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      Feature tracking cardiac magnetic resonance in systemic light chain amyloidosis

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          Abstract

          Background Systemic light chain amyloidosis (AL) is associated with a high cardiovascular morbidity and mortality. Cardiovascular involvement and determination of prognosis is underestimated by standard imaging parameters. Recently, cardiac deformation analysis of global circumferential and longitudinal strain has been shown to have great clinical impact on the assessment of prognosis and survival in this rare disease. For quantification of cardiac deformation analysis we applied a novel non-invasive post-processing feature tracking algorithm (FTI) on pre-acquired regular CMR SSFP images in healthy volunteers and in patients with AL and sought to investigate wall motion differences between both groups. Methods 65 patients (mean age 58 ± 11 years; 41 male, 24 female patients) with biopsy proven systemic AL were scanned on a clinical 1.5 T CMR scanner (Philips Achieva). Short axis slices covering entirely both ventricles as well as 2-, 3- and 4-chamber were acquired using standard SSFP-sequences before initiation of specific pharmaceutical AL therapies. The control group consisted of 50 healthy subjects (mean age 58 ± 5 years; 23 male, 27 female). Besides the standard CMR parameters for volumes, ejection fraction (EF) and myocardial mass and wall thickness we measured global circumferential and longitudinal strain on SSFP images by the application of the post-processing feature tracking algorithm. Results Global circumferential strain and global longitudinal strain correlated well with left ventricular ejection fraction (r^2=0.64, p<0.05; r^2=0.47, p<0.05). In patients with AL global longitudinal strain was significantly reduced compared to healthy subjects (-16.9±5.1% vs -23±3.3%, p<0.05), whereas global circumferential strain was not (-25.1±7.0% vs -27.1±5.0%, n.s.). In the subgroup analysis of AL patients without cardiac involvement (mean wall thickness ≤ 12mm) global longitudinal strain showed significantly reduced values in comparison to healthy control subjects (-20.3±4.7% vs -23±3.3%, p<0.05), whereas global circumferential strain did not show a significant difference. Patients with an ejection fraction ≥50% already had reduced global longitudinal strains (-18.5±4.5% vs -23±3.3%, p<0.05), again global circumferential strain did not show a significant difference. Conclusions FTI strain analysis derived from regular SSFP sequences offers the possibility for a retrospective or prospective fast quantitative wall motion assessment of myocardial deformation patterns without specific and time-consuming strain imaging techniques. FTI allows distinguishing between healthy subjects and subjects with AL. Further investigations are necessary to analyze the impact of this new method on clinical outcome in AL patients. Funding none

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          Author and article information

          Conference
          J Cardiovasc Magn Reson
          J Cardiovasc Magn Reson
          Journal of Cardiovascular Magnetic Resonance
          BioMed Central
          1097-6647
          1532-429X
          2013
          30 January 2013
          : 15
          : Suppl 1
          : P97
          Affiliations
          [1 ]University of Heidelberg, Heidelberg, Germany
          [2 ]TomTec Imaging Systems, Munich, Germany
          Article
          1532-429X-15-S1-P97
          10.1186/1532-429X-15-S1-P97
          3560040
          bc5b7f65-4b59-48bf-b723-3fe90cf8302c
          Copyright ©2013 Kammerer et al; licensee BioMed Central Ltd.

          This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

          16th Annual SCMR Scientific Sessions
          San Francisco, CA, USA
          31 January-3 February 2013
          History
          Categories
          Poster Presentation

          Cardiovascular Medicine
          Cardiovascular Medicine

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