mtDNA Mutation Load Analysis in Mesoangioblasts

Mitochondrial Myopathies Clinical Trial

— MABS05  

Official title:

Assess the mtDNA Mutation Load in Mesoangioblasts of mtDNA Mutation Carriers

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05199740
• Other study ID #: NL78411.068.21
• Status: Recruiting
• Start date: December 20, 2022
• Est. completion date: July 1, 2026

Study information

• Verified date: January 2024
• Source: Maastricht University
• Contact: Florence van Tienen, PhD
• Phone: 314332918
• Email: florence.vantienen[@]maastrichtuniversity.nl
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Mitochondrial diseases caused by defects in oxidative phosphorylation (OXPHOS) due to heteroplasmic mitochondrial DNA (mtDNA) mutations are rare (frequency 1/5,000), but severe multi-system disorders. Clinical manifestations are highly variable, but predominantly affect energy demanding tissues, like brain and muscle. Myopathy is a common feature of mtDNA disorders, being present in more than 50% of the mtDNA mutation carriers, and seriously affects patients' general well-being and quality of life. Currently, no treatment is available for these patients, although the induction of muscle regeneration by exercise treatment has been shown to alleviate their myopathy. This implies that these patients can produce muscle fibres that perform better, most likely because the mutation load is lower. Mesoangioblasts (MABs) are myogenic precursors that have been recognized as a source for development of a systemic myogenic stem-cell therapy. Autologous MABs may be feasible for half of the mtDNA mutation carriers of 6 different mtDNA mutations, as their mtDNA mutation load in mesoangioblasts was (nearly) absent (<10%). However, there are many more mtDNA mutations in the 16.5kb mtDNA and the aim of this study is to determine the mtDNA mutation load in mesoangioblasts of other mtDNA mutation carriers and identify the patients or mutations for which this is a feasible approach.

Description:

Rationale: Mitochondrial diseases caused by defects in oxidative phosphorylation (OXPHOS) due to heteroplasmic mitochondrial DNA (mtDNA) mutations are rare (frequency 1/5,000), but severe multi-system disorders. Clinical manifestations are highly variable, but predominantly affect energy demanding tissues, like brain and muscle. Myopathy is a common feature of mtDNA disorders, being present in more than 50% of the mtDNA mutation carriers, and seriously affects patients' general well-being and quality of life. Currently, no treatment is available for these patients, although the induction of muscle regeneration by exercise treatment has been shown to alleviate their myopathy. This implies that these patients can produce muscle fibres that perform better, most likely because the mutation load is lower. Mesoangioblasts (MABs) are myogenic precursors that have been recognized as a source for development of a systemic myogenic stem-cell therapy, and allogeneic transplantation has been successfully applied to mice and dogs with Duchenne muscular dystrophy. A subsequent phase I/II clinical study in boys with DMD demonstrated that donor MABs treatment was relatively safe, but did not result in clinical improvement, which can partly be attributed to the required use of immunosuppressive agents. The use of autologous MABs would circumvent this and a previous study of our group demonstrated that this is feasible for half of the mtDNA mutation carriers of 6 different mtDNA mutations, as their mtDNA mutation load in mesoangioblasts was (nearly) absent (<10%). However, there are many more mtDNA mutations in the 16.5kb mtDNA and the aim of this study is to determine the mtDNA mutation load in mesoangioblasts of other mtDNA mutation carriers and identify the patients or mutations for which this is a feasible approach.

Objective: The primary objectives of this project is to assess the mtDNA mutation load in mesoangioblasts of mtDNA mutation carriers and identify which patients display no/low (<10%) mtDNA mutation load in mesoangioblasts. Secondary objectives aim at determining the proliferation, myogenic differentiation and OXPHOS capacity of mesoangioblasts, their systemic inflammation status and assessment of the mtDNA mutation load in satellite cells.

Study design: Mono-centre observation study. Study population: 30 adult carriers of a heteroplasmic mtDNA point-mutation or large-scale mtDNA deletion (>2kb).

Intervention: From each participant, a 30mg skeletal muscle biopsy and a 20ml venous blood sample will be collected.

Main study parameters/endpoints: Assess the mtDNA mutation load in skeletal muscle derived mesoangioblasts.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: July 1, 2026
• Est. primary completion date: July 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria all participants:

• Written informed consent

• Age: 18+

• Sex: male/female

• Carriers of a heteroplasmic mtDNA mutation load >20% in skeletal muscle or >1% in blood

Exclusion Criteria all participants:

• No informed consent

• Use of anti-coagulants, anti-thrombotics and other medication influencing coagulation

• Have a weekly alcohol intake of = 35 units (men) or = 24 units (women)

• Current history of drug abuse

• A history of strokes

• Significant concurrent illness

• Ongoing participation in other clinical trials that contain an intervention

• Major surgery within 4 weeks of the visit

• Pregnant or lactating women

• Patients unable and/or unwilling to comply with treatment and study instructions

Related Conditions & MeSH terms

• Mitochondrial Myopathies

Intervention

Other:
• in vitro analysis
in vitro analysis of mesoangioblasts from mtDNA mutation carriers

Locations

Country	Name	City	State
Netherlands	Maastricht University	Maastricht

Sponsors (1)

Lead Sponsor	Collaborator
Maastricht University

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assess mtDNA mutation load in mesoangioblasts	Isolate mesoangioblasts and quantify mtDNA mutation load using GeneScan analysis	1 day
Secondary	Assess level of systemic inflammation marker TNFa in blood plasma	TNFa measurement in plasma (pg/ml)	1 day
Secondary	Assess level of systemic tissue damage marker CK in blood plasma	CK measurement in plasma (U/l)	1 day
Secondary	Assess level of systemic inflammation marker IL-6 in blood plasma	IL-6 measurement in plasma (pg/ml)	1 day
Secondary	Assess level of systemic inflammation marker SDF-1 in blood plasma	SDF-1 measurement in plasma (pg/ml)	1 day
Secondary	Assess mitochondrial function in mesoangioblasts	Assess mtDNA copynumber and OXPHOS capacity in mesoangioblasts	1 day
Secondary	Assess myogenic differentiation capacity of mesoangioblasts	Assess myogenic fusion index of mesoangioblasts isolated from a muscle biopsy	1 day
Secondary	Assess mtDNA mutation load in satellite cells	Isolate satellite cells and quantify mtDNA mutation load using GeneScan analysis	1 day