Development of a New Technique for Quantifying Mitochondrial DNA in Single Muscle Fibers

Официальное название

Development of a New Technique for Quantifying Mitochondrial DNA in Single Muscle Fibers, as a Tool for Interpreting Variants of Uncertain Significance in Mitochondrial Diseases

Обзор

Mitochondrial diseases (MDs) are the most common metabolic disorders. Due to their great clinical and genetic heterogeneity, their diagnosis relies exclusively on the identification of pathogenic variants in nuclear genes or in mitochondrial DNA (mtDNA). However, to date, 50% of affected patients remain without a definitive diagnosis. The advent of next-generation sequencing (NGS) has improved diagnostic yield, but many identified variants remain of uncertain significance (VUS), preventing a definitive diagnosis. The clinical interpretation of these newly identified rare variants therefore represents a major challenge. In the context of MDs, one of the major criteria for mtDNA variant pathogenicity is a good correlation between heteroplasmy level and tissue or cellular involvement. Heteroplasmy refers to the coexistence, within the same cell or tissue, of mutated and non-mutated mtDNA molecules. Pathogenic mtDNA variants are most often heteroplasmic, with the most affected tissues harboring a higher proportion of mutated mtDNA. In muscle biopsies from patients with MDs, muscle fibers may show a cytochrome c oxidase (COX) enzymatic deficiency (COX-negative fibers), reflecting dysfunction of the mitochondrial respiratory chain (MRC). Single-fiber analysis makes it possible to isolate muscle fibers by LASER microdissection and to quantify the heteroplasmy level of a variant within them. The presence of a high heteroplasmy level in COX-negative fibers, in contrast to fibers without deficiency (COX-positive fibers), is strong evidence supporting the pathogenicity of the variant. In previous projects, we tested two variant quantification techniques (PCR-RFLP and NGS), but these methods remain too labor-intensive or costly and are therefore difficult to maintain in routine practice. This pilot study aims to develop a new method for quantifying heteroplasmy levels using digital PCR. Faster and less expensive, this approach could simplify technical implementation and reduce analysis costs, thereby facilitating its integration into clinical practice. Initially, a feasibility study will begin with validation of digital PCR on DNA extracted from blood samples of two patients carrying pathogenic variants identified in a previous study (AOI 2017 IDRCB: 2017-A00688-45). This validation will compare digital PCR with the PCR-RFLP method for heteroplasmy quantification and assess the reliability and reproducibility of the technique. Once validation is achieved, digital PCR will be tested on DNA extracted from microdissected muscle fibers from the same patients to evaluate its feasibility at the single-fiber level, with comparison to PCR-RFLP results. If feasibility at the single-fiber level is confirmed, the method will then be tested in four new patients from the Mitochondrial Diseases Reference Center, in whom variants of uncertain significance have been identified and for whom muscle biopsies with COX-negative fibers are available. Additional samples (blood, urine, and buccal swabs) will be collected to assess heteroplasmy levels across different tissues. If validated, this technique could be applied to a larger number of patients and integrated into the diagnostic strategy for mitochondrial diseases. Moreover, digital PCR could also be used to quantify mtDNA copy number, an essential biomarker for monitoring patients with MDs. To this end, mtDNA is partitioned into thousands of nanowells, and absolute quantification is obtained by counting fluorescent signals emitted by positive partitions, with a nuclear DNA probe serving as an internal control. This validation will be performed using the same blood samples and muscle fibers, by comparing digital PCR results with those obtained using the reference method, quantitative PCR (qPCR). The primary objective of this study is to reduce diagnostic odysseys by simplifying existing methods. In addition, the application of digital PCR to quantify mtDNA copy number could offer new perspectives, particularly as a biomarker for patient monitoring and the development of clinical trials.

Вмешательства

• Диагностический тест Quantification of Mitochondrial DNA Heteroplasmy and Copy Number by Digital PCR in Mitochondrial Diseases
  The intervention consists of using digital PCR (dPCR) to quantify mitochondrial DNA (mtDNA) heteroplasmy levels and mtDNA copy number. dPCR will be performed on DNA extracted from blood, urine, and buccal (saliva) samples, as well as from laser-microdissected single muscle fibers obtained from muscle biopsies. The method will be validated by comparison with reference techniques (PCR-RFLP for heteroplasmy and quantitative PCR for mtDNA copy number) to assess its accuracy and reproducibility. dPC

Первичные конечные точки

• Validate a new digital PCR technique to quantify the heteroplasmy level of a variant in single muscle fibers in order to improve diagnostic yield. [Срок оценки: Inclusion visit]

Вторичные конечные точки (1)

• Validate a new digital PCR technique for quantifying the number of mitochondrial DNA (mtDNA) copies [Срок оценки: Inclusion visit]

Критерии участия

Критерии включения

• major or minor patients, sporadic or isolated cases
• Signature of informed consent, for minor patients : signature of both parents or holders of parental authority, unless it is impossible to obtain the consent of one of the parents within a reasonable period of time
• Affiliation to a social security system
• Suspicion of a mitochondrial disorder, as assessed by the clinician at the Mitochondrial Diseases Reference Center, based on at least one of the following:

• Clinical presentation suggestive of a mitochondrial disorder (unusual combination of symptoms, specific syndromes such as MELAS, muscle weakness, ptosis, etc.) and/or
• Metabolic workup indicative of respiratory chain involvement and/or
• Identification of a deficit affecting one or more respiratory chain complexes in a muscle biopsy.
• Patient with a previously identified mitochondrial DNA variant of uncertain significance (VUS).
• Histological analysis of muscle biopsy showing at least 5 COX-negative fibers.
• Muscle biopsy available and possibility to retrieve slides from the pathology laboratory.

Критерии исключения

• Refusal to sign the study consent.
• Individuals admitted to a healthcare or social facility for purposes other than research participation.
• Adults subject to legal guardianship (guardianship, conservatorship)
• Pregnant or breastfeeding women

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Диагностика

Центры проведения

Франция · 3 центра

• CHU de Nice - Service de Génétique Médicale — Nice
• Groupement Hospitalier Est Hospices civils de Lyon - Service de génétique médicale — Bron
• Hôpital Gui de Chauliac - Service de Neurologie — Montpellier

Идентификаторы

NCT: NCT07511608 · 25-AOIP-01

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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