Serum Asymmetric and Symmetric Dimethylarginine and Morbidity and Mortality in Hemodialysis Patients

被引:27
作者
Shafi, Tariq [1 ,2 ]
Hostetter, Thomas H. [3 ]
Meyer, Timothy W. [4 ,5 ]
Hwang, Seungyoung [1 ]
Hai, Xin [3 ]
Melamed, Michal L. [6 ,7 ]
Banerjee, Tanushree [8 ]
Coresh, Josef [1 ,2 ,9 ,10 ]
Powe, Neil R. [8 ]
机构
[1] Johns Hopkins Univ, Dept Med, 301 Mason Lord Dr,Ste 2500, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Welch Ctr Prevent Epidemiol & Clin Res, 301 Mason Lord Dr,Ste 2500, Baltimore, MD 21224 USA
[3] Case Western Univ, Sch Med, Dept Med, Cleveland, OH USA
[4] Palo Alto Vet Affairs Hlth Care Syst, Dept Med, Palo Alto, CA USA
[5] Stanford Univ, Palo Alto, CA 94304 USA
[6] Albert Einstein Coll Med, Dept Med, Bronx, NY USA
[7] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[8] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[9] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[10] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
Cardiovascular mortality; dialysis outcomes; asymmetric dimethylarginine (ADMA); symmetric dimethylarginine (SDMA); hemodialysis; end-stage renal disease (ESRD); uremic toxins; cardiovascular morbidity; cardiac death; sudden cardiac death; CARDIOVASCULAR RISK-FACTOR; STAGE RENAL-DISEASE; ALL-CAUSE MORTALITY; NITRIC-OXIDE; L-ARGININE; ONLINE HEMODIAFILTRATION; ENDOGENOUS INHIBITOR; GUANIDINO COMPOUNDS; ADMA; DEATH;
D O I
10.1053/j.ajkd.2016.10.033
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: Asymmetric (ADMA) and symmetric dimethylarginine (SDMA) are putative uremic toxins that may exert toxicity by a number of mechanisms, including impaired nitric oxide synthesis and generation of reactive oxygen species. The study goal was to determine the association between these metabolites and cardiovascular outcomes in hemodialysis patients. Study Design: Post hoc analysis of the Hemodialysis (HEMO) Study. Setting & Participants: 1,276 prevalent hemodialysis patients with available samples 3 to 6 months after randomization. Predictor: ADMA and SDMA measured in stored specimens. Outcomes: Cardiac death, sudden cardiac death, first cardiovascular event, and any-cause death. Association with predictors analyzed using Cox regression adjusted for potential confounders (including demographics, clinical characteristics, comorbid conditions, albumin level, and residual kidney function). Results: Mean age of patients was 57 +/- 14 (SD) years, 63% were black, and 57% were women. Mean ADMA (0.9 +/- 0.2 mmol/L) and SDMA levels (4.3 +/- 1.4 mu mol/L) were moderately correlated (r = 0.418). Higher dialysis dose or longer session length were not associated with lower predialysis ADMA or SDMA concentrations. In fully adjusted models, each doubling of ADMA level was associated with higher risk (HR per 2-fold higher concentration; 95% CI) of cardiac death (1.83; 1.29-2.58), sudden cardiac death (1.79; 1.19-2.69), first cardiovascular event (1.50; 1.20-1.87), and any-cause death (1.44; 1.13-1.83). Compared to the lowest ADMA quintile (<0.745 mu mol/L), the highest ADMA quintile (>= 1.07 mu mol/L) was associated with higher risk (HR; 95% CI) of cardiac death (2.10; 1.44-3.05), sudden cardiac death (2.06; 1.46-2.90), first cardiovascular event (1.75; 1.35-2.27), and any-cause death (1.56; 1.21-2.00). SDMA level was associated with higher risk for cardiac death (HR, 1.40; 95% CI, 1.03-1.92), but this was no longer statistically significant after adjusting for ADMA level (HR, 1.20; 95% CI, 0.86-1.68). Limitations: Single time-point measurement of ADMA and SDMA. Conclusions: ADMA and, to a lesser extent, SDMA levels are associated with cardiovascular outcomes in hemodialysis patients. (C) 2016 by the National Kidney Foundation, Inc.
引用
收藏
页码:48 / 58
页数:11
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