Analysis of a second-tier test panel in dried blood spot samples using liquid chromatography-tandem mass spectrometry in Catalonia's newborn screening programme

dc.contributor.author
Pajares García, Sonia
dc.contributor.author
González de Aledo-Castillo, José Manuel
dc.contributor.author
Flores Jiménez, José Eduardo
dc.contributor.author
Collado, Tatiana
dc.contributor.author
Pérez, Judit
dc.contributor.author
Paredes Fuentes, Abraham José
dc.contributor.author
Argudo Ramírez, Ana
dc.contributor.author
López Galera, Rosa Ma.
dc.contributor.author
Prats, Blanca
dc.contributor.author
García Villoria, Judit
dc.date.issued
2024-05-27T07:51:56Z
dc.date.issued
2024-10-06T05:10:10Z
dc.date.issued
2023-10-06
dc.date.issued
2024-05-15T13:58:45Z
dc.identifier
1437-4331
dc.identifier
https://hdl.handle.net/2445/211941
dc.identifier
9380624
dc.identifier
37794778
dc.description.abstract
Objectives: Acylcarnitine and amino acid analyses of dried blood spot (DBS) samples using tandem mass spectrometry in newborn screening (NBS) programmes can generate false positive (FP) results. Therefore, implementation of second-tier tests (2TTs) using DBS samples has become increasingly important to avoid FPs. The most widely used 2TT metabolites include methylmalonic acid, 3-hydroxypropionic acid, methylcitric acid, and homocysteine.Methods: We simultaneously measured 46 underivatised metabolites, including organic acids, acylglycine and acylcarnitine isomers, homocysteine, and orotic acid, in DBS samples using tandem mass spectrometry. To validate this method, we analysed samples from 147 healthy newborns, 160 patients with genetic disorders diagnosed via NBS, 20 patients with acquired vitamin B12 deficiency, 10 newborns receiving antibiotic treatment, and nine external quality control samples.Results: The validation study revealed that 31 metabolites showed good analytical performance. Furthermore, this method detected key metabolites for all diseases associated with increased levels of the following acylcarnitines: C3, C4, C5, C4DC\C5OH, and C5DC. The sensitivity of this method to detect all diseases was 100 %, and the specificity was 74-99 %, except for glutaric aciduria type 1. This method can also be used to diagnose mitochondrial fatty acid beta-oxidation disorders (FAODs) and urea cycle defects (UCDs).Conclusions: We have described a 2TT panel of 31 metabolites in DBS samples based on an easy and rapid method without derivatisation. Its implementation allowed us to distinguish between different organic acidurias, some FAODs, and UCDs. This new strategy has increased the efficiency of our NBS programme by reducing FP and false negative results, second sample requests, and the time required for diagnosis.
dc.format
12 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
De Gruyter
dc.relation
Versió preprint del document publicat a: https://doi.org/10.1515/cclm-2023-0216
dc.relation
Clinical Chemistry And Laboratory Medicine, 2023, vol. 62, num. 3, p. 493-505
dc.relation
https://doi.org/10.1515/cclm-2023-0216
dc.rights
(c) De Gruyter, 2023
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject
Neonatologia
dc.subject
Malalties cerebrals
dc.subject
Neonatology
dc.subject
Brain diseases
dc.title
Analysis of a second-tier test panel in dried blood spot samples using liquid chromatography-tandem mass spectrometry in Catalonia's newborn screening programme
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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