Coronary microvascular dysfunction in hypertrophy and heart failure

Author:

Camici Paolo G1,Tschöpe Carsten234,Di Carli Marcelo F567,Rimoldi Ornella18ORCID,Van Linthout Sophie23

Affiliation:

1. Vita Salute University and San Raffaele Hospital, Milano, Italy

2. Berlin Institute of Health Center for Regenerative Therapies (BCRT), Charité—Universitätsmedizin Berlin, Berlin, Germany

3. German Center for Cardiovascular Research (DZHK), Partner Site Berlin, Berlin, Germany

4. Department of Cardiology, Charité—Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany

5. Cardiovascular Imaging Program, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

6. Department of Radiology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

7. Cardiovascular Division, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

8. CNR IBFM, Segrate, Italy

Abstract

Abstract Left ventricular (LV) hypertrophy (LVH) is a growth in left myocardial mass mainly caused by increased cardiomyocyte size. LVH can be a physiological adaptation to physical exercise or a pathological condition either primary, i.e. genetic, or secondary to LV overload. Patients with both primary and secondary LVH have evidence of coronary microvascular dysfunction (CMD). The latter is mainly due to capillary rarefaction and adverse remodelling of intramural coronary arterioles due to medial wall thickening with an increased wall/lumen ratio. An important feature of this phenomenon is the diffuse nature of this remodelling, which generally affects the coronary microvessels in the whole of the left ventricle. Patients with LVH secondary to arterial hypertension can develop both heart failure with preserved ejection fraction (HFpEF) and heart failure with reduced ejection fraction (HFrEF). These patients can develop HFrEF via a ‘direct pathway’ with an interval myocardial infarction and also in its absence. On the other hand, patients can develop HFpEF that can then progress to HFrEF with or without interval myocardial infarction. A similar evolution towards LV dysfunction and both HFpEF and HFrEF can occur in patients with hypertrophic cardiomyopathy, the most common genetic cardiomyopathy with a phenotype characterized by massive LVH. In this review article, we will discuss both the experimental and clinical studies explaining the mechanisms responsible for CMD in LVH as well as the evidence linking CMD with HFpEF and HFrEF.

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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