{Reference Type}: Journal Article
{Title}: Epidemiology of Spinal Muscular Atrophy Based on the Results of a Large-Scale Pilot Project on 202,908 Newborns.
{Author}: Efimova IY;Zinchenko RA;Marakhonov AV;Balinova NV;Mikhalchuk KA;Shchagina OA;Polyakov AV;Mudaeva DA;Saydaeva DH;Matulevich SA;Parshintseva PD;Belyashova EY;Yakubovskiy GI;Tebieva IS;Gabisova YV;Irinina NA;Jamschikova AV;Nurgalieva LR;Saifullina EV;Nevmerzhitskaya KS;Belyaeva TI;Romanova OS;Voronin SV;Kutsev SI;
{Journal}: Pediatr Neurol
{Volume}: 156
{Issue}: 0
{Year}: 2024 Jul 24
{Factor}: 4.21
{DOI}: 10.1016/j.pediatrneurol.2024.04.015
{Abstract}: BACKGROUND: This study presents the findings of a newborn screening (NBS) pilot project for 5q-spinal muscular atrophy (5q-SMA) in multiple regions across Russia for during the year 2022. The aim was to assess the feasibility and reproducibility of NBS for SMA5q in diverse populations and estimate the real prevalence of 5q-SMA in Russia as well as the distribution of patients with different number of SMN2 copies.
METHODS: The pilot project of NBS here was based on data, involving the analysis of 202,908 newborns. SMA screening assay was performed using a commercially available real-time polymerase chain reaction kit, the Eonis SCID-SMA.
RESULTS: In one year, 202,908 newborns were screened, identifying 26 infants with homozygous deletion of SMN1 exon 7, yielding an estimated 5q-SMA incidence of 1:7804 newborns. It was found that 38.46% had two SMN2 copies, 42.31% had three copies, 15.38% had four copies, and 3.85% had five copies of SMN2. Immediate treatment was proposed for patients with two or three SMN2 copies. Infants with four or more SMN2 copies warranted further investigation on management and treatment. Short-term monitoring after gene therapy showed motor function improvements. Delays in treatment initiation were observed, including the testing for adeno-associated virus 9 antibodies and nonmedical factors.
CONCLUSIONS: The study emphasizes the need for a standardized algorithm for early diagnosis and management through NBS to benefit affected families. Overall, the NBS program for 5q-SMA in Russia demonstrated the potential to improve outcomes and transform SMA from a devastating disease to a chronic condition with evolving medical requirements.