José Carlos Nicolau

ORCID: 0000-0002-9680-3689
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About
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Research Areas
  • Acute Myocardial Infarction Research
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Cardiac Imaging and Diagnostics
  • Coronary Interventions and Diagnostics
  • Salivary Gland Disorders and Functions
  • Atrial Fibrillation Management and Outcomes
  • Lipoproteins and Cardiovascular Health
  • Cardiovascular Function and Risk Factors
  • Venous Thromboembolism Diagnosis and Management
  • Heart Failure Treatment and Management
  • Cardiac Health and Mental Health
  • Cardiac Valve Diseases and Treatments
  • Oral microbiology and periodontitis research
  • Diabetes Treatment and Management
  • Cardiac Structural Anomalies and Repair
  • Health Systems, Economic Evaluations, Quality of Life
  • Cancer, Hypoxia, and Metabolism
  • Healthcare during COVID-19 Pandemic
  • Laser Applications in Dentistry and Medicine
  • COVID-19 Clinical Research Studies
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Cardiac pacing and defibrillation studies
  • Cardiac Arrest and Resuscitation
  • Dental Health and Care Utilization
  • Adipokines, Inflammation, and Metabolic Diseases

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2013-2025

Instituto do Coração
2013-2025

Universidade de São Paulo
2015-2024

Université Paris Cité
2024

Radboud University Medical Center
2024

Brigham and Women's Hospital
2013-2024

Beth Israel Deaconess Medical Center
2024

Radboud University Nijmegen
2024

Harvard University
2024

Hôpital Bichat-Claude-Bernard
2024

Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, inflammatory hypothesis atherothrombosis has remained unproved.We conducted a randomized, double-blind trial canakinumab, therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction high-sensitivity C-reactive protein level 2 mg or more per liter. The compared three doses canakinumab...

10.1056/nejmoa1707914 article EN New England Journal of Medicine 2017-08-27

The potential benefit of dual antiplatelet therapy beyond 1 year after a myocardial infarction has not been established. We investigated the efficacy and safety ticagrelor, P2Y12 receptor antagonist with established an acute coronary syndrome, in this context.We randomly assigned, double-blind 1:1:1 fashion, 21,162 patients who had to 3 years earlier ticagrelor at dose 90 mg twice daily, 60 or placebo. All were receive low-dose aspirin followed for median 33 months. primary end point was...

10.1056/nejmoa1500857 article EN New England Journal of Medicine 2015-03-14
Paul M. Ridker Jean MacFadyen Tom Thurén Giulia Renda Peter Libby and 95 more Robert J. Glynn Paul M. Ridker Alberto J. Lorenzatti Henry Krum George Varigos Peter Siostrzonek Peter Sinnaeve Francisco Antônio Helfenstein Fonseca José Carlos Nicolau Nina Gotcheva Jacques Genest Yong Huo Miguel Urina‐Triana Davor Miličić Renata Cífková Riina Vettus Wolfgang Köenig S.D. Anker Athanasios Manolis Fernando Wyss Tamás Forster Axel F. Sigurðsson Prem Pais Alessandro Fucili Hisao Ogawa Hiroaki Shimokawa Irina Veze Birutė Petrauskienė Leon Salvador John J.P. Kastelein Jan H. Cornel Tor Ole Klemsdal Félix Medina Andrzej Budaj L Vida-Simiti Zhanna Kobalava Petar Otašević Daniel Pella Mitja Lainščak Ki‐Bae Seung Patrick Commerford Mikael Dellborg Marc Y. Donath Juey‐Jen Hwang Hakan Kültürsay Marcus Flather Christie M. Ballantyne Seth Bilazarian William H. Chang Cara East Giulia Renda Les B. Forgosh Robert J. Glynn Barry Harris Peter Libby M Ligueros Tom Thurén Erin A. Bohula Bindu Charmarthi Susan Cheng Sherry Chou Jacqueline Suk Danik Graham T. McMahon Bradley A. Maron MingMing Ning Benjamin A. Olenchock Reena L. Pande Todd S. Perlstein Aruna D. Pradhan Natalia S. Rost Aneesh B. Singhal Viviany R. Taqueti Nancy Wei Howard A. Burris Angela Cioffi Anne Marie Dalseg Nilanjan Ghosh Julie R. Gralow Tina Mayer Hope S. Rugo Vance G. Fowler Ajit P. Limaye Sara E. Cosgrove Donald P. Levine Renato D. Lópes John Scott Tom Thurén M Ligueros Robert Hilkert Georgia Tamesby Carolyn Mickel Brian Manning Julian Woelcke Monique Tan S Manfreda

10.1016/s0140-6736(17)32247-x article EN The Lancet 2017-08-27

Thrombin potently activates platelets through the protease-activated receptor PAR-1. Vorapaxar is a novel antiplatelet agent that selectively inhibits cellular actions of thrombin antagonism PAR-1.We randomly assigned 26,449 patients who had history myocardial infarction, ischemic stroke, or peripheral arterial disease to receive vorapaxar (2.5 mg daily) matching placebo and followed them for median 30 months. The primary efficacy end point was composite death from cardiovascular causes,...

10.1056/nejmoa1200933 article EN New England Journal of Medicine 2012-03-24

The assessment of myocardial viability has been used to identify patients with coronary artery disease and left ventricular dysfunction in whom coronary-artery bypass grafting (CABG) will provide a survival benefit. However, the efficacy this approach is uncertain.In substudy who were enrolled randomized trial medical therapy or without CABG, we single-photon-emission computed tomography (SPECT), dobutamine echocardiography, both assess on basis prespecified thresholds.Among 1212 trial, 601...

10.1056/nejmoa1100358 article EN New England Journal of Medicine 2011-04-04

The effect of intensified platelet inhibition for patients with unstable angina or myocardial infarction without ST-segment elevation who do not undergo revascularization has been delineated.In this double-blind, randomized trial, in a primary analysis involving 7243 under the age 75 years receiving aspirin, we evaluated up to 30 months treatment prasugrel (10 mg daily) versus clopidogrel (75 daily). In secondary 2083 older, 5 clopidogrel.At median follow-up 17 months, end point death from...

10.1056/nejmoa1205512 article EN New England Journal of Medicine 2012-08-26

Vorapaxar is a new oral protease-activated-receptor 1 (PAR-1) antagonist that inhibits thrombin-induced platelet activation.In this multinational, double-blind, randomized trial, we compared vorapaxar with placebo in 12,944 patients who had acute coronary syndromes without ST-segment elevation. The primary end point was composite of death from cardiovascular causes, myocardial infarction, stroke, recurrent ischemia rehospitalization, or urgent revascularization.Follow-up the trial terminated...

10.1056/nejmoa1109719 article EN New England Journal of Medicine 2011-11-13

The cholesteryl ester transfer protein inhibitor evacetrapib substantially raises the high-density lipoprotein (HDL) cholesterol level, reduces low-density (LDL) and enhances cellular efflux capacity. We sought to determine effect of on major adverse cardiovascular outcomes in patients with high-risk vascular disease.

10.1056/nejmoa1609581 article EN New England Journal of Medicine 2017-05-17

10.1590/s0066-782x2007000700002 article PT cc-by-nc Arquivos Brasileiros de Cardiologia 2007-04-01
Piotr Ponikowski Bridget‐Anne Kirwan Stefan D. Anker Theresa A. McDonagh Maria Dorobanțu and 95 more Jarosław Dróżdż Vincent Fabien Gerasimos Filippatos Udo Michael Göhring Andre Keren Irakli Khintibidze Hans Kragten Felipe A. Martínez Marco Metra Davor Miličić José Carlos Nicolau Marcus Ohlsson Alexander Parkhomenko Domingo A. Pascual‐Figal Frank Ruschitzka David Sim Hadi Skouri Peter van der Meer Basil S. Lewis Josep Comín‐Colet Stephan von Haehling Alain Cohen‐Solal Nicolas Danchin Wolfram Doehner Henry J. Dargie Michael Motro Javed Butler Tim Friede Klaus H. Jensen Stuart J. Pocock Ewa A. Jankowska Guillermo Moisés Azize Anna Mollar Fernández GO Zapata P. García Pacho Anne‐Marie Glenny F Ferre Pacora ML Parody Joseph de Bono C Beltrano Alejandro Hershson N Vita Luquez Ha HG Cestari H. Fernández Armando Pérez de Prado Mario A Berli Ruben Garcia Duran Jorge Thierer Mirta Díez L. Lobo Marquez RR Borelli MÁ Hominal Marco Metra Pietro Ameri Piergiuseppe Agostoni Alessandra Salvioni Luciano Fattore Edoardo Gronda Stefano Ghio F Turrini Mariagrazia Uguccioni M Di Biase Massimo Piepoli Stefano Savonitto Andrea Mortara Pierfranco Terrosu Alessandro Fucili Giuseppe Boriani Paolo Midi Enrico Passamonti F Cosmi Peter van der Meer P. Van Bergen M van de Wetering NYY al-Windy Wilco Tanis M. F. L. Meijs RGEJ Groutars HKS The Bas Kietselaer HAM van Kesteren DPW Beelen Jan Heymeriks Ruud van de Wal Jeroen Schaap Mireille E. Emans Paul H. Westendorp P.R. Nierop Rian M. Nijmeijer Olivier C. Manintveld Maria Dorobanțu DA Darabantiu Mihnea Zdrenghea DM Toader

10.1016/s0140-6736(20)32339-4 article EN The Lancet 2020-11-13

Bococizumab is a humanized monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and reduces levels of low-density lipoprotein (LDL) cholesterol. We sought to evaluate the efficacy bococizumab in patients at high cardiovascular risk.In two parallel, multinational trials with different entry criteria for LDL cholesterol levels, we randomly assigned 27,438 combined receive (at dose 150 mg) subcutaneously every 2 weeks or placebo. The primary end point was...

10.1056/nejmoa1701488 article EN New England Journal of Medicine 2017-03-17
Patrick R. Lawler Ewan C. Goligher Jeffrey S. Berger Matthew D. Neal Bryan J. McVerry and 95 more José Carlos Nicolau Michelle N. Gong Marc Carrier Robert S Rosenson Harmony R. Reynolds Alexis F. Turgeon Jorge Escobedo David T. Huang Charlotte Bradbury Brett L. Houston Lucy Z. Kornblith Anand Kumar Susan R. Kahn Mary Cushman Zoe McQuilten Arthur S. Slutsky Keri S. Kim Anthony Gordon Bridget‐Anne Kirwan Maria M. Brooks Alisa M. Higgins Roger Lewis Elizabeth Lorenzi Scott Berry Lindsay R. Berry Aaron W. Aday Farah Al-Beidh Djillali Annane Yaseen M. Arabi Diptesh Aryal Lisa Baumann Kreuziger Abi Beane Zahra Bhimani Shailesh Bihari Henny H. Billett Lindsay Bond Marc J. M. Bonten Frank Brunkhorst Meredith Buxton Adrian Buzgau Lana A. Castellucci Sweta Chekuri Jen‐Ting Chen Allen C. Cheng Tamta Chkhikvadze Benjamin Coiffard Todd W. Costantini Sophie de Brouwer Lennie Derde Michelle A. Detry Abhijit Duggal Vladimír Džavík Mark B. Effron Lise J Estcourt Brendan M. Everett Dean Fergusson Mark Fitzgerald Robert Fowler J.‐P. Galanaud Benjamin Galen Sheetal Gandotra Sebastián García‐Madrona Timothy D. Girard Lucas C. Godoy Andrew L. Goodman Herman Goossens Cameron Green Yonatan Greenstein Peter L Gross Naomi M. Hamburg Rashan Haniffa George P. Hanna Nicholas Hanna Sheila M. Hegde Carolyn M. Hendrickson R. Duncan Hite Alexander Hindenburg Aluko A. Hope James M Horowitz Christopher M. Horvat Kristin Hudock Beverley J. Hunt Mansoor Husain Robert C. Hyzy Vivek N. Iyer Jeffrey R. Jacobson Devachandran Jayakumar Norma Keller Akram Khan Yuri Kim Andrei Kindzelski Andrew J. King M. Margaret Knudson Aaron E. Kornblith Vidya Krishnan

Thrombosis and inflammation may contribute to the risk of death complications among patients with coronavirus disease 2019 (Covid-19). We hypothesized that therapeutic-dose anticoagulation improve outcomes in noncritically ill who are hospitalized Covid-19.In this open-label, adaptive, multiplatform, controlled trial, we randomly assigned were Covid-19 not critically (which was defined as an absence critical care-level organ support at enrollment) receive pragmatically regimens either...

10.1056/nejmoa2105911 article EN New England Journal of Medicine 2021-08-04

Elevated lipoprotein-associated phospholipase A2 activity promotes the development of vulnerable atherosclerotic plaques, and elevated plasma levels this enzyme are associated with an increased risk coronary events. Darapladib is a selective oral inhibitor A2.In double-blind trial, we randomly assigned 15,828 patients stable heart disease to receive either once-daily darapladib (at dose 160 mg) or placebo. The primary end point was composite cardiovascular death, myocardial infarction,...

10.1056/nejmoa1315878 article EN New England Journal of Medicine 2014-03-30

Additional treatments are needed for heart failure with reduced ejection fraction (HFrEF). Sodium-glucose cotransporter 2 (SGLT2) inhibitors may be an effective treatment patients HFrEF, even those without diabetes.To evaluate the effects of dapagliflozin in HFrEF and diabetes.Exploratory analysis a phase 3 randomized trial conducted at 410 sites 20 countries. Patients New York Heart Association classification II to IV less than or equal 40% elevated plasma N-terminal pro B-type natriuretic...

10.1001/jama.2020.1906 article EN JAMA 2020-03-27

Patients with diabetes mellitus (DM) have high platelet reactivity and are at increased risk of ischaemic events bleeding post-acute coronary syndromes (ACS). In the PLATelet inhibition patient Outcomes (PLATO) trial, ticagrelor reduced primary composite endpoint cardiovascular death, myocardial infarction, or stroke, but similar rates major compared clopidogrel. We aimed to investigate outcome vs. clopidogrel in patients DM poor glycaemic control. analysed pre-existing (n = 4662), including...

10.1093/eurheartj/ehq325 article EN European Heart Journal 2010-08-29

Background: Ezetimibe, when added to simvastatin, reduces cardiovascular events after acute coronary syndrome. We explored outcomes stratified by diabetes mellitus (DM). Methods: In IMPROVE-IT (Improved Reduction of Outcomes: Vytorin Efficacy International Trial), 18 144 patients syndrome with low-density lipoprotein cholesterol 50 125 mg/dL were randomized 40 mg ezetimibe/simvastatin (E/S) or placebo/simvastatin. The primary composite end point was death, major events, and stroke. DM a...

10.1161/circulationaha.117.030950 article EN Circulation 2017-12-20

Patients with stable coronary artery disease and diabetes mellitus who have not had a myocardial infarction or stroke are at high risk for cardiovascular events. Whether adding ticagrelor to aspirin improves outcomes in this population is unclear.

10.1056/nejmoa1908077 article EN New England Journal of Medicine 2019-09-01

Goals of management in patients with heart failure and reduced ejection fraction include reducing death hospitalizations, improving health status (symptoms, physical function, quality life). In the DAPA-HF trial (Dapagliflozin Prevention Adverse-Outcomes Heart Failure), sodium-glucose cotransporter-2 inhibitor, dapagliflozin, improved symptoms fraction. this analysis, we examine effects dapagliflozin on a broad range outcomes, using Kansas City Cardiomyopathy Questionnaire (KCCQ).KCCQ was...

10.1161/circulationaha.119.044138 article EN cc-by Circulation 2019-11-17

Background: Sodium glucose transporter-2 inhibitors reduce the risk of major adverse cardiovascular events (MACE) in patients with type 2 diabetes mellitus and a history atherosclerotic disease. Because their baseline risk, previous myocardial infarction (MI) may derive even greater benefit from sodium inhibitor therapy. Methods: DECLARE-TIMI 58 (Dapagliflozin Effect on Cardiovascular Events–Thrombolysis Myocardial Infarction 58) randomized 17 160 either established disease (n=6974) or...

10.1161/circulationaha.119.039996 article EN Circulation 2019-03-18
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