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Completed

NCT Number: NCT06080568

Human Mitochondrial Stress-driven Obesity Resistance

The overarching aim of this observational study is to determine alterations in energy balance while exploring the underlying cellular mechanisms in human genetic models of mitochondrial stress.

In a case-control design, individuals with pathogenic mitochondrial DNA mutations will be compared to healthy controls matched for sex, age, and physical activity level. Participants will attend a screening visit and an experimental trial including assessments of energy expenditure, appetite sensation, energy intake, and muscle and subcutaneous adipose tissue biopsy samples.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Rigshospitalet

Copenhagen, Denmark, 2100

About this study

Background: Pre-clinical models of mitochondrial stress are resistant to diet-induced obesity. Likewise, humans with primary mitochondrial diseases present a high prevalence of underweight (42%) as compared to a very low prevalence of obesity (2%). In this direction, recent data show a lower BMI across 17 cohorts of patients with mitochondrial diseases compared to national averages, suggesting mitochondrial stress-induced increments in resting energy expenditure as the primary driver of the lean phenotype. In recent years, the study of humans with genetic mutations has shown enormous potential to establish the mechanistic link between two physiological variables; indeed, if the mutation has a functional impact on one of those variables, then the direction of causality can be readily ascribed. Taken together, studies integrating assessments of energy balance with mitochondrial phenotyping in patients with rare mitochondrial disorders hold the potential to uncover putative mechanisms conferring protection from obesity in humans.

Objective: To determine alterations in energy expenditure/intake while exploring the underlying cellular mechanisms in individuals harboring mitochondrial DNA (mtDNA) mutations associated with mitochondrial stress.

Study design: Case-control study in individuals with mtDNA mutations (n=15) and healthy controls (n=15) matched for sex, age, and physical activity level.

Endpoint: Differences between individuals with mtDNA mutations and controls.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Eligibility criteria for individuals with mitochondrial DNA mutations

Inclusion criteria

  • Known mtDNA point mutations

Exclusion criteria

  • Use of antiarrhythmic medications or other medications which, in the opinion of the investigators, have the potential to affect outcome measures.
  • Diagnosed severe heart disease, dysregulated thyroid gland conditions, or other dysregulated endocrinopathies, or other conditions which, in the opinion of the investigators, have the potential to affect outcome measures.
  • Pregnancy

Eligibility criteria for controls

Exclusion criteria

  • Current and regular use of antidiabetic medications or other medications which, in the opinion of the investigators, have the potential to affect outcome measures.
  • Diagnosed heart disease, symptomatic asthma, liver cirrhosis or -failure, chronic kidney disease, dysregulated thyroid gland conditions or other dysregulated endocrinopathies, or other conditions which, in the opinion of the investigators, have the potential to affect outcome measures
  • Daily use of tobacco products
  • Excessive alcohol consumption
  • Pregnancy

Treatment and study plan

Primary outcomes

  1. Resting energy expenditure

    Time frame: Before (baseline) and 60-180 minutes after ingestion of a glucose solution

    Resting energy expenditure is measured in the fasting and fed state by indirect calorimetry

  2. Appetite

    Time frame: Before (baseline) and 60-180 minutes after ingestion of a glucose solution as well as immediately after an ad libitum meal test

    Subjective appetite sensations are measured in the fasting and fed state by visual analogue scale (VAS) ratings

  3. Energy intake

    Time frame: 180 minutes after ingestion of a glucose solution

    Energy intake is measured by quantifying the amount of food ingested during an ad libitum meal test

Secondary outcomes

  1. Plasma hormones and cytokines modulating appetite and energy expenditure

    Time frame: Before (baseline) and 0-180 minutes after ingestion of a glucose solution

    Plasma levels of FGF21, GDF15, GLP-1, PYY, ghrelin, glucagon, and GIP are measured in the fasting and fed state

  2. Plasma adipokines modulating appetite and energy expenditure

    Time frame: Baseline

    Plasma levels of leptin and adiponectin are measured in the fasting state

  3. Muscle mitochondrial leak respiration

    Time frame: Baseline

    Mitochondrial O2 flux is measured by high-resolution respirometry in permeabilized muscle fibers

  4. Muscle mitochondrial efficiency

    Time frame: Baseline

    Mitochondrial P/O ratio is measured by high-resolution respirometry in isolated mitochondria

  5. Muscle mitochondrial membrane potential

    Time frame: Baseline

    Mitochondrial membrane potential is measured by high-resolution fluorometry in isolated mitochondria

Other outcomes

  1. Body composition

    Time frame: Baseline

    Fat free mass and fat mass are determined by dual-energy X-ray absorptiometry

  2. Physical activity level

    Time frame: Baseline

    Physical activity level is measured by wrist-worn accelerometers

  3. Self-reported physical activity

    Time frame: Baseline

    Self-reported physical activity is measured by the International Physical Activity Questionnaire - Short Form (IPAQ-SF)

  4. Cardiorespiratory fitness

    Time frame: Baseline

    Pulmonary maximal oxygen uptake (VO2max) is determined during an incremental exercise test to exhaustion

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Collaborators

  • University of Copenhagen

Registry information

Official study title

Energy Balance and Mitochondrial Function in Human Genetic Models of Mitochondrial Stress-mediated Obesity Resistance

Acronym: MITO-OB-RES

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Oct 12, 2023
Registry last updated
Jun 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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