Achieving glycemic control in patients with type 2 diabetes and renal impairment

被引:20
作者
Avogaro, Angelo [1 ]
Schernthaner, Guntram [2 ]
机构
[1] Univ Padua, Sch Med, Dept Med, I-35128 Padua, Italy
[2] Rudolfstiftung, Dept Med 1, Vienna, Austria
关键词
Glycemic control; Type; 2; diabetes; Chronic kidney disease; Renal impairment; Oral anti-diabetes drugs; CHRONIC KIDNEY-DISEASE; MULTIFACTORIAL INTERVENTION; MELLITUS; PHARMACOKINETICS; NEPHROPATHY; OUTCOMES; RISK; EXENATIDE; MODERATE; TRIAL;
D O I
10.1007/s00592-012-0442-x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Defining optimal regimens for the management of diabetes among patients with renal impairment is often clinically challenging, and guidance on the optimal management of these patients in clinical practice can vary considerably. Moreover, as many anti-diabetes agents are predominantly excreted renally, treatment options to control blood glucose levels are limited for patients with type 2 diabetes and concomitant chronic kidney disease. Many of the widely used and more established anti-diabetes drugs cannot be used in this population either or must be down-titrated to reduce the increased risk of severe hypoglycemic episodes. A number of more recently available anti-diabetes drugs are indicated for use in patients with type 2 diabetes and chronic kidney disease. Newer drugs that may improve the currently very limited treatment options for patients with type 2 diabetes and renal impairment include the glucagon-like peptide-1 receptor agonists and the dipeptidyl peptidase-4 inhibitors. This review paper, based on a literature search for both original and review articles (Medline), relevant clinical practice/regulatory guidelines and integrating our own knowledge of the field, provides an up-to-date examination of the current treatment options available. However, further studies with larger populations of patients with type 2 diabetes and chronic kidney disease are needed to clarify the efficacy and safety of the different treatment options, including newer drugs.
引用
收藏
页码:283 / 291
页数:9
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