Attitudes of Individuals with Gaucher Disease toward Substrate Reduction Therapies
- PMID: 28803392
- PMCID: PMC5794801
- DOI: 10.1007/s10897-017-0137-0
Attitudes of Individuals with Gaucher Disease toward Substrate Reduction Therapies
Abstract
Type 1 Gaucher disease (GD) is the most common lysosomal storage disorder. Previously, treatment for GD was limited to intravenous enzyme replacement therapies (ERTs). More recently, oral substrate reduction therapies (SRTs) were approved for treatment of GD. Although both therapies alleviate disease symptoms, attitudes toward SRTs and patient perceptions of health while using SRT have not been well established. Electronic surveys were administered to adults with GD and asked about treatment history, attitudes toward SRTs, and perception of health while using SRTs as compared to ERTs, if applicable to the participant. ERT users that were offered treatment with SRTs cited potential side effects, wanting more research on SRTs, and satisfaction with their current treatment regimen as reasons for declining SRTs. SRT users expressed convenience and less invasiveness as reasons for choosing SRTs. Additionally, those using SRTs most often perceived their health to be similar to when they previously used ERT. Participant responses illustrate that attitudes toward SRTs can be variable and that one particular treatment may not be ideal for all patients with GD depending on individual perceptions of factors such as convenience, invasiveness, or side effects. Thus, individuals with GD should be counseled adequately by healthcare providers about both ERTs and SRTs for treatment of GD now that SRTs are clinically available.
Keywords: Enzyme replacement therapy; Gaucher disease; Genetic counseling; Patient preferences; Substrate reduction therapy; Therapy preferences; Type 1 Gaucher disease.
Conflict of interest statement
Conflict of Interest
Victoria F. Wagner, Hope Northrup, S. Shahrukh Hashmi, Joanne M. Nguyen, Mary Kay Koenig, and Jessica M. Davis received funding from Sanofi Genzyme for this project. They declare that they have no additional conflicts of interest.
Funding
This study was funded by Sanofi Genzyme (GZ-2015-11365).
Human Studies and Informed Consent
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000. Informed consent was obtained from all participants included in the study.
Animal Studies
No animal studies were carried out by the authors for this article.
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