Cyril Ruwende
University of Michigan
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Atherosclerosis | 2010
Erdal Cavusoglu; Cyril Ruwende; Vineet Chopra; Shyam Poludasu; Sunitha Yanamadala; William H. Frishman; Calvin Eng; David J. Pinsky; Jonathan D. Marmur
BACKGROUND Patients with diabetes mellitus (DM) have been shown to have higher levels of asymmetric dimethylarginine (ADMA), an endogenous inhibitor of endothelial nitric oxide (NO) synthase. Higher plasma levels of ADMA have been implicated in the pathogenesis of endothelial dysfunction and atherosclerosis by lowering NO levels. High baseline plasma levels of ADMA in patients with DM have been shown to predict diabetes related complications. However, there are limited data on the prognostic significance of baseline ADMA levels in patients with established DM. METHODS The present study investigated the long-term prognostic significance of baseline plasma ADMA levels in a well-characterized cohort of 170 high-risk diabetic men with known or suspected coronary artery disease who were referred for coronary angiography. All patients were followed prospectively for the development of vascular outcomes, including all-cause mortality. RESULTS After controlling for a variety of baseline variables (including established biomarkers such as hs-CRP and fibrinogen), plasma ADMA levels (analyzed as the upper tertile of baseline values compared with the lower two tertiles) were a strong and independent predictor of all-cause mortality (HR 2.63, 95% CI 1.13-6.11, p=0.0247) when using a Cox proportional hazards model. In addition, baseline ADMA values were also an independent predictor of the composite outcome of all-cause mortality or MI (fatal or non-fatal) (HR 2.44, 95% CI 1.26-4.72, p=0.0079), as well as the composite outcome of all-cause mortality, MI (fatal or nonfatal), or stroke (HR 2.00, 95% CI 1.10-3.62, p=0.0232). CONCLUSION These data demonstrate that elevated baseline levels of ADMA are a strong and independent predictor of cardiovascular outcomes (including all-cause mortality) in patients with DM.
The American Journal of Medicine | 2011
Erdal Cavusoglu; Jonathan D. Marmur; Mohammad R. Hojjati; Vineet Chopra; Mitul Butala; Rakesh Subnani; Mohammad S. Huda; Sunitha Yanamadala; Cyril Ruwende; Calvin Eng; David J. Pinsky
UNLABELLED PURPOSE OR BACKGROUND: Interleukin (IL)-10 is an immunoregulatory cytokine that is produced by a variety of cell types, such as macrophages and activated monocytes. IL-10 possesses numerous anti-inflammatory, anti-thrombotic and anti-atherosclerotic properties. Furthermore, patients with acute coronary syndrome have been demonstrated to have reduced levels of IL-10 compared to their stable counterparts. For these reasons, it has been proposed that IL-10 plays a protective role in both atherogenesis and plaque vulnerability. However, 2 short-term studies on the prognostic utility of IL-10 in patients with acute coronary syndrome have provided conflicting results, with one study showing that reduced levels of IL-10 were predictors of adverse outcomes and another showing that elevated levels predicted poor outcomes. The objective of the present study was to investigate the long-term prognostic significance of baseline IL-10 levels in patients with acute coronary syndrome. METHODS Baseline plasma IL-10 levels were measured in 193 well-characterized male patients with acute coronary syndrome who were referred for coronary angiography and followed prospectively for 5 years for the development of major adverse cardiovascular events. RESULTS After controlling for a variety of baseline variables (including established biomarkers such as high-sensitivity C-reactive protein and N-terminal-pro-B-type natriuretic peptide), plasma IL-10 levels (whether analyzed as a continuous variable or as a categorical variable using receiver operating characteristic-derived cut point) were a strong and independent predictor of the composite outcome of death or non-fatal myocardial infarction when using a Cox proportional hazards model. CONCLUSIONS These data demonstrate that, despite biologic plausibility for IL-10 as being a cardioprotective cytokine, elevated baseline plasma levels of IL-10 are a strong and independent predictor of long-term adverse cardiovascular outcomes in patients with acute coronary syndrome.
Coronary Artery Disease | 2009
Erdal Cavusoglu; Cyril Ruwende; Vineet Chopra; Sunitha Yanamadala; Calvin Eng; David J. Pinsky; Jonathan D. Marmur
BackgroundNitric oxide (NO) is produced from L-arginine by NO synthase and is an important molecule with antiatherogenic properties. Asymmetric dimethylarginine (ADMA) acts as an endogenous inhibitor of endothelial NO synthase. As such, it has been associated with endothelial dysfunction and elevated circulating levels of ADMA have been found in patients with cardiovascular risk factors. In addition, high baseline plasma levels of ADMA have been shown to be an independent predictor of adverse outcomes in a variety of patient populations. However, there are very limited data in patients with acute coronary syndromes (ACS). MethodsThis study investigated the long-term prognostic significance of baseline plasma ADMA levels in a well-characterized cohort of 193 men with ACS who were referred for coronary angiography. All patients were followed up prospectively for the development of vascular outcomes. ResultsAfter controlling for a variety of baseline variables (including established biomarkers such as high-sensitivity C-reactive protein and fibrinogen), plasma ADMA levels (analyzed as the upper tertile of baseline values compared with the lower two tertiles) were a strong and independent predictor of each of the individual endpoints of all-cause mortality [hazard ratio (HR): 2.45, 95% confidence interval (CI): 1.08–5.57; P=0.0325] and myocardial infarction (HR: 2.28, 95% CI: 1.14–4.57; P=0.0204) when using a Cox proportional hazards model. In addition, baseline ADMA values were also an independent predictor of the composite outcome of all-cause mortality, fatal or nonfatal myocardial infarction, or stroke (HR: 1.81, 95% CI: 1.01–3.25; P=0.0482). ConclusionThese data show that elevated baseline levels of ADMA are a strong and independent predictor of cardiovascular outcomes (including mortality) in patients with ACS.
American Journal of Cardiology | 2008
Erdal Cavusoglu; Vineet Chopra; Venkata Battala; Cyril Ruwende; Sunitha Yanamadala; Calvin Eng; David J. Pinsky; Jonathan D. Marmur
The objective of the present study was to determine the association between plasma adiponectin and left ventricular (LV) systolic function. Baseline plasma adiponectin was measured in 389 patients undergoing coronary angiography for a variety of indications at a Veterans Affairs Medical Center. Detailed demographic, clinical, laboratory, and angiographic data were available for patients. LV systolic function was assessed using ventriculography, and patients were grouped into those with normal or mild dysfunction (ejection fraction > or =45%) versus those with moderate to severe systolic dysfunction (ejection fraction <45%). After adjusting for a variety of clinically relevant covariates known to affect LV systolic function, adiponectin was independently associated with LV systolic function in the entire cohort of patients (p = 0.0002) using multivariate linear regression analysis. In addition, using multivariate logistic regression analysis, adiponectin was an independent predictor of the presence of moderate to severe LV dysfunction (odds ratio 1.54, 95% confidence interval 1.21 to 1.97, p = 0.0005). Moreover, baseline adiponectin was also independently associated with LV function in both the myocardial infarction (MI) and non-MI subpopulations of patients (p = 0.0401 and p= 0.0023, respectively). Finally, in the non-MI subpopulation, baseline adiponectin was an independent predictor of moderate to severe LV systolic dysfunction (odds ratio 1.52, 95% confidence interval 1.15 to 2.02, p = 0.0034). In conclusion, baseline plasma adiponectin was an independent predictor of LV systolic dysfunction in a population of patients referred for coronary angiography.
American Journal of Hypertension | 2009
Erdal Cavusoglu; Vineet Chopra; Amit Gupta; Palak U. Choksi; Cyril Ruwende; Sunitha Yanamadala; William H. Frishman; David J. Pinsky; Jonathan D. Marmur
BACKGROUND In experimental animal studies, potassium has been demonstrated to protect against the development of atherosclerosis through a variety of mechanisms. Data regarding the role of potassium in the development of human atherosclerosis are sparse. The objective of this study was to determine the association between plasma potassium levels and angiographically defined coronary artery disease (CAD). METHODS In a cohort of 389 male patients undergoing coronary angiography for a variety of clinical indications, the association between baseline serum potassium levels and the extent of angiographically defined atherosclerosis was analyzed. Adjustments were made for clinical and laboratory variables (including inflammatory markers) known to be associated with atherosclerosis. RESULTS By multivariate logistic regression analysis, baseline serum potassium levels were an independent predictor of the presence of multivessel disease (odds ratio (OR) 1.31, 95% confidence interval (CI) 1.01-1.69; P < 0.05). In addition, in the non-myocardial infarction subpopulation of patients, serum potassium was also an independent predictor of the presence of multivessel disease by multivariate logistic regression analysis (OR 1.34, 95% CI, 1.02-1.76; P < 0.05). In the myocardial infarction (MI) subpopulation, serum potassium was not a predictor of multivessel disease, possibly due to the confounding effect of hypokalemia known to be present during MI. CONCLUSIONS These data demonstrate that a simple baseline serum potassium level is independently associated with the presence of multivessel disease, even in the context of clinical CAD risk factors and other established inflammatory markers.
Journal of the American College of Cardiology | 2015
Nadia R. Sutton; Milan Seth; Cyril Ruwende; Hitinder S. Gurm
Results: A history of AF was present in 10,760 patients (12%). Patients with AF were older (72 vs. 64 years) and more likely to have chronic lung disease (28% vs. 18%) and congestive heart failure (38% vs. 13%). Patients with AF were more likely to be treated with a bare metal stent (28% vs. 17%) or balloon angioplasty only (12% vs. 10%). Patients with AF were also more likely to have in-hospital complications or die (3% vs. 1%). In risk adjusted matched analysis, the presence of AF was associated with an increased risk of requiring blood transfusion, bleeding, development of cardiogenic shock, and in-hospital mortality (figure). No difference was seen in risk of requiring dialysis after PCI.
European Heart Journal | 2006
Erdal Cavusoglu; Cyril Ruwende; Vineet Chopra; Sunitha Yanamadala; Calvin Eng; Luther T. Clark; David J. Pinsky; Jonathan D. Marmur
American Heart Journal | 2006
Erdal Cavusoglu; Cyril Ruwende; Vineet Chopra; Sunitha Yanamadala; Calvin Eng; Luther T. Clark; David J. Pinsky; Jonathan D. Marmur
American Journal of Cardiology | 2007
Erdal Cavusoglu; Cyril Ruwende; Calvin Eng; Vineet Chopra; Sunitha Yanamadala; Luther T. Clark; David J. Pinsky; Jonathan D. Marmur
Journal of the American College of Cardiology | 2007
Erdal Cavusoglu; Elizabeth Kornecki; Malgorzata B. Sobocka; Anna Babinska; Yigal H. Ehrlich; Vineet Chopra; Sunitha Yanamadala; Cyril Ruwende; Moro O. Salifu; Luther T. Clark; Calvin Eng; David J. Pinsky; Jonathan D. Marmur