Publication:
Our Journey from Individual Efforts to Nationwide Support: Implementing Newborn Screening for Spinal Muscular Atrophy in Serbia

dc.contributor.authorBrkušanin, Miloš (55659956500)
dc.contributor.authorGarai, Nemanja (58998128000)
dc.contributor.authorKaranović, Jelena (56055635600)
dc.contributor.authorŠljivančanin Jakovljević, Tamara (57207933278)
dc.contributor.authorDimitrijević, Aleksandra (14008428400)
dc.contributor.authorJovanović, Kristina (57201635836)
dc.contributor.authorMitrović, Tanja Lazić (36191969100)
dc.contributor.authorMiković, Željko (7801694296)
dc.contributor.authorBrajušković, Goran (55508235500)
dc.contributor.authorNikolić, Dimitrije Mihailo (8279362600)
dc.contributor.authorSavić-Pavićević, Dušanka (57212301497)
dc.date.accessioned2025-06-12T11:40:51Z
dc.date.available2025-06-12T11:40:51Z
dc.date.issued2024
dc.description.abstractInnovative treatments for spinal muscular atrophy (SMA) yield the utmost advantages only within the presymptomatic phase, underlining the significance of newborn screening (NBS). We aimed to establish statewide NBS for SMA in Serbia. Our stepwise implementation process involved technical validation of a screening assay, collaboration with patient organizations and medical professionals, a feasibility study, and negotiation with public health representatives. Over 12,000 newborns were tested during the 17-month feasibility study, revealing two unrelated SMA infants and one older sibling. All three children received therapeutic interventions during the presymptomatic phase and have shown no signs of SMA. No false-negative results were found among the negative test results. As frontrunners in this field in Serbia, we established screening and diagnostic algorithms and follow-up protocols and raised awareness among stakeholders about the importance of early disease detection, leading to the incorporation of NBS for SMA into the national program on 15 September 2023. Since then, 54,393 newborns have been tested, identifying six SMA cases and enabling timely treatment. Our study demonstrates that effective collaborations between academia, non-profit organizations, and industry are crucial in bringing innovative healthcare initiatives to fruition, and highlights the potential of NBS to revolutionize healthcare outcomes for presymptomatic SMA infants and their families. © 2024 by the authors.
dc.identifier.urihttps://doi.org/10.3390/ijns10030057
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85205070790&doi=10.3390%2fijns10030057&partnerID=40&md5=ee2fbf381075251ae9f6c78e77dfb166
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/898
dc.subjectfeasibility study
dc.subjectgenetic testing
dc.subjectmotor neuron disease
dc.subjectneonatal screening
dc.subjectnewborn screening
dc.subjectpopulation screening
dc.subjectpublic health
dc.subjectreal-time PCR
dc.subjectSMN1
dc.subjectspinal muscular atrophy
dc.titleOur Journey from Individual Efforts to Nationwide Support: Implementing Newborn Screening for Spinal Muscular Atrophy in Serbia
dspace.entity.typePublication

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