Results of the Hungarian Newborn Screening Pilot Program for Spinal Muscular Atrophy

The growing need to identify spinal muscular atrophy (SMA) patients as early as possible has shifted attention to newborn screening (NBS). The aim of the present study was to evaluate the possibility of including the SMA-NBS in the Hungarian screening panel. As the first step, a government-funded pilot program started in November 2022 and continued until the end of 2023. Evaluation of the first 14 months was followed by the decision to lengthen the program until the end of 2024, which was further supported by the needs of society. Screening tests were performed in both Hungarian national screening laboratories uniformly using the combined EONIS SCID-SMA real-time PCR assay kit by Revvity, for the newborns whose parents gave written consent for the analysis. Altogether, 155,985 newborns were screened during the 26 months of the program, which was 87% of all newborns involved in the national neonatal screens of the same period. All 19 newborns identified on the screen were diagnosed with SMA, confirmed by a multiplex ligation-dependent probe amplification assay (MLPA). The favorable results of the pilot study support the inclusion of the SMA in the national screening panel at the earliest possible date.

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Publication Details

Journal
International Journal of Neonatal Screening
Published
2025-04-23
DOI
https://doi.org/10.3390/ijns11020029
Citations
2
Primary Topic
Neurogenetic and Muscular Disorders Research
Type
article
Field-Weighted Citation Impact
3.25

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article

Results of the Hungarian Newborn Screening Pilot Program for Spinal Muscular Atrophy

István Lénárt, Csaba Bereczki, Péter Monostori, Szabolcs Udvari et al.
2 citations
International Journal of Neonatal Screening
Neurogenetic and Muscular Disorders Research
3.25
article

Results of the Hungarian Newborn Screening Pilot Program for Spinal Muscular Atrophy

István Lénárt, Csaba Bereczki, Péter Monostori, Szabolcs Udvari, Ildikó Szatmári, Ákos Baráth, Attila Jozsef Szabo, Borbála Mikos, Krisztina Hegedűs, Mária Judit Molnár, Andrea Xue, Adrienn Géresi
article en
2 citations

Abstract

The growing need to identify spinal muscular atrophy (SMA) patients as early as possible has shifted attention to newborn screening (NBS). The aim of the present study was to evaluate the possibility of including the SMA-NBS in the Hungarian screening panel. As the first step, a government-funded pilot program started in November 2022 and continued until the end of 2023. Evaluation of the first 14 months was followed by the decision to lengthen the program until the end of 2024, which was further supported by the needs of society. Screening tests were performed in both Hungarian national screening laboratories uniformly using the combined EONIS SCID-SMA real-time PCR assay kit by Revvity, for the newborns whose parents gave written consent for the analysis. Altogether, 155,985 newborns were screened during the 26 months of the program, which was 87% of all newborns involved in the national neonatal screens of the same period. All 19 newborns identified on the screen were diagnosed with SMA, confirmed by a multiplex ligation-dependent probe amplification assay (MLPA). The favorable results of the pilot study support the inclusion of the SMA in the national screening panel at the earliest possible date.

International Journal of Neonatal ScreeningVol. 11(2)
Semmelweis University (HU), University of Szeged (HU)
Emberi Eroforrások Minisztériuma, Magyarország Kormánya, Medical Research Council
Reduced inequalities
Openalex Percentile: Top 9%
Neurogenetic and Muscular Disorders Research
3.25
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