Brkušanin Miloš, Garai Nemanja, Karanović Jelena, Šljivančanin Jakovljević Tamara, Dimitrijević Aleksandra, Jovanović Kristina, Mitrović Tanja Lazić, Miković Željko, Brajušković Goran, Nikolić Dimitrije Mihailo, Savić-Pavićević Dušanka
Centre for Human Molecular Genetics, Faculty of Biology, University of Belgrade, 11000 Belgrade, Serbia.
Department of Neonatology, Obstetrics and Gynaecology Clinic Narodni Front, 11000 Belgrade, Serbia.
Int J Neonatal Screen. 2024 Aug 15;10(3):57. doi: 10.3390/ijns10030057.
Innovative 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.
脊髓性肌肉萎缩症(SMA)的创新疗法仅在症状前阶段能带来最大益处,这凸显了新生儿筛查(NBS)的重要性。我们旨在在塞尔维亚建立全国性的SMA新生儿筛查项目。我们的逐步实施过程包括对筛查检测方法进行技术验证、与患者组织及医学专业人员合作、开展可行性研究以及与公共卫生代表进行协商。在为期17个月的可行性研究中,对超过12,000名新生儿进行了检测,发现了两名无亲缘关系的SMA婴儿以及一名年长的同胞。这三名儿童均在症状前阶段接受了治疗干预,且未出现SMA症状。在阴性检测结果中未发现假阴性情况。作为塞尔维亚该领域的先驱,我们制定了筛查和诊断算法以及后续随访方案,并提高了利益相关者对早期疾病检测重要性的认识,从而促使SMA新生儿筛查于2023年9月15日纳入国家项目。自那时起,已有54,393名新生儿接受了检测,确诊了6例SMA病例并实现了及时治疗。我们的研究表明,学术界、非营利组织和行业之间的有效合作对于推动创新医疗举措取得成果至关重要,并凸显了新生儿筛查为症状前SMA婴儿及其家庭带来医疗变革的潜力。