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Clinical Trials/NCT06120647
NCT06120647
Recruiting
Not Applicable

Molecular Mechanisms Underpinning Sarcopenic Obesity

The Swedish School of Sport and Health Sciences1 site in 1 country60 target enrollmentJanuary 28, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sarcopenic Obesity
Sponsor
The Swedish School of Sport and Health Sciences
Enrollment
60
Locations
1
Primary Endpoint
Fiber type-specific cell signalling
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The coexistence of obesity and sarcopenia results in sarcopenic obesity, a high-risk geriatric condition associated with metabolic perturbations and several co-morbidities. Despite the rising numbers of older adults diagnosed with sarcopenic obesity, few studies have characterized this condition on the muscle cell and systemic level. This study sought to comprehensively assess the influence of sarcopenic obesity on muscle and blood-related parameters and compare it to non-sarocopenic obese and non-sarcopenic lean older adults.

Registry
clinicaltrials.gov
Start Date
January 28, 2020
End Date
December 30, 2025
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
The Swedish School of Sport and Health Sciences
Responsible Party
Principal Investigator
Principal Investigator

William Apro

Associate Professor

The Swedish School of Sport and Health Sciences

Eligibility Criteria

Inclusion Criteria

  • Body fat % in accordance with previously defined criteria
  • Free of smoking (since 10 years)
  • Able to walk without assistance
  • Able to perform bilateral leg extension exercise

Exclusion Criteria

  • History of or present disease of myocardial, vascular, endocrine, hepatic, renal, pulmonary or neuromuscular origin
  • Uncontrolled hypo/hypertension
  • Use of anticoagulants (Warfarin, Trombyl)
  • Use of metformin or other anti-diabetic medications
  • Poor appetite and unexplained weight loss (4,5 kg) over the past 6 months
  • Active malignancy
  • Present infection
  • Dementia or delirium
  • Other conditions that may interfere with the study protocol in the opinion of the PI

Outcomes

Primary Outcomes

Fiber type-specific cell signalling

Time Frame: 1 hour after ingestion of essential amino acids and resistance exercise

This measure will be investigated during an experimental trial in which the participants are subjected to an acute bout of resistance exercise followed by the ingestion of essential amino acids (240 mg/kg lean mass). During this 3 hour time period, the participants will donate two muscle biopsies, one before exercise and the second one 1 hour after exercise. Cell signalling networks related to muscle mass regulation will be examined in these biopsy samples. The signal will be measured using Western blotting and the signal obtained is expressed in relation to baseline (adjusted volume intensity).

Secondary Outcomes

  • Whole body glucose tolerance(2 hours)
  • Accelerometer-assessed physical activity levels(1 week)
  • Isometric and isokinetic leg muscle strength(1 hour)
  • Skeletal muscle fiber characteristics(1 hour prior to ingestion of essential amino acids and resistance exercise)
  • Whole body muscle volume(1 hour)

Study Sites (1)

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