Journal of diabetes investigation

Initial patient characteristics in a real-world study of oral semaglutide for adults with type 2 diabetes in Japan

Updated

Abstract

A total of 624 participants initiated the study on oral semaglutide for type 2 diabetes.

  • The mean age of participants was 64.1 years, with a standard deviation of 14.1 years.
  • Participants had a mean body weight of 72.4 kg and a mean body mass index of 27.5 kg/m².
  • The median duration of type 2 diabetes among participants was 9.3 years.
  • Most participants (75.6%) were already taking glucose-lowering medications at baseline, with metformin being the most common.
  • A significant majority (86.0%) had a target for glycemic control of glycated hemoglobin ≤7%.
  • Younger participants (<75 years) had a higher mean body mass index compared to older participants (≥75 years), but glycated hemoglobin levels were similar.

Simplified

Key numbers

64.1 years
Mean Age
Mean age of participants enrolled in the study.
75.6%
Proportion on Glucose-Lowering Medications
Percentage of participants taking glucose-lowering medications at baseline.
27.5 kg/m²
Mean BMI
Mean body mass index of participants at baseline.

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Funding

Competing interests

RS received lecture fees from Novo Nordisk. HA and AM‐P report employment with, and being shareholders in, Novo Nordisk. DY received consulting/lecture fees from Novo Nordisk Pharma Ltd, Nippon Boehringer Ingelheim, Eli Lilly Japan K.K., and Kyowa Kirin Co. Ltd; and grants from Arkray Inc., Novo Nordisk Pharma Ltd, Nippon Boehringer Ingelheim, Taisho Pharmaceutical Co. Ltd, and Terumo Corporation. DY is an Editorial Board member of the Journal of Diabetes Investigation and a co‐author of this article. To minimize bias, they were excluded from all editorial decision‐making related to the acceptance of this article for publication. Approval of the research protocol: The protocol for this research project has been approved by suitably constituted Ethics Committees or Institutional Review Boards of the institutions and it conforms to the provisions of the Declaration of Helsinki. Ethics Committees, Institutional Review Boards and approval numbers are listed in the Supporting Information. Informed consent: All informed consent was obtained from the participants and/or guardians. Registration no. of the study/trial: This study is registered with ClinicalTrials.gov (NCT04878393; first submitted May 5, 2021). Animal studies: Not applicable.
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