TY - JOUR
T1 - Relationship between the efficacy of oral antidiabetic drugs and clinical features in type 2 diabetic patients (JDDM38)
AU - Japan Diabetes Clinical Data Management Study Group (JDDM)
AU - Kanatsuka, Azuma
AU - Sato, Yasunori
AU - Kawai, Koichi
AU - Hirao, Koichi
AU - Kobayashi, Masashi
AU - Kashiwagi, Atsunori
AU - Abe, Nobuyuki
AU - Arai, Keiko
AU - Fujiya, Hiroshi
AU - Fukumoto, Yoshihide
AU - Dake, Fumihiko
AU - Iizumi, Tomohiro
AU - Ito, Masaaki
AU - Iwasaki, Koichi
AU - Kanamori, Akira
AU - Kato, Sumio
AU - Kato, Masakazu
AU - Kawara, Akira
AU - Kimura, Kenichi
AU - Chikamori, Kazumasa
AU - Iemitsu, Kotaro
AU - Kou, Shigetake
AU - Kudo, Mikihiko
AU - Kurihara, Yoshio
AU - Lee, Gendai
AU - Tsuruoka, Akira
AU - Manda, Naoki
AU - Matoba, Kiyokazu
AU - Hayashi, Hiroshi
AU - Minami, Masae
AU - Kuribayashi, Nobuichi
AU - Miyazawa, Kazuhiro
AU - Chiba, Yasuko
AU - Osonoi, Takeshi
AU - Nakamura, Shin
AU - Sasaki, Hideo
AU - Komori, Katsutoshi
AU - Oishi, Mariko
AU - Okada, Akira
AU - Okuguchi, Fuminobu
AU - Yanagisawa, Morifumi
AU - Sugimoto, Hidekatsu
AU - Sugiyama, Hiromichi
AU - Takai, Masahiko
AU - Takaki, Masato
AU - Takamura, Hiroshi
AU - Takeda, Hiroshi
AU - Tanaka, Kokichi
AU - Miwa, Takashi
AU - Tomonaga, Osamu
N1 - Publisher Copyright:
© 2016 Asian Association for the Study of Diabetes and John Wiley & Sons Australia, Ltd.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Aims/Introduction: We carried out an observational cohort study to examine the relationship between the efficacy of oral antidiabetic drugs and clinical features in type 2 diabetics. Materials and Methods: We analyzed the CoDiC® database of the Japan Diabetes Data Management Study Group across 67 institutions in Japan. In a total of 3,698 drug-naïve patients who were initiated with metformin, dipeptidyl peptidase-4 inhibitor (DPP-4i) or sulfonylurea (SU) from 2007 to 2012, we evaluated body mass index (BMI) and hemoglobin A1c (HbA1c). The patients were stratified according to their clinical features, and matched using a propensity score to adjust for baseline factors. Results: HbA1c was reduced with all drugs, with the largest effect elicited by DPP-4i and the smallest by SU (P = 0.00). HbA1c increased with SU after 6 months in the patients stratified by an age-of-onset of <50 years (P = 0.00). BMI increased with SU in the patients stratified by a BMI of <25 (P = 0.00), and decreased with metformin in the patients with a BMI >25 (P = 0.00). The reduction in HbA1c was larger in patients with HbA1c of ≥8%, compared with that in patients with HbA1c of <8% (P = 0.00). HbA1c during the study period was higher in patients who were added to or swapped with other drug(s), than in patients continued on the original drug (P = 0.00). Conclusions: The effect on bodyweight and glycemic control differed among metformin, DPP-4i and SU, and the difference was associated with clinical features.
AB - Aims/Introduction: We carried out an observational cohort study to examine the relationship between the efficacy of oral antidiabetic drugs and clinical features in type 2 diabetics. Materials and Methods: We analyzed the CoDiC® database of the Japan Diabetes Data Management Study Group across 67 institutions in Japan. In a total of 3,698 drug-naïve patients who were initiated with metformin, dipeptidyl peptidase-4 inhibitor (DPP-4i) or sulfonylurea (SU) from 2007 to 2012, we evaluated body mass index (BMI) and hemoglobin A1c (HbA1c). The patients were stratified according to their clinical features, and matched using a propensity score to adjust for baseline factors. Results: HbA1c was reduced with all drugs, with the largest effect elicited by DPP-4i and the smallest by SU (P = 0.00). HbA1c increased with SU after 6 months in the patients stratified by an age-of-onset of <50 years (P = 0.00). BMI increased with SU in the patients stratified by a BMI of <25 (P = 0.00), and decreased with metformin in the patients with a BMI >25 (P = 0.00). The reduction in HbA1c was larger in patients with HbA1c of ≥8%, compared with that in patients with HbA1c of <8% (P = 0.00). HbA1c during the study period was higher in patients who were added to or swapped with other drug(s), than in patients continued on the original drug (P = 0.00). Conclusions: The effect on bodyweight and glycemic control differed among metformin, DPP-4i and SU, and the difference was associated with clinical features.
KW - Oral antidiabetic drug
KW - Propensity score-matched cohort study
KW - Type 2 diabetes mellitus
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U2 - 10.1111/jdi.12430
DO - 10.1111/jdi.12430
M3 - Article
C2 - 27330726
AN - SCOPUS:84948168962
SN - 2040-1116
VL - 7
SP - 386
EP - 395
JO - Journal of Diabetes Investigation
JF - Journal of Diabetes Investigation
IS - 3
ER -