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Published on: February 17, 2018
Pathophysiology and imaging of heart failure in women with autoimmune rheumatic diseases
Sophie I Mavrogeni1, George Markousis-Mavrogenis2, Loukia Koutsogeorgopoulou3
1Onassis Cardiac Surgery Center, 50 Esperou Street, 175-61 P. Faliro, Athens, Greece. soma13@otenet.gr.
Insights
Cardiovascular disease is a major concern in autoimmune rheumatic diseases (ARDs), particularly heart failure (HF). Cardiovascular magnetic resonance (CMR) offers superior tissue characterization for diagnosing HF in ARDs compared to echocardiography.
Area of Science:
- Rheumatology and Cardiology
- Noninvasive Cardiac Imaging
Background:
- Autoimmune rheumatic diseases (ARDs) affect 8% of the population, predominantly women.
- Cardiovascular disease (CVD), including heart failure (HF), is a significant complication and leading cause of death in ARDs.
- HF in ARDs often presents silently and typically with preserved ejection fraction.
Purpose of the Study:
- To compare the utility of echocardiography and cardiovascular magnetic resonance (CMR) in evaluating HF in patients with ARDs.
- To highlight the need for advanced imaging modalities for detailed cardiac assessment in ARDs.
Main Methods:
- Review of noninvasive imaging modalities for HF evaluation in ARDs.
- Focus on echocardiography as the current standard and CMR for advanced tissue characterization.
Main Results:
- Echocardiography is operator-dependent and limited in tissue characterization.
- CMR provides reproducible, operator-independent assessment of myocardial function and tissue characteristics (edema, ischemia, fibrosis).
- CMR enables detailed diagnosis of myocardial inflammation and fibrosis, crucial for understanding HF pathophysiology in ARDs.
Conclusions:
- CMR offers superior insights into the pathophysiological basis of heart failure in autoimmune rheumatic diseases compared to echocardiography.
- Advanced tissue characterization by CMR facilitates personalized cardiac and anti-rheumatic treatment strategies for ARDs patients with HF.
Abstract:
Autoimmune rheumatic diseases (ARDs) affect 8% of the population, and approximately 78% of them are women. Cardiovascular disease (CVD) in ARDs encompasses different pathophysiologic processes, such as endothelial dysfunction, myocardial/vascular inflammation and accelerated atherosclerosis with silent clinical presentation, leading to heart failure (HF), usually with preserved ejection fraction. Echocardiography and cardiovascular magnetic resonance (CMR) are the two most commonly used noninvasive imaging modalities for the evaluation of HF in patients with ARDs. Echocardiography currently represents the main diagnostic tool for cardiac imaging in clinical practice. However, the demand for more efficient and prompt diagnostic and therapeutic approach in this specific population necessitates the implementation of modalities capable of providing a more detailed and quantified information from the point of tissue characterization. Furthermore, echocardiography is an operator and acoustic window depended modality, with relatively low reproducibility and unable to perform tissue characterization. CMR is a noninvasive modality without radiation that can give reproducible and operator-independent information about both myocardial function and tissue characterization. By providing quantification of oedema, stress perfusion defects and fibrosis, CMR can diagnose myocardial inflammation, micro-macro-vascular myocardial ischemia and replacement or diffuse fibrosis, respectively. Tissue characterization allows for moving beyond the cardiac function to the assessment of intra- and inter-cellular alterations and promotes the development of personalized cardiac and anti-rheumatic treatment in ARDs with HF. ARDs are mainly female diseases. Cardiac involvement leading in HF is not unusual in ARDs and remains the main cause of death. Noninvasive, nonradiating imaging modalities such as echocardiography and CMR represent the main diagnostic tools. Specifically, echocardiography represents the first diagnostic approach; however, it is CMR that gives information about the pathophysiologic background behind HF in ARDs.
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