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Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa

Preliminary data suggest a positive effect of taliglucerase alfa on the bone marrow infiltration of Gaucher cells. In this investigator-initiated study, we report the impact of taliglucerase alfa on the bone marrow fat fraction (FF) in 26 patients assessed by quantitative chemical shift imaging (QCS...

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Autores principales: Zimran, Ari, Dinur, Tama, Revel-Vilk, Shoshana, Akkerman, Eric M., van Dussen, Laura, Hollak, Carla E. M., Maayan, Hannah, Altarescu, Gheona, Chertkoff, Raul, Maas, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326976/
https://www.ncbi.nlm.nih.gov/pubmed/30066229
http://dx.doi.org/10.1007/s10545-018-0195-y
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author Zimran, Ari
Dinur, Tama
Revel-Vilk, Shoshana
Akkerman, Eric M.
van Dussen, Laura
Hollak, Carla E. M.
Maayan, Hannah
Altarescu, Gheona
Chertkoff, Raul
Maas, Mario
author_facet Zimran, Ari
Dinur, Tama
Revel-Vilk, Shoshana
Akkerman, Eric M.
van Dussen, Laura
Hollak, Carla E. M.
Maayan, Hannah
Altarescu, Gheona
Chertkoff, Raul
Maas, Mario
author_sort Zimran, Ari
collection PubMed
description Preliminary data suggest a positive effect of taliglucerase alfa on the bone marrow infiltration of Gaucher cells. In this investigator-initiated study, we report the impact of taliglucerase alfa on the bone marrow fat fraction (FF) in 26 patients assessed by quantitative chemical shift imaging (QCSI). Of 15 treatment-naïve patients (median age 48 [range 24–68] years), eight had baseline FF ≤ 0.3, six of those with a FF ≤ 0.23 (‘bone at risk’). All significantly improved from a median baseline FF of 0.24 (0.15–0.32) to 1st year FF of 0.37 (0.25–0.54) and 2nd year FF of 0.42 (0.27–0.59) (p = 0.01). Among the 11 ‘switch-over’ patients (median age 42 [range 33–69] years; median imiglucerase exposure 8 [range 1–17] years), eight had baseline FF ≤ 0.3, five of those with FF < 0.23. All, but one, significantly improved from a median baseline FF of 0.17 (0.08–0.28) to 1st year FF of 0.3 (0.05–0.34) and 2nd year FF of 0.34 (0.08–0.44) (p = 0.03). Two elderly female patients (age 43 and 58 years, with 17 years imiglucerase exposure) who remained at the same enzyme replacement therapy dose, increased from baseline FF of 0.13 and 0.19 to 0.26 at 1 year. Although the number of observations is small, we hypothesize that switching to taliglucerase may result in an improved bone marrow response. A larger study is needed to assess the early benefit of taliglucerase alfa in adult patients with type 1 Gaucher disease on the bone marrow compartment.
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spelling pubmed-63269762019-01-25 Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa Zimran, Ari Dinur, Tama Revel-Vilk, Shoshana Akkerman, Eric M. van Dussen, Laura Hollak, Carla E. M. Maayan, Hannah Altarescu, Gheona Chertkoff, Raul Maas, Mario J Inherit Metab Dis Original Article Preliminary data suggest a positive effect of taliglucerase alfa on the bone marrow infiltration of Gaucher cells. In this investigator-initiated study, we report the impact of taliglucerase alfa on the bone marrow fat fraction (FF) in 26 patients assessed by quantitative chemical shift imaging (QCSI). Of 15 treatment-naïve patients (median age 48 [range 24–68] years), eight had baseline FF ≤ 0.3, six of those with a FF ≤ 0.23 (‘bone at risk’). All significantly improved from a median baseline FF of 0.24 (0.15–0.32) to 1st year FF of 0.37 (0.25–0.54) and 2nd year FF of 0.42 (0.27–0.59) (p = 0.01). Among the 11 ‘switch-over’ patients (median age 42 [range 33–69] years; median imiglucerase exposure 8 [range 1–17] years), eight had baseline FF ≤ 0.3, five of those with FF < 0.23. All, but one, significantly improved from a median baseline FF of 0.17 (0.08–0.28) to 1st year FF of 0.3 (0.05–0.34) and 2nd year FF of 0.34 (0.08–0.44) (p = 0.03). Two elderly female patients (age 43 and 58 years, with 17 years imiglucerase exposure) who remained at the same enzyme replacement therapy dose, increased from baseline FF of 0.13 and 0.19 to 0.26 at 1 year. Although the number of observations is small, we hypothesize that switching to taliglucerase may result in an improved bone marrow response. A larger study is needed to assess the early benefit of taliglucerase alfa in adult patients with type 1 Gaucher disease on the bone marrow compartment. Springer Netherlands 2018-07-31 2018 /pmc/articles/PMC6326976/ /pubmed/30066229 http://dx.doi.org/10.1007/s10545-018-0195-y Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Zimran, Ari
Dinur, Tama
Revel-Vilk, Shoshana
Akkerman, Eric M.
van Dussen, Laura
Hollak, Carla E. M.
Maayan, Hannah
Altarescu, Gheona
Chertkoff, Raul
Maas, Mario
Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa
title Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa
title_full Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa
title_fullStr Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa
title_full_unstemmed Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa
title_short Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa
title_sort improvement in bone marrow infiltration in patients with type i gaucher disease treated with taliglucerase alfa
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326976/
https://www.ncbi.nlm.nih.gov/pubmed/30066229
http://dx.doi.org/10.1007/s10545-018-0195-y
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