Association of trimethylamineN-Oxide with cardiovascular and all-cause mortality in hemodialysis patients

被引:21
|
作者
Zhang, Pan [1 ,2 ,3 ,4 ,5 ]
Zou, Jian-Zhou [1 ,2 ,3 ,4 ,5 ]
Chen, Jun [6 ]
Tan, Xiao [1 ,2 ,3 ,4 ,5 ]
Xiang, Fang-Fang [1 ,2 ,3 ,4 ,5 ]
Shen, Bo [1 ,2 ,3 ,4 ,5 ]
Hu, Jia-Chang [1 ,2 ,3 ,4 ,5 ]
Wang, Jia-Lin [1 ,2 ,3 ,4 ,5 ]
Wang, Ya-Qiong [1 ,2 ,3 ,4 ,5 ]
Yu, Jin-Bo [1 ,2 ,3 ,4 ,5 ]
Nie, Yu-Xin [1 ,2 ,3 ,4 ,5 ]
Chen, Xiao-Hong [1 ,2 ,3 ,4 ,5 ]
Yu, Jia-Wei [1 ,2 ,3 ,4 ,5 ]
Zhang, Zhen [1 ,2 ,3 ,4 ,5 ]
Lv, Wen-Lv [1 ,2 ,3 ,4 ,5 ]
Xie, Ye-Qing [1 ,2 ,3 ,4 ,5 ]
Cao, Xue-Sen [1 ,2 ,3 ,4 ,5 ]
Ding, Xiao-Qiang [1 ,2 ,3 ,4 ,5 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Nephrol, Shanghai, Peoples R China
[2] Hemodialysis Qual Control Ctr Shanghai, Shanghai, Peoples R China
[3] Shanghai Key Lab Kidney & Blood Purificat, Shanghai, Peoples R China
[4] Shanghai Inst Kidney & Dialysis, Shanghai, Peoples R China
[5] Shanghai Clin Med Ctr Kidney Dis, Shanghai, Peoples R China
[6] Fudan Univ, Sch Pharm, Dept Pharmaceut, Shanghai, Peoples R China
关键词
Uremic toxins; trimethylamine N-oxide; cardiovascular mortality; all-cause mortality; hemodialysis; P-CRESYL SULFATE; N-OXIDE; INDOXYL SULFATE; UREMIC TOXICITY; DISEASE; INFLAMMATION; RISK; ATHEROSCLEROSIS; METABOLISM; PHOSPHATIDYLCHOLINE;
D O I
10.1080/0886022X.2020.1822868
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Trimethylamine-N-Oxide (TMAO) is a proatherogenic and prothrombotic metabolite. Our study examined the association of plasma TMAO level with cardiovascular and all-cause mortality in hemodialysis (HD) patients. Methods Patients who were at least 18 years-old and received HD for at least 6 months were enrolled within 6 months. Patients with coronary heart disease, congestive heart failure, arrhythmia, or stroke within 3 months before study onset were excluded. The primary endpoints were cardiovascular and all-cause death, and the secondary endpoint was cerebrovascular death. Results We recruited 252 patients and divided them into a high-TMAO group (>4.73 mu g/mL) and a low-TMAO group (<= 4.73 mu g/mL). The median follow-up time was 73.4 months (interquartile range: 42.9, 108). A total of 123 patients died, 39 from cardiovascular disease, 19 from cerebrovascular disease, and 65 from other causes. Kaplan-Meier analysis indicated that the high-TMAO group had a greater incidence of cardiovascular death (Log-Rank:p = 0.006) and all-cause death (Log-Rank:p < 0.001). Cox regression analysis showed that high TMAO level was significantly associated with cardiovascular and all-cause mortality. After adjustment for confounding, this association remained significant for cardiovascular mortality (TMAO as a continuous variable: HR: 1.18, 95%CI: 1.07, 1.294,p < 0.001; TMAO as a dichotomous variable: HR: 3.44, 95%CI: 1.68, 7.08,p < 0.001) and all-cause mortality (TMAO as a continuous variable: HR: 1.14, 95%CI: 1.08, 1.21,p < 0.001; TMAO as a dichotomous variable: HR: 2.54, 95%CI: 1.71, 3.76,p < 0.001). Conclusions High plasma TMAO level is significantly and independently associated with cardiovascular and all-cause mortality in HD patients.
引用
收藏
页码:1004 / 1014
页数:11
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