Clinical and prognostic implications of capillary density in patients with cardiac light chain amyloidosis

Darae Kim1, Jin-Oh Choi1, Kihyun Kim2

  • 1Division of Cardiology, Department of Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-Ro Gangnam-gu, Seoul, 06351, Republic of Korea.

ESC Heart Failure
|September 16, 2021
PubMed

Insights

Capillary density in heart biopsies is linked to outcomes in light chain amyloidosis. Lower capillary density indicates a higher risk of death and improves current staging systems for cardiac amyloidosis.

Area of Science:

  • Cardiology
  • Oncology
  • Pathology

Background:

  • Cardiac involvement is a critical determinant of outcomes in light chain (AL) amyloidosis.
  • Assessing cardiac function and prognosis in AL amyloidosis is essential for patient management.

Purpose of the Study:

  • To evaluate the association between capillary density (CD) in endomyocardial biopsies and cardiac parameters in AL amyloidosis.
  • To determine if CD improves the prognostic value of existing staging systems for cardiac AL amyloidosis.

Main Methods:

  • Prospective enrollment of 67 patients with biopsy-proven AL cardiac amyloidosis.
  • Transthoracic echocardiography, 2D strain echocardiography, and endomyocardial biopsy (EBM) were performed.
  • Capillary density and amyloid load were quantified from EBM.

Main Results:

  • Capillary density correlated significantly with left ventricle global longitudinal strain, N-terminal pro-B type natriuretic peptide, and amyloid load.
  • Patients with lower capillary density (≤220/mm²) had a significantly higher risk of death.
  • A staging model incorporating CD demonstrated improved discrimination and reclassification compared to the 2012 Mayo staging system alone.

Conclusions:

  • Capillary density is significantly related to myocardial amyloid deposit severity.
  • Capillary density offers incremental prognostic value beyond the current 2012 Mayo staging system in cardiac AL amyloidosis.
Abstract

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