Bone marrow involvement in Gaucher disease at MRI : what long-term evolution can we expect under enzyme replacement therapy?

2015 ◽  
Vol 25 (10) ◽  
pp. 2969-2975 ◽  
Author(s):  
Benjamin Fedida ◽  
Sébastien Touraine ◽  
Jerôme Stirnemann ◽  
Nadia Belmatoug ◽  
Jean-Denis Laredo ◽  
...  
2015 ◽  
Vol 114 (2) ◽  
pp. S20-S21
Author(s):  
Nadia Belmatoug ◽  
Benjamin Fedida ◽  
Sebastien Touraine ◽  
Jerôme Stirnemann ◽  
Jean-Denis Laredo ◽  
...  

Blood ◽  
2006 ◽  
Vol 108 (3) ◽  
pp. 830-835 ◽  
Author(s):  
Maaike de Fost ◽  
Carla E. M. Hollak ◽  
Johanna E. M. Groener ◽  
Johannes M. F. G. Aerts ◽  
Mario Maas ◽  
...  

AbstractDosing of enzyme replacement therapy (ERT) for Gaucher disease type 1 is still a subject of debate and varies from 15 to 130 U/kg/mo, making a huge economic difference of US $70 000 to US $380 000 (€55 000-300 000) per patient per year. To investigate whether this difference in dosing ultimately translates into a different response, we retrospectively compared long-term outcome of ERT at 2 large European treatment centers, Academic Medical Center, Amsterdam, The Netherlands (n = 49, median dose, 15-30 U/kg/4 wks) and Heinrich-Heine University, Duesseldorf, Germany (n = 57, median dose, 80 U/kg/4 wks). These adult cohorts had a similar genetic background. All follow-up parameters were matched separately at baseline, to avoid bias with respect to disease severity. Improvement in hemoglobin, platelet count, and hepatosplenomegaly was not significantly different between both cohorts, whereas plasma chitotriosidase and bone marrow involvement by magnetic resonance imaging improved more quickly and was more pronounced in the higher-dosed group. Major bone complications rarely occurred in both groups. In conclusion, different dosing regimens of ERT do not affect outcome of hematologic and visceral parameters, but higher dosing leads to accelerated decrease of chitotriosidase and better objective bone response in adult type 1 Gaucher disease.


2018 ◽  
Vol 231 (02) ◽  
pp. 52-59
Author(s):  
André Lollert ◽  
Katharina Laudemann ◽  
Eugen Mengel ◽  
Christian Hoffmann ◽  
Larissa Moos ◽  
...  

Abstract Purpose We retrospectively assessed bone and visceral manifestations in patients with Gaucher disease type 1 (GD1) with whole-body magnetic resonance imaging (WB-MRI) to determine the effects of different timing in initiating long-term enzyme replacement therapy. Materials and Methods In 17 patients with GD1, we performed 2 WB-MRI examinations at a median interval of 13 months. Patients had received enzyme replacement therapy with alglucerase/imiglucerase for a median of 13 years prior to the first examination. MRI results were retrospectively stratified based on treatment initiation into 2 groups: “early” (age ≤12 years, median 5 years) and “late” (during adulthood, median 32 years). We evaluated occurrence of irreversible avascular necroses (AVN) and applied several semi-quantitative scores, including the Bone-Marrow-Burden (BMB) score, the Düsseldorf-Gaucher score (DGS), the Vertebra-Disc-Ratio (VDR), and the Gaucher disease type 1 Severity Scoring System (GD-DS3). Results MRI assessments showed no AVN in the “early” group. AVN were observed in 2 patients of the “late” group; one also had a splenic Gaucheroma. The follow-up examinations showed slight improvements in the BMB-score, DGS, and VDR, with similar tendencies in both treatment groups. The GD-DS3 score only improved in “late” group. Conclusion This retrospective study supported the ongoing clinical value of enzyme replacement therapy with alglucerase/imiglucerase, as WB-MRI-based scores stayed constant or slightly improved even after long-term treatment. Secondary complications were only observed in the late treatment group. Our results suggest that “early initiation” of enzyme replacement therapy may protect the bone.


1997 ◽  
Vol 7 (4) ◽  
pp. 486-491 ◽  
Author(s):  
S. Magnaldi ◽  
R. Longo ◽  
M. Ukmar ◽  
M. Zanatta ◽  
M. Bottega ◽  
...  

2014 ◽  
Vol 37 (6) ◽  
pp. 961-968 ◽  
Author(s):  
L. J. Anderson ◽  
W. Henley ◽  
K. M. Wyatt ◽  
V. Nikolaou ◽  
S. Waldek ◽  
...  

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