted in accordance with the Declaration of Helsinki and its subsequent revisions.
PubMed

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