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 De...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 61(2023), 6 vom: 02. Juni, Seite 515-519
1. Verfasser: Jiang, J J (VerfasserIn)
Weitere Verfasser: Zheng, X, Ma, M S, Cui, X G, Jian, S, Tang, X Y, Bao, X D, Zhang, S M, Ma, J R, Song, H M, Qiu, Z Q
Format: Online-Aufsatz
Sprache:Chinese
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:English Abstract Journal Article empagliflozin HDC1R2M35U
LEADER 01000naa a22002652 4500
001 NLM358141168
003 DE-627
005 20231226074119.0
007 cr uuu---uuuuu
008 231226s2023 xx |||||o 00| ||chi c
024 7 |a 10.3760/cma.j.cn112140-20230131-00067  |2 doi 
028 5 2 |a pubmed24n1193.xml 
035 |a (DE-627)NLM358141168 
035 |a (NLM)37312462 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a chi 
100 1 |a Jiang, J J  |e verfasserin  |4 aut 
245 1 0 |a Short-term efficacy of empagliflozin in children with glycogen storage disease type Ⅰb 
264 1 |c 2023 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 15.06.2023 
500 |a Date Revised 15.06.2023 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a 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 
650 4 |a English Abstract 
650 4 |a Journal Article 
650 7 |a empagliflozin  |2 NLM 
650 7 |a HDC1R2M35U  |2 NLM 
700 1 |a Zheng, X  |e verfasserin  |4 aut 
700 1 |a Ma, M S  |e verfasserin  |4 aut 
700 1 |a Cui, X G  |e verfasserin  |4 aut 
700 1 |a Jian, S  |e verfasserin  |4 aut 
700 1 |a Tang, X Y  |e verfasserin  |4 aut 
700 1 |a Bao, X D  |e verfasserin  |4 aut 
700 1 |a Zhang, S M  |e verfasserin  |4 aut 
700 1 |a Ma, J R  |e verfasserin  |4 aut 
700 1 |a Song, H M  |e verfasserin  |4 aut 
700 1 |a Qiu, Z Q  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Zhonghua er ke za zhi = Chinese journal of pediatrics  |d 1960  |g 61(2023), 6 vom: 02. Juni, Seite 515-519  |w (DE-627)NLM136249191  |x 0578-1310  |7 nnns 
773 1 8 |g volume:61  |g year:2023  |g number:6  |g day:02  |g month:06  |g pages:515-519 
856 4 0 |u http://dx.doi.org/10.3760/cma.j.cn112140-20230131-00067  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_11 
912 |a GBV_ILN_20 
912 |a GBV_ILN_22 
912 |a GBV_ILN_24 
912 |a GBV_ILN_31 
912 |a GBV_ILN_39 
912 |a GBV_ILN_40 
912 |a GBV_ILN_50 
912 |a GBV_ILN_61 
912 |a GBV_ILN_65 
912 |a GBV_ILN_69 
912 |a GBV_ILN_70 
912 |a GBV_ILN_72 
912 |a GBV_ILN_120 
912 |a GBV_ILN_130 
912 |a GBV_ILN_227 
912 |a GBV_ILN_244 
912 |a GBV_ILN_285 
912 |a GBV_ILN_294 
912 |a GBV_ILN_350 
912 |a GBV_ILN_665 
912 |a GBV_ILN_813 
951 |a AR 
952 |d 61  |j 2023  |e 6  |b 02  |c 06  |h 515-519