Shimada Shingo, Miyake Katsunori, Venkat Deepak, Gonzalez Humberto, Moonka Dilip, Yoshida Atsushi, Abouljoud Marwan, Nagai Shunji
Division of Transplant and Hepatobiliary Surgery Henry Ford Health System Detroit Michigan USA.
Division of Gastroenterology and Hepatology Henry Ford Health System Detroit Michigan USA.
Ann Gastroenterol Surg. 2024 Jan 19;8(3):383-393. doi: 10.1002/ags3.12775. eCollection 2024 May.
We aimed to identify the characteristics of new-onset diabetes after liver transplantation (LT) (NODAT) and investigate its impacts on post-transplant outcomes.
Adult LT patients between 2014 and 2020 who used tacrolimus as initial immunosuppression and survived 3 months at least were evaluated. Patients who developed NODAT within 3 months after LT were classified as NODAT group. Also, patients were further classified as history of diabetes before LT (PHDBT) and non-diabetes (ND) groups. Patient characteristics, post-LT outcomes, and cardiovascular and/or pulmonary complications were compared.
A total of 83, 225, and 263 patients were classified into NODAT, PHDBT, and ND groups. The proportion of cholestatic liver disease and rejection within 90 days were higher in NODAT group. Mean serum tacrolimus concentration trough level in the first week after LT was 7.12, 6.12, and 6.12 ng/mL ( < 0.001). Duration of corticosteroids was significantly longer in NODAT compared to PHDBD or ND (416, 289, and 228 days, < 0.001). Three-year graft and patient survival were significantly worse in NODAT than ND (80.5% vs. 95.0%, < 0.001: 82.0% vs. 95.4%, < 0.001) but similar to PHDBT. Adjusted risks of 3-year graft loss and patient death using Cox regression analysis were significantly higher in NODAT compared to ND (adjusted hazard ratio [aHR] 3.41, = 0.004; aHR 3.61, = 0.004). Incidence rates of cardiovascular or pulmonary complications after LT in NODAT were significantly higher than ND but similar to PHDBT.
Higher initial tacrolimus concentration and early rejection might be risk factors for NODAT. NODAT was associated with worse post-transplant outcomes.
我们旨在确定肝移植(LT)后新发糖尿病(NODAT)的特征,并研究其对移植后结局的影响。
对2014年至2020年间使用他克莫司作为初始免疫抑制且至少存活3个月的成年LT患者进行评估。LT后3个月内发生NODAT的患者被分类为NODAT组。此外,患者还被进一步分类为LT前糖尿病史(PHDBT)组和非糖尿病(ND)组。比较患者特征、LT后结局以及心血管和/或肺部并发症。
总共83、225和263例患者被分类为NODAT组、PHDBT组和ND组。NODAT组90天内胆汁淤积性肝病和排斥反应的比例更高。LT后第一周的平均血清他克莫司谷浓度分别为7.12、6.12和6.12 ng/mL(<0.001)。与PHDBT组或ND组相比,NODAT组的皮质类固醇使用时间明显更长(416、289和228天,<0.001)。NODAT组的三年移植物和患者生存率明显低于ND组(80.5%对95.0%,<0.001;82.0%对95.4%,<0.001),但与PHDBT组相似。使用Cox回归分析,NODAT组三年移植物丢失和患者死亡的调整风险明显高于ND组(调整后的风险比[aHR] 3.41,P = 0.004;aHR 3.61,P = 0.004)。LT后NODAT组心血管或肺部并发症的发生率明显高于ND组,但与PHDBT组相似。
较高的初始他克莫司浓度和早期排斥反应可能是NODAT的危险因素。NODAT与较差的移植后结局相关。