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Feasibility of newborn screening for guanidinoacetate methyltransferase (GAMT) deficiency

Overview of attention for article published in Journal of Inherited Metabolic Disease, November 2013
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Title
Feasibility of newborn screening for guanidinoacetate methyltransferase (GAMT) deficiency
Published in
Journal of Inherited Metabolic Disease, November 2013
DOI 10.1007/s10545-013-9662-7
Pubmed ID
Authors

Marzia Pasquali, Elisabeth Schwarz, Maren Jensen, Tatiana Yuzyuk, Irene DeBiase, Harper Randall, Nicola Longo

Abstract

Guanidinoacetate methyltransferase (GAMT) deficiency causes brain creatine deficiency characterized by developmental delays, speech delay, seizures and autism-like behavior. Identification and therapy at birth because of a positive family history has prevented intellectual disability and seizures in all cases reported. The objective of this study was to develop a method to identify patients with GAMT deficiency from newborn screening blood spots. Creatine and guanidinoacetate were extracted from 10,000 deidentified blood spots using the same protocol routinely used for newborn screening and quantified by stable isotope dilution using deuterated creatine and guanidinoacetate as internal standards. Residual dried blood spots from three infants with GAMT deficiency were used to evaluate the sensitivity of the method. A second tier test using UPLC-MS/MS was performed to analyze samples with a concentration of guanidinoacetate >2.44 μmol/L (99.5th centile of the normal population). Fifty four blood spots required second tier testing in addition to seven blood spots from three patients with GAMT deficiency retrospectively analyzed. With second tier testing, only the samples from GAMT deficiency patients had elevated concentration of guanidinoacetate. Our results show that GAMT deficiency can be identified in newborns using routine extraction methods. The cost of this additional screening is minimal, as it does not require additional instrumentation, procedure, or sample collection. The use of a second tier test can reduce the false positive rate to a minimum. Summary Brain creatine deficiency syndromes cause mental retardation that can be prevented if therapy is initiated early in life. This manuscript reports that infants with GAMT deficiency (one of the brain creatine deficiency syndromes) can be identified from elevated guanidinoacetate in newborn blood spots with virtually absent false-positive results using a second tier test.

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Mendeley readers

The data shown below were compiled from readership statistics for 70 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Germany 1 1%
Unknown 69 99%

Demographic breakdown

Readers by professional status Count As %
Researcher 14 20%
Student > Ph. D. Student 9 13%
Student > Master 9 13%
Student > Bachelor 5 7%
Student > Postgraduate 5 7%
Other 11 16%
Unknown 17 24%
Readers by discipline Count As %
Medicine and Dentistry 13 19%
Psychology 10 14%
Agricultural and Biological Sciences 6 9%
Biochemistry, Genetics and Molecular Biology 5 7%
Social Sciences 3 4%
Other 15 21%
Unknown 18 26%