Left ventricular assessment in patients with systemic light chain amyloidosis: a 3-dimensional speckle tracking transthoracic echocardiographic study

  • Sarah Pradel
  • Julien Magne
  • Arnaud Jaccard
  • Bahaa M. Fadel
  • Cyrille Boulogne
  • Vera Maria Cury Salemi
  • Thibaud Damy
  • Victor Aboyans
  • Dania MohtyEmail author
Original Paper


Cardiac involvement in systemic light chain (AL) amyloidosis carries a poor prognosis mainly through involvement of the left ventricular (LV) myocardium. Despite its limitations, two-dimensional transthoracic echocardiography (2D-TTE) remains the main tool used for the assessment of LV systolic function in AL patients. We hypothesize that 3D-TTE coupled with speckle tracking imaging allows earlier detection of LV systolic dysfunction than 2D-TTE in AL amyloidosis. We prospectively studied 71 subjects including 58 patients with confirmed AL amyloidosis (mean age 66 ± 10 years, 60% male) and 21 healthy control (mean age 64 ± 7 years, 48% male) from 2011 to 2014 at the University Hospital of Limoges. The AL patients were divided into three groups according to Mayo Clinic (MC) staging and all subjects underwent 2D-TTE and 3D-TTE at the same setting. Using 2D-TTE, there was no significant difference in LV ejection fraction (EF) between the groups [LVEF = 63 ± 7% (control), 59 ± 6% (MC stage I), 60 ± 8% (MC stage II) and 57 ± 14% (MC stage III) (p = 0.24)]. In contrast, 3D-TTE demonstrated significantly worse LV systolic function in stage II and III patients using 3D-LVEF [MC II and III 45 ± 8% and 39 ± 12% vs. control 53 ± 8% (p < 0.0001)], global longitudinal strain (GLS) [MC II and III − 11 ± 4% and − 8 ± 3% vs. control − 15 ± 3% (p < 0.0001)] and global radial strain (GRS) [MC II and III 14 ± 9% and 10 ± 8% vs. control 25 ± 10% (p < 0.0001)]. Furthermore, MC III patients had significantly worse global circumferential strain and area tracking [− 17 ± 6% and − 25 ± 8% vs. − 24 ± 7% and − 36 ± 7% for control (p < 0.0001)]. Additionally, MC I had significantly better 3D GLS, GRS and global strain (− 15 ± 3%, 25 ± 10% and 28 ± 12%) than MC II (− 11 ± 4%, 14 ± 9% and 16 ± 10%) and MC III patients (− 8 ± 3%, 10 ± 8% and 12 ± 8%), respectively. Despite an apparently preserved LVEF by 2D-TTE, AL patients in MC stage II and III demonstrate evidence of LV systolic dysfunction by 3D imaging using LVEF and strain analysis. Worse LV involvement by AL amyloidosis was associated with more impaired 3D-TTE LV systolic parameters.


Light chain amyloidosis 3-Dimensional echocardiography Left ventricular function 



Mrs. Frederique Wittmer, M.Sc., for her help in some data analysis. Dr. David Lavergne, Ph.D., from the National amyloidosis referral center, for his help in data collection. Mr. David Gibson, Ph.D., for his help in the correction of the manuscript.


Toshiba provided a complementary machine “Artida Medical System” allowing performance of 2D and 3D TTE in our patient population.

Compliance with ethical standards

Conflict of interest

All authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. All ethical standards were respected during this work.

Research involving human and animal rights

No animals were involved in our study.

Informed consent

Informed consent was obtained from all individual participants included in the study.


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Copyright information

© Springer Nature B.V. 2019

Authors and Affiliations

  • Sarah Pradel
    • 1
  • Julien Magne
    • 1
  • Arnaud Jaccard
    • 2
  • Bahaa M. Fadel
    • 3
  • Cyrille Boulogne
    • 1
  • Vera Maria Cury Salemi
    • 4
  • Thibaud Damy
    • 5
  • Victor Aboyans
    • 1
  • Dania Mohty
    • 1
    • 2
    • 3
    Email author
  1. 1.Department of CardiologyDupuytren University HospitalLimogesFrance
  2. 2.Department of Hematology, National Reference Center of Light-Chain Systemic AmyloidosisDupuytren University HospitalLimogesFrance
  3. 3.Heart CenterKing Faisal Specialist Hospital & Research CenterRiyadhSaudi Arabia
  4. 4.Hospital das Clínicas da Faculdade de Medicina da Universidade de São PauloSão PauloBrazil
  5. 5.Department of CardiologyAP-HP, Henri Mondor University HospitalCreteilFrance

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