Fussner Lynn A, Heimbach Julie K, Fan Chun, Dierkhising Ross, Coss Elizabeth, Leise Michael D, Watt Kymberly D
Department of Internal Medicine, Transplant Center, Mayo Clinic, Rochester, MN.
Surgery, Transplant Center, Mayo Clinic, Rochester, MN.
Liver Transpl. 2015 Jul;21(7):889-96. doi: 10.1002/lt.24137.
The evolution of metabolic and cardiovascular disease (CVD) complications after liver transplantation (LT) is poorly characterized. We aim to illustrate the prevalence of obesity and metabolic syndrome (MS), define the cumulative incidence of CVD, and characterize risk factors associated with these comorbidities after LT. A retrospective review of 455 consecutive LT recipients from 1999 to 2004 with an 8- to 12-year follow-up was performed. Obesity increased from 23.8% (4 months) to 40.8% (3 years) after LT. Increase in body mass index predicted MS at 1 year after LT (odds ratio, 1.1; P < 0.001, per point). CVD developed in 10.6%, 20.7%, and 30.3% of recipients within 1, 5, and 8 years, respectively. Age, diabetes, hypertension, glomerular filtration rate < 60 mL/minute, prior CVD, ejection fraction < 60%, left ventricular hypertrophy, and serum troponin (TN) > 0.07 ng/mL were associated with CVD on univariate analysis. Age (hazard ratio [HR], 1.03; 95% confidence interval [CI], 1.01-1.06; P = 0.019), diabetes (HR, 1.78; 95% CI, 1.09-2.92; P = 0.022), prior history of CVD (HR, 2.46; 95% CI, 1.45-4.16; P < 0.001), and serum TN > 0.07 ng/mL (HR, 1.98; 95% CI, 1.23-3.18; P = 0.005) were independently associated with CVD in the long term. Smoking history (ever), sex, hyperlipidemia, and serum ferritin levels were not predictive of CVD. Tacrolimus use versus noncalcineurin-based immunosuppression (HR, 0.26; 95% CI, 0.14-0.49; P < 0.001) was associated with reduced risk of CVD but not versus cyclosporine (HR, 0.67; 95% CI, 0.30-1.49; P = 0.322). CVD is common after LT. Independent of MS, more data are needed to identify nonconventional risk factors and biomarkers like serum TN. Curbing weight gain in the early months after transplant may impact MS and subsequent CVD in the long term.
肝移植(LT)后代谢和心血管疾病(CVD)并发症的演变情况目前尚不清楚。我们旨在阐明肥胖和代谢综合征(MS)的患病率,确定CVD的累积发病率,并描述LT后与这些合并症相关的危险因素。对1999年至2004年连续455例LT受者进行回顾性研究,并进行8至12年的随访。LT后肥胖率从23.8%(4个月)增至40.8%(3年)。体重指数增加可预测LT后1年发生MS(优势比为1.1;每增加1个单位,P<0.001)。分别有10.6%、20.7%和30.3%的受者在1年、5年和8年内发生CVD。单因素分析显示,年龄、糖尿病、高血压、肾小球滤过率<60 mL/分钟、既往CVD、射血分数<60%、左心室肥厚和血清肌钙蛋白(TN)>0.07 ng/mL与CVD相关。长期来看,年龄(风险比[HR]为1.03;95%置信区间[CI]为1.01-1.06;P=0.019)、糖尿病(HR为1.78;95%CI为1.09-2.92;P=0.022)、既往CVD病史(HR为2.46;95%CI为1.45-4.16;P<0.001)和血清TN>0.07 ng/mL(HR为1.98;95%CI为1.23-3.18;P=0.005)与CVD独立相关。吸烟史(曾经吸烟)、性别、高脂血症和血清铁蛋白水平不能预测CVD。使用他克莫司与非钙调神经磷酸酶抑制剂免疫抑制相比(HR为0.26;95%CI为0.14-0.49;P<0.001)与CVD风险降低相关,但与环孢素相比无此关联(HR为0.67;95%CI为0.30-1.49;P=0.322)。LT后CVD很常见。除MS外,还需要更多数据来确定非传统危险因素和生物标志物,如血清TN。在移植后的最初几个月控制体重增加可能会对长期的MS和随后的CVD产生影响。