Elenga Narcisse, Yassin Mohamed A
Paediatric Department, Centre Hospitalier de Cayenne, Cayenne, France.
Hematology Section, Medical Oncology Department, Hamad Medical Corporation, Doha, Qatar.
Front Med (Lausanne). 2023 Dec 6;10:1243870. doi: 10.3389/fmed.2023.1243870. eCollection 2023.
Sickle cell disease (SCD) is a rare genetic blood condition affecting millions worldwide. Oxidative stress is a key player in the pathogenesis of SCD and its comorbid consequences. Renal function impairment is a common complication of SCD in both pediatric and adult patients with serious consequences leading to increased risk of mortality. In this observational real-world study, we are reporting the long-term (120 weeks) renal function in 10 patients treated with L-glutamine.
Ten patients (4 pediatric and 6 adults), with confirmed diagnoses of SCD (HbSS genotype), were enrolled, these included four patients from Qatar with Arab Indian haplotype and six patients from French Guiana with African haplotype. All patients were treated with L-glutamine oral powder (~0.3 g/kg body weight, Endari) twice daily for 120 weeks. Clinical events and laboratory parameters (renal function, hemoglobin, reticulocytes, and lactate dehydrogenase [LDH]) were measured at baseline, 48, and 120 weeks.
The study showed that with L-glutamine treatment there were improvements in renal and hematological parameters with no vaso-occlusive crisis at both 48-and 120-week follow-up time points in all 10 patients. Improvements were seen in the albumin creatinine ratio (ACR) from baseline to 48 weeks (mean [Standard deviation SD] ACR: -4.19 [9.81] mg/g) and 120 weeks (mean [SD] ACR: -12.31 [21.09] mg/g). Mean (SD) increase in hemoglobin concentrations from baseline to 48 weeks and 120 weeks was 0.72 (1) g/dL and 1.41 (0.79) g/dL, respectively. Mean (SD) reticulocyte counts and LDH levels decreased from baseline to 48 weeks (mean [SD] change from baseline to 48 weeks, reticulocyte counts: -40.30 [101.58] × 10 cells/L; LDH levels: -259 [154.93] U/L) and 120 weeks (mean [SD] change from baseline to 120 weeks, reticulocyte counts: -58.30 [128.38] × 10 cells/L; LDH levels: -344.80 [274.63] U/L).
This is one of the first studies that assessed the long-term renal outcomes in SCD using L-glutamine. L-glutamine improved the renal function in patients with SCD along with improvements in clinical outcomes and hemolysis, from 48 weeks and sustained through 120 weeks of treatment.
镰状细胞病(SCD)是一种罕见的遗传性血液疾病,影响着全球数百万人。氧化应激是SCD发病机制及其合并症后果的关键因素。肾功能损害是SCD在儿科和成年患者中的常见并发症,会导致严重后果,增加死亡风险。在这项观察性的真实世界研究中,我们报告了10例接受L-谷氨酰胺治疗患者的长期(120周)肾功能情况。
纳入10例确诊为SCD(HbSS基因型)的患者(4例儿科患者和6例成年患者),其中包括4例来自卡塔尔、具有阿拉伯印度单倍型的患者以及6例来自法属圭亚那、具有非洲单倍型的患者。所有患者每天两次口服L-谷氨酰胺粉末(约0.3 g/kg体重,Endari),持续120周。在基线、48周和120周时测量临床事件和实验室参数(肾功能、血红蛋白、网织红细胞和乳酸脱氢酶[LDH])。
研究表明,接受L-谷氨酰胺治疗后,所有10例患者在48周和120周的随访时间点,肾功能和血液学参数均有改善,且未发生血管闭塞性危机。从基线到48周(白蛋白肌酐比值[ACR]:平均[标准差SD]-4.19[9.81]mg/g)和120周(平均[SD]ACR:-12.31[·21.09]mg/g),ACR有所改善。从基线到48周和120周,血红蛋白浓度的平均(SD)增加值分别为0.72(1)g/dL和1.41(0.79)g/dL。从基线到48周(从基线到48周的平均[SD]变化,网织红细胞计数:-40.30[101.58]×10⁹细胞/L;LDH水平:-259[154.9·3]U/L)和120周(从基线到120周的平均[SD]变化,网织红细胞计数:-58.30[128.38]×10⁹细胞/L;LDH水平:-344.80[274.63]U/L),网织红细胞计数和LDH水平均从基线下降。
这是首批使用L-谷氨酰胺评估SCD长期肾脏结局的研究之一。L-谷氨酰胺改善了SCD患者的肾功能,同时临床结局和溶血情况也得到改善,从48周开始并持续至120周的治疗期。