首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Glucagon-like peptide-1 receptor agonists as insulin add-on therapy in patients with inadequate glycemic control in type 2 diabetes mellitus: lixisenatide as a new therapeutic option
【24h】

Glucagon-like peptide-1 receptor agonists as insulin add-on therapy in patients with inadequate glycemic control in type 2 diabetes mellitus: lixisenatide as a new therapeutic option

机译:胰高血糖素样肽-1受体激动剂在2型糖尿病患者血糖控制不足的患者中作为胰岛素的补充疗法:利西拉来作为一种新的治疗选择

获取原文
获取原文并翻译 | 示例
           

摘要

Despite the variety of therapeutic options for the management of type 2 diabetes mellitus, many patients fail to meet glycated hemoglobin (HbA1c) targets. The relative contribution of postprandial plasma glucose (PPG) to overall HbA1c is estimated at 40-60%, with the effect of PPG on HbA1c, being prominent in patients on basal insulin. The development of glucagon-like peptide-1 receptor agonists (GLP-1RA5) has been an important achievement in diabetes management and has become an established treatment. Of available GLP-1RAs, lixisenatide is a once-daily prandial GLP-1RA that has been shown to produce a reduction in HbA(lc) with a pronounced postprandial effect, suggesting a complementary effect between lixisenatide and basal insulin on PPG and fasting plasma glucose, resulting in a beneficial effect on body weight in all populations. Therefore, lixisenatide will make an important addition to current options for treating diabetes, especially for patients not achieving glycemic targets with basal insulin therapy.
机译:尽管治疗2型糖尿病的治疗选择多种多样,但许多患者仍未达到糖化血红蛋白(HbA1c)指标。餐后血浆葡萄糖(PPG)对总HbA1c的相对贡献估计为40-60%,PPG对HbA1c的影响在基础胰岛素患者中尤为突出。胰高血糖素样肽-1受体激动剂(GLP-1RA5)的开发已成为糖尿病治疗中的重要成就,并已成为公认的治疗方法。在所有可用的GLP-1RA中,利西拉来是每日一次的餐后GLP-1RA,已显示可降低HbA(lc),具有明显的餐后作用,提示利西拉来和基础胰岛素对PPG和空腹血糖的补充作用,对所有人群的体重都有有益的影响。因此,利西拉来将为当前治疗糖尿病的方法提供重要的补充,特别是对于那些未通过基础胰岛素治疗达到血糖目标的患者。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号