Citrulline in the management of patients with urea cycle disorders

被引:1
|
作者
Imbard, Apolline [1 ,2 ]
Bouchereau, Juliette [3 ]
Arnoux, Jean-Baptiste [3 ]
Brassier, Anais [3 ]
Schiff, Manuel [3 ,4 ,5 ]
Berat, Claire-Marine [1 ,4 ]
Pontoizeau, Clement [1 ,4 ]
Benoist, Jean-Francois [1 ,2 ]
Josse, Constant [6 ]
Montestruc, Francois [6 ]
de Lonlay, Pascale [3 ,4 ,7 ]
机构
[1] AP HP, Dept Biochem, Paris, France
[2] Univ Paris Saclay, Paris, France
[3] Hop Necker Enfants Malad, AP HP, Reference Ctr Inborn Error Metab, Dept Pediat,G2M Network,MetabERN, Paris, France
[4] Univ Paris, Paris, France
[5] INSERM, Inst Imagine, UMR S1163, Paris, France
[6] eXYSTAT, F-92240 Malakoff, France
[7] INSERM, Inst Necker Enfants Malad INEM, UMR S1151, Paris, France
关键词
Ammonia; Arginine; Citrulline; Urea cycle disorders; ARGININE;
D O I
10.1186/s13023-023-02800-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
BackgroundTreatment recommendations for urea cycle disorders (UCDs) include supplementation with amino acids involved in the urea cycle (arginine and/or citrulline, depending on the enzyme deficiency), to maximize ammonia excretion through the urea cycle, but limited data are available regarding the use of citrulline. This study retrospectively reviewed clinical and biological data from patients with UCDs treated with citrulline and/or arginine at a reference center since 1990. The aim was to describe the prescription, impact, and safety of these therapies. Data collection included patient background, treatment details, changes in biochemical parameters (plasma ammonia and amino acids concentrations), decompensations, and patient outcomes.ResultsOverall, 79 patients (median age at diagnosis, 0.9 months) received citrulline and/or arginine in combination with a restricted protein diet, most with ornithine transcarbamylase (n = 57, 73%) or carbamoyl phosphate synthetase 1 (n = 15, 19%) deficiencies. Most patients also received ammonium scavengers. Median follow-up was 9.5 years and median exposure to first treatment with arginine + citrulline, citrulline monotherapy, or arginine monotherapy was 5.5, 2.5, or 0.3 years, respectively. During follow-up, arginine or citrulline was administered at least once (as monotherapy or in combination) in the same proportion of patients (86.1%); the overall median duration of exposure was 5.9 years for arginine + citrulline, 3.1 years for citrulline monotherapy, and 0.6 years for arginine monotherapy. The most common switch was from monotherapy to combination therapy (41 of 75 switches, 54.7%). During treatment, mean ammonia concentrations were 35.9 & mu;mol/L with citrulline, 49.8 & mu;mol/L with arginine, and 53.0 & mu;mol/L with arginine + citrulline. Mean plasma arginine concentrations increased significantly from the beginning to the end of citrulline treatment periods (from 67.6 & mu;mol/L to 84.9 & mu;mol/L, P < 0.05). At last evaluation, mean height and weight for age were normal and most patients showed normal or adapted behavior (98.7%) and normal social life (79.0%). Two patients (2.5%) experienced three treatment-related gastrointestinal adverse reactions.ConclusionsThis study underlines the importance of citrulline supplementation, either alone or together with arginine, in the management of patients with UCDs. When a monotherapy is considered, citrulline would be the preferred option in terms of increasing plasma arginine concentrations.
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页数:12
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