Untargeted metabolomic profiling reveals multiple pathway perturbations and new clinical biomarkers in urea cycle disorders

被引:44
作者
Burrage, Lindsay C. [1 ,2 ]
Thistlethwaite, Lillian [3 ]
Stroup, Bridget M. [1 ]
Sun, Qin [1 ]
Miller, Marcus J. [1 ,6 ]
Nagamani, Sandesh C. S. [1 ,2 ]
Craigen, William [1 ,2 ]
Scaglia, Fernando [1 ,2 ,4 ]
Sutton, V. Reid [1 ,2 ]
Graham, Brett [1 ,2 ,6 ]
Kennedy, Adam D. [5 ,7 ]
Milosavljevic, Aleksandar [1 ,3 ]
Lee, Brendan H. [1 ,2 ]
Elsea, Sarah H. [1 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Houston, TX 77030 USA
[3] Baylor Coll Med, Program Quantitat & Computat Biosci, Houston, TX 77030 USA
[4] Prince Wales Hosp, BCM CUHK Ctr Med Genet, ShaTin, Hong Kong, Peoples R China
[5] Metabolon Inc, Durham, NC USA
[6] Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[7] Baebies Inc, Durham, NC USA
关键词
metabolomics; urea cycle disorder; arginase deficiency; branched-chain amino acids; guanidino compounds; GUANIDINO COMPOUNDS; CEREBROSPINAL-FLUID; CEREBRAL-CORTEX; INBORN-ERRORS; DEFICIENCY; MUTATIONS; ARGININE; THERAPY; PLASMA; URINE;
D O I
10.1038/s41436-019-0442-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Untargeted metabolomic analysis is increasingly being used in the screening and management of individuals with inborn errors of metabolism (IEM). We aimed to test whether untargeted metabolomic analysis in plasma might be useful for monitoring the disease course and management of urea cycle disorders (UCDs). Methods: Untargeted mass spectrometry-based metabolomic analysis was used to generate z-scores for more than 900 metabolites in plasma from 48 individuals with various UCDs. Pathway analysis was used to identify common pathways that were perturbed in each UCD. Results: Our metabolomic analysis in plasma identified multiple potentially neurotoxic metabolites of arginine in arginase deficiency and, thus, may have utility in monitoring the efficacy of treatment in arginase deficiency. In addition, we were also able to detect multiple biochemical perturbations in all UCDs that likely reflect clinical management, including metabolite alterations secondary to dietary and medication management. Conclusion: In addition to utility in screening for IEM, our results suggest that untargeted metabolomic analysis in plasma may be beneficial for monitoring efficacy of clinical management and off-target effects of medications in UCDs and potentially other IEM.
引用
收藏
页码:1977 / 1986
页数:10
相关论文
共 38 条
[1]   Treatment of arginase deficiency revisited: guanidinoacetate as a therapeutic target and biomarker for therapeutic monitoring [J].
Amayreh, Wajdi ;
Meyer, Uta ;
Das, Anibh M. .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2014, 56 (10) :1021-1024
[2]   Aromatic L-amino acid decarboxylase deficiency diagnosed by clinical metabolomic profiling of plasma [J].
Atwal, Paldeep S. ;
Donti, Taraka R. ;
Cardon, Aaron L. ;
Bacino, C. A. ;
Sun, Qin ;
Emrick, L. ;
Sutton, V. Reid ;
Elsea, Sarah H. .
MOLECULAR GENETICS AND METABOLISM, 2015, 115 (2-3) :91-94
[3]   In vitro effects of L-arginine and guanidino compounds on NTPDase1 and 5′-nucleotidase activities from rat brain synaptosomes [J].
Balz, D ;
Wyse, ATD ;
Morsch, VM ;
da Silva, AC ;
Vieira, VL ;
Morsch, ALB ;
Schetinger, MRC .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2003, 21 (02) :75-82
[4]   A longitudinal study of urea cycle disorders [J].
Batshaw, Mark L. ;
Tuchman, Mendel ;
Summar, Marshall ;
Seminara, Jennifer .
MOLECULAR GENETICS AND METABOLISM, 2014, 113 (1-2) :127-130
[5]   Phenylbutyrate therapy for maple syrup urine disease [J].
Brunetti-Pierri, Nicola ;
Lanpher, Brendan ;
Erez, Ayelet ;
Ananieva, Elitsa A. ;
Islam, Mohammad ;
Marini, Juan C. ;
Sun, Qin ;
Yu, Chunli ;
Hegde, Madhuri ;
Li, Jun ;
Wynn, R. Max ;
Chuang, David T. ;
Hutson, Susan ;
Lee, Brendan .
HUMAN MOLECULAR GENETICS, 2011, 20 (04) :631-640
[6]   Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency [J].
Burrage, Lindsay C. ;
Sun, Qin ;
Elsea, Sarah H. ;
Jiang, Ming-Ming ;
Nagamani, Sandesh C. S. ;
Frankel, Arthur E. ;
Stone, Everett ;
Alters, Susan E. ;
Johnson, Dale E. ;
Rowlinson, Scott W. ;
Georgiou, George ;
Lee, Brendan H. .
HUMAN MOLECULAR GENETICS, 2015, 24 (22) :6417-6427
[7]   Sodium phenylbutyrate decreases plasma branched-chain amino acids in patients with urea cycle disorders [J].
Burrage, Lindsay C. ;
Jain, Mahim ;
Gandolfo, Laura ;
Lee, Brendan H. ;
Nagamani, Sandesh C. S. .
MOLECULAR GENETICS AND METABOLISM, 2014, 113 (1-2) :131-135
[8]   Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet [J].
Cappuccio, Gerarda ;
Pinelli, Michele ;
Alagia, Marianna ;
Donti, Taraka ;
Day-Salvatore, Debra-Lynn ;
Veggiotti, Pierangelo ;
De Giorgis, Valentina ;
Lunghi, Simona ;
Vari, Maria Stella ;
Striano, Pasquale ;
Brunetti-Pierri, Nicola ;
Kennedy, Adam D. ;
Elsea, Sarah H. .
PLOS ONE, 2017, 12 (09)
[9]   Next-generation metabolic screening: targeted and untargeted metabolomics for the diagnosis of inborn errors of metabolism in individual patients [J].
Coene, Karlien L. M. ;
Kluijtmans, Leo A. J. ;
van der Heeft, Ed ;
Engelke, Udo F. H. ;
de Boer, Siebolt ;
Hoegen, Brechtje ;
Kwast, Hanneke J. T. ;
van de Vorst, Maartje ;
Huigen, Marleen C. D. G. ;
Keularts, Irene M. L. W. ;
Schreuder, Michiel F. ;
van Karnebeek, Clara D. M. ;
Wortmann, Saskia B. ;
de Vries, Maaike C. ;
Janssen, Mirian C. H. ;
Gilissen, Christian ;
Engel, Jasper ;
Wevers, Ron A. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2018, 41 (03) :337-353
[10]  
Csardi G., 2005, Int J Comp Syst, V1695, P1