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两例1型戈谢病患者联合使用米格鲁司他和酶替代疗法:两例病例报告

Combined miglustat and enzyme replacement therapy in two patients with type 1 Gaucher disease: two case reports.

作者信息

Amato Dominick, Patterson Mary Anne

机构信息

Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.

Department of Medicine, Mount Sinai Hospital, 60 Murray Street, Room L-315, Box 34, Toronto, ON, M5G 1X5, Canada.

出版信息

J Med Case Rep. 2018 Jan 27;12(1):19. doi: 10.1186/s13256-017-1541-7.

Abstract

BACKGROUND

Intravenous enzyme replacement therapy is a first-line therapy for Gaucher disease type 1, and substrate reduction therapy represents an oral treatment alternative. Both enzyme replacement therapy and substrate reduction therapy are generally used as monotherapies in Gaucher disease. However, one randomized study and several case reports have described combination therapy over short time periods.

CASE PRESENTATION

We report two female Gaucher disease type 1 patients of mainly Anglo-Saxon descent, where combined enzyme replacement therapy and miglustat substrate reduction therapy were administered to overcome refractory clinical symptoms. The first patient was diagnosed at age 17 and developed Gaucher disease-related bone manifestations that worsened despite starting imiglucerase enzyme replacement therapy. After switching to miglustat substrate reduction therapy, her bone symptoms improved, but she developed tremors and eventually switched back to enzyme replacement therapy. Miglustat was later recommenced in combination with ongoing enzyme replacement therapy due to continued bone pain, and her bone symptoms improved along with maintained visceral manifestations. Enzyme replacement therapy was subsequently tapered off and the patient has since been successfully maintained on miglustat. The second patient was diagnosed aged 3, and commenced imiglucerase enzyme replacement therapy aged 15. After 9 years on enzyme replacement therapy she switched to miglustat substrate reduction therapy and her core symptoms were maintained/stable for 3 years. Imiglucerase enzyme replacement therapy was later added as a boost to therapy and her symptoms were subsequently maintained over a 2.3-year period. However, miglustat was discontinued due to her relocation, necessitating an increase in enzyme replacement therapy dose. Overall, both patients benefited from combination therapy.

CONCLUSION

While the majority of Gaucher disease type 1 patients will not need treatment with both substrate reduction therapy and enzyme replacement therapy, the current case reports demonstrate that judicious use of combination therapy may be of benefit in some cases.

摘要

背景

静脉内酶替代疗法是1型戈谢病的一线治疗方法,而底物减少疗法是一种口服治疗选择。酶替代疗法和底物减少疗法在戈谢病中通常都作为单一疗法使用。然而,一项随机研究和几例病例报告描述了短时间内的联合治疗。

病例介绍

我们报告了两名主要为盎格鲁-撒克逊血统的1型戈谢病女性患者,她们接受了酶替代疗法和米格列醇底物减少疗法的联合治疗,以克服难治性临床症状。第一名患者在17岁时被诊断出患有戈谢病,尽管开始使用伊米苷酶进行酶替代疗法,但仍出现了与戈谢病相关的骨骼表现且病情恶化。在改用米格列醇底物减少疗法后,她的骨骼症状有所改善,但出现了震颤,最终又换回了酶替代疗法。由于持续的骨痛,后来再次开始使用米格列醇并与持续的酶替代疗法联合使用,她的骨骼症状得到改善,同时内脏表现也得以维持。随后逐渐减少酶替代疗法的剂量,此后患者一直成功地使用米格列醇维持治疗。第二名患者3岁时被诊断出患有戈谢病,15岁时开始使用伊米苷酶进行酶替代疗法。在接受酶替代疗法9年后,她改用米格列醇底物减少疗法,其核心症状维持/稳定了3年。后来添加伊米苷酶进行强化治疗,随后她的症状在2.3年的时间里得以维持。然而,由于她搬迁,停用了米格列醇,这就需要增加酶替代疗法的剂量。总体而言,两名患者均从联合治疗中获益。

结论

虽然大多数1型戈谢病患者不需要同时使用底物减少疗法和酶替代疗法,但目前的病例报告表明,在某些情况下明智地使用联合治疗可能有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/639c/5787317/7195e34bbd0c/13256_2017_1541_Fig1_HTML.jpg

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