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Novel insights into antithrombin deficiency enabled by mass spectrometry-based precision diagnostics

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dc.contributor.author Kruijt, Mirjam
dc.contributor.author de-la-Morena-Barrio, María-Eugenia
dc.contributor.author Corral, Javier
dc.contributor.author Cobbaert, Christa-M
dc.contributor.author Ruhaak, L-Renee
dc.date.accessioned 2026-03-10T11:45:47Z
dc.date.available 2026-03-10T11:45:47Z
dc.date.issued 2025-01
dc.identifier.citation Kruijt M, De La Morena-Barrio ME, Corral J, Cobbaert CM, Ruhaak LR. Novel insights into antithrombin deficiency enabled by mass spectrometry-based precision diagnostics. Journal of Thrombosis and Haemostasis. enero de 2025;23(1):210-21. doi:10.1016/j.jtha.2024.10.005
dc.identifier.issn 1538-7933
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/25204
dc.description.abstract BACKGROUND: Although P5 (preventive, personalized, predictive, participatory, psychocognitive) medicine and patient-focused healthcare are gaining ground in various healthcare areas, the diagnosis of antithrombin deficiency (ATD) is still based on crude diagnostic tests, clustering patients into clinically heterogeneous subgroups whereby relevant thrombophilia phenotypes may go unnoticed. Clinical pathways and the majority of evidence are based on these tests; therefore, generic treatment is still the norm. OBJECTIVES: To unravel the heterogeneity of ATD, a mass spectrometry (liquid chromatography coupled to multiple-reaction-monitoring mass spectrometry [LC-MRM-MS])-based test for antithrombin was developed allowing molecular characterization of the antithrombin proteoforms in patient plasma. This study provides the first insight into the tests' clinical performance. METHODS: Plasma from 91 unrelated ATD patients and 41 patients with a congenital disorder of glycosylation affecting antithrombin glycosylation were characterized functionally, genetically, and analyzed by LC-MRM-MS. An established data analysis strategy was applied for quantitation and molecular characterization of antithrombin proteoforms. RESULTS: The test recognized patients with a quantitative defect, discriminated between type I and type II ATD, and identified variant proteoforms. Overall, the diagnostic sensitivity for ATD was 100% for LC-MRM-MS compared with 81.1% by the functional test. Type II ATD, a subtype prone to misdiagnosis, revealed an even larger difference of 100% identification by LC-MRM-MS vs 56.8% by functional test. CONCLUSION: The qualitative and quantitative mass spectrometry-based AT-test can serve as a platform for investigating the molecular basis of the clinical heterogeneity of ATD. This "precision diagnostics" approach for ATD can lower diagnostic uncertainty and modernize the ATD diagnostic and clinical pathways.
dc.language.iso eng
dc.publisher ELSEVIER SCIENCE INC
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es
dc.subject.mesh Humans
dc.subject.mesh Antithrombin III Deficiency/diagnosis/blood/genetics
dc.subject.mesh Mass Spectrometry/methods
dc.subject.mesh Chromatography, Liquid
dc.subject.mesh Antithrombin III/genetics
dc.subject.mesh Female
dc.subject.mesh Male
dc.subject.mesh Glycosylation
dc.subject.mesh Adult
dc.subject.mesh Middle Aged
dc.subject.mesh Precision Medicine
dc.subject.mesh Phenotype
dc.subject.mesh Antithrombins/blood
dc.subject.mesh Biomarkers/blood
dc.subject.mesh Predictive Value of Tests
dc.title Novel insights into antithrombin deficiency enabled by mass spectrometry-based precision diagnostics
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 39423957
dc.relation.publisherversion https://linkinghub.elsevier.com/retrieve/pii/S1538783624006111
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1016/j.jtha.2024.10.005
dc.journal.title Journal of Thrombosis and Haemostasis
dc.identifier.essn 1538-7836


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