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      Benzene Derivatives from Ink Lead to False Positive Results in Neonatal Hyperphenylalaninemia Screening with Ninhydrin Fluorometric Method

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          Abstract

          Ninhydrin-based fluorometric quantification of phenylalanine is one of the most widely used methods for hyperphenylalaninemia (HPA) screening in neonates due to its high sensitivity, high accuracy, and low cost. Here we report an increase of false positive cases in neonatal HPA screening with this method, caused by contamination of blood specimen collection devices during the printing process. Through multiple steps of verification, the contaminants were identified from ink circles printed on the collection devices to indicate the positions and sizes of blood drops. Blood specimens from HPA-negative persons collected on these contaminated collection devices showed positive results in the fluorometric tests, but negative results in tandem mass spectroscopy (MS/MS) experiments. Contaminants on the collection devices could be extracted by 80% ethanol and showed an absorption peak around 245 nm, suggesting that these contaminants may contain benzene derivatives with similar structure to phenylalanine. High-performance liquid chromatography (HPLC) analysis of the ethanol extracts from contaminated collection devices identified two prominent peaks specifically from the devices. Methyl-2-benzoylbenzoate (MBB, CAS#606-28-0) was found as one of the major chemicals from contaminated collection devices. This report aims to remind colleagues in the field of this potential contamination and call for tighter regulation and quality control of specimen collection devices.

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          Most cited references14

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          Genetics of Phenylketonuria: Then and Now.

          Nenad Blau (2016)
          More than 950 phenylalanine hydroxylase (PAH) gene variants have been identified in people with phenylketonuria (PKU). These vary in their consequences for the residual level of PAH activity, from having little or no effect to abolishing PAH activity completely. Advances in genotyping technology and the availability of locus-specific and genotype databases have greatly expanded our understanding of the correlations between individual gene variant, residual PAH activity, tetrahydrobiopterin (BH4 ) responsiveness, and the clinical PKU phenotype. Most patients (∼76%) have compound heterozygous PAH gene variants and one mutated allele may markedly influence the activity of the second mutated allele, which in turn may influence either positively or negatively the activity of the biologically active heterotetrameric form of the PAH. While it is possible to predict the level of BH4 responsiveness (∼71%) and PKU severity (∼78%) from the nature of the underlying gene variants, these relationships remain complex and incompletely understood. A greater understanding of these relationships may increase the potential for individualized management of PKU in future. Inherited deficiencies in BH4 metabolism account for about 1%-2% of all hyperphenylalaninemias and are clinically more severe than PKU. Almost 90% of all patients are deficient in 6-pyruvoyl-tetrahydropterin synthase and dihydropteridine reductase.
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            Phenylketonuria: Direct and indirect effects of phenylalanine.

            High phenylalanine concentrations in the brain due to dysfunctional phenylalanine hydroxylase (Pah) are considered to account for mental retardation in phenylketonuria (PKU). In this study, we treated hippocampal cultures with the amino acid in order to determine the role of elevated levels of phenylalanine in PKU-related mental retardation. Synapse density and dendritic length were dramatically reduced in hippocampal cultures treated with phenylalanine. Changes in cofilin expression and phosphorylation status, which were restored by NMDA, as well as reduced activation of the small GTPase Rac1, likely underlie these structural alterations. In the Pah(enu2) mouse, which carries a mutated Pah gene, we previously found higher synaptic density due to delayed synaptic pruning in response to insufficient microglia function. Microglia activity and C3 complement expression, both of which were reduced in the Pah(enu2) mouse, however, were unaffected in hippocampal cultures treated with phenylalanine. The lack of a direct effect of phenylalanine on microglia is the key to the opposite effects regarding synapse stability in vitro and in the Pah(enu2) mouse. Judging from our data, it appears that another player is required for the inactivation of microglia in the Pah(enu2) mouse, rather than high concentrations of phenylalanine alone. Altogether, the data underscore the necessity of a lifelong phenylalanine-restricted diet.
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              Sapropterin treatment does not enhance the health-related quality of life of patients with phenylketonuria and their parents.

              Sapropterin causes reductions in blood phenylalanine concentrations in sensitive patients with phenylketonuria (PKU). We examined whether the subsequent relaxation of dietary restrictions influenced the quality of life (QoL) of patients and parents.
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                Author and article information

                Journal
                Int J Neonatal Screen
                Int J Neonatal Screen
                IJNS
                International Journal of Neonatal Screening
                MDPI
                2409-515X
                29 February 2020
                March 2020
                : 6
                : 1
                : 14
                Affiliations
                [1 ]Tianjin Women’s and Children’s Health Centre, Tianjin 300070, China; yaojingyi82@ 123456126.com (J.Y.); cuilan68@ 123456126.com (L.C.); panlei2121@ 123456126.com (L.P.); xinli66@ 123456126.com (L.X.)
                [2 ]Newborn Screening and Molecular Biology Branch, Division of Laboratory Sciences, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA; jvm0@ 123456cdc.gov
                [3 ]Department of Biology, College of Life Sciences, Tianjin University, Tianjin 300072, China; yanglululu@ 123456tju.edu.cn (L.Y.); zefangwang@ 123456tju.edu.cn (Z.W.)
                [4 ]Department of Basic Medicine, Tianjin Medical College, Tianjin 300222, China; luoping62@ 123456163.com
                [5 ]Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin 300308, China; douding.wxn@ 123456gmail.com
                [6 ]Binhai Genomics Institute, BGI-Tianjin, BGI-Shenzhen, Tianjin 300308, China; yuanwang@ 123456genomics.cn
                Author notes
                [* ]Correspondence: rustyfengsr@ 123456hotmail.com ; Tel.: +86-22-58297982
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0003-1619-3436
                Article
                IJNS-06-00014
                10.3390/ijns6010014
                7422975
                33073012
                d658b358-caf4-48a8-9ac7-ad716d19452e
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 27 November 2019
                : 18 February 2020
                Categories
                Article

                neonatal screening,hyperphenylalaninemia (hpa), false-positive,ninhydrin fluorometric test,specimen collection devices,filter paper,newborns,dried blood spots

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