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Published in: Clinical Research in Cardiology 3/2015

01-03-2015 | Original Paper

Improvement of risk assessment in systemic light-chain amyloidosis using human placental growth factor

Authors: Arnt V. Kristen, Johannes Rinn, Ute Hegenbart, David Lindenmaier, Corina Merkle, Christoph Röcken, Stefan Hardt, Evangelos Giannitsis, Hugo A. Katus

Published in: Clinical Research in Cardiology | Issue 3/2015

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Abstract

Background

Vascular amyloid deposition is common in light-chain amyloidosis resulting in endothelial dysfunction. Human placental growth factor (PlGF), a member of the vascular endothelial growth factor family was found to be altered in diverse pathological conditions, e.g. endothelial dysfunction. This study evaluated the clinical role of PlGF in light-chain amyloidosis.

Methods

PlGF (cobas-PlGF, Roche Diagnostics, Mannheim, Germany) was analyzed in 125 consecutive patients with AL and correlated with diverse clinical parameters including mortality.

Results

Kidney (n = 76) and heart (n = 57) were predominantly affected by amyloid deposition. Median PlGF was 26.3 (21.1–42.1) ng/L, NT-proBNP 3649 (1124–8581) pg/mL, and hs-TnT 42 (21–107) ng/L. PlGF increased with number of organs involved and with deterioration of renal function. A significant correlation of PlGF with hs-TnT (ρ = 0.306; p = 0.0007) and NT-proBNP (ρ = 0.315; p = 0.0006) was observed, but no correlation was observed with clinical, echocardiography, and electrocardiography parameters of cardiac involvement. In this cohort 1-year all-cause mortality was 19.2 %. The best cutoff discriminating survivors and non-survivors was 28.44 ng/L (sensitivity 66.7 %; specificity 78.1 %). A three-step risk model including hs-TnT and NT-proBNP revealed a better discrimination if patients at intermediary risk were additionally stratified by PlGF. Net reclassification index was 37.2 % (p = 0.002). Multivariate analysis revealed PlGF, difference of involved and uninvolved light chain, number of organs involved and risk class according to troponin T and NT-proBNP as independent predictors of mortality.

Conclusion

Plasma PlGF values in AL are invariably associated with the number of involved organs, but not with clinical, echocardiography, and electrocardiography parameters of cardiac involvement. PlGF provide useful information for risk stratification of patients at intermediary risk according to hs-TnT and NT-proBNP.
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Metadata
Title
Improvement of risk assessment in systemic light-chain amyloidosis using human placental growth factor
Authors
Arnt V. Kristen
Johannes Rinn
Ute Hegenbart
David Lindenmaier
Corina Merkle
Christoph Röcken
Stefan Hardt
Evangelos Giannitsis
Hugo A. Katus
Publication date
01-03-2015
Publisher
Springer Berlin Heidelberg
Published in
Clinical Research in Cardiology / Issue 3/2015
Print ISSN: 1861-0684
Electronic ISSN: 1861-0692
DOI
https://doi.org/10.1007/s00392-014-0779-y

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