Sitagliptin reduces albuminuria in patients with type 2 diabetes

被引:138
作者
Hattori, Sachiko [1 ]
机构
[1] Tsunemi Cho Clin, Ashikaga, Tochigi 3260022, Japan
关键词
DPP-4; inhibitor; Albuminuria; eGFR; INFLAMMATION; LIRAGLUTIDE; COMBINATION; GLIMEPIRIDE; INHIBITOR; METFORMIN; MELLITUS;
D O I
10.1507/endocrj.K10E-382
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the inhibitory effect of sitagliptin on albuminuria in patients with type 2 diabetes. Thirty-six patients (19 men and 17 women) whose HbA 1c was higher than 6.5% (NGSP) despite receiving education on diet and exercise and medical treatment for at least 6 months at our clinic were enrolled into this study and were successfully followed over 6 months of sitagliptin treatment. Sitagliptin (50 mg/day) treatment significantly lowered both systolic and diastolic blood pressures, fasting blood glucose and postprandial blood glucose, HbA I c, and glycated albumin at 3 months and 6 months. Significant reductions in highly sensitive C-reactive protein and soluble vascular cell adhesion molecule 1 were also observed at 6 months. Urinary albumin excretion (measured as urinary albumin-to-creatinine ratio (ACR: mg/g Cr)) did not change in the 6 months before sitagliptin treatment (Delta ACR: 2.3 +/- 19.9) and decreased in the 6 months after sitagliptin treatment (Delta ACR: -20.6 +/- 24.6); these differences were statistically significant. At 6 months, the ACR decreased from 11.6 +/- 8.4 to 4.5 +/- 5.0 in 13 patients with normoalbuminuria (ACR < 30), from 98.4 +/- 79 to 24.9 +/- 20 in 15 patients with microalbuminuria (30 < ACR < 300), and from 1263 +/- 492 to 561 +/- 89 in 8 patients with macroalbuminuria (ACR > 300). Thus, the present findings strongly suggest that sitagliptin reduces albuminuria without lowering the estimated glomerular filtration rate, most likely depending on known factors such as blood sugar reduction, blood pressure reduction, and inflammation reduction, as well as yet undetermined factors caused by an increase in active glucagon-like peptide-1.
引用
收藏
页码:69 / 73
页数:5
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共 14 条
[11]   (R)-8-(3-amino-piperidin-1-yl)-7-but-2-ynyl-3-methyl-1(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydro-purine-2,6-dione (BI 1356), a novel xanthine-based dipeptidyl peptidase 4 inhibitor, has a superior potency and longer duration of action compared with other dipeptidyl peptidase-4 inhibitors [J].
Thomas, Leo ;
Eckhardt, Matthias ;
Langkopf, Elke ;
Tadayyon, Moh ;
Himmelsbach, Frank ;
Mark, Michael .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 325 (01) :175-182
[12]   Reversal of New-Onset Diabetes through Modulating Inflammation and Stimulating β-Cell Replication in Nonobese Diabetic Mice by a Dipeptidyl Peptidase IV Inhibitor [J].
Tian, Lei ;
Gao, Jie ;
Hao, Jianqiang ;
Zhang, Yu ;
Yi, Huimin ;
O'Brien, Timothy D. ;
Sorenson, Robert ;
Luo, Jian ;
Guo, Zhiguang .
ENDOCRINOLOGY, 2010, 151 (07) :3049-3060
[13]   Liraglutide provides similar glycaemic control as glimepiride (both in combination with metformin) and reduces body weight and systolic blood pressure in Asian population with type 2 diabetes from China, South Korea and India: a 16-week, randomized, double-blind, active control trial [J].
Yang, W. ;
Chen, L. ;
Ji, Q. ;
Liu, X. ;
Ma, J. ;
Tandon, N. ;
Bhattacharyya, A. ;
Kumar, A. ;
Kim, K. -W. ;
Yoon, K. -H. ;
Bech, O. M. ;
Zychma, M. .
DIABETES OBESITY & METABOLISM, 2011, 13 (01) :81-88
[14]   Severe Hypoglycemia and Risks of Vascular Events and Death. [J].
Zoungas, Sophia ;
Patel, Anushka ;
Chalmers, John ;
de Galan, Bastiaan E. ;
Li, Qiang ;
Billot, Laurent ;
Woodward, Mark ;
Ninomiya, Toshiharu ;
Neal, Bruce ;
MacMahon, Stephen ;
Grobbee, Diederick E. ;
Kengne, Andre Pascal ;
Marre, Michel ;
Heller, Simon .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (15) :1410-1418