Funabashi Ayana, Ito Hitoshi, Maeda Mamoru, Hasegawa Yoshitaka, Tsukioka Ryota, Onda Mitsuko
AIN PHARMACIEZ INC, 2-4-30 Higashisapporo 5-jo, Shiroishi-ku, Sapporo, 003- 0005, Hokkaido, Japan.
Faculty of Pharmacy, Department of Social and Administrative Pharmacy, Osaka Medical and Pharmaceutical University, 4-20-1, Nasahara, Takatsuki, 569-1094, Osaka, Japan.
Sci Rep. 2025 Apr 3;15(1):11494. doi: 10.1038/s41598-025-96103-6.
Dipeptidyl peptidase-4 inhibitors (DPP-4is) are widely used in Japan; however, their incretin activity raise concerns about gastrointestinal adverse events (GAEs). Therefore, we aimed to investigate GAEs symptoms commonly associated with DPP-4is and associated symptomatic treatment, to enable community pharmacists in charge of pharmaceutical management of outpatient prescriptions in Japan to strengthen patient intervention strategies. Therefore, we conducted a prescription sequence symmetry analysis (PSSA) using a prescription claims database (2018-2022) of a domestic chain pharmacy to evaluate the association between DPP-4is and GAEs. Adjusted sequence ratios (ASRs), a safety index, were calculated based on three treatment groups: prokinetic agents (dopamine D2 receptor blockers and serotonin 5-HT4 receptor agonists), gastric acid suppressants (histamine H2 receptor blockers and proton pump inhibitors), and laxatives, and the order in which DPP-4is were prescribed. The ASR was calculated for 90, 180, and 360 days, and subgroup analyses were performed for prokinetic agents and gastric acid suppressants groups based on their mechanism of action. ASR values > 1 indicated significant association with DPP-4is. PSSA results showed DPP-4is association across all observation periods for prokinetic agents and laxatives, but not for gastric acid suppressants. Subgroup analyses indicated a similar trend, suggesting that DPP-4is are associated with nausea and constipation owing to functional impairment rather than gastric acid secretion. Additionally, prescription data confirmed the possibility of adding gastrointestinal medications, which could cause a potential prescribing cascade, after prescribing DPP-4is. These findings highlight the importance of strengthening follow-up between patient visits to facilitate the early detection of GAEs caused by DPP-4is, and carefully considering the risks and benefits of symptomatic treatment.
二肽基肽酶-4抑制剂(DPP-4is)在日本被广泛使用;然而,其肠促胰岛素活性引发了对胃肠道不良事件(GAEs)的担忧。因此,我们旨在调查与DPP-4is常见相关的GAEs症状及相关对症治疗方法,以使负责日本门诊处方药物管理的社区药剂师能够加强患者干预策略。因此,我们使用一家国内连锁药店的处方索赔数据库(2018 - 2022年)进行了处方序列对称性分析(PSSA),以评估DPP-4is与GAEs之间的关联。基于三个治疗组计算调整序列比(ASRs),这是一个安全指标:促动力药(多巴胺D2受体阻滞剂和5-羟色胺5-HT4受体激动剂)、胃酸抑制剂(组胺H2受体阻滞剂和质子泵抑制剂)、泻药以及DPP-4is的处方顺序。分别计算了90天、180天和360天的ASR,并根据促动力药和胃酸抑制剂组的作用机制进行了亚组分析。ASR值>1表明与DPP-4is有显著关联。PSSA结果显示,在所有观察期内,促动力药和泻药与DPP-4is有关联,但胃酸抑制剂与DPP-4is无关联。亚组分析表明了类似趋势,提示DPP-4is与恶心和便秘相关是由于功能障碍而非胃酸分泌。此外,处方数据证实了在开具DPP-4is后添加胃肠道药物可能导致潜在的处方级联反应。这些发现凸显了加强患者就诊期间随访以促进早期发现DPP-4is引起的GAEs以及仔细考虑对症治疗的风险和益处的重要性。