Multimodality imaging approach to left ventricular dysfunction in diabetes: an expert consensus document from the European Association of Cardiovascular Imaging

Author:

Marwick Thomas H1,Gimelli Alessia2ORCID,Plein Sven3ORCID,Bax Jeroen J4ORCID,Charron Phillippe56,Delgado Victoria7ORCID,Donal Erwan89ORCID,Lancellotti Patrizio1011ORCID,Levelt Eylem12,Maurovich-Horvat Pal13,Neubauer Stefan14ORCID,Pontone Gianluca15ORCID,Saraste Antti1617,Cosyns Bernard18ORCID,Edvardsen Thor1920ORCID,Popescu Bogdan A21,Galderisi Maurizio22,Derumeaux Genevieve23,Bäck Magnus,Bertrand Philippe B,Dweck Marc,Keenan Niall,Magne Julien,Neglia Danilo,Stankovic Ivan,

Affiliation:

1. Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia

2. Fondazione Toscana Gabriele Monasterio, Via Moruzzi, 1, 56124 Pisa, Italy

3. Multidisciplinary Cardiovascular Research Center & Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK

4. Department of Cardiology, Leiden University Medical Centre (LUMC), Leiden, The Netherlands

5. Sorbonne Université, INSERM UMRS 1166 and ICAN Institute, Paris, France

6. APHP, Centre de référence pour les maladies cardiaques héréditaires ou rares, Hôpital Pitié-Salpêtrière, Paris, France

7. Department of Cardiology, Leiden University Medical Centre, Albinusdreef 2, Leiden 2300RC, The Netherlands

8. Service de Cardiologie Et Maladies Vasculaires Et CIC-IT 1414, CHU Rennes, 35000 Rennes, France

9. Université de Rennes 1, LTSI, 35000 Rennes, France

10. Department of Cardiology, University of Liège Hospital, GIGA Cardiovascular Sciences, CHU SartTilman, Liège, Belgium

11. Gruppo Villa Maria Care and Research, Maria Cecilia Hospital, Cotignola, and Anthea Hospital, Bari, Italy

12. Department of Cardiovascular Sciences, University of Leicester, Glenfield Hospital , Groby Road, Leicester LE3 9QF, UK

13. MTA-SE Cardiovascular Imaging Research Group, Medical Imaging Centre, Semmelweis University, 2 Koranyi u., 1083 Budapest, Hungary

14. Radcliffe Department of Medicine, University of Oxford Centre for Clinical Magnetic Resonance Research, University of Oxford, Headley Way, Oxford OX3 9DU, UK

15. Centro Cardiologico Monzino IRCCS, University of Milan, Cardiovascular Imaging, Milan, Italy

16. Turku PET Centre, University of Turku, Turku, Finland

17. Heart Center, Turku University Hospital, Turku, Finland

18. Cardiology, CHVZ (Centrum voor Hart en Vaatziekten), ICMI (In Vivo Cellular and Molecular Imaging) Laboratory, Universitair ziekenhuis Brussel, 109 Laarbeeklaan, Brussels 1090, Belgium

19. Department of Cardiology, Oslo University Hospital, Rikshospitalet, Postbox 4950 Nydalen, Sognsvannsveien 20, NO-0424 Oslo, Norway

20. Institute for clinical medicine, University of Oslo, Sognsvannsveien 20, NO-0424 Oslo, Norway

21. Department of Cardiology, University of Medicine and Pharmacy “Carol Davila”, Euroecolab, Emergency Institute for Cardiovascular Diseases “Prof. Dr. C. C. Iliescu”, Bucharest, Romania

22. Department of Advanced Biomedical Sciences, Federico II University, Naples, Italy

23. IMRB – Inserm U955 Senescence, metabolism and cardiovascular diseases 8, rue du Général Sarrail, 94010 Créteil, France

Abstract

Abstract Heart failure (HF) is among the most important and frequent complications of diabetes mellitus (DM). The detection of subclinical dysfunction is a marker of HF risk and presents a potential target for reducing incident HF in DM. Left ventricular (LV) dysfunction secondary to DM is heterogeneous, with phenotypes including predominantly systolic, predominantly diastolic, and mixed dysfunction. Indeed, the pathogenesis of HF in this setting is heterogeneous. Effective management of this problem will require detailed phenotyping of the contributions of fibrosis, microcirculatory disturbance, abnormal metabolism, and sympathetic innervation, among other mechanisms. For this reason, an imaging strategy for the detection of HF risk needs to not only detect subclinical LV dysfunction (LVD) but also characterize its pathogenesis. At present, it is possible to identify individuals with DM at increased risk HF, and there is evidence that cardioprotection may be of benefit. However, there is insufficient justification for HF screening, because we need stronger evidence of the links between the detection of LVD, treatment, and improved outcome. This review discusses the options for screening for LVD, the potential means of identifying the underlying mechanisms, and the pathways to treatment.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine

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