Spinal Muscular Atrophy (SMA)
Conditions
Keywords
SMA, SMN1, long read, cis duplication, genetic counselling
Brief summary
Spinal Muscular Atrophy (SMA) is a severe neuromuscular disease caused by deletion of the SMN1 gene, with the most severe form leading to death in children without treatment. Genetic counselling to detect couples where both partners are carriers is particularly important. In some countries, preconception screening is offered. However, some carriers escape detection due to the existence of two copies of the SMN1 gene side-by-side (2+0 genotype). Currently, no molecular genetic methods used for diagnostic purposes can detect these 2+0 genotypes, which pose a significant challenge in genetic counselling. This study aims to use new technologies based on the analysis of ultra-long molecules to detect side-by-side duplications of the SMN1 gene to detect heterozygous subjects not identified by current techniques and improve genetic counselling.
Detailed description
Spinal Muscular Atrophy (SMA) is a severe autosomal recessive neuromuscular disease, with the most severe form leading to death in children without treatment. Genetic counseling to detect couples where both partners are heterozygous is particularly important. In some countries, preconception screening is offered. However, some individuals' heterozygous status escape detection due to the existence of a cis duplication of the SMN1 gene on the second allele (\[2+0\] genotype). Currently, no molecular genetic methods used for diagnostic purposes can detect these \[2+0\] genotypes, which poses a significant challenge in genetic counseling. The SMN1 gene, responsible for SMA, is located in the 5q11q13 region, which remains poorly understood in the human reference genome (dark region). The architecture of this inverted duplicated region favors recombination events that lead to deletions, duplications, and gene conversions. The SMN1 gene, located in the telomeric region, has a very homologous copy, the SMN2 gene, located in the centromeric region. The lack of detailed knowledge about duplication events hinders the development of molecular tools aimed at improving genetic counseling. This study aims to use new technologies based on the analysis of ultra-long molecules to detect cis duplication of the SMN1 gene. We will assess the usefulness of optical mapping (Bionano) to analyze this complex region.
Interventions
GENETICblood sample
For subjects who agree to participate in the study, a blood sample will be taken (2x5 mL on EDTA) and sent the same day at 4°C to the genetics laboratory at Rouen University Hospital using a carrier that guarantees delivery on D+1
Sponsors
Agence de La Biomédecine
University Hospital, Rouen
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
• Adult Subject: * Subject with either: * 1 or 3 copies of the SMN1 gene (control group) and a variable number of copies of the SMN2 gene * 2 copies of the SMN1 gene in cis (2+0 genotype) (test group) * Affiliation to French health insurance * Signed consent form
Exclusion criteria
* Pregnant or breastfeeding women * Individuals deprived of liberty by an administrative or judicial decision, or those under guardianship or curatorship
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Ability to identify a [2+0] SMN1 genotype | From enrollment until the end of the analyses (36 months) |
Secondary
| Measure | Time frame |
|---|---|
| Ability to perform assembly of ultra-long molecules of DNA | From enrollment until the end of the analyses (36 months) |
Countries
France
Contacts
Primary ContactPascale Saugier-Veber, PharmD PhD
Outcome results
None listed