A Prospective Study Of Biomarkers Of Skeletal Muscle Atrophy

NCT ID: NCT02839460

Last Updated: 2019-04-11

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 30 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2016-11-30
• Study Completion Date: 2019-03-31

Brief Summary

This is a single center, prospective biomarker study to evaluate serum levels of TWEAK and expression levels of TWEAK and Fn14 in muscle biopsies from patients with sarcopenia as well as healthy, physically active controls.

Conditions

Sarcopenia

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

subjects with sarcopenia

Screening Procedures (Physical Exam, Height & Weight, Vitals, Medical History, CHAMPS, DXA Scan, Physical Performance Testing, Muscle Strength Testing, Blood Collection)

Day 1 (target +/- 2 days) Outpatient Muscle Biopsy (Vitals, Blood Collection, Muscle Biopsy, update Concomitant Therapy and Procedure-Related AEs/SAEs)

Day 14 (target +/- 2 days) Safety Follow-up Visit (Vitals, Blood Collection, update Concomitant Therapy and Procedure-Related AEs/SAEs)

Outpatient Muscle Biopsy

Intervention Type: PROCEDURE

Outpatient Muscle Biopsy involving skeletal muscle sample collected from the vastus lateralis muscle

healthy, physically-active controls

Screening Procedures (Physical Exam, Height & Weight, Vitals, Medical History, CHAMPS, DXA Scan, Physical Performance Testing, Muscle Strength Testing, Blood Collection)

Day 1 (target +/- 2 days) Outpatient Muscle Biopsy (Vitals, Blood Collection, Muscle Biopsy, update Concomitant Therapy and Procedure-Related AEs/SAEs)

Day 14 (target +/- 2 days) Safety Follow-up Visit (Vitals, Blood Collection, update Concomitant Therapy and Procedure-Related AEs/SAEs)

Outpatient Muscle Biopsy

Intervention Type: PROCEDURE

Outpatient Muscle Biopsy involving skeletal muscle sample collected from the vastus lateralis muscle

Interventions

Outpatient Muscle Biopsy

Outpatient Muscle Biopsy involving skeletal muscle sample collected from the vastus lateralis muscle

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

To be eligible to participate in this study, all candidates must meet the following eligibility criteria at Baseline or at the time point specified in the individual eligibility criterion listed:

All Participants

1. Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information in accordance with national and local subject privacy regulations

Subjects with Sarcopenia

1. Men and postmenopausal women of 65 years of age or older

2. Gait speed measured over 4 meters of <1.0 m/s OR grip strength < 26 kg for men or < 16 kg for women.

3. Appendicular skeletal muscle adjusted for BMI by DXA ≤ 0.789 for men and ≤ 0.512 for women.

4. Weigh at least 40kg;

5. Self-reported difficulty climbing 10 steps OR walking outside on level ground for 1/4 mile

Healthy Controls

1. Men and postmenopausal women of 65 Years of age or older

2. Body mass index (BMI) between 18.5 and 30 kg/m2 inclusive at the time of Screening

3. Measures of Physical Performance and Lean Mass exceed thresholds defined for Sarcopenia group.

4. ≥ 150 minutes/week moderate-intensity physical activity OR regular engagement in resistance training ≥ 2 days/week

5. Willing to maintain a consistent diet and pattern of physical activity for the duration of the study

Exclusion Criteria

1. History of human immunodeficiency virus (HIV), hepatitis B or C, or tuberculosis (TB)

2. Immunocompromized subjects, as determined by the Investigator, based on medical history, physical examination, or laboratory testing, or due to prior or current immunosuppressive or immunomodulating treatment, including, but not limited to, HIV infection, history of organ transplantation, and anti-rejection therapy

3. Acute infection (urinary, respiratory, other) within past week or hospitalization within one month

4. Participation in any interventional clinical study within 12 weeks

5. A lower limb fracture in the past 6 months or any impairment or disease severely affecting gait (e.g. stroke with hemiparesis, myasthenia gravis, Parkinson's disease, peripheral polyneuropathy, intermittent claudication in advanced peripheral vascular disease, spinal stenosis, or severe osteoarthritis of the knee or hip);

6. Any underlying muscle disease including active myopathy or muscular dystrophy.

7. Confirmed diagnosis of heart failure classified as New York Heart Association Class III and IV (e.g. cardiomyopathy) or hypertrophic cardiomyopathy.

8. Type I diabetes or uncontrolled Type 2 diabetes (HA1C ≥ 9).

9. Requires regular assistance from another person for general activities of daily living (e.g. bathing, dressing)

10. Moderate to Vigorous Exercise performed in week prior to study visits (temporary exclusion - will be rescheduled)

11. Any other condition judged by the Principal Investigator or Study Physician to preclude safe participation in the study

• Minimum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Biogen

INDUSTRY

Sponsor Role: collaborator

University of Florida

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stephen D Anton, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Locations

University of Florida Institute on Aging

Gainesville, Florida, United States

Countries

United States

Other Identifiers

TWEAK

Identifier Type: -

Identifier Source: org_study_id