Mitochondrial DNA and Exercise in Young Adults Born Preterm
This study is looking at why some young adults born prematurely (before 37 weeks of pregnancy) don't get fitter from exercise, even when they follow recommended guidelines. We know that young adults born very prematurely (32 weeks or earlier) often don't improve their fitness (maximal aerobic capacity) after exercise training. This study will have participants follow a moderate-intensity aerobic exercise program 4-5 days a week for 40-60 minutes per session. Researchers will measure changes in their mitochondrial DNA (the genetic material inside the energy-producing parts of cells) and their maximal aerobic capacity before and after the exercise program. The goal is to understand if specific mitochondrial DNA patterns are linked to how well someone responds to exercise. You can join if you are 18-35 years old, were born prematurely, and are currently inactive. There is also a control group of inactive young adults born at full term.
- Study design
- This is an interventional study with 60 participants. It includes young adults born prematurely and a control group born at full term.
- What's involved
- Participants will follow a moderate-intensity aerobic exercise training program for 4-5 days per week, for 40-60 minutes each session. Measurements will be taken immediately after the exercise training intervention and at an initial visit.
- Compensation
- Not stated in the trial record.
- Follow-up
- Mitochondrial DNA and aerobic capacity will be measured immediately after the aerobic exercise training intervention.
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Mitochondrial DNA Signatures of Poor Aerobic Exercise Trainability in Young Adults Born Preterm
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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Inclusion
What this trial measures
- Mitochondrial DNA heteroplasmyImmediately after aerobic exercise training intervention; change in pre- to post-frequency
The full-length mitochondrial DNA sequence will be analyzed and assessed for heteroplasmic sites in the mitochondrial genome. Briefly, mitochondrial DNA exists in many copies, and heteroplasmy is noted when the amino acid sequence changes from the major read 2% or more across the DNA copies. The change in the mean heteroplasmy frequency and the mean number of sites with heteroplasmy with aerobic exercise training by comparing these changes in young adults born preterm to those born at term.
- Mitochondrial DNA sequence variantsImmediately after visit 1
The full-length mitochondrial DNA sequence will be determined in participants who report being born prematurely, which will be compared to their biological birth mother. In this comparison, we will assess for variants. We deem a site as an 'informative' mitochondrial DNA variant in young adults born prematurely as a change in amino acid sequence from the biological birth mother.
- Change in maximal aerobic capacityImmediately after aerobic exercise training intervention; change in pre- to post-frequency
The change in maximal aerobic capacity will be assessed via the modified Balke-graded exercise test before and after the aerobic exercise training program.
- Change in mitochondrial oxidative capacity in peripheral blood mononuclear cellsImmediately after aerobic exercise training intervention; change in pre- to post-frequency
Mitochondrial maximal respiration (i.e., oxidative capacity) will be measured in isolated peripheral blood mononuclear cells.