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依帕列净治疗 1b 型糖原贮积症的疗效和安全性:国际问卷调查数据。

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire.

机构信息

Department of General Pediatrics, Adolescent Medicine and Neonatology, Medical Centre-University of Freiburg, Faculty of Medicine, Freiburg, Germany.

Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center of Groningen, University of Groningen, Groningen, The Netherlands.

出版信息

Genet Med. 2022 Aug;24(8):1781-1788. doi: 10.1016/j.gim.2022.04.001. Epub 2022 May 3.

DOI:10.1016/j.gim.2022.04.001
PMID:35503103
Abstract

PURPOSE

This paper aims to report collective information on safety and efficacy of empagliflozin drug repurposing in individuals with glycogen storage disease type Ib (GSD Ib).

METHODS

This is an international retrospective questionnaire study on the safety and efficacy of empagliflozin use for management of neutropenia/neutrophil dysfunction in patients with GSD Ib, conducted among the respective health care providers from 24 countries across the globe.

RESULTS

Clinical data from 112 individuals with GSD Ib were evaluated, representing a total of 94 treatment years. The median age at start of empagliflozin treatment was 10.5 years (range = 0-38 years). Empagliflozin showed positive effects on all neutrophil dysfunction-related symptoms, including oral and urogenital mucosal lesions, recurrent infections, skin abscesses, inflammatory bowel disease, and anemia. Before initiating empagliflozin, most patients with GSD Ib were on G-CSF (94/112; 84%). At the time of the survey, 49 of 89 (55%) patients previously treated with G-CSF had completely stopped G-CSF, and another 15 (17%) were able to reduce the dose. The most common adverse event during empagliflozin treatment was hypoglycemia, occurring in 18% of individuals.

CONCLUSION

Empagliflozin has a favorable effect on neutropenia/neutrophil dysfunction-related symptoms and safety profile in individuals with GSD Ib.

摘要

目的

本文旨在报告依帕列净药物再利用在 1 型糖原贮积病(GSD Ib)个体中的安全性和疗效的综合信息。

方法

这是一项针对依帕列净用于治疗 GSD Ib 患者中性粒细胞减少症/中性粒细胞功能障碍的安全性和疗效的国际回顾性问卷调查研究,在全球 24 个国家的各自医疗保健提供者中进行。

结果

评估了 112 名 GSD Ib 个体的临床数据,共代表 94 年治疗。依帕列净治疗开始时的中位年龄为 10.5 岁(范围为 0-38 岁)。依帕列净对所有与中性粒细胞功能障碍相关的症状均有积极影响,包括口腔和泌尿生殖黏膜病变、复发性感染、皮肤脓肿、炎症性肠病和贫血。在开始依帕列净治疗之前,大多数 GSD Ib 患者正在接受 G-CSF(94/112;84%)治疗。在调查时,89 名曾接受 G-CSF 治疗的患者中有 49 名(55%)已完全停止 G-CSF 治疗,另有 15 名(17%)能够减少剂量。依帕列净治疗期间最常见的不良事件是低血糖,发生在 18%的个体中。

结论

依帕列净对 GSD Ib 个体的中性粒细胞减少症/中性粒细胞功能障碍相关症状和安全性具有良好的影响。

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