Chronic Disease Research Group, Minneapolis Medical Research Foundation, Minneapolis, MN 55415, USA.
Transpl Int. 2012 Jul;25(7):748-57. doi: 10.1111/j.1432-2277.2012.01488.x. Epub 2012 Apr 30.
Metabolic syndrome is associated with coronary heart disease (CHD) and new-onset diabetes after kidney transplant (NODAT). Using data collected from transplant centers worldwide for the Patient Outcomes in Renal Transplantation study, we examined associations of metabolic syndrome (n = 2253 excluding recipients with diabetes pretransplant), CHD (n = 2253), and NODAT (n = 1840 further excluding recipients with diabetes in the first year post-transplant), with the primary outcome of allograft failure. We assessed risk factors associated with secondary outcomes of metabolic syndrome, NODAT, and CHD after adjusting for type of baseline immunosuppression and transplant center effects. Metabolic syndrome prevalence was 39.8% at 12-24 months post-transplant and 35.4% at 36-48 months. Metabolic syndrome was independently associated with NODAT (hazard ratio 3.46, 95% confidence interval 2.40-4.98, P < 0.0001), CHD (2.03, 1.16-3.52, P = 0.013), and allograft failure (1.36, 1.03-1.79, P = 0.028). Allograft failure occurred in 218 patients (14.6%). After adjustment for metabolic syndrome, NODAT (1.63, 1.18-2.24, P = 0.003) and CHD (5.48, 3.27-9.20, P < 0.0001) remained strongly associated with increased risk of allograft failure. Metabolic syndrome, NODAT, and CHD are risk factors for allograft failure. NODAT and CHD are risk factors for allograft failure, independent of metabolic syndrome.
代谢综合征与冠心病(CHD)和肾移植后新发糖尿病(NODAT)有关。利用全球移植中心收集的数据,进行了一项名为“患者肾脏移植结局研究”,我们检查了代谢综合征(n = 2253,排除移植前患有糖尿病的患者)、CHD(n = 2253)和 NODAT(n = 1840,进一步排除移植后第一年患有糖尿病的患者)与移植物失功的主要结局之间的关联。我们评估了代谢综合征、NODAT 和 CHD 的次要结局的相关风险因素,这些因素在调整了基线免疫抑制类型和移植中心效应后进行了评估。移植后 12-24 个月时,代谢综合征的患病率为 39.8%,36-48 个月时为 35.4%。代谢综合征与 NODAT(风险比 3.46,95%置信区间 2.40-4.98,P < 0.0001)、CHD(2.03,1.16-3.52,P = 0.013)和移植物失功(1.36,1.03-1.79,P = 0.028)独立相关。218 例患者(14.6%)发生移植物失功。在调整了代谢综合征后,NODAT(1.63,1.18-2.24,P = 0.003)和 CHD(5.48,3.27-9.20,P < 0.0001)与移植物失功风险增加仍密切相关。代谢综合征、NODAT 和 CHD 是移植物失功的危险因素。NODAT 和 CHD 是移植物失功的危险因素,独立于代谢综合征。