Aftermath of the pilot project on neonatal screening for spinal muscular atrophy in the City of Saint Petersburg, Russia. Organizational, diagnostic and clinical aspects

A. Glotov, A. Kiselev, M. Maretina, L.M. Shchyugareva, S. Shtykalova, N. Maslyanyuk, M.V. Plokhikh, T.V. Kabakova, A. Andreeva, L. Koroleva, O.B. Sokolova, T.A. Antsiferova, M.E. Orlovskaya, A. Kyanksep, O. Nevmerzhitskaya, E. S. Kuznetsova, E.N. Slastenova, S. Vinogradova, Y. Pavlenko, M. Kruchina, N. A. Filatova, V. Bezhenar, O.Yu. Krishtofik, M.B. Fedotova, S.A. Fomin, S. V. Moiseev, I. Sosnina, A. Koroteev, Yuu V Gorelik, O. Bespalova, I. Kogan, V. Baranov
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Abstract

Spinal muscular atrophy (SMA) is one of the most frequent and severe hereditary diseases that leads to the destruction of motor neurons in the spinal cord and muscle weakness and is resulted from mutations in the SMN1 gene. The purpose of this research was to identify homo- and heterozygous mutations in the SMN1 gene in newborns. Materials and methods used: a multicenter prospective open continuous screening study of newborns at the age of 4 DoL (for full-term)/7 DoL (for preterm). The screening was carried out in Dec. 30, 2021-Nov. 17, 2022 on the basis of 21 obstetrics facilities located within the City of Saint Petersburg (Russia). Results: 36,140 participants (17,687 (49%) boys/18,453 (51%) girls) of the neonatal screening; 77 (0.21%) parents/caretakers have refused to participate. A technique for detecting homo- and heterozygous deletions in the SMN1 gene was developed based on rapid DNA extraction from dried blood spots followed by the real-time PCR. The project had identified 4 patients with SMA, two of whom had two and the other two had three copies of the SMN2 gene. The period of time needed to set the diagnosis ranged from 7th to 14th DoL. All of these patients have received the gene replacement therapy for a period of 3 to 5 months. There was a positive trend as a result of the therapy in all of the cases. 772 SMA carriers were also identified during the screening. 51% of their parents/caretakers have been followingly consulted on the possible risks of the disease. The frequency of SMA in the City of Saint Petersburg was 1 in 9035 newborns with a carrier frequency of 1 in 47. The sensitivity and specificity of the test were determined, which were 99.74% and 100%, respectively. Conclusion: SMA screening has been tested and put into practice. The conducted project of neonatal screening for SMA in the City of Saint Petersburg has demonstrated the readiness of its residents and the municipal healthcare system, the practitioners and organizers to this type of medical solution. The described developed methodology has demonstrated its effectiveness in terms of early detection of patients and carriers of this disease.
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俄罗斯圣彼得堡市新生儿脊髓性肌萎缩症筛查试点项目的结果。组织,诊断和临床方面
脊髓性肌萎缩症(SMA)是由SMN1基因突变引起的最常见和最严重的遗传性疾病之一,可导致脊髓运动神经元的破坏和肌肉无力。本研究的目的是鉴定新生儿中SMN1基因的同源和杂合突变。使用的材料和方法:一项针对4岁(足月)/7岁(早产儿)新生儿的多中心前瞻性开放式连续筛查研究。影片放映时间为2021年12月30日至11月30日。在位于圣彼得堡市(俄罗斯)的21个产科设施的基础上,于2022年17日。结果:36140名新生儿筛查参与者(17687名(49%)男孩/ 18453名(51%)女孩);77名(0.21%)家长/监护人拒绝参与。建立了一种检测SMN1基因同源和杂合缺失的技术,该技术基于从干血斑中快速提取DNA并进行实时PCR。该项目已经确定了4名患有SMA的患者,其中两人有两个,另外两人有三个SMN2基因拷贝。设定诊断所需的时间范围为第7 ~第14个DoL。所有这些患者都接受了3到5个月的基因替代治疗。在所有病例中,治疗的结果都是积极的趋势。在筛查过程中还发现了772名SMA携带者。51%的父母/看护人随后接受了关于该疾病可能风险的咨询。圣彼得堡市新生儿罹患SMA的频率为1 / 9035,携带者频率为1 / 47。试验的灵敏度和特异性分别为99.74%和100%。结论:SMA筛查已得到检验和应用。在圣彼得堡市开展的新生儿SMA筛查项目表明,该市居民和市政卫生保健系统、从业人员和组织者对这类医疗解决方案已经做好了准备。所描述的开发方法已证明其在早期发现这种疾病的患者和携带者方面的有效性。
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来源期刊
Pediatriya - Zhurnal im G.N. Speranskogo
Pediatriya - Zhurnal im G.N. Speranskogo Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.60
自引率
0.00%
发文量
150
期刊介绍: Journal “Pediatria” named after G.N. Speransky (the official short names of the Journal are “Journal «Pediatria»,” “Pediatria,” and “«Pediatria,» the Journal”) is the oldest Soviet-and-Russian (in the Russian Federation, the CIS and former Soviet Union) scientific and practical medical periodical assigned for pediatricians that is published continuously since May, 1922, and distributed worldwide. Our mission statement specifies that we aim to the ‘raising the level of skills and education of pediatricians, organizers of children’s health protection services, medicine scientists, lecturers and students of medical institutes for higher education, universities and colleges worldwide with an emphasis on Russian-speaking audience and specific, topical problems of children’s healthcare in Russia, the CIS, Baltic States and former Soviet Union Countries and their determination with the use of the World’s best practices in pediatrics.’ As part of this objective, the Editorial of the Journal «Pediatria» named after G.N. Speransky itself adopts a neutral position on issues treated within the Journal. The Journal serves to further academic discussions of topics, irrespective of their nature - whether religious, racial-, gender-based, environmental, ethical, political or other potentially or topically contentious subjects. The Journal is registered with the ISSN, - the international identifier for serials and other continuing resources, in the electronic and print world: ISSN 0031-403X (Print), and ISSN 1990-2182 (Online). The Journal was founded by the Academician, Dr. Georgiy Nestorovich SPERANSKY, in May, 1922. Now (since 1973) the Journal bears his honorary name.
期刊最新文献
ORGANIZING PNEUMONIA IN CHILDREN: EPIDEMIOLOGY, ETIOLOGICAL STRUCTURE, CLINICAL AND COMPUTED TOMOGRAPHIC SEMIOTICS, COMORBIDITY, THERAPY INTERSTITIAL LUNG DISEASES IN CHILDREN: MODERN CLASSIFICATION, DIAGNOSTIC ALGORITHM, COMMON THERAPEUTIC APPROACHES CARDIOVASCULAR SYSTEM IN NEWBORNS BORN TO MOTHERS WHO HAD A NEW CORONAVIRUS INFECTION DURING PREGNANCY SOCIAL AND MEDICAL ASPECTS OF THE COVID-19 PANDEMIC. MANIFESTATION PARTICULARITIES OF THE NEWLY DIAGNOSED TYPE 1 DIABETES MELLITUS IN CHILDREN AND ADOLESCENTS DURING THE COVID-19 PANDEMIC IMPACT OF AGE AND GENDER ON SPIROMETRIC PARAMETERS IN ADOLESCENTS WITH BRONCHIAL ASTHMA
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