Scientific Reports (Feb 2023)

A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patients

  • Shahram Savad,
  • Mahmoud Reza Ashrafi,
  • Niusha Samadaian,
  • Morteza Heidari,
  • Mohammad-Hossein Modarressi,
  • Gholamreza Zamani,
  • Saloomeh Amidi,
  • Sarang Younesi,
  • Mohammad Mahdi Taheri Amin,
  • Pourandokht Saadati,
  • Alireza Ronagh,
  • Hossein Shojaaldini Ardakani,
  • Solat Eslami,
  • Soudeh Ghafouri-Fard

DOI
https://doi.org/10.1038/s41598-023-30449-7
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 11

Abstract

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Abstract Spinal muscular atrophy (SMA) is among the most common autosomal recessive disorders with different incidence rates in different ethnic groups. In the current study, we have determined SMN1, SMN2 and NAIP copy numbers in an Iranian population using MLPA assay. Cases were recruited from Genome-Nilou Laboratory, Tehran, Iran and Pars-Genome Laboratory, Karaj, Iran during 2012–2022. All enrolled cases had a homozygous deletion of exon 7 of SMN1. Moreover, except for 11 cases, all other cases had a homozygous deletion of exon 8 of SMN1. Out of 186 patients, 177 (95.16%) patients showed the same copy numbers of exons 7 and 8 of SMN2 gene. In addition, 53 patients (28.49%) showed 2 copies, 71 (38.17%) showed 3 copies and 53 patients (28.49%) showed 4 copies of SMN2 gene exons 7 and 8. The remaining 9 patients showed different copy numbers of exons 7 and 8 of SMN2 gene. The proportions of SMA patients with different numbers of normal NAIP were 0 copy in 73 patients (39.24%), 1 copy in 59 patients (31.72%), 2 copies in 53 patients (28.49%) and 4 copies in one patient (0.5%). These values are different from values reported in other populations. Integration of the data of the SMN1/2 and NAIP genes showed 17 genotypes. Patients with genotype 0-0-3-3-1 (0 copies of SMN1 (E7,8), 3 copies of SMN2 (E7,8) and 1 copy of NAIP (E5)) were the most common genotype in this study. Patients with 0-0-2-2-0 genotype were more likely to have type I SMA. The results of the current study have practical significance, particularly in the genetic counseling of at-risk families.