3 results on '"Celia Maria Cassaro Strunz"'
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2. Troponin in diabetic patients with and without chronic coronary artery disease
- Author
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Whady Hueb, Carlos Alexandre Segre, Roberto Kalil Filho, Alessandra Roggério, Ana Luiza de Oliveira Carvalho, José Antonio Franchini Ramires, Rosa Maria Rahmi Garcia, Desiderio Favarato, Marília da Costa Oliveira Sprandel, Raul C. Maranhão, Paulo Cury Rezende, and Celia Maria Cassaro Strunz
- Subjects
Male ,medicine.medical_specialty ,medicine.drug_class ,Coronary Artery Disease ,Coronary artery disease ,Troponin C ,Diabetes mellitus ,Risk Factors ,Internal medicine ,Natriuretic Peptide, Brain ,medicine ,Natriuretic peptide ,Humans ,Aged ,Peroxidase ,Angiology ,Biological markers ,biology ,business.industry ,Case-control study ,Cholesterol, LDL ,Middle Aged ,medicine.disease ,Troponin ,Cardiac surgery ,DOENÇAS CARDIOVASCULARES ,Diabetes Mellitus, Type 2 ,Case-Control Studies ,Cardiology ,biology.protein ,Tyrosine ,Female ,Cardiology and Cardiovascular Medicine ,business ,Oxidation-Reduction ,Biomarkers ,Research Article - Abstract
Background Cardiac-specific troponin detected with the new high-sensitivity assays can be chronically elevated in response to cardiovascular comorbidities and confer important prognostic information, in the absence of unstable coronary syndromes. Both diabetes mellitus and coronary artery disease are known predictors of troponin elevation. It is not known whether diabetic patients with coronary artery disease have different levels of troponin compared with diabetic patients with normal coronary arteries. To investigate this question, we determined the concentrations of a level 1 troponin assay in two groups of diabetic patients: those with multivessel coronary artery disease and those with angiographically normal coronary arteries. Methods We studied 95 diabetic patients and compared troponin in serum samples from 50 patients with coronary artery disease (mean age = 63.7, 58 % male) with 45 controls with angiographically normal coronary arteries. Brain natriuretic peptide and the oxidative stress biomarkers myeloperoxidase, nitrotyrosine and oxidized LDL were also determined. Results Diabetic patients with coronary artery disease had higher levels of troponin than did controls (median values, 12.0 pg/mL (95 % CI:10–16) vs 7.0 pg/mL (95 % CI: 5.9-8.5), respectively; p = 0.0001). The area under the ROC curve for the diagnosis of CAD was 0.712 with a sensitivity of 70 % and a specificity of 66 %. Plasma BNP levels and oxidative stress variables (myeloperoxidase, nitrotyrosine, and oxidized LDL) were not different between the two groups. In a multivariate analysis, gender (p = 0.04), serum glucose (0.03) and Troponin I (p = 0.01) had independent statistical significance. Conclusion Troponin elevation is related to the presence of chronic coronary artery disease in diabetic patients with multiple associated cardiovascular risk factors. Troponin may serve as a biomarker in this high-risk population. Trial registration http://www.controlled-trials.com Registration number:ISRCTN26970041
- Published
- 2015
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3. Hypotheses, rationale, design, and methods for prognostic evaluation in type 2 diabetic patients with angiographically normal coronary arteries. The MASS IV-DM Trial
- Author
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Pedro A. Lemos, Raul C. Maranhão, Paulo R. Soares, José R. Parga, Eduardo Gomes Lima, Alexandre C. Pereira, Claudio Meneguetti, Ricardo D'Oliveira Vieira, Whady Hueb, Cibele Larrosa Garzillo, Augusto Ushida, Jeane M. Tsutsui, Alexandre Ciappina Hueb, Bernard J. Gersh, Celia Maria Cassaro Strunz, José A. F. Ramires, Rosa Rhami Garcia, Neuza Lopes, and Dalton de Alencar Fischer Chamone
- Subjects
medicine.medical_specialty ,lcsh:Diseases of the circulatory (Cardiovascular) system ,Type 2 diabetes ,Coronary Artery Disease ,Coronary Angiography ,Kidney ,Coronary artery disease ,Study Protocol ,Internal medicine ,medicine ,Humans ,Genetic Predisposition to Disease ,Platelet activation ,Coronary atherosclerosis ,Angiology ,Macrovascular disease ,Ultrasonography ,Inflammation ,Metabolic Syndrome ,Polymorphism, Genetic ,business.industry ,Thrombosis ,medicine.disease ,Prognosis ,Coronary Vessels ,Coronary arteries ,Oxidative Stress ,medicine.anatomical_structure ,Diabetes Mellitus, Type 2 ,lcsh:RC666-701 ,Research Design ,Cardiology ,Arterial stiffness ,business ,Cardiology and Cardiovascular Medicine ,Follow-Up Studies - Abstract
Background The MASS IV-DM Trial is a large project from a single institution, the Heart Institute (InCor), University of São Paulo Medical School, Brazil to study ventricular function and coronary arteries in patients with type 2 diabetes mellitus. Methods/Design The study will enroll 600 patients with type 2 diabetes who have angiographically normal ventricular function and coronary arteries. The goal of the MASS IV-DM Trial is to achieve a long-term evaluation of the development of coronary atherosclerosis by using angiograms and coronary-artery calcium scan by electron-beam computed tomography at baseline and after 5 years of follow-up. In addition, the incidence of major cardiovascular events, the dysfunction of various organs involved in this disease, particularly microalbuminuria and renal function, will be analyzed through clinical evaluation. In addition, an effort will be made to investigate in depth the presence of major cardiovascular risk factors, especially the biochemical profile, metabolic syndrome inflammatory activity, oxidative stress, endothelial function, prothrombotic factors, and profibrinolytic and platelet activity. An evaluation will be made of the polymorphism as a determinant of disease and its possible role in the genesis of micro- and macrovascular damage. Discussion The MASS IV-DM trial is designed to include diabetic patients with clinically suspected myocardial ischemia in whom conventional angiography shows angiographically normal coronary arteries. The result of extensive investigation including angiographic follow-up by several methods, vascular reactivity, pro-thrombotic mechanisms, genetic and biochemical studies may facilitate the understanding of so-called micro- and macrovascular disease of DM.
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