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依替膦森在一名患有杜氏肌营养不良症和镰状细胞贫血症男孩中的应用。

Eteplirsen Use in a Boy with Duchenne Muscular Dystrophy and Sickle Cell Anemia.

作者信息

Aiello Gregory M, Cartwright Michael Stephen

机构信息

Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.

Department of Neurology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.

出版信息

Case Rep Neurol. 2022 Oct 24;14(3):404-407. doi: 10.1159/000527358. eCollection 2022 Sep-Dec.


DOI:10.1159/000527358
PMID:36644004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9834637/
Abstract

Eteplirsen is an antisense oligonucleotide used in the treatment of Duchenne muscular dystrophy (DMD). The safety of eteplirsen use in individuals with rare comorbid conditions is not known. We present the case of a 4-year-old boy with a DMD exon deletion amenable to treatment with eteplirsen and comorbid sickle cell anemia. He has received eteplirsen treatment for 3 years with no clear adverse effects, including no increase in sickle cell crises.

摘要

依特普瑞森是一种用于治疗杜氏肌营养不良症(DMD)的反义寡核苷酸。在患有罕见合并症的个体中使用依特普瑞森的安全性尚不清楚。我们报告了一名4岁男孩的病例,他患有可使用依特普瑞森治疗的DMD外显子缺失,并合并镰状细胞贫血。他接受依特普瑞森治疗已3年,没有明显的不良反应,包括镰状细胞危象没有增加。

相似文献

[1]
Eteplirsen Use in a Boy with Duchenne Muscular Dystrophy and Sickle Cell Anemia.

Case Rep Neurol. 2022-10-24

[2]
Safety, tolerability and pharmacokinetics of eteplirsen in young boys aged 6-48 months with Duchenne muscular dystrophy amenable to exon 51 skipping.

Neuromuscul Disord. 2023-6

[3]
Open-Label Evaluation of Eteplirsen in Patients with Duchenne Muscular Dystrophy Amenable to Exon 51 Skipping: PROMOVI Trial.

J Neuromuscul Dis. 2021

[4]
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J Neuromuscul Dis. 2021

[5]
Pharmacology and toxicology of eteplirsen and SRP-5051 for DMD exon 51 skipping: an update.

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[6]
Survival among patients receiving eteplirsen for up to 8 years for the treatment of Duchenne muscular dystrophy and contextualization with natural history controls.

Muscle Nerve. 2024-7

[7]
Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy.

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[8]
Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy.

Ann Neurol. 2016-2

[9]
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[10]
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引用本文的文献

[1]
Duchenne muscular dystrophy caused by a deletion (c.5021del) in exon 35 of the DMD gene: A case report and review of the literature.

Heliyon. 2024-3-27

本文引用的文献

[1]
Casimersen: First Approval.

Drugs. 2021-5

[2]
Standard of care versus new-wave corticosteroids in the treatment of Duchenne muscular dystrophy: Can we do better?

Orphanet J Rare Dis. 2021-3-4

[3]
Current and emerging therapies for Duchenne muscular dystrophy and spinal muscular atrophy.

Pharmacol Ther. 2021-4

[4]
Mechanisms and Clinical Applications of Glucocorticoid Steroids in Muscular Dystrophy.

J Neuromuscul Dis. 2021

[5]
Sickle cell disease.

Nat Rev Dis Primers. 2018-3-15

[6]
Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease.

Molecules. 2017-4-5

[7]
Eteplirsen in the treatment of Duchenne muscular dystrophy.

Drug Des Devel Ther. 2017-2-28

[8]
Safety of antisense oligonucleotide and siRNA-based therapeutics.

Drug Discov Today. 2017-5

[9]
Antisense oligonucleotide therapies: the promise and the challenges from a toxicologic pathologist's perspective.

Toxicol Pathol. 2015-1

[10]
Serum transaminase levels in boys with Duchenne and Becker muscular dystrophy.

Pediatrics. 2010-12-13

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