Literature DB >> 27839985

Reported outcomes of 453 pregnancies in patients with Gaucher disease: An analysis from the Gaucher outcome survey.

Heather Lau1, Nadia Belmatoug2, Patrick Deegan3, Ozlem Goker-Alpan4, Ida Vanessa D Schwartz5, Suma P Shankar6, Zoya Panahloo7, Ari Zimran8.   

Abstract

Gaucher disease (GD) may worsen during pregnancy, leading to the discussion of continuing treatment during pregnancy. We examined fetal outcomes of pregnancies reported in the Gaucher Outcome Survey, an international GD-specific registry established in 2010. A total of 453 pregnancies were reported. Most pregnancies (336/453, 74.2%) were in women who did not receive GD-specific treatment during pregnancy, while enzyme replacement therapy (ERT) was received during 117/453 (25.8%) pregnancies. No pregnancies exposed to substrate reduction therapy were reported. The percentage of normal outcomes (live birth delivered at term with no congenital abnormalities) was similar in untreated and treated pregnancies (92.9% vs. 91.4%). The percentage of spontaneous abortions in untreated pregnancies was 3.6% (95% CI, 1.9%- 6.2%) compared with 6.9% (95% CI, 3.0%-13.1%) in treated pregnancies (p=0.1866). In women who received velaglucerase alfa <1month prior to conception and/or during pregnancy, 34/36 (94.4%) pregnancies had normal outcomes and 2 (5.6%) ended in spontaneous abortion. Normal outcomes were observed in the 20 pregnancies with velaglucerase alfa exposure starting <1month prior to conception and continuing through all trimesters. These observations, in addition to information in the literature, suggest that continuation of ERT during pregnancy may be appropriate for GD patients.
Copyright © 2016 Shire Human Genetic Therapies, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Enzyme replacement therapy; Gaucher disease; Pregnancy; Velaglucerase alfa

Mesh:

Substances:

Year:  2016        PMID: 27839985     DOI: 10.1016/j.bcmd.2016.10.003

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  6 in total

1.  Recent advances in the diagnosis and management of Gaucher disease.

Authors:  Sam E Gary; Emory Ryan; Alta M Steward; Ellen Sidransky
Journal:  Expert Rev Endocrinol Metab       Date:  2018-03-12

Review 2.  Gaucher disease: Basic and translational science needs for more complete therapy and management.

Authors:  Gregory A Grabowski; Armand H M Antommaria; Edwin H Kolodny; Pramod K Mistry
Journal:  Mol Genet Metab       Date:  2020-12-29       Impact factor: 4.797

3.  Characteristics of 26 patients with type 3 Gaucher disease: A descriptive analysis from the Gaucher Outcome Survey.

Authors:  Ida Vanessa D Schwartz; Özlem Göker-Alpan; Priya S Kishnani; Ari Zimran; Lydie Renault; Zoya Panahloo; Patrick Deegan
Journal:  Mol Genet Metab Rep       Date:  2017-12-27

4.  Demographics and patient characteristics of 1209 patients with Gaucher disease: Descriptive analysis from the Gaucher Outcome Survey (GOS).

Authors:  Ari Zimran; Nadia Belmatoug; Bruno Bembi; Patrick Deegan; Deborah Elstein; Diego Fernandez-Sasso; Pilar Giraldo; Ozlem Goker-Alpan; Heather Lau; Elena Lukina; Zoya Panahloo; Ida Vanessa D Schwartz
Journal:  Am J Hematol       Date:  2017-12-12       Impact factor: 10.047

5.  Safety and effectiveness of taliglucerase alfa in patients with Gaucher disease: an interim analysis of real-world data from a multinational drug registry (TALIAS).

Authors:  Lina Titievsky; Tilman Schuster; Ronnie Wang; Muhammad Younus; Andrew Palladino; Kabir Quazi; Michael P Wajnrajch; Betina Hernandez; Pamela S Becker; Neal J Weinreb; Christina Chambers; Roy Mansfield; Louise Taylor; Li-Jung Tseng; Paige Kaplan
Journal:  Orphanet J Rare Dis       Date:  2022-04-01       Impact factor: 4.123

Review 6.  The Importance of a Multidisciplinary Approach in the Management of a Patient with Type I Gaucher Disease.

Authors:  Miguel-Ángel Torralba-Cabeza; Susana Olivera-González; José-Luis Sierra-Monzón
Journal:  Diseases       Date:  2018-07-26
  6 in total

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