The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X.
The pathophysiology of cardiac syndrome X is multifactorial and endothelial dysfunction has been implicated as important contributing factor. Asymmetric dimethylarginine (ADMA), characterized as a circulating endogenous inhibitor of nitric oxide synthase, may have been implicated as an important con...
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doaj-da7970fd26c24c988fca302a4f51533e2020-11-24T22:17:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011212e018899510.1371/journal.pone.0188995The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X.Tse-Min LuTzong-Shyuan LeeShing-Jong LinWan-Leong ChanChiao-Po HsuThe pathophysiology of cardiac syndrome X is multifactorial and endothelial dysfunction has been implicated as important contributing factor. Asymmetric dimethylarginine (ADMA), characterized as a circulating endogenous inhibitor of nitric oxide synthase, may have been implicated as an important contributing factor for the development of endothelial dysfunction. In this study, we aim to assess the predictive power of ADMA for long-term prognosis in patients with cardiac syndrome X.We enrolled 239 consecutive patients with cardiac syndrome X diagnosed by coronary angiography. The mean age was 58.7±10.1 years. The patients were grouped into tertiles according to the plasma ADMA levels: <0.38 μmol/l (tertile I), 0.38-0.44 μmol/l (tertile II), and >0.44 μmol/l (tertile III). All patients were followed up for a mean period of 6.5±1.5 years (median: 6.3 years, inter-quartile range: 5.7-8.0 years). During the follow-up period, major adverse events (MAE) were observed in 15 patients (6.3%), including 13 deaths. The plasma ADMA levels in patients who developed MAE were significantly higher than those who did not (0.48±0.06 μmol/l vs. 0.42±0.08 μmol/l, p = 0.005). In multivariate Cox regression analysis adjusted for age, eGFR and LVEF, ADMA tertile I and II were identify to be associated with a significantly lower risk of MAE compared to ADMA tertile III (p = 0.017). By considering the plasma ADMA level as a continuous variable, the plasma ADMA level remained a significant independent predictor for outcomes of MAE, and the relative risk of MACE increased by 50% when plasma ADMA level increased by 1 SD of value (p = 0.018).In patients with cardiac syndrome X, elevated plasma ADMA levels appeared to be an independent predictor of long-term adverse clinical outcomes.http://europepmc.org/articles/PMC5716529?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tse-Min Lu Tzong-Shyuan Lee Shing-Jong Lin Wan-Leong Chan Chiao-Po Hsu |
spellingShingle |
Tse-Min Lu Tzong-Shyuan Lee Shing-Jong Lin Wan-Leong Chan Chiao-Po Hsu The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X. PLoS ONE |
author_facet |
Tse-Min Lu Tzong-Shyuan Lee Shing-Jong Lin Wan-Leong Chan Chiao-Po Hsu |
author_sort |
Tse-Min Lu |
title |
The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X. |
title_short |
The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X. |
title_full |
The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X. |
title_fullStr |
The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X. |
title_full_unstemmed |
The prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome X. |
title_sort |
prognostic value of asymmetric dimethylarginine in patients with cardiac syndrome x. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2017-01-01 |
description |
The pathophysiology of cardiac syndrome X is multifactorial and endothelial dysfunction has been implicated as important contributing factor. Asymmetric dimethylarginine (ADMA), characterized as a circulating endogenous inhibitor of nitric oxide synthase, may have been implicated as an important contributing factor for the development of endothelial dysfunction. In this study, we aim to assess the predictive power of ADMA for long-term prognosis in patients with cardiac syndrome X.We enrolled 239 consecutive patients with cardiac syndrome X diagnosed by coronary angiography. The mean age was 58.7±10.1 years. The patients were grouped into tertiles according to the plasma ADMA levels: <0.38 μmol/l (tertile I), 0.38-0.44 μmol/l (tertile II), and >0.44 μmol/l (tertile III). All patients were followed up for a mean period of 6.5±1.5 years (median: 6.3 years, inter-quartile range: 5.7-8.0 years). During the follow-up period, major adverse events (MAE) were observed in 15 patients (6.3%), including 13 deaths. The plasma ADMA levels in patients who developed MAE were significantly higher than those who did not (0.48±0.06 μmol/l vs. 0.42±0.08 μmol/l, p = 0.005). In multivariate Cox regression analysis adjusted for age, eGFR and LVEF, ADMA tertile I and II were identify to be associated with a significantly lower risk of MAE compared to ADMA tertile III (p = 0.017). By considering the plasma ADMA level as a continuous variable, the plasma ADMA level remained a significant independent predictor for outcomes of MAE, and the relative risk of MACE increased by 50% when plasma ADMA level increased by 1 SD of value (p = 0.018).In patients with cardiac syndrome X, elevated plasma ADMA levels appeared to be an independent predictor of long-term adverse clinical outcomes. |
url |
http://europepmc.org/articles/PMC5716529?pdf=render |
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