Rigshospitalet
Copenhagen, Denmark, 2100
NCT Number: NCT06080568
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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Notify Me18 year and older
All sexes
Observational
Copenhagen, Denmark, 2100
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.
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
Exclusion criteria
Eligibility criteria for controls
Exclusion criteria
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
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
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
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
Time frame: Baseline
Plasma levels of leptin and adiponectin are measured in the fasting state
Time frame: Baseline
Mitochondrial O2 flux is measured by high-resolution respirometry in permeabilized muscle fibers
Time frame: Baseline
Mitochondrial P/O ratio is measured by high-resolution respirometry in isolated mitochondria
Time frame: Baseline
Mitochondrial membrane potential is measured by high-resolution fluorometry in isolated mitochondria
Time frame: Baseline
Fat free mass and fat mass are determined by dual-energy X-ray absorptiometry
Time frame: Baseline
Physical activity level is measured by wrist-worn accelerometers
Time frame: Baseline
Self-reported physical activity is measured by the International Physical Activity Questionnaire - Short Form (IPAQ-SF)
Time frame: Baseline
Pulmonary maximal oxygen uptake (VO2max) is determined during an incremental exercise test to exhaustion
Rigshospitalet, Denmark
Other
Energy Balance and Mitochondrial Function in Human Genetic Models of Mitochondrial Stress-mediated Obesity Resistance
Acronym: MITO-OB-RES
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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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