- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02166307
Clinical Verification of Peptide Biomarkers for Human Aging
June 17, 2014 updated by: Yulin Deng, Beijing Institute of Technology
Clinical Verification of Peptide Biomarkers for Human Aging by Standard-Free, Label-Free LC-MS/MS Quanification of Aldehyde-modified Peptides
Aging in human physically refers to a multidimensional process that all the changes were accumulated in a person over time.
These aging changes are responsible for the progressive increases in the chance of disease and death associated with them.
So far, there are several theories have been developed to understand the aging process, such as cross-linking, which is led by Maillard Reactions.
Maillard Reaction is a complex series of reactions between reducing sugar/aldehydes and amino groups on proteins.
Under physiological conditions, aldehydes are products of various exogenous and endogenous amines catalyzed by semicarbazide-sensitive amine oxidase (SSAO), a family of heterogeneous enzyme.
It was reported that SSAO shows a significant higher catalytic activity, producing more aldehydes in age-related diseases.
However, SSAO is not a perfect candidate to be monitored for evaluating aging, because it is widely distributed in tissues, which are not readily accessible sample-sources for clinical applications.
In this work, the investigators have found 6 biomarker candidates by developing a standard-free, label-free MS-based proteomics method based on standard protein (human serum albumin, the highest abundance protein in human plasma) model in vitro.
Then, the investigators wanted to verify these biomarker candidates by clinical plasma samples to see if there is significant quantitative difference among people with different ages.
Study Overview
Status
Completed
Conditions
Detailed Description
The procedure of clinical study was:
- to get plasma samples from hospital;
- digestion of plasma protein-mixture by trypsin in lab;
- run mass spectrometry and monitor the amount of target HSA-peptides.
Study Type
Observational
Enrollment (Actual)
253
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
23 years to 72 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
university hospital, plasma samples of physical examination, faculties and staff of a certain university
Description
Inclusion Criteria:
- Cases with different ages
Exclusion Criteria:
- Cases with Diabetes Mellitus and Hepatitis B
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
measurement of the amount of plasma peptides
Time Frame: two years
|
The investigators have found 6 biomarker candidates by developing a standard-free, label-free MS-based proteomics method based on standard protein (human serum albumin, the highest abundance protein in human plasma) model in vitro.
Then, the investigators wanted to verify these biomarker candidates by clinical plasma samples to see if there is significant quantitative difference among people with different ages.
|
two years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yulin Deng, Ph.D, School of Life Science, BIT
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2009
Primary Completion (Actual)
December 1, 2011
Study Completion (Actual)
December 1, 2011
Study Registration Dates
First Submitted
June 16, 2014
First Submitted That Met QC Criteria
June 17, 2014
First Posted (Estimate)
June 18, 2014
Study Record Updates
Last Update Posted (Estimate)
June 18, 2014
Last Update Submitted That Met QC Criteria
June 17, 2014
Last Verified
June 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- deng02
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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