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

Author:

Pajares-García Sonia12,González de Aledo-Castillo José Manuel1ORCID,Flores-Jiménez José Eduardo1,Collado Tatiana1,Pérez Judit1,Paredes-Fuentes Abraham José1,Argudo-Ramírez Ana1,López-Galera Rosa María123,Prats Blanca4,García-Villoria Judit123

Affiliation:

1. Department of Biochemistry and Molecular Genetics, Section of Inborn Errors of Metabolism-IBC , Hospital Clinic , Barcelona , Spain

2. Center for Biomedical Research Network on Rare Diseases (CIBERER) , Madrid , Spain

3. Biomedical Research Institute , August Pi i Sunyer (IDIBAPS) , Barcelona , Spain

4. Health Department, Maternal and Child Health Service, Public Health Agency of Catalonia , The Government of Catalonia , Barcelona , Spain

Abstract

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 β-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.

Funder

Agència de Gestió d’Ajuts Universitaris i de Recerca (AGAUR) and the CERCA Programme/Generalitat de Catalunya

Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), an initiative of the Instituto de Salud Carlos III

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Reference41 articles.

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