Development of Targeted RNA-Seq for Amyotrophic Lateral Sclerosis Diagnosis

Recruiting

• Conditions: Amyotrophic Lateral Sclerosis
• Interventions: Other: RNA sequencing

• Registration Number: NCT06083584
• Lead Sponsor: Centre Hospitalier Universitaire de Nīmes

Brief Summary

Genetic diagnosis of Amyotrophic Lateral Sclerosis (ALS) could identify the origin of the disease, potentially allowing the patient to pursue targeted/gene therapy. However, many familial forms of ALS are genetically undiagnosed, either because no variant has been detected in the genes of interest, or because the detected variant(s) have uncertain significance. Currently, molecular diagnosis takes place in two stages: 1) Search for the GGGGCC expansion in the C9ORF72 gene by RP-PCR; 2) Analysis of the coding regions by high-throughput sequencing of a panel of 30 genes involved in ALS.

Many of these variants of uncertain significance affect splicing. Their impact can be predicted using in silico tools, but only an analysis of the patient's RNA can confirm their pathogenic nature. Currently, the analysis of transcripts is only done a posteriori, when a variant predicted to impact splicing is detected on the patient's DNA. RT-PCR followed by Sanger sequencing then verifies the impact of the splice variants. This method confirmed the impact of certain splice variants in patients. However, this method is time-consuming and requires custom development, and is mutation/gene/patient-dependent. In contrast, high-throughput RNA sequencing (RNA-Seq) simultaneously analyzes the splicing of numerous genes, with a global approach, applicable to all patients. This approach avoids the custom design of primers, which can be biased by the interpretation of splicing predictions, while RNA-Seq systematically captures and sequences all the transcripts. Finally, RNA-Seq provides additional information compared to DNA sequencing such as the detection of exon skipping, intron inclusion, and the creation of fusion transcripts.

In the GTEx project (GTEx Consortium, 2013), expression levels of human genome transcripts were quantified by RNA-Seq. Using these results, the study investigators measured expression of transcripts of known ALS genes in whole blood. Applying a threshold value of 0.5 transcripts per million reads (TPM), 25 of the 30 ALS genes currently analyzed by NGS in routine diagnostics at Nîmes University Hospital could be eligible for a complete analysis by RNA-Seq. None of the French laboratories carrying out genetic analyzes of ALS has yet developed RNA-Seq as a routine diagnostic tool. The study laboratory receives more than 600 requests for genetic diagnosis of ALS patients per year. The aim of this study is therefore to develop a global method for analyzing RNA transcripts of ALS genes to categorize the mutations to improve the diagnostic management of patients.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2023-10-09
• Study First Submitted QC: 2023-10-09
• Study First Posted: 2023-10-16
• Study Start: 2023-11-22
• Status Verified: 2025-05
• Last Update Submitted: 2025-05-15
• Last Update Posted: 2025-05-20
• Primary Completion: 2027-05
• Study Completion: 2027-05

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 192

Inclusion Criteria

• Have a prescription for a genetic diagnosis of ALS (or familial hypercholesterolemia for the control cohort)
• Have given their informed consent for the genetic study and the biobank
• The patient must be a member or beneficiary of a health insurance plan

Exclusion Criteria

• The patient is under safeguard of justice or state guardianship

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Positive controls	RNA sequencing	6 patients already in database. The 6 confirmed splicing mutations are: DCTN1 (NM_004082.5): c.3209G\>T, OPTN (NM_001008211.1) : c.1613-7T\>G, FUS (NM_004960.4) : c.764+8T\>A, GRN (NM_002087.4): c.835+1G\>A, GRN (NM_002087.4): c.709-3C\>G, SPG11 (NM_025137.4): c.3039-5T\>G
Negative controls	RNA sequencing	30 patients with familial hypercholesterolemia. The absence of splicing anomalies in the SLA genes after confirmation by RT-PCR followed by Sanger sequencing of the absence of anomalies for the 6 variants listed above for each of the 30 individuals.
Exploratory cohort	RNA sequencing	156 ALS: 20 ALS patients with splice variants predicted to be deleterious by in silico prediction software; 136 panel-analysis-negative ALS patients (priority will be given to familial ALS)

Primary Outcome Measures

Name	Time	Method
Concordance between the RNA-Seq results (index text) versus RT-PCR followed by Sanger sequencing (reference technique) on positive plus negative controls	Day 0	Sashimi Plot visualized in Integrative Genomics Viewer

Secondary Outcome Measures

Name	Time	Method
Frequency of splicing anomalies detected in ALS patients in the "exploratory cohort" versus negative controls.	Day 0	Frequency

Trial Locations

Locations (7)

CHU de Montpellier; 🇫🇷 Montpellier, France

CHU de Nîmes; 🇫🇷 Nîmes, France

CHU de Lyon; 🇫🇷 Lyon, France

CHU de Toulouse; 🇫🇷 Toulouse, France

La Timone; 🇫🇷 Marseille, France

CHU de Bordeaux; 🇫🇷 Bordeaux, France

CHU de Clermont-Ferrand; 🇫🇷 Clermont-Ferrand, France