[依帕列净治疗糖原储存病Ⅰ型患儿的近期疗效]。

J J Jiang, X Zheng, M S Ma, X G Cui, S Jian, X Y Tang, X D Bao, S M Zhang, J R Ma, H M Song, Z Q Qiu
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Their clinical symptoms such as height and weight increase, abdominal pain, diarrhea, oral ulcer, infection times, and drug applications were recorded at 2 weeks, 1 month, 2 months, 3 months, 6 months, 9 months, 12 months, and 15 months after treatment to assess the therapeutic effect. The liquid chromatography-tandem mass spectrometry method was used to monitor the changes in 1, 5-anhydroglucitol (1, 5AG) concentration in plasma. At the same time, adverse reactions such as hypoglycemia and urinary tract infection were closely followed up and monitored. <b>Results:</b> The 4 patients with GSD Ⅰb were 15, 14, 4 and 14 years old, respectively at the beginning of empagliflozin treatment, and were followed up for 15, 15, 12 and 6 months, respectively. Maintenance dose range of empagliflozin was 0.24-0.39 mg/(kg·d). The frequency of diarrhea and abdominal pain decreased in cases 2, 3, and 4 at 1, 2 and 3 months of treatment, respectively. 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引用次数: 0

摘要

目的:分析恩格列净治疗糖原沉积病Ⅰb型(GSDⅠb)的短期疗效。方法:在这项前瞻性、开放标签单臂研究中,收集2020年12月至2022年12月北京协和医院儿科4例患者的数据。均经基因测序诊断为中性粒细胞减少症。这些患者接受恩格列净治疗。分别于治疗后2周、1个月、2个月、3个月、6个月、9个月、12个月、15个月记录患者身高、体重增加、腹痛、腹泻、口腔溃疡、感染次数、用药情况等临床症状,评价治疗效果。采用液相色谱-串联质谱法监测血浆中1,5 -无氢葡萄糖醇(1,5 ag)浓度的变化。同时密切随访监测低血糖、尿路感染等不良反应。结果:4例GSDⅠb患者开始恩格列净治疗时年龄分别为15、14、4、14岁,随访时间分别为15、15、12、6个月。依帕列净维持剂量范围为0.24 ~ 0.39 mg/(kg·d)。病例2、3、4分别在治疗1、2、3个月时腹泻和腹痛次数减少。他们的身高和体重都有不同程度的增加。中性粒细胞绝对计数分别从0.84×109、0.50×109、0.48×109、0.48×109/L增加到1.48×109、3.04×109、1.10×109、0.73×109/L。粒细胞集落刺激因子1例逐渐降低,3例停止。2例患儿在给予恩格列净后血浆1,5 AG水平显著降低(病例2从46.3 mg/L降至9.6 mg/L,病例3从56.1 mg/L降至15.0 mg/L), 4例患者均未发生低血糖、肝肾功能异常、泌尿系统感染等不良反应。结论:经短期观察,恩格列净可改善GSDⅠb口腔溃疡、腹痛、腹泻、反复感染等症状,并可缓解中性粒细胞减少症,降低血浆中1,5 ag浓度,安全性较好。
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[Short-term efficacy of empagliflozin in children with glycogen storage disease type Ⅰb].

Objective: To analyze the short-time efficacy of empagliflozin in the treatment of glycogen storage disease type Ⅰb (GSD Ⅰb). Methods: In this prospective open-label single-arm study, the data of 4 patients were collected from the pediatric department in Peking Union Medical College Hospital from December 2020 to December 2022. All of them were diagnosed by gene sequencing and had neutropenia. These patients received empagliflozin treatment. Their clinical symptoms such as height and weight increase, abdominal pain, diarrhea, oral ulcer, infection times, and drug applications were recorded at 2 weeks, 1 month, 2 months, 3 months, 6 months, 9 months, 12 months, and 15 months after treatment to assess the therapeutic effect. The liquid chromatography-tandem mass spectrometry method was used to monitor the changes in 1, 5-anhydroglucitol (1, 5AG) concentration in plasma. At the same time, adverse reactions such as hypoglycemia and urinary tract infection were closely followed up and monitored. Results: The 4 patients with GSD Ⅰb were 15, 14, 4 and 14 years old, respectively at the beginning of empagliflozin treatment, and were followed up for 15, 15, 12 and 6 months, respectively. Maintenance dose range of empagliflozin was 0.24-0.39 mg/(kg·d). The frequency of diarrhea and abdominal pain decreased in cases 2, 3, and 4 at 1, 2 and 3 months of treatment, respectively. Their height and weight increased at different degrees.The absolute count of neutrophils increased from 0.84×109, 0.50×109, 0.48×109, 0.48×109/L to 1.48×109, 3.04×109, 1.10×109, 0.73×109/L, respectively. Granulocyte colony-stimulating factor was gradually reduced in 1 patients and stopped in 3 patient. Plasma 1, 5 AG levels in 2 children were significantly decreased after administration of empagliflozin (from 46.3 mg/L to 9.6 mg/L in case 2, and from 56.1 mg/L to 15.0 mg/L in case 3). All 4 patients had no adverse reactions such as hypoglycemia, abnormal liver or kidney function, or urinary system infection. Conclusion: In short-term observation, empagliflozin can improve the symptoms of GSD Ⅰb oral ulcers, abdominal pain, diarrhea, and recurrent infection, also can alleviate neutropenia and decrease 1, 5AG concentration in plasma, with favorable safety.

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