Association between oxidative stress and atrial fibrillation.
Association between oxidative stress and atrial fibrillation.
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DOI:
10.1016/j.hrthm.2017.07.028
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发表时间:
2017-12
期刊:
影响因子:
5.5
通讯作者:
Quyyumi AA
中科院分区:
文献类型:
--
作者:
Samman Tahhan A;Sandesara PB;Hayek SS;Alkhoder A;Chivukula K;Hammadah M;Mohamed-Kelli H;O'Neal WT;Topel M;Ghasemzadeh N;Ko YA;Aida H;Gafeer M;Sperling L;Vaccarino V;Liang Y;Jones DP;Quyyumi AA
Oxidative stress (OS) may be a key mechanism underlying the development of atrial fibrillation (AF) in experimental studies, but data in humans remain limited. Systemic OS can be estimated by measurements of circulating levels of the aminothiols including glutathione, cysteine, and their oxidized products. We tested the hypothesis that the redox potentials of glutathione (EhGSH) and cysteine will be associated with prevalent and incident AF. Plasma levels of aminothiols were measured in 1439 patients undergoing coronary angiography, of whom 148 (10.3%) had a diagnosis of AF. After a median follow-up of 6.3 years, 104 of 917 patients (11.5%) developed incident AF. Multivariate logistic regression and Cox regression models were used to determine whether OS markers were independent predictors of prevalent and incident AF after adjustment for traditional risk factors, heart failure, coronary artery disease, and high-sensitivity C-reactive protein level. For each 10% increase in EhGSH, the odds of prevalent AF was 30% higher (odds ratio [OR] 1.3; 95% confidence interval [CI] 1.1–1.7; P = .02) and 90% higher (OR 1.9; 95% CI 1.3–2.7; P = .004) when the median was used as a cutoff. The EhGSH level above the median was more predictive of chronic AF (OR 4.0; 95% CI 1.3– 12.9; P = .01) than of paroxysmal AF (OR 1.7; 95% CI 1.1–2.7; P = .03). Each 10% increase in EhGSH level was associated with a 40% increase in the risk of incident AF (hazard ratio 1.4; 95% CI 1.1– 1.7; P = .01). Increased OS measured by the redox potentials of glutathione is associated with prevalent and incident AF. Therapies that modulate OS need to be investigated to treat and prevent AF.
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37.8
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Patel RS;Ghasemzadeh N;Eapen DJ;Sher S;Arshad S;Ko YA;Veledar E;Samady H;Zafari AM;Sperling L;Vaccarino V;Jones DP;Quyyumi AA
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影响因子:
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