Omics Gaucher Study: Multiomic Approach

Active, not recruiting

• Conditions: Gaucher Disease
• Interventions: Other: Genetic testing and Omics analysis

• Registration Number: NCT05526664
• Lead Sponsor: CENTOGENE GmbH Rostock

Brief Summary

The study aims to investigate the transcriptomic and metabolomic changes in blood, plasma and isolated monocytes from Gaucher patients and healthy controls.

Detailed Description

Gaucher disease is one of the most common lysosomal storage disorders (LSD) and is an autosomal recessive inherited disorder, primed by mutation in the GBA1 gene which leads to a deficiency in β-glucocerebrosidase (GCase) activity and accumulation of its substrate glucosylceramide (GluCer)/-sphingosine (GluSph). The macrophages are the main cell type exhibiting a Gaucher disease phenotype. The large accumulation of GluCer and to a lesser extent that of GluSph lead to dysfunction in organs such as spleen, liver, bone marrow, and lungs.

However, a validated, reproducible, and broadly applicable tool to classify Gaucher Disease at any stage of the disease is still missing.

The development of new technologies, such as genomic analysis by next generation sequencing (NGS) and other "omics technologies," has advanced the molecular understanding and diagnosis of Rare Diseases

The current study will analyze the transcriptional and metabolomic profiles in blood, plasma and isolated monocytes from Gaucher patients and healthy controls with the aim to compare these profiles and to define how much a patient profile differs from a healthy one.

Study Timeline

• Study First Submitted: 2022-08-31
• Study First Submitted QC: 2022-08-31
• Study First Posted: 2022-09-02
• Study Start: 2022-10-06
• Status Verified: 2023-09
• Last Update Submitted: 2024-06-27
• Last Update Posted: 2024-06-28
• Primary Completion: 2024-12
• Study Completion: 2025-12

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

Gaucher Type 1 participants:

• Informed consent
• The participant is older than 18 years old
• The participant was diagnosed with Gaucher Type 1 disease

Gaucher Type 3 participants:

• Informed consent
• The participant is older than 18 years old
• The participant was diagnosed with Gaucher type 3 disease

Healthy participants:

• Informed consent
• The participant is older than 18 years old
• Healthy participants

Exclusion Criteria

Gaucher Type I participants:

• The participant had any other clinically significant disease
• The participant had a recent (within 14 days) acute infection and/or vaccination

Gaucher Type 3 participants:

• Diagnosis of a significant CNS disease or cardiovascular disease other than Gaucher type 3
• The participant had a recent (within 14 days) acute infection and/or vaccination

Healthy participants:

• The participant had a recent (within 14 days) acute infection and/or vaccination

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Healthy Volunteer	Genetic testing and Omics analysis	* Healthy participants * Adults only
Gaucher Type 1	Genetic testing and Omics analysis	* The participant was diagnosed with Gaucher type 1 disease * Adults only
Gaucher Type 3	Genetic testing and Omics analysis	* The participant was diagnosed with Gaucher type 3 disease * Adults only

Primary Outcome Measures

Name	Time	Method
OMICS DATA	12 months	investigate the transcriptomic and metabolomic changes in blood, plasma and isolated monocytes from Gaucher patients and healthy controls.

Trial Locations

Locations (1)

UKE; 🇩🇪 Hamburg, Germany