PMID- 37005303 OWN - NLM STAT- MEDLINE DCOM- 20230404 LR - 20230404 IS - 1347-5215 (Electronic) IS - 0918-6158 (Linking) VI - 46 IP - 4 DP - 2023 TI - Prescription Trends for the Antidiabetic Agents Used to Treat Type 2 Diabetes Mellitus in Japan from 2012-2020: a Time-Series Analysis. PG - 592-598 LID - 10.1248/bpb.b22-00710 [doi] AB - In April 2014, sodium-glucose cotransporter 2 inhibitor (SGLT-2i) was introduced in Japan. In May 2015, the prescription limitation for SGLT-2i was lifted. Subsequently, SGLT-2i was shown to reduce cardiovascular events in patients with type 2 diabetes mellitus (T2DM). SGLT-2i prescription is expected to increase and consequently affect the prescription trends for other antidiabetic agents. Therefore, we evaluated the trends for antidiabetic agent prescriptions in Japan from April 2012 to March 2020. In this study, a dynamic cohort consisting of patients with T2DM derived from the Japan Medical Data Center health insurance database and with at least one antidiabetic agent prescription was investigated. The prescription rates were calculated monthly (/1000 person-months) for each class of antidiabetic agent. The eligible cohort comprised 34333 patients. The prescription rate for dipeptidyl peptidase-4 inhibitor increased from 424.0 in April 2012 to 656.3 in May 2015, and slightly decreased to 635.4 in March 2020. The prescription rate for biguanide consistently increased from 347.2 in April 2012 to 500.1 in March 2020. The prescription rate for sulfonylurea consistently decreased from 393.8 in April 2012 to 172.5 in March 2020. The prescription rate for SGLT-2i consistently increased from 4.1 in April 2014 to 363.1 in March 2020. SGLT-2i prescription increased and may affect the prescription trends for dipeptidyl peptidase-4 inhibitor and sulfonylurea after May 2015, when the prescription limitation for SGLT-2i was lifted. Biguanide prescriptions increased regardless of the introduction of SGLT-2i. The treatment of T2DM in Japan is clearly changing, with a focus on SGLT-2i and biguanide. FAU - Iketani, Ryo AU - Iketani R AD - Center for Outcomes Research and Economic Evaluation for Health, National Institute of Public Health. FAU - Imai, Shinobu AU - Imai S AD - Division of Pharmacoepidemiology, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University. LA - eng PT - Journal Article PL - Japan TA - Biol Pharm Bull JT - Biological & pharmaceutical bulletin JID - 9311984 RN - 0 (Hypoglycemic Agents) RN - 0 (Sodium-Glucose Transporter 2 Inhibitors) RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Sulfonylurea Compounds) RN - 0 (Biguanides) RN - EC 3.4.14.- (Dipeptidyl-Peptidases and Tripeptidyl-Peptidases) SB - IM MH - Humans MH - Hypoglycemic Agents/therapeutic use/pharmacology MH - *Diabetes Mellitus, Type 2/drug therapy MH - Japan MH - *Sodium-Glucose Transporter 2 Inhibitors/therapeutic use/pharmacology MH - *Dipeptidyl-Peptidase IV Inhibitors/therapeutic use MH - Sulfonylurea Compounds MH - Prescriptions MH - Biguanides/therapeutic use MH - Dipeptidyl-Peptidases and Tripeptidyl-Peptidases OTO - NOTNLM OT - administrative claims data OT - antidiabetic agent OT - sodium-glucose cotransporter-2 inhibitor OT - time-series analysis OT - type 2 diabetes mellitus EDAT- 2023/04/03 06:00 MHDA- 2023/04/04 06:42 CRDT- 2023/04/02 22:34 PHST- 2023/04/04 06:42 [medline] PHST- 2023/04/02 22:34 [entrez] PHST- 2023/04/03 06:00 [pubmed] AID - 10.1248/bpb.b22-00710 [doi] PST - ppublish SO - Biol Pharm Bull. 2023;46(4):592-598. doi: 10.1248/bpb.b22-00710.