Combined Genome and RNA Sequencing for Genetic Diagnosis of Parkinsonism (ParkOmic)

University Hospital, Strasbourg, France

Status

Not yet enrolling

Conditions

Parkinson's Disease

Treatments

Diagnostic Test: Combiner whole genome and RNA sequencing

Study type

Interventional

Funder types

Other

Identifiers

NCT06576713

9320

Details and patient eligibility

About

Despite the increasing availability and advances in the analysis of high-throughput DNA sequencing, the majority of patients with early-onset or familial parkinsonism remain without a molecular diagnosis.

Studying the genetic forms of parkinsonian syndromes presents numerous clinical, scientific and therapeutic interests. In clinical practice, identifying the genetic cause in a patient allow to provide genetic counseling and estimate the risk of recurrence in their relatives. Establishing correlations between the genotype and phenotype of patients with genetically determined parkinsonism, allow to better anticipate the evolution of the disease, or even to highlight biomarkers during the presymptomatic phases. Finally, the proteins encoded by the genes implicated in familial parkinsonism represent potential therapeutic targets likely to be modulated by neuroprotective pharmacological agents, even in sporadic Parkinson's disease.

In this work,investigators aimed at elucidating the missing genetic causes of parkinsonism through the application of combined RNA and whole genome sequencing.

Full description

Investigators selected 14 patients with early-onset parkinsonism for whom no variant of certain pathogenicity had been identified after exome sequencing.

Patients and their relatives will have a blood sample collection following the inclusion visit for DNA extraction, patients will receive a skin biopsy for fibroblast culture and RNA extraction for RNA sequencing. The genome sequencing will be performed on an Illumina® HiSeq4000 sequencer.

Investigators will also perform skin biopsies on patients for fibroblast cultures in order to extract RNA for RNA sequencing. The choice of fibroblast analysis for the study of the transcriptome is justified by the fact that genes expressed in the brain likely to be associated with neurodegenerative diseases are more frequently expressed in the skin than in the other clinically accessible tissues such as blood. Skin biopsies will be performed by the referring clinicians, and RNA extraction will be carried out using the Quiagen® RNeasy kit.

Transcriptome analysis by RNA sequencing including sequencing and bioinformatics processing of data, including detection of aberrant splicing (LeafCutter), aberrant expressions (DESeq) and identification of variants (GATK + Varank) will also be carried out Genome data will be integrated with data from RNA sequencing. Investigators plan to analyze all 14 patients according to this strategy.

Enrollment

14 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Extrapyramidal syndrome beginning before or at the age of 40 or associated with a family history:
Dopaminergic denervation proven by ioflupane brain scintigraphy (DaTscan®)
DNAs from both asymptomatic parents available in biobank
Subject affiliated to a social protection health insurance scheme or beneficiary or beneficiary
Subject able to understand the objectives and risks related to the research and to give dated and signed informed consent

Exclusion criteria

- Contraindication for performing a superficial skin biopsy provided for by the protocol
Molecular cause of parkinsonism previously identified
Absence of prior genetic exploration by high-throughput DNA sequencing
Patient with late-onset sporadic parkinsonian syndrome (> 40 years) without family history
Patient with Parkinson's syndrome associated with a specific diagnosis (genetic or non-genetic pathology: exposure to neuroleptics, toxic origin)
Impossibility of providing the subject with informed information
Subject under judicial protection
Subject under guardianship or curatorship