Nunome Hideo, Sakura Hiroshi, Hashimoto Naotake, Sasamoto Kazuo, Ohashi Hiroshi, Hasumi Sumiko, Ujihara Noriko, Kasahara Tadasu, Tomonaga Osamu, Honda Masashi, Iwamoto Yasuhiko
1Diabetes Center, Edogawa Hospital, Medical Plaza Shinozaki, SK Building, 7-15-12, Shinozaki-machi, Edogawa-ku, Tokyo, 133-0057 Japan.
2Department of Medicine, Tokyo Women's Medical University, Medical Center East, 2-1-10 Nishiogu, Arakawa-ku, Tokyo, 116-8567 Japan.
Diabetol Int. 2017 Dec 16;9(3):158-167. doi: 10.1007/s13340-017-0340-0. eCollection 2018 Jul.
As a subanalysis of the Januvia Multicenter Prospective Trial in Type 2 Diabetes (JAMP study), we examined factors that decreased blood glucose control effect of sitagliptin after 3 months and patients requiring an addition or increase of diabetes treatment.
We selected patients in whom glycated hemoglobin (HbA1c) levels decreased by month 3 after initiation of sitagliptin treatment and conducted two analyses: (1) in patients who did not change drugs until month 12, we compared changes in HbA1c levels between concomitant drugs and examined factors that decreased blood glucose control effect of sitagliptin; (2) compared changes in HbA1c levels and backgrounds between patients who did and did not require an addition to or increased dose of the antidiabetic agent.
Four hundred and ninety-eight patients were chosen. In 369 patients without drug change until month 12, changes in HbA1c levels during months 3-12 were not significantly different among concomitant drugs; factors causing rebound HbA1c were smoking and weight gain. Patient characteristics were compared between those who did and did not require an additional drug or a dose increase ( = 114) ( = 384). Drug changes were associated with longer disease duration, younger age, higher rate of smoking, and higher degree of insulin resistance but not with concomitantly administered drugs.
Smoking and weight gain were factors that decreased the effect of sitagliptin on reducing blood glucose levels. Differences in concomitant drugs did not affect sitagliptin's effects on glycemic control. A dose increase or the addition of the antidiabetic drug was not associated with concomitant drugs.
作为西他列汀治疗2型糖尿病多中心前瞻性试验(JAMP研究)的一项亚分析,我们研究了3个月后降低西他列汀血糖控制效果的因素以及需要增加或调整糖尿病治疗方案的患者情况。
我们选择了西他列汀治疗开始后第3个月糖化血红蛋白(HbA1c)水平下降的患者,并进行了两项分析:(1)在12个月前未更换药物的患者中,我们比较了联合用药期间HbA1c水平的变化,并研究了降低西他列汀血糖控制效果的因素;(2)比较了需要增加或提高抗糖尿病药物剂量的患者与不需要的患者之间HbA1c水平和背景情况的变化。
共选取498例患者。在369例12个月前未更换药物的患者中,联合用药期间3至12个月HbA1c水平变化无显著差异;导致HbA1c反弹的因素为吸烟和体重增加。比较了需要增加药物剂量或提高剂量的患者(n = 114)与不需要的患者(n = 384)的患者特征。药物更换与病程较长、年龄较轻、吸烟率较高和胰岛素抵抗程度较高有关,但与联合使用的药物无关。
吸烟和体重增加是降低西他列汀降血糖效果的因素。联合用药的差异不影响西他列汀的血糖控制效果。增加抗糖尿病药物剂量或加用抗糖尿病药物与联合用药无关。