New ratio as a useful marker for early diagnosis of proximal urea cycle disorders

被引:1
|
作者
Messina, MariaAnna [1 ]
Raudino, Federica [1 ]
Iacobacci, Riccardo [1 ]
Meli, Concetta [1 ]
Fiumara, Agata [1 ,2 ]
机构
[1] Univ Gaspare Rodolico San Marco, Pediat Clin, Referral Ctr Inherited Metab Disorders, Expanded Newborn Screening Lab, Catania, Italy
[2] Univ Catania, Clin & Expt Med Dept, Catania, Italy
关键词
ORNITHINE TRANSCARBAMYLASE DEFICIENCY; DRIED BLOOD SPOTS; QUANTIFICATION; GLUTAMINE; PLASMA;
D O I
10.1016/j.cca.2021.06.011
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background and aims: Proximal urea cycle disorders (PUCDs) are not included in most newborn screening programs due to the lack of adequate markers to monitor. Failure to alter citrulline and glutamine levels, the prognostic markers commonly used, can results in high false negative. Therefore, new biomarkers, prognostic of PUCDs, are strongly desirable. Materials and methods: We used tandem mass spectrometry to analyze blood spot from PUCDs patients during their follow up in our referral center focusing on glutamine to glutamate (Gln/Glu) ratio. We reanalyzed the same specimens of three patients after two months and the specimen of a new patient with suspicious of PUCD disorder. Results: Specimens of our patients shown a significant elevation of the ratio Gln/Glu compared to that of a healthy population (p < 0.05) as well as the specimens analyzed after two months, while the glutamine concentration dropped. New patient, showing high value of the ratio, was molecularly confirmed as PUCD patient. We further analyzed the blood spots from a neonatal population in order to fix a cut-off value and include it in a newborn screening panel. Conclusion: Our preliminary results suggest that the Gln/Glu ratio could be a very useful diagnostic marker, more stable over time than glutamine, which could improve the performance in early PUCDs identification.
引用
收藏
页码:154 / 159
页数:6
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