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Author(s)
Third
Department of Internal Medicine, Division of Diabetes, Endocrinology
and Metabolism, Kyorin University School of Medicine, Tokyo, Japan.
Foundation for Biomedical Research and Innovation, Hyogo, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Watanabe Medical Clinic, Hiroshima, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Department of Internal Medicine, Saitama Social Insurance Hospital, Saitama, Japan.
Sakado Central Hospital, Saitama, Japan.
Sakado Central Hospital, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Third Department of Internal Medicine, Division of Diabetes, Endocrinology and Metabolism, Kyorin University School of Medicine, Tokyo, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Third Department of Internal Medicine, Division of Diabetes, Endocrinology and Metabolism, Kyorin University School of Medicine, Tokyo, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Foundation for Biomedical Research and Innovation, Hyogo, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Watanabe Medical Clinic, Hiroshima, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Department of Internal Medicine, Saitama Social Insurance Hospital, Saitama, Japan.
Sakado Central Hospital, Saitama, Japan.
Sakado Central Hospital, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Third Department of Internal Medicine, Division of Diabetes, Endocrinology and Metabolism, Kyorin University School of Medicine, Tokyo, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Third Department of Internal Medicine, Division of Diabetes, Endocrinology and Metabolism, Kyorin University School of Medicine, Tokyo, Japan.
Division of Endocrinology and Diabetes, Saitama Medical University, Saitama, Japan.
Japanese type 2 diabetic
patients were treated with sitagliptin to evaluate the efficacy of this agent,
and also to investigate the clinical characteristics of those who responded to
sitagliptin. In total, 1001 diabetic patients, inadequately controlled (HbA1c ≥
6.5%) with oral hypoglycemic agents (OHA) other than DPP-4 inhibitors or with
diet and exercise only, were enrolled. We added 50mg of sitagliptin to the
therapeutic regimens of 410 patients including 68 OHA naive patients, while the
other 591 patients were switched from a single OHA to 50 mg of sitagliptin.
After 6 months, glycemic control was significantly improved due to both reduced
insulin resistance, as demonstrated by a significant HOMA-R reduction, and
recovery of pancreatic β cell function, as assessed by HOMA-β and the proinsulin/insulin (PI/I)
ratio. In the bivariable analysis, a good response, defined as an HbA1c
reduction during the 6 months of at least 0.9%, was associated with high HbA1c
and PI/I at baseline and combination treatments with sulfonylurea, biguanide
and α-glucosidase
inhibitors, but not with obesity. On the other hand, in the multivariable
regression analysis, only high baseline HbA1c and combination treatment with anα-glucosidase
inhibitor were significantly associated with a good response to sitagliptin. In
patients with type 2 diabetes, the addition of sitagliptin or switching from
another OHA to this agent achieved an HbA1c reduction without overloading β cells.
In particular, we suggest that a good response to sitagliptin can be expected
when this agent is combined with an α-glucosidase
inhibitor (UMIN No. #000014157).
KEYWORDS
Cite this paper
Inukai, K. , Hirata, T. , Sumita, T. , Watanabe, M. ,
Ikegami, Y. , Ito, D. , Kurihara, S. , Yasukawa, N. , Morimoto, J. ,
Takata, N. , Kanazawa, K. , Neda, T. , Sumitani, Y. , Inoue, K. ,
Noguchi, Y. , Hosaka, T. , Ishida, H. and Katayama, S. (2014)
Clinical Characteristics of Japanese Type 2 Diabetic Patients Responsive
to Sitagliptin. Journal of Diabetes Mellitus, 4, 172-178. doi: 10.4236/jdm.2014.43025.
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