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A False-Positive Case of Methylmalonic Aciduria by Tandem Mass Spectrometry Newborn Screening Dependent on Maternal Malnutrition in Pregnancy

Bibliographic Data

ID15463102
AuthorsCláudia Rossi (0000-0003-0949-0280, University of Chieti-Pescara, corresponding author), Ilaria Cicalini (0000-0002-9792-2225, University of Chieti-Pescara), Cristiano Rizzo (0000-0002-5954-9749, Bambino Gesù Children's Hospital), Mirco Zucchelli (0000-0002-4242-5627, University of Chieti-Pescara), Ada Consalvo (0000-0003-3860-9404, University of Chieti-Pescara), Silvia Valentinuzzi (0000-0002-1561-3542, University of Chieti-Pescara), Daniela Semeraro (0000-0002-3881-5251, University of Chieti-Pescara), Giorgia Gasparroni (0000-0001-9495-5577, University of Chieti-Pescara), Patrizia Brindisino (University of Chieti-Pescara), Diego Gazzolo (0000-0002-0643-2555, University of Chieti-Pescara), Carlo Dionisi‐Vici (0000-0002-0007-3379, Bambino Gesù Children's Hospital), Vincenzo De Laurenzi (0000-0002-7506-1743, University of Chieti-Pescara), Damiana Pieragostino (0000-0003-1015-3484, University of Chieti-Pescara)
Year2020
Volume17
Issue10
Pages3601-3601
Publication date2020-05-20
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph17103601
PMID32443888
OpenAlexW3026629077
LanguageEN
Citations received1

Methylmalonic Acidurias (MMAs) are a group of inborn errors of metabolism (IEMs), specifically of propionate catabolism characterized by gastrointestinal and neurometabolic manifestations resulting from a deficiency in the function of methylmalonyl-CoA mutase, methylmalonyl-CoA epimerase, and cobalamin metabolism. In Expanded Newborn Screening (NBS), increased levels of propionylcarnitine (C3) and/or of its ratios by MS/MS analysis of dried blood spots (DBS) samples are suggestive for either Propionic Acidemia or MMAs. C3 elevation is not considered a specific marker for these disorders, resulting in high false-positive rates. The use of analyte ratios improves specificity, but it still cannot resolve the diagnostic issue. Second-tier testing are strongly recommended as confirmation of primary NBS results and for a differential diagnosis. LC-MS/MS analysis allows the quantification of more specific markers of the disorder. Here, we report the case of a newborn with a suspected MMA at Expanded NBS and at second-tier test. Given the urgent situation, in-depth diagnostic investigations were performed. Further investigations surprisingly revealed a Vitamin B12 deficiency due to a maternal malnutrition during pregnancy. This case emphasized that metabolic alterations at NBS may not only be influenced by genome and related to IEMs, but also to external factors and to maternal conditions

Biology · cobalamin · Mass spectrometry · Methylmalonic acid · Methylmalonic acidemia · Methylmalonic aciduria · Newborn screening · Pregnancy · Tandem mass spectrometry · Vitamin B12 · Chemistry · Folate and B Vitamins Research · Medicine · Metabolism and Genetic Disorders · Neonatal Health and Biochemistry · Endocrinology · Genetics · Internal Medicine · Pediatrics

  • Partial Biotinidase Deficiency Revealed Imbalances in Acylcarnitines Profile at Tandem Mass Spectrometry Newborn Screening

    Open Access•Ilaria Cicalini, Damiana Pieragostino et al.•International Journal of…•2021

Citations per year0.2
Citation span2021 - 2021 (1)
Highly citedNo

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