Cardiovascular Magnetic Resonance Reveals Cardiac Pathophysiology in Autoimmune Rheumatic Diseases

George Markousis-Mavrogenis1, Petros P Sfikakis2,3, Loukia Koutsogeorgopoulou3

  • 1Onassis Cardiac Surgery Center, Athens, Greece.

Insights

Cardiovascular magnetic resonance (CMR) detects early cardiovascular disease (CVD) in autoimmune rheumatic diseases (ARDs), aiding personalized treatment. This imaging technique identifies inflammation and fibrosis, crucial for managing high-risk patients.

Area of Science:

  • Cardiology
  • Rheumatology
  • Medical Imaging

Background:

  • Autoimmune rheumatic diseases (ARDs) significantly increase cardiovascular disease (CVD) incidence and mortality.
  • Early detection of CVD in ARD patients is critical for improving outcomes.
  • Cardiovascular magnetic resonance (CMR) offers a non-invasive method for early CVD assessment in ARD.

Purpose of the Study:

  • To review the diagnostic capabilities of CMR in identifying CVD in ARD patients.
  • To highlight how CMR findings guide treatment decisions for ARD patients.
  • To summarize the role of CMR in the personalized management of ARD.

Main Methods:

  • Utilizing balanced steady-state free precession (bSSFP) for cardiac anatomy and function assessment.
  • Employing T2-weighted imaging (T2-W) and T2 mapping for myocardial edema detection.
  • Applying late gadolinium enhancement (LGE) and T1 mapping/extracellular volume fraction (ECV) for fibrosis quantification.

Main Results:

  • CMR parameters effectively identify myocardial edema and fibrosis in ARD patients.
  • These parameters are instrumental in making informed treatment decisions.
  • Despite the absence of multicenter studies, CMR applications are widespread in ARD management.

Conclusions:

  • Tissue characterization with CMR enables early and reliable identification of CVD in ARD patients.
  • CMR contributes significantly to the personalized management strategies for ARD patients.
  • CMR imaging is a valuable tool for risk stratification and therapeutic guidance in this population.
Abstract

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