Analysis of a second-tier test panel in dried blood spot samples using liquid chromatography-tandem mass spectrometry in Catalonia’s newborn screening programme
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 FP...
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creator | Pajares-García, Sonia González de Aledo-Castillo, José Manuel Flores-Jiménez, José Eduardo Collado, Tatiana Pérez, Judit Paredes-Fuentes, Abraham José Argudo-Ramírez, Ana López-Galera, Rosa María Prats, Blanca García-Villoria, Judit |
description | 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.
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.
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).
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. |
doi_str_mv | 10.1515/cclm-2023-0216 |
format | Article |
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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.
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).
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.</description><identifier>ISSN: 1434-6621</identifier><identifier>EISSN: 1437-4331</identifier><identifier>DOI: 10.1515/cclm-2023-0216</identifier><identifier>PMID: 37794778</identifier><language>eng</language><publisher>Germany: De Gruyter</publisher><subject>Aciduria ; acylcarnitines ; acylglycines ; Amino Acid Metabolism, Inborn Errors ; Amino acids ; Antibiotics ; Blood ; Brain Diseases, Metabolic ; Carnitine - analogs & derivatives ; Chromatography ; Chromatography, Liquid - methods ; Disorders ; Dried Blood Spot Testing - methods ; Genetic disorders ; Glutaryl-CoA Dehydrogenase - deficiency ; Homocysteine ; Humans ; Infant, Newborn ; Isomers ; Liquid chromatography ; Mass spectrometry ; Mass spectroscopy ; Medical screening ; Metabolites ; Neonatal Screening - methods ; Neonates ; newborn screening ; Organic acids ; Orotic acid ; Oxidation ; Quality control ; Scientific imaging ; second-tier test ; Spain ; Tandem Mass Spectrometry - methods ; Urea ; Vitamin B12 ; Vitamin deficiency</subject><ispartof>Clinical chemistry and laboratory medicine, 2024-02, Vol.62 (3), p.493-505</ispartof><rights>2023 Walter de Gruyter GmbH, Berlin/Boston.</rights><rights>2023 Walter de Gruyter GmbH, Berlin/Boston</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-d45db54948e0faea8dc997b4f822ccfdad6b5cb9c2bfb026b66803e620b71dff3</citedby><cites>FETCH-LOGICAL-c376t-d45db54948e0faea8dc997b4f822ccfdad6b5cb9c2bfb026b66803e620b71dff3</cites><orcidid>0000-0002-7622-417X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.degruyter.com/document/doi/10.1515/cclm-2023-0216/pdf$$EPDF$$P50$$Gwalterdegruyter$$H</linktopdf><linktohtml>$$Uhttps://www.degruyter.com/document/doi/10.1515/cclm-2023-0216/html$$EHTML$$P50$$Gwalterdegruyter$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,66754,68538</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37794778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pajares-García, Sonia</creatorcontrib><creatorcontrib>González de Aledo-Castillo, José Manuel</creatorcontrib><creatorcontrib>Flores-Jiménez, José Eduardo</creatorcontrib><creatorcontrib>Collado, Tatiana</creatorcontrib><creatorcontrib>Pérez, Judit</creatorcontrib><creatorcontrib>Paredes-Fuentes, Abraham José</creatorcontrib><creatorcontrib>Argudo-Ramírez, Ana</creatorcontrib><creatorcontrib>López-Galera, Rosa María</creatorcontrib><creatorcontrib>Prats, Blanca</creatorcontrib><creatorcontrib>García-Villoria, Judit</creatorcontrib><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</title><title>Clinical chemistry and laboratory medicine</title><addtitle>Clin Chem Lab Med</addtitle><description>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.
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.
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).
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.</description><subject>Aciduria</subject><subject>acylcarnitines</subject><subject>acylglycines</subject><subject>Amino Acid Metabolism, Inborn Errors</subject><subject>Amino acids</subject><subject>Antibiotics</subject><subject>Blood</subject><subject>Brain Diseases, Metabolic</subject><subject>Carnitine - analogs & derivatives</subject><subject>Chromatography</subject><subject>Chromatography, Liquid - methods</subject><subject>Disorders</subject><subject>Dried Blood Spot Testing - methods</subject><subject>Genetic disorders</subject><subject>Glutaryl-CoA Dehydrogenase - deficiency</subject><subject>Homocysteine</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Isomers</subject><subject>Liquid chromatography</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Medical screening</subject><subject>Metabolites</subject><subject>Neonatal Screening - methods</subject><subject>Neonates</subject><subject>newborn screening</subject><subject>Organic acids</subject><subject>Orotic acid</subject><subject>Oxidation</subject><subject>Quality control</subject><subject>Scientific imaging</subject><subject>second-tier test</subject><subject>Spain</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Urea</subject><subject>Vitamin B12</subject><subject>Vitamin deficiency</subject><issn>1434-6621</issn><issn>1437-4331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkcuKFTEQhhtRnItuXUrAjZsec-ukG9wMBx2FATe6bnKpPpMh6fQkaYaz8zXc-mg-iWnPqCCuUpCvvqLqb5oXBF-QjnRvjPGhpZiyFlMiHjWnhDPZcsbI4181b4Wg5KQ5y_kWY9J1XD5tTpiUA5eyP22-X87KH7LLKE5IoQwmzrYtDhIqkAta1AweuRnZ5MAi7WO0KC-xoKzC4iGjNbt5j7y7W51F5ibFoErcJ7XcHNqiZgsBBZVzbQJT6i-UdNiEO1WUj7NTP75-y2iGex3TjLJJAPNmXNJmCQGeNU8m5TM8f3jPmy_v333efWivP1193F1et4ZJUVrLO6s7PvAe8KRA9dYMg9R86ik1ZrLKCt0ZPRiqJ42p0EL0mIGgWEtip4mdN6-P3jr5bq3Lj8FlA97XE8Q1j7SXjHaEY1LRV_-gt3FN9ZKVGkiPO86prNTFkTIp5pxgGpfkgkqHkeBxS2_c0hu39MYtvdrw8kG76gD2D_47rgq8PQL3yhdIFvZpPdTi7_j_mwVlfGDsJ3ZFr14</recordid><startdate>20240226</startdate><enddate>20240226</enddate><creator>Pajares-García, Sonia</creator><creator>González de Aledo-Castillo, José Manuel</creator><creator>Flores-Jiménez, José Eduardo</creator><creator>Collado, Tatiana</creator><creator>Pérez, Judit</creator><creator>Paredes-Fuentes, Abraham José</creator><creator>Argudo-Ramírez, Ana</creator><creator>López-Galera, Rosa María</creator><creator>Prats, Blanca</creator><creator>García-Villoria, Judit</creator><general>De Gruyter</general><general>Walter De Gruyter & Company</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7622-417X</orcidid></search><sort><creationdate>20240226</creationdate><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</title><author>Pajares-García, Sonia ; González de Aledo-Castillo, José Manuel ; Flores-Jiménez, José Eduardo ; Collado, Tatiana ; Pérez, Judit ; Paredes-Fuentes, Abraham José ; Argudo-Ramírez, Ana ; López-Galera, Rosa María ; Prats, Blanca ; García-Villoria, Judit</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-d45db54948e0faea8dc997b4f822ccfdad6b5cb9c2bfb026b66803e620b71dff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aciduria</topic><topic>acylcarnitines</topic><topic>acylglycines</topic><topic>Amino Acid Metabolism, Inborn Errors</topic><topic>Amino acids</topic><topic>Antibiotics</topic><topic>Blood</topic><topic>Brain Diseases, Metabolic</topic><topic>Carnitine - analogs & derivatives</topic><topic>Chromatography</topic><topic>Chromatography, Liquid - methods</topic><topic>Disorders</topic><topic>Dried Blood Spot Testing - methods</topic><topic>Genetic disorders</topic><topic>Glutaryl-CoA Dehydrogenase - deficiency</topic><topic>Homocysteine</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Isomers</topic><topic>Liquid chromatography</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Medical screening</topic><topic>Metabolites</topic><topic>Neonatal Screening - methods</topic><topic>Neonates</topic><topic>newborn screening</topic><topic>Organic acids</topic><topic>Orotic acid</topic><topic>Oxidation</topic><topic>Quality control</topic><topic>Scientific imaging</topic><topic>second-tier test</topic><topic>Spain</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>Urea</topic><topic>Vitamin B12</topic><topic>Vitamin deficiency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pajares-García, Sonia</creatorcontrib><creatorcontrib>González de Aledo-Castillo, José Manuel</creatorcontrib><creatorcontrib>Flores-Jiménez, José Eduardo</creatorcontrib><creatorcontrib>Collado, Tatiana</creatorcontrib><creatorcontrib>Pérez, Judit</creatorcontrib><creatorcontrib>Paredes-Fuentes, Abraham José</creatorcontrib><creatorcontrib>Argudo-Ramírez, Ana</creatorcontrib><creatorcontrib>López-Galera, Rosa María</creatorcontrib><creatorcontrib>Prats, Blanca</creatorcontrib><creatorcontrib>García-Villoria, Judit</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical chemistry and laboratory medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pajares-García, Sonia</au><au>González de Aledo-Castillo, José Manuel</au><au>Flores-Jiménez, José Eduardo</au><au>Collado, Tatiana</au><au>Pérez, Judit</au><au>Paredes-Fuentes, Abraham José</au><au>Argudo-Ramírez, Ana</au><au>López-Galera, Rosa María</au><au>Prats, Blanca</au><au>García-Villoria, Judit</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of a second-tier test panel in dried blood spot samples using liquid chromatography-tandem mass spectrometry in Catalonia’s newborn screening programme</atitle><jtitle>Clinical chemistry and laboratory medicine</jtitle><addtitle>Clin Chem Lab Med</addtitle><date>2024-02-26</date><risdate>2024</risdate><volume>62</volume><issue>3</issue><spage>493</spage><epage>505</epage><pages>493-505</pages><issn>1434-6621</issn><eissn>1437-4331</eissn><abstract>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.
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.
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).
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.</abstract><cop>Germany</cop><pub>De Gruyter</pub><pmid>37794778</pmid><doi>10.1515/cclm-2023-0216</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-7622-417X</orcidid></addata></record> |
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subjects | Aciduria acylcarnitines acylglycines Amino Acid Metabolism, Inborn Errors Amino acids Antibiotics Blood Brain Diseases, Metabolic Carnitine - analogs & derivatives Chromatography Chromatography, Liquid - methods Disorders Dried Blood Spot Testing - methods Genetic disorders Glutaryl-CoA Dehydrogenase - deficiency Homocysteine Humans Infant, Newborn Isomers Liquid chromatography Mass spectrometry Mass spectroscopy Medical screening Metabolites Neonatal Screening - methods Neonates newborn screening Organic acids Orotic acid Oxidation Quality control Scientific imaging second-tier test Spain Tandem Mass Spectrometry - methods Urea Vitamin B12 Vitamin deficiency |
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 |
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