Rickels Michael R, Ballou Cassandra M, Foster Nicole C, Alejandro Rodolfo, Baidal David A, Bellin Melena D, Eggerman Thomas L, Hering Bernhard J, Kandeel Fouad, Brand Adam, Miller Kellee M, Barton Franca B, Payne Elizabeth H
Institute for Diabetes, Obesity & Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
The Emmes Company, LLC, Rockville, MD.
Diabetes Care. 2025 May 1;48(5):737-744. doi: 10.2337/dc24-1915.
Islet transplantation was recently approved by the U.S. Food and Drug Administration for adults with type 1 diabetes complicated by recurrent severe hypoglycemia events (SHEs). We sought to understand the long-term benefit for glycemic control and risk of immunosuppression to kidney function associated with islet transplantation compared with ongoing standard of care.
We performed a case-control analysis of prospectively collected data from patients in the Collaborative Islet Transplant Registry (CITR) with at least one SHE in the year (2000-2014) before transplantation (case subjects) and compared them with data from patients in the T1D Exchange (T1DX) Registry with at least one SHE in the year (2010-2012) before enrollment (control subjects), with both cohorts observed over 5 years. SHEs were restricted to those resulting in seizure or loss of consciousness.
Case subjects from CITR (n = 71) compared with control subjects from T1DX (n = 213) more often achieved the primary outcome of HbA1c <7.0% and absence of an SHE (71-80% vs. 21-33% over 5 years; P < 0.001) and the outcome of HbA1c ≤6.5% and absence of an SHE (60-75% vs. 10-20%; P < 0.001) while requiring significantly less insulin (majority in CITR were insulin independent). Kidney function, measured by estimated glomerular filtration rate, declined from baseline to a greater extent in CITR than in T1DX (-8.8 to -20 vs. -1.3 to -6.5 mL ⋅ min-1 ⋅ 1.73 m-2 over 5 years; P < 0.001).
Islet transplantation for adults with type 1 diabetes complicated by SHEs results in near-normal glycemic control in the absence of SHEs more often than observed with standard of care, but at the cost of greater reduction in kidney function.
胰岛移植最近已获美国食品药品监督管理局批准,用于治疗患有1型糖尿病并伴有复发性严重低血糖事件(SHEs)的成人患者。我们试图了解与持续的标准治疗相比,胰岛移植对血糖控制的长期益处以及免疫抑制对肾功能的风险。
我们对协作胰岛移植登记处(CITR)中在移植前一年(2000 - 2014年)至少发生一次SHEs的患者的前瞻性收集数据进行了病例对照分析(病例组),并将其与T1D交换(T1DX)登记处中在入组前一年(2010 - 2012年)至少发生一次SHEs的患者的数据进行比较(对照组),两个队列均观察了5年。SHEs仅限于导致癫痫发作或意识丧失的事件。
CITR的病例组(n = 71)与T1DX的对照组(n = 213)相比,更常实现糖化血红蛋白(HbA1c)<7.0%且无SHEs的主要结局(5年期间分别为71 - 80%对21 - 33%;P < 0.001)以及HbA1c≤6.5%且无SHEs的结局(60 - 75%对10 - 20%;P < 0.001),同时所需胰岛素显著减少(CITR中的大多数患者无需胰岛素)。通过估算肾小球滤过率衡量的肾功能,在CITR中从基线下降的程度比在T1DX中更大(5年期间分别为-8.8至-20对-1.3至-6.5 mL·min-1·1.73 m-2;P < 0.001)。
对于患有1型糖尿病并伴有SHEs的成人患者,胰岛移植比标准治疗更常导致在无SHEs的情况下血糖接近正常控制,但代价是肾功能下降幅度更大。