期刊文献+

DPP4抑制剂对糖尿病的作用:远远超过控制血糖 被引量:3

Effect of DPP4-inhabitor on diabetes mellitus: beyond glycemic control
下载PDF
导出
摘要 糖尿病的患病人数在全世界持续上升,2型糖尿病早期的特点是胰岛素代谢信号降低、胰岛素抵抗。另外,糖尿病会增加相关心血管疾病和慢性肾脏疾病的风险,会导致心肾性代谢综合征。近年来出现的二肽基肽酶4(DPP4)抑制剂为治疗糖尿病提供了新的选择。该文通过分析胰岛素抵抗、免疫功能、心肾性代谢综合征之间的关联,来阐明DPP4抑制剂作为治疗糖尿病的新途径的可能作用机制,其不仅仅能控制血糖,并能改善胰岛素代谢信号和胰岛素抵抗,还能保护心血管,降低血压。 The population of diabetes continues to rise in worldwide.The characteristic of early type 2 diabetes is insulin resistance caused by decreased insulin metabolic signaling.Diabetes is a very important factor for high risk of cardiovascular disease (CVD)and chronic kidney disease (CKD)and might lead to car-dio-renal metabolic syndrome (CRS).After investigating the relationship among insulin resistance,immune modulation and CRS,it is suggested that the effect of DPP4 inhibition on diabetes may be more beneficial than glycemic control.DPP4 inhibition can improve insulin metabolic system,as well as insulin resistance signal, protect the cardiovascular system,lower blood pressure.
作者 朱路 李华荣
出处 《新医学》 2014年第2期79-82,共4页 Journal of New Medicine
关键词 DPP4抑制剂 胰岛素抵抗 免疫调节 心肾性代谢综合征 DPP4-inhabitor Insulin resistance Immunomodulatory Cardiorenal metabolic syndrome
  • 相关文献

同被引文献37

  • 1Danaei G, Finucane MM, Lu Y, et al. National, re- gional, and global trends in fasting plasma glucose and diabetes prevalence since 1980: systematicanalysis ofhealth examination surveys and epidemiological studies with 370 country-years and 2"7 millionparticipants. Lancet, 2011, 378: 31-40.
  • 2Caporali A, Meloni M, Mitic T, et al. 524p75NTR-de- pendent activation of NF-kB is required for the traffic- king and transcriptional regulation of microRNA-503 in microvascular complications of diabetes. Cardiovasc Res, 2014, 103:S96.
  • 3Shah P, Ardestani A, Dharmadhikari G, et al. The DPP-4 inhibitor linagliptin restores β-cell function and survival in human isolated islets through GLP-1 stabili- zation. J Clin Endocrinol Metab, 2013, 98: E1163- 72.
  • 4Avogaro A, de Kreutzenberg S, Fadini G. Dipeptidyl- peptidase 4 inhibition: linking metabolic control to car- diovascular protection. Curr Pharm Des, 2014, 20: 2387-2394.
  • 5Barnett AH. The role of GLP-1 mimetics and basal insu- lin analogues in type 2 diabetes mellitus: guidance from studies ofliraglutide. Diabetes Obes Metab, 2012, 14: 304 -314.
  • 6Bhavsar S, Mudaliar S, Cherrington A. Evolution of ex- enatide as a diabetes therapeutic. Curr Diabetes Rev, 2013, 9:161-193.
  • 7Sehramm TK, Gislason GH, Vaag A, et al. Mortality and cardiovascular risk associated with different insulin seeretagogues eompared with metformin in type 2 diabe- tes, with or without a previous myocardial infarction: a nationwide study. Eur Heart J, 2011, 32: 1900- 1908.
  • 8Gore MO, Meguire DK. Resolving drug effects from class effects among drugs for type 2 diabetes mellitus: more support forcardiovaseular outcome assessments. Eur Heart J, 2011, 32: 1832-1834.
  • 9DeYoung MB, Macconell L, Sarin V, et al. Encapsula- tion of exenatide in poly- (D, L-lactide-co-glycolide) microspheres produced an investigational long-acting once-weekly formulation for type 2 diabetes. Diabetes Technol Ther, 2011, 13: 1145-1154.
  • 10Zinman B, Schmidt WE, Moses A, et al. Achieving a clinically relevant composite outcome of an HbAlc of < 7% without weight gain or hypoglycaemiain type 2 dia- betes: a meta-analysis of the liraglutide clinical trial programme. Diabetes Obes Metab, 2012, 14: 77-82.

引证文献3

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部