TY - JOUR
T1 - Bezafibrate reduces blood glucose in type 2 diabetes mellitus
AU - Ogawa, Susumu
AU - Takeuchi, Kazuhisa
AU - Sugimura, Kazuhiko
AU - Fukuda, Motoshi
AU - Lee, Ribun
AU - Ito, Sadayoshi
AU - Sato, Tokutaro
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2000
Y1 - 2000
N2 - The clinical efficacy of bezafibrate was examined with special reference to glucose metabolism in patients with type 2 diabetes mellitus (DM2). In protocol 1,342 patients with DM2 and hyperlipidemias were randomly divided into 2 groups, 16-week bezafibrate treatment (n = 174) and no bezafibrate treatment (n = 168). In protocol 2, 20 DM2 patients were randomly divided into 2 groups, 8-week bezafibrate treatment (n = 10) and no bezafibrate treatment (n = 10), and a meal tolerance test (MTT) was performed. In protocol 1, bezafibrate treatment significantly reduced the fasting levels of triglyceride (TG) by 50% ± 1.6%, total cholesterol (TC) by 12% ± 1.1%, plasma glucose (PG) from 151.3 ± 3.5 to 128.6 ± 3.4 mg/dL, and hemoglobin A(1c) (HbA(1c)) from 7.2% ± 0.1% to 6.9% ± 0.1%, and significantly increased high-density lipoprotein cholesterol (HDL-C) by 20% ± 0.8%. In protocol 2, fasting TG, PG, and insulin levels were significantly reduced by bezafibrate treatment. Moreover, in the MTT, postprandial increments of TG were significantly blunted after bezafibrate treatment, whereas postprandial PG and insulin levels were not significantly changed. Leptin levels were significantly decreased, while tumor necrosis factor alpha (TNF-α) levels were not changed. In conclusion, both hyperglycemia and hyperlipidemia can be improved by bezafibrate treatment in DM2. (C) 2000 by W.B. Saunders Company.
AB - The clinical efficacy of bezafibrate was examined with special reference to glucose metabolism in patients with type 2 diabetes mellitus (DM2). In protocol 1,342 patients with DM2 and hyperlipidemias were randomly divided into 2 groups, 16-week bezafibrate treatment (n = 174) and no bezafibrate treatment (n = 168). In protocol 2, 20 DM2 patients were randomly divided into 2 groups, 8-week bezafibrate treatment (n = 10) and no bezafibrate treatment (n = 10), and a meal tolerance test (MTT) was performed. In protocol 1, bezafibrate treatment significantly reduced the fasting levels of triglyceride (TG) by 50% ± 1.6%, total cholesterol (TC) by 12% ± 1.1%, plasma glucose (PG) from 151.3 ± 3.5 to 128.6 ± 3.4 mg/dL, and hemoglobin A(1c) (HbA(1c)) from 7.2% ± 0.1% to 6.9% ± 0.1%, and significantly increased high-density lipoprotein cholesterol (HDL-C) by 20% ± 0.8%. In protocol 2, fasting TG, PG, and insulin levels were significantly reduced by bezafibrate treatment. Moreover, in the MTT, postprandial increments of TG were significantly blunted after bezafibrate treatment, whereas postprandial PG and insulin levels were not significantly changed. Leptin levels were significantly decreased, while tumor necrosis factor alpha (TNF-α) levels were not changed. In conclusion, both hyperglycemia and hyperlipidemia can be improved by bezafibrate treatment in DM2. (C) 2000 by W.B. Saunders Company.
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U2 - 10.1016/S0026-0495(00)90176-8
DO - 10.1016/S0026-0495(00)90176-8
M3 - Article
C2 - 10726910
AN - SCOPUS:0034064204
SN - 0026-0495
VL - 49
SP - 331
EP - 334
JO - Metabolism: Clinical and Experimental
JF - Metabolism: Clinical and Experimental
IS - 3
ER -