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Cardiometabolic risk management: insights from a European Society of Cardiology Cardiovascular Round Table.
Cosentino, Francesco; Verma, Subodh; Ambery, Philip; Treppendahl, Marianne Bach; van Eickels, Martin; Anker, Stefan D; Cecchini, Michele; Fioretto, Paola; Groop, Per-Henrik; Hess, David; Khunti, Kamlesh; Lam, Carolyn S P; Richard-Lordereau, Isabelle; Lund, Lars H; McGreavy, Paul; Newsome, Philip N; Sattar, Naveed; Solomon, Scott; Weidinger, Franz; Zannad, Faiez; Zeiher, Andreas.
Afiliación
  • Cosentino F; Cardiology Unit, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital, Solna, 171 76 Stockholm, Sweden.
  • Verma S; Division of Cardiac Surgery, St Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada.
  • Ambery P; Late-stage Development, CVRM, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Treppendahl MB; Cardiovascular Diseases, Global Medical Affairs, Novo Nordisk A/S, Søborg, Denmark.
  • van Eickels M; Thrombosis & Hematology, Medical Affairs, Bayer AG, Berlin, Germany.
  • Anker SD; Department of Cardiology (CVK), Berlin Institute of Health Center for Regenerative Therapies (BCRT), and German Centre for Cardiovascular Research (DZHK) Partner Site Berlin, Charité Universitätsmedizin, Berlin, Germany.
  • Cecchini M; Health Division, Organisation for Economic Co-operation and Development (OECD), Paris, France.
  • Fioretto P; Department of Medicine, University of Padova, Padova, Italy.
  • Groop PH; Department of Nephrology, University of Helsinki, Helsinki University Hospital, Helsinki, Finland.
  • Hess D; Folkhälsan Institute of Genetics, Helsinki, Finland.
  • Khunti K; Department of Diabetes, Monash University, Melbourne, Australia.
  • Lam CSP; Department of Physiology and Pharmacology, University of Western Ontario, Robarts Research Institute, London, ON, Canada.
  • Richard-Lordereau I; Department of Pharmacology, University of Toronto, Division of Vascular Surgery, St Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada.
  • Lund LH; Leicester Diabetes Centre, University of Leicester, Leicester, UK.
  • McGreavy P; National Heart Centre Singapore, Duke-National University of Singapore, Singapore.
  • Newsome PN; General Medicine Europe, Amgen Europe, Rotkreutz ZG, Switzerland.
  • Sattar N; Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
  • Solomon S; ESC Patients Forum, Sheffield, UK.
  • Weidinger F; National Institute for Health Research, Birmingham Biomedical Research Centre at University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Zannad F; Centre for Liver & Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
  • Zeiher A; School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
Eur Heart J ; 44(39): 4141-4156, 2023 Oct 14.
Article en En | MEDLINE | ID: mdl-37448181
Metabolic comorbidities are common in patients with cardiorenal disease; they can cause atherosclerotic cardiovascular disease (ASCVD), speed progression, and adversely affect prognosis. Common comorbidities are Type 2 diabetes mellitus (T2DM), obesity/overweight, chronic kidney disease (CKD), and chronic liver disease. The cardiovascular system, kidneys, and liver are linked to many of the same risk factors (e.g. dyslipidaemia, hypertension, tobacco use, diabetes, and central/truncal obesity), and shared metabolic and functional abnormalities lead to damage throughout these organs via overlapping pathophysiological pathways. The COVID-19 pandemic has further complicated the management of cardiometabolic diseases. Obesity, T2DM, CKD, and liver disease are associated with increased risk of poor outcomes of COVID-19 infection, and conversely, COVID-19 can lead to worsening of pre-existing ASCVD. The high rates of these comorbidities highlight the need to improve recognition and treatment of ASCVD in patients with obesity, insulin resistance or T2DM, chronic liver diseases, and CKD and equally, to improve recognition and treatment of these diseases in patients with ASCVD. Strategies to prevent and manage cardiometabolic diseases include lifestyle modification, pharmacotherapy, and surgery. There is a need for more programmes at the societal level to encourage a healthy diet and physical activity. Many pharmacotherapies offer mechanism-based approaches that can target multiple pathophysiological pathways across diseases. These include sodium-glucose cotransporter-2 inhibitors, glucagon-like peptide-1 receptor agonists, selective mineralocorticoid receptor antagonists, and combined glucose-dependent insulinotropic peptide/glucagon-like peptide-1 receptor agonist. Non-surgical and surgical weight loss strategies can improve cardiometabolic disorders in individuals living with obesity. New biomarkers under investigation may help in the early identification of individuals at risk and reveal new treatment targets.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Eur Heart J Año: 2023 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Eur Heart J Año: 2023 Tipo del documento: Article País de afiliación: Suecia
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