Providence Medical Research Center, Providence Health Care, Spokane, Washington.
Division of Nephrology, Kidney Research Institute, and Institute of Translational Health Sciences, University of Washington, Seattle, Washington.
Diabetes Obes Metab. 2020 Jul;22(7):1014-1023. doi: 10.1111/dom.13986. Epub 2020 Feb 20.
Type 2 diabetes is the leading cause of chronic kidney disease (CKD). The prevalence of CKD is growing in parallel with the rising number of patients with type 2 diabetes globally. At present, the optimal approach to glycaemic control in patients with type 2 diabetes and advanced CKD (categories 4 and 5) remains uncertain, as these patients were largely excluded from clinical trials of glucose-lowering therapies. Nonetheless, clinical trial data are available for the use of incretin therapies, dipeptidyl peptidase-4 inhibitors and glucagon-like peptide-1 receptor agonists, for patients with type 2 diabetes and advanced CKD. This review discusses the role of incretin therapies in the management of these patients. Because the presence of advanced CKD in patients with type 2 diabetes is associated with a markedly elevated risk of cardiovascular disease (CVD), treatment strategies must include the reduction of both CKD and CVD risks because death, particularly from cardiovascular causes, is more probable than progression to end-stage kidney disease. The management of hyperglycaemia is essential for good diabetes care even in advanced CKD. Current evidence supports an individualized approach to glycaemic management in patients with type 2 diabetes and advanced CKD, taking account of the needs of each patient, including the presence of co-morbidities and concomitant therapies. Although additional studies are needed to establish optimal strategies for glycaemic control in patients with type 2 diabetes and advanced CKD, treatment regimens with currently available pharmacotherapy can be individually tailored to meet the needs of this growing patient population.
2 型糖尿病是慢性肾脏病(CKD)的主要病因。随着全球 2 型糖尿病患者数量的增加,CKD 的患病率也在同步增长。目前,对于 2 型糖尿病合并晚期 CKD(类别 4 和 5)患者的血糖控制最佳方法仍不确定,因为这些患者在很大程度上被排除在降血糖治疗的临床试验之外。尽管如此,仍有临床试验数据可用于 2 型糖尿病合并晚期 CKD 患者使用肠促胰岛素治疗、二肽基肽酶-4 抑制剂和胰高血糖素样肽-1 受体激动剂。本文讨论了肠促胰岛素治疗在这些患者管理中的作用。由于 2 型糖尿病合并晚期 CKD 患者的心血管疾病(CVD)风险显著升高,因此治疗策略必须包括降低 CKD 和 CVD 风险,因为死亡,尤其是心血管原因导致的死亡,比进展为终末期肾病的可能性更大。即使在晚期 CKD 中,控制高血糖对于良好的糖尿病管理也至关重要。目前的证据支持对 2 型糖尿病合并晚期 CKD 患者进行个体化血糖管理,考虑到每位患者的需求,包括合并症和伴随治疗的存在。尽管需要进一步的研究来确定 2 型糖尿病合并晚期 CKD 患者的最佳血糖控制策略,但目前可用的药物治疗方案可以根据患者的需求进行个体化调整,以满足这一不断增长的患者群体的需求。