PMID- 37103055 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230501 IS - 2308-3425 (Electronic) IS - 2308-3425 (Linking) VI - 10 IP - 4 DP - 2023 Apr 18 TI - Retrospective Analysis of the Effectiveness of Oral Semaglutide in Type 2 Diabetes Mellitus and Its Effect on Cardiometabolic Parameters in Japanese Clinical Settings. LID - 10.3390/jcdd10040176 [doi] LID - 176 AB - Glucagon-like peptide-1 receptor agonists (GLP-1RA) have a more potent glycated hemoglobin (HbA1c)-lowering effect than existing therapies and are widely used for treating type 2 diabetes mellitus (T2DM). Once-daily oral semaglutide is the world's first oral GLP-1RA. This study aimed to provide real-world data on oral semaglutide in Japanese patients with T2DM and its effects on cardiometabolic parameters. This was a single-center retrospective observational study. We examined changes in HbA1c and body weight (BW) and the rate of achieving HbA1c < 7% after 6 months of oral semaglutide treatment in Japanese patients with T2DM. Furthermore, we examined differences in the efficacy of oral semaglutide with multiple patient backgrounds. A total of 88 patients were included in this study. Overall, the mean (standard error of the mean) HbA1c at 6 months decreased by -1.24% (0.20%) from baseline, and BW at 6 months (n = 85) also decreased by -1.44 kg (0.26 kg) from baseline. The percentage of patients who achieved HbA1c < 7% changed significantly from 14% at baseline to 48%. HbA1c decreased from baseline regardless of age, sex, body mass index, chronic kidney disease, or diabetes duration. Additionally, alanine aminotransferase, total cholesterol, triglyceride, and non-high-density lipoprotein cholesterol were significantly reduced from baseline. Oral semaglutide may be an effective option for the intensification of therapy in Japanese patients with T2DM who have inadequate glycemic control with existing therapy. It may also reduce BW and improve cardiometabolic parameters. FAU - Yamada, Hodaka AU - Yamada H AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Yoshida, Masashi AU - Yoshida M AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Funazaki, Shunsuke AU - Funazaki S AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Morimoto, Jun AU - Morimoto J AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Tonezawa, Shiori AU - Tonezawa S AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Takahashi, Asuka AU - Takahashi A AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Nagashima, Shuichi AU - Nagashima S AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Masahiko, Kimura AU - Masahiko K AD - Department of Pharmacy, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Kiyoshi, Otsuka AU - Kiyoshi O AD - Department of Pharmacy, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. FAU - Hara, Kazuo AU - Hara K AD - Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical University Saitama Medical Center, 1-847 Amanuma-cho, Omiya-ku, Saitama 330-8503, Japan. LA - eng GR - 19K18012/JSPS KAKENHI/ PT - Journal Article DEP - 20230418 PL - Switzerland TA - J Cardiovasc Dev Dis JT - Journal of cardiovascular development and disease JID - 101651414 PMC - PMC10141082 OTO - NOTNLM OT - cardiometabolic risk factors OT - glucagon-like peptide-1 receptor agonist OT - oral semaglutide OT - real-world data OT - type 2 diabetes mellitus COIS- The authors declare no conflict of interest. EDAT- 2023/04/27 12:41 MHDA- 2023/04/27 12:42 PMCR- 2023/04/18 CRDT- 2023/04/27 10:33 PHST- 2023/03/18 00:00 [received] PHST- 2023/04/09 00:00 [revised] PHST- 2023/04/16 00:00 [accepted] PHST- 2023/04/27 12:42 [medline] PHST- 2023/04/27 12:41 [pubmed] PHST- 2023/04/27 10:33 [entrez] PHST- 2023/04/18 00:00 [pmc-release] AID - jcdd10040176 [pii] AID - jcdd-10-00176 [pii] AID - 10.3390/jcdd10040176 [doi] PST - epublish SO - J Cardiovasc Dev Dis. 2023 Apr 18;10(4):176. doi: 10.3390/jcdd10040176.