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Protocol of the Berlin Long-term Observation of Vascular Events (BeLOVE): a prospective cohort study with deep phenotyping and long-term follow up of cardiovascular high-risk patients.
Weber, Joachim E; Ahmadi, Michael; Boldt, Leif-Hendrik; Eckardt, Kai-Uwe; Edelmann, Frank; Gerhardt, Holger; Grittner, Ulrike; Haubold, Kathrin; Hübner, Norbert; Kollmus-Heege, Jil; Landmesser, Ulf; Leistner, David M; Mai, Knut; Müller, Dominik N; Nolte, Christian H; Pieske, Burkert; Piper, Sophie K; Rattan, Simrit; Rauch, Geraldine; Schmidt, Sein; Schmidt-Ott, Kai M; Schönrath, Katharina; Schulz-Menger, Jeanette; Schweizerhof, Oliver; Siegerink, Bob; Spranger, Joachim; Ramachandran, Vasan S; Witzenrath, Martin; Endres, Matthias; Pischon, Tobias.
Afiliación
  • Weber JE; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany joachim.weber@bih-charite.de.
  • Ahmadi M; Department of Neurology, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Boldt LH; Center for Stroke Research (CSB), Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Eckardt KU; German Center for Cardiovascular Research (DZHK), partner site Berlin, Berlin, Germany.
  • Edelmann F; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Gerhardt H; Department of Neurology, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Grittner U; German Center for Cardiovascular Research (DZHK), partner site Berlin, Berlin, Germany.
  • Haubold K; Department of Internal Medicine and Cardiology, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Hübner N; Department of Cardiology, Angiology and Intensive Care Medicine, Deutsches Herzzentrum der Charité (DHZC), Berlin, Germany.
  • Kollmus-Heege J; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Landmesser U; Department of Nephrology and Medical Intensive Care, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Leistner DM; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Mai K; German Center for Cardiovascular Research (DZHK), partner site Berlin, Berlin, Germany.
  • Müller DN; Department of Internal Medicine and Cardiology, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Nolte CH; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Pieske B; German Center for Cardiovascular Research (DZHK), partner site Berlin, Berlin, Germany.
  • Piper SK; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Rattan S; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Rauch G; Institute of Biometry and Clinical Epidemiology, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Schmidt S; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Schmidt-Ott KM; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Schönrath K; German Center for Cardiovascular Research (DZHK), partner site Berlin, Berlin, Germany.
  • Schulz-Menger J; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Schweizerhof O; Experimental and Clinical Research Center (ECRC), a cooperation of Charité - Universitätsmedizin Berlin and Max Delbrück Center for Molecular Medicine (MDC), Berlin, Germany.
  • Siegerink B; Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Spranger J; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Ramachandran VS; Institute of Biometry and Clinical Epidemiology, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
  • Witzenrath M; Berlin Institute of Health (BIH) at Charité- Universitätsmedizin Berlin, Berlin, Germany.
  • Endres M; German Center for Cardiovascular Research (DZHK), partner site Berlin, Berlin, Germany.
  • Pischon T; Department of Cardiology, Charité- Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.
BMJ Open ; 13(10): e076415, 2023 10 31.
Article en En | MEDLINE | ID: mdl-37907297
INTRODUCTION: The Berlin Long-term Observation of Vascular Events is a prospective cohort study that aims to improve prediction and disease-overarching mechanistic understanding of cardiovascular (CV) disease progression by comprehensively investigating a high-risk patient population with different organ manifestations. METHODS AND ANALYSIS: A total of 8000 adult patients will be recruited who have either suffered an acute CV event (CVE) requiring hospitalisation or who have not experienced a recent acute CVE but are at high CV risk. An initial study examination is performed during the acute treatment phase of the index CVE or after inclusion into the chronic high risk arm. Deep phenotyping is then performed after ~90 days and includes assessments of the patient's medical history, health status and behaviour, cardiovascular, nutritional, metabolic, and anthropometric parameters, and patient-related outcome measures. Biospecimens are collected for analyses including 'OMICs' technologies (e.g., genomics, metabolomics, proteomics). Subcohorts undergo MRI of the brain, heart, lung and kidney, as well as more comprehensive metabolic, neurological and CV examinations. All participants are followed up for up to 10 years to assess clinical outcomes, primarily major adverse CVEs and patient-reported (value-based) outcomes. State-of-the-art clinical research methods, as well as emerging techniques from systems medicine and artificial intelligence, will be used to identify associations between patient characteristics, longitudinal changes and outcomes. ETHICS AND DISSEMINATION: The study was approved by the Charité-Universitätsmedizin Berlin ethics committee (EA1/066/17). The results of the study will be disseminated through international peer-reviewed publications and congress presentations. STUDY REGISTRATION: First study phase: Approved WHO primary register: German Clinical Trials Register: https://drks.de/search/de/trial/DRKS00016852; WHO International Clinical Registry Platform: http://apps.who.int/trialsearch/Trial2.aspx?TrialID=DRKS00016852. Recruitment started on July 18, 2017.Second study phase: Approved WHO primary register: German Clinical Trials Register DRKS00023323, date of registration: November 4, 2020, URL: http://www.drks.de/ DRKS00023323. Recruitment started on January 1, 2021.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / COVID-19 Límite: Adult / Humans País/Región como asunto: Europa Idioma: En Revista: BMJ Open Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / COVID-19 Límite: Adult / Humans País/Región como asunto: Europa Idioma: En Revista: BMJ Open Año: 2023 Tipo del documento: Article País de afiliación: Alemania
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