Park Woo Yeong, Koh Eun Sil, Kim Su-Hyun, Kim Young Ok, Jin Dong Chan, Song Ho Chul, Choi Euy Jin, Kim Yong-Lim, Kim Yon-Su, Kang Shin-Wook, Kim Nam-Ho, Yang Chul Woo, Kim Yong Kyun
Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Internal Medicine, College of Medicine, Chung-Ang University, Seoul, Korea.
PLoS One. 2015 Sep 16;10(9):e0138159. doi: 10.1371/journal.pone.0138159. eCollection 2015.
Gamma-glutamyltransferase (GGT) is a biomarker of liver injury. GGT has also been reported to be a marker of oxidative stress and a predictor of mortality in the general population. Hemodialysis (HD) patients suffer from oxidative stress. The aim of our study was to investigate the relationship between serum GGT levels and clinical outcomes in HD patients.
A total of 1,634 HD patients were enrolled from the Clinical Research Center registry for end-stage renal disease, a prospective cohort in Korea. Patients were categorized into three groups by tertiles of serum GGT levels. The primary outcome was all-cause, cardiovascular, or infection-related mortality and hospitalization.
During the median follow-up period of 30 months, the highest tertile of serum GGT levels had a significantly higher risk for all-cause mortality (hazard ratio (HR) 2.39, 95% confidence interval (CI), 1.55-3.69, P<0.001), cardiovascular mortality (HR 2.14, 95% CI, 1.07-4.26, P = 0.031) and infection-related mortality (HR 3.07, 95% CI, 1.30-7.25, P = 0.011) using tertile 1 as the reference group after adjusting for clinical variables including liver diseases. The highest tertile also had a significantly higher risk for first hospitalization (HR 1.22, 95% CI, 1.00-1.48, P = 0.048) and cardiovascular hospitalization (HR 1.42, 95% CI, 1.06-1.92, P = 0.028).
Our data demonstrate that high serum GGT levels were an independent risk factor for all-cause, cardiovascular, and infection-related mortality, as well as cardiovascular hospitalization in HD patients. These findings suggest that serum GGT levels might be a useful biomarker to predict clinical outcomes in HD patients.
γ-谷氨酰转移酶(GGT)是肝损伤的生物标志物。据报道,GGT也是氧化应激的标志物和普通人群死亡率的预测指标。血液透析(HD)患者存在氧化应激。我们研究的目的是探讨HD患者血清GGT水平与临床结局之间的关系。
从韩国一个前瞻性队列——终末期肾病临床研究中心登记处招募了总共1634例HD患者。根据血清GGT水平的三分位数将患者分为三组。主要结局是全因、心血管或感染相关的死亡率及住院率。
在30个月的中位随访期内,以第一三分位数为参照组,在对包括肝脏疾病在内的临床变量进行校正后,血清GGT水平最高的三分位数组全因死亡率(风险比(HR)2.39,95%置信区间(CI),1.55 - 3.69,P<0.001)、心血管死亡率(HR 2.14,95%CI,1.07 - 4.26,P = 0.031)和感染相关死亡率(HR 3.07,95%CI,1.30 - 7.25,P = 0.011)的风险显著更高。血清GGT水平最高的三分位数组首次住院(HR 1.22,95%CI,1.00 - 1.48,P = 0.048)和心血管住院(HR 1.42,95%CI,1.06 - 1.92,P = 0.028)的风险也显著更高。
我们的数据表明,高血清GGT水平是HD患者全因、心血管和感染相关死亡率以及心血管住院的独立危险因素。这些发现提示血清GGT水平可能是预测HD患者临床结局的有用生物标志物。