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本文引用的文献

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Daily Glucose Profiles after Switching from Injectable to Oral Semaglutide in Patients with Type 2 Diabetes Mellitus.每日血糖谱在 2 型糖尿病患者从注射用转为口服司美格鲁肽后的变化。
Intern Med. 2024 Jan 1;63(1):43-50. doi: 10.2169/internalmedicine.1441-22. Epub 2023 May 24.
2
Cost-Effectiveness of Semaglutide vs. Empagliflozin, Canagliflozin, and Sitagliptin for Treatment of Patients with Type 2 Diabetes in Denmark: A Decision-Analytic Modelling Study.司美格鲁肽与恩格列净、卡格列净和西他列汀治疗丹麦2型糖尿病患者的成本效益:一项决策分析模型研究
Pharmacoecon Open. 2023 Jul;7(4):579-591. doi: 10.1007/s41669-023-00416-z. Epub 2023 May 13.
3
Retrospective Analysis of the Effectiveness of Oral Semaglutide in Type 2 Diabetes Mellitus and Its Effect on Cardiometabolic Parameters in Japanese Clinical Settings.口服司美格鲁肽治疗2型糖尿病有效性及其对日本临床环境中心血管代谢参数影响的回顾性分析
J Cardiovasc Dev Dis. 2023 Apr 18;10(4):176. doi: 10.3390/jcdd10040176.
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A consensus statement from the Japan Diabetes Society (JDS): a proposed algorithm for pharmacotherapy in people with type 2 diabetes.日本糖尿病学会(JDS)的共识声明:2型糖尿病患者药物治疗的建议算法。
Diabetol Int. 2022 Dec 23;14(1):1-14. doi: 10.1007/s13340-022-00605-x. eCollection 2023 Jan.
5
A Significant Effect of Oral Semaglutide on Cardiovascular Risk Factors in Patients With Type 2 Diabetes.口服司美格鲁肽对2型糖尿病患者心血管危险因素有显著影响。
Cardiol Res. 2022 Oct;13(5):303-308. doi: 10.14740/cr1441. Epub 2022 Oct 25.
6
First-Line Therapy for Type 2 Diabetes With Sodium-Glucose Cotransporter-2 Inhibitors and Glucagon-Like Peptide-1 Receptor Agonists : A Cost-Effectiveness Study.钠-葡萄糖共转运蛋白 2 抑制剂和胰高血糖素样肽-1 受体激动剂治疗 2 型糖尿病的一线治疗:成本效益研究。
Ann Intern Med. 2022 Oct;175(10):1392-1400. doi: 10.7326/M21-2941. Epub 2022 Oct 4.
7
Efficacy and safety of oral semaglutide in patients with non-alcoholic fatty liver disease complicated by type 2 diabetes mellitus: A pilot study.口服司美格鲁肽治疗非酒精性脂肪性肝病合并2型糖尿病患者的疗效与安全性:一项试点研究。
JGH Open. 2022 Jun 16;6(7):503-511. doi: 10.1002/jgh3.12780. eCollection 2022 Jul.
8
Efficacy and safety of oral semaglutide in Japanese patients with type 2 diabetes: A subgroup analysis by baseline variables in the PIONEER 9 and PIONEER 10 trials.口服司美格鲁肽在日本 2 型糖尿病患者中的疗效和安全性:PIONEER 9 和 PIONEER 10 试验中按基线变量的亚组分析。
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9
Efficacy and safety of oral semaglutide by baseline age in Japanese patients with type 2 diabetes: A subgroup analysis of the PIONEER 9 and 10 Japan trials.在日本 2 型糖尿病患者中,根据基线年龄评估口服司美格鲁肽的疗效和安全性:PIONEER 9 和 10 日本试验的亚组分析。
Diabetes Obes Metab. 2022 Feb;24(2):321-326. doi: 10.1111/dom.14571. Epub 2021 Nov 9.
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Levels of circulating semaglutide determine reductions in HbA1c and body weight in people with type 2 diabetes.血清素水平决定了 2 型糖尿病患者的 HbA1c 和体重的降低。
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日本2型糖尿病患者从二肽基肽酶-4抑制剂转换为口服司美格鲁肽的疗效和安全性。

Efficacy and safety of switching from a dipeptidyl peptidase-4 inhibitor to oral semaglutide in Japanese patients with type 2 diabetes mellitus.

作者信息

Yoneda Chihiro, Kobayashi Junji, Kuribayashi Nobuichi

机构信息

Misaki Internal Medicine Clinic, 6-44-9 Futawa-Higashi, Funabashi, Chiba 274-0805 Japan.

出版信息

Diabetol Int. 2024 May 30;15(3):569-576. doi: 10.1007/s13340-024-00734-5. eCollection 2024 Jul.

DOI:10.1007/s13340-024-00734-5
PMID:39101186
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11291808/
Abstract

BACKGROUND

Dipeptidyl peptidase-4 inhibitors (DPP-4is) are the most widely used oral hypoglycemic drugs in Japan. However, once-daily oral semaglutide has been reported to reduce glycated hemoglobin (HbA1c) and body weight (BW) without causing significant hypoglycemia. Here, we aimed to evaluate the efficacy and safety of switching from a DPP-4i to oral semaglutide in Japanese patients with type 2 diabetes (T2D).

METHODS

We performed a single-center retrospective study of the changes in HbA1c and BW in 68 patients with T2D who were switched from a DPP-4i and took oral semaglutide for  ≥ 6 months, without changes in any other oral hypoglycemic agent.

RESULTS

Mean HbA1c decreased from 7.8 to 7.0% ( < 0.001) and BW decreased from 74.2 to 71.2 kg ( < 0.001) over 6 months. The decrease in HbA1c was more pronounced in participants with high baseline HbA1c ( =  - 0.542,  < 0.001). There was also a trend ( = 0.236,  = 0.052) toward a decrease in BW in individuals with shorter disease duration. There were reductions in either HbA1c or BW in 65 participants (95.6%). In addition, the larger the decrease in HbA1c was, the greater was the decrease in BW ( = 0.480,  < 0.001). Eighteen participants (20.1%) discontinued the drug within 6 months, of whom 10 (11.6% of the total) did so because of suspected adverse effects and the discontinuation rate was the highest in older, non-obese patients.

CONCLUSIONS

Switching from a DPP-4i to oral semaglutide may be useful for Japanese patients with T2D who have inadequate glycemic or BW control. However, its utility may be limited by gastrointestinal adverse effects in certain patients.

摘要

背景

二肽基肽酶-4抑制剂(DPP-4i)是日本使用最广泛的口服降糖药物。然而,据报道,每日一次口服司美格鲁肽可降低糖化血红蛋白(HbA1c)和体重(BW),且不会引起显著低血糖。在此,我们旨在评估日本2型糖尿病(T2D)患者从DPP-4i转换为口服司美格鲁肽的疗效和安全性。

方法

我们对68例从DPP-4i转换而来并服用口服司美格鲁肽≥6个月的T2D患者的HbA1c和BW变化进行了单中心回顾性研究,且未改变任何其他口服降糖药物。

结果

在6个月内,平均HbA1c从7.8%降至7.0%(<0.001),BW从74.2kg降至71.2kg(<0.001)。基线HbA1c较高的参与者中,HbA1c的下降更为明显(= -0.542,<0.001)。病程较短的个体体重也有下降趋势(= 0.236,= 0.052)。65名参与者(95.6%)的HbA1c或BW有所降低。此外,HbA1c下降幅度越大,BW下降幅度越大(= 0.480,<0.001)。18名参与者(20.1%)在6个月内停药,其中10名(占总数的11.6%)因疑似不良反应停药,停药率在老年非肥胖患者中最高。

结论

对于血糖或体重控制不佳的日本T2D患者,从DPP-4i转换为口服司美格鲁肽可能有用。然而,其效用可能会受到某些患者胃肠道不良反应的限制。