Novel Methodology to Measure Protein Accumulation

Sponsor
Mayo Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT01505621
Collaborator
(none)
24
1
20
1.2

Study Details

Study Description

Brief Summary

Accumulation of damaged proteins is thought to underlie many degenerative conditions, including aging, diabetes, Alzheimer's disease, cataracts, and others. Over time, proteins can be irreversibly damaged by a variety of factors, such as reactive oxygen species, and without timely degradation they can accumulate and aggregate. We believe this can contribute to the development of chronic degenerative disorders.

The purpose of this study is to develop a novel methodology for measuring protein accumulation and test it in two groups of people: young (18-30 years) and old (≥65 years). This methodology will require that people drink a solution of essential amino acids that includes isotopically labeled L[ring-13C6]phenylalanine. We will then collect blood and muscle samples, to isolate plasma and skeletal muscle proteins. Participants will return to the study center four more times on a weekly interval.

We hypothesize that older proteins, which persisted in circulation and accumulated over time, will have a higher degree of post-translational oxidative damage than newly synthesized proteins.

Condition or Disease Intervention/Treatment Phase
  • Other: L[ring-13C6]phenylalanine

Study Design

Study Type:
Observational
Actual Enrollment :
24 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Novel Methodology to Measure Protein Accumulation
Study Start Date :
Dec 1, 2011
Actual Primary Completion Date :
Aug 1, 2013
Actual Study Completion Date :
Aug 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Young

Healthy adults 18-30 years old

Other: L[ring-13C6]phenylalanine
Oral drink composed of essential amino acids including L[ring-13C6]phenylalanine

Elderly

Healthy adults greater than 65 years old

Other: L[ring-13C6]phenylalanine
Oral drink composed of essential amino acids including L[ring-13C6]phenylalanine

Outcome Measures

Primary Outcome Measures

  1. Isotopic enrichment of plasma and skeletal muscle proteins achieved by oral ingestion of [13C6]-phenylalanine [3 weeks]

    Administration of an oral amino acid mixture containing isotopically-labeled [13C6]-phenylalanine (13C-Phe) will result in 13C-Phe incorporation into newly synthesized proteins. Measuring isotopic enrichment (IE) of 13C-Phe immediately after administration and weekly for 3 consecutive weeks will allow for estimation of protein accumulation.

  2. Degree of post-translational modifications in plasma and muscle proteins [3 weeks]

    The abundance of post-translational modifications of plasma and muscle proteins will be measured using mass spectrometry.

Secondary Outcome Measures

  1. Assess differences in protein accumulation as a function of age [3 weeks]

    Use the newly developed methodology to assess whether otherwise healthy older adults (≥65 years old) have greater accumulation of plasma and muscle proteins compared to healthy young adults (18-30 years old).

  2. Assess differences in protein modification/damage as a function of age [3 weeks]

    The abundance of post-translational modification/damage of plasma and muscle proteins will be measured using mass spectrometry in young (18-30 years old)and older (>65 years old) adults.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age 18-30 years

  • Age greater than 65 years

Exclusion Criteria:
  • Active or uncontrolled cardiovascular disease

  • Chronic kidney disease with serum creatinine ≥ 1.4 mg/dL for women and ≥ 1.5 mg/dL for men

  • Chronic liver disease (elevation in serum transaminases ≥ 3 times the upper limit of normal)

  • Any debilitating chronic illness, including malignancy

  • Significant malabsorptive state, including prior gastric bypass surgery or inflammatory bowel disease

  • Diabetes mellitus (types 1 or 2) or glucose ≥ 110 mg/dL.

  • Obesity (BMI ≥ 31 kg/m2)

  • Anticoagulant therapy (warfarin or heparin) or bleeding disorder that increases risk of bleeding during a muscle biopsy.

  • Anemia (hemoglobin ≤ 11 g/dL)

  • Use of medications known to modulate protein synthesis, mitochondrial function, and/or glucose homeostasis (including β-blockers and corticosteroids).

  • Participation in another study where the 13CPhe was administered during the past 6 months.

  • Moderate or high level of structured exercise (on average, ≥ 30 minutes per day and ≥ 2 days per week)

  • Pregnancy

  • Daily use of tobacco products (smoking or chewing); or smoking ≥7 cigarettes per week, on average. Abstinence from tobacco for ≥3 months is required before enrollment in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
K. Sreekumaran Nair, Professor of Medicine, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01505621
Other Study ID Numbers:
  • 11-004969
First Posted:
Jan 6, 2012
Last Update Posted:
Apr 10, 2014
Last Verified:
Apr 1, 2014
Keywords provided by K. Sreekumaran Nair, Professor of Medicine, Mayo Clinic

Study Results

No Results Posted as of Apr 10, 2014