Montada-Atin Tess, Prasad G V Ramesh
Kidney Transplant Program, St. Michael's Hospital, Toronto M5C 2T2, Ontario, Canada.
World J Diabetes. 2021 May 15;12(5):541-555. doi: 10.4239/wjd.v12.i5.541.
A common challenge in managing kidney transplant recipients (KTR) is post-transplant diabetes mellitus (PTDM) or diabetes mellitus (DM) newly diagnosed after transplantation, in addition to known pre-existing DM. PTDM is an important risk factor for post-transplant cardiovascular (CV) disease, which adversely affects patient survival and quality of life. CV disease in KTR may manifest as ischemic heart disease, heart failure, and/or left ventricular hypertrophy. Available therapies for PTDM include most agents currently used to treat type 2 diabetes. More recently, the use of sodium glucose co-transporter 2 inhibitors (SGLT2i), glucagon-like peptide-1 receptor agonists (GLP-1 RA), and dipeptidyl peptidase 4 inhibitors (DPP4i) has cautiously extended to KTR with PTDM, even though KTR are typically excluded from large general population clinical trials. Initial evidence from observational studies seems to indicate that SGLT2i, GLP-1 RA, and DPP4i may be safe and effective for glycemic control in KTR, but their benefit in reducing CV events in this otherwise high-risk population remains unproven. These newer drugs must still be used with care due to the increased propensity of KTR for intravascular volume depletion and acute kidney injury due to diarrhea and their single-kidney status, pre-existing burden of peripheral vascular disease, urinary tract infections due to immunosuppression and a surgically altered urinary tract, erythrocytosis from calcineurin inhibitors, and reduced kidney function from acute or chronic rejection.
管理肾移植受者(KTR)的一个常见挑战是移植后糖尿病(PTDM),即移植后新诊断出的糖尿病(DM),此外还有已知的移植前已存在的DM。PTDM是移植后心血管(CV)疾病的重要危险因素,对患者的生存和生活质量产生不利影响。KTR中的CV疾病可能表现为缺血性心脏病、心力衰竭和/或左心室肥厚。PTDM的现有治疗方法包括目前用于治疗2型糖尿病的大多数药物。最近,钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)、胰高血糖素样肽-1受体激动剂(GLP-1 RA)和二肽基肽酶4抑制剂(DPP4i)已谨慎地扩展用于患有PTDM的KTR,尽管KTR通常被排除在大型普通人群临床试验之外。观察性研究的初步证据似乎表明,SGLT2i、GLP-1 RA和DPP4i可能对KTR的血糖控制安全有效,但它们在降低这一高危人群CV事件方面的益处仍未得到证实。由于KTR因腹泻导致血管内容量减少和急性肾损伤的倾向增加,以及其单肾状态、既往外周血管疾病负担、免疫抑制和手术改变的尿路导致的尿路感染、钙调神经磷酸酶抑制剂引起的红细胞增多症以及急性或慢性排斥导致的肾功能下降,这些新药仍必须谨慎使用。