- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04300504
Muscle in Obesity: Imaging, Function and microRNA
Growing evidence suggests that dynapenic abdominal obesity is associated with a greater risk of falls, functional disability and hospitalisation compared to those with dynapenia, obesity or neither phenotype. Understanding the pathogenesis underlying this phenotype has the potential to inform potential treatment strategies.
MicroRNAs can act as messengers at the cellular level to promote or block processes for muscle growth and repair, amongst other things. There is evidence that ageing changes microRNA levels in the muscle and that these changes may result in reduced muscle quality and quantity. However, it is not known whether being obese can change microRNA levels in muscle and how this relates to physical performance.
The aim of this study is to investigate the effect of dynapenic abdominal obesity on microRNA levels in serum and muscle quality and quantity in the legs of older women.
This is an observational, cross-sectional study. The investigators will recruit 4 groups of older women: normal weight, normal weight with dynapenia, obese and obese with dynapenia. The investigators will measure the microRNA levels in serum. The investigators will measure the quantity and fat content of muscle in the legs using magnetic resonance imaging. Muscle strength, fatigue and balance will be measured using gait (walking) analysis, balance tests, and a machine designed to measure leg strength and fatigue.
The investigators will measure and compare microRNA levels between groups. The investigators will use databases and computer programmes to look at all of the microRNAs which are different between groups and see how they affect the muscle. The investigators will compare muscle strength, size and fatigue between groups. The investigators will explore relationships of muscle quantity and quality measures with microRNA changes in the muscle. This approach will allow the investigators to understand how obesity affects the microRNA profile of muscle and whether this translates into impairment of function and mobility.
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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South Yorkshire
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Sheffield, South Yorkshire, United Kingdom
- University of Sheffield/Sheffield Teaching Hospitals
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion criteria:
- Caucasian
- Female
- BMI 18.5-25 or 30-40kg/m2
- Ages 60-80 years
- Sufficiently mobile to undergo scanning and biomechanical testing
- Able to remain motionless during scans
- Able and willing to participate in the study and provide written informed consent
Exclusion Criteria:
- BMI 18.5-25kg/m2 AND waist circumference >88cm i.e. normal weight AND abdominally obese
- BMI 30-40kg/m2 AND waist circumference <88cm i.e. obese AND not abdominally obese
- History of any long-term immobilisation (duration greater than 2 weeks in the past 12 months)
- History of hospital admission in the past 3 months
- History of recent significant weight loss (5% in 3 months or 10% in 6 months)
- Diabetes mellitus
History of current conditions which may affect muscle metabolism
- Malabsorption syndromes e.g. inflammatory bowel disease, pancreatic insufficiency etc.
- Chronic renal disease
- Diagnosed eating disorder
- Conditions which prevent the undertaking or analysis of the MRI and DXA scans or the interpretation of their results e.g. hip prosthesis, metal implants etc.
- Conditions which prevent the undertaking of the fatigue protocols e.g. hypertension etc.
Use of medications or treatment known to affect muscle metabolism
o Anabolic steroids, glucocorticoids, antiretrovirals etc.
- Excessive alcohol intake defined as greater than 21 units per week
- Competitive athlete, defined as participating in competitive sport at amateur or professional level
- Conditions which prevent the undertaking of a 6-minute walking test e.g. unstable angina or myocardial infarction during the previous month.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
normal weight, not dynapenic
BMI 18.5 to 25kg/m2, waist circumference <= 88cm, healthy women aged 60-80 years, time to complete 5 chair stands <15 seconds
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observational study
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|
normal weight, dynapenic
BMI 18.5 to 25kg/m2, waist circumference <= 88cm,healthy women aged 60-80 years, time to complete 5 chair stands >15 seconds
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observational study
|
|
obese, not dynapenic
BMI 30 to 40kg/m2, waist circumference > 88cm, healthy women aged 60-80 years, time to complete 5 chair stands <15 seconds
|
observational study
|
|
obese, dynapenic
BMI 30 to 40kg/m2, waist circumference > 88cm, women aged 60-80 years, time to complete 5 chair stands >15 seconds
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observational study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Differential microRNA expression, expressed as fold-change and p-values, measured using real time quantitative polymerase chain reaction (RT-qPCR) between normal weight and obese groups, further stratified by dynapenia
Time Frame: 1 day (one measurement )
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Serum analyses
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1 day (one measurement )
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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mean difference in distance walked during 6 minute walk test between normal weight and obese, further stratified by dynapenia
Time Frame: 1 day (one measurement )
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6 Minute walk test
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1 day (one measurement )
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mean difference in muscle mass and volume measures between normal weight and obese, further stratified by dynapenia MRI
Time Frame: 1 day (one measurement )
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MRI (Magnetic Resonance Imaging)
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1 day (one measurement )
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mean difference in muscle mass and volume measures between normal weight and obese, further stratified by dynapenia DXA
Time Frame: 1 day (one measurement )
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DXA (dual energy X-ray absorptiometry)
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1 day (one measurement )
|
|
mean difference in muscle strength between normal weight and obese, further stratified by dynapenia
Time Frame: 1 day (one measurement )
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Isokinetic dynamometer
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1 day (one measurement )
|
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mean difference in fatigue between normal weight and obese, further stratified by dynapenia
Time Frame: 1 day (one measurement )
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kinetic change in gait parameters from Opal accelerometers
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1 day (one measurement )
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Collaborators and Investigators
Investigators
- Principal Investigator: Jennifer Walsh, University of Sheffield
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STH21022
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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