- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02077127
Monocyte Chemoattractant Protein-1 2518A/G Polymorphism (MCP-1)
March 3, 2014 updated by: Li Dong, Harbin Medical University
Association of Monocyte Chemoattractant Protein-1 (MCP-1)2518A/G Polymorphism With Proliferative Diabetic Retinopathy in Northern Chinese Type 2 Diabetes
The pathogenesis of proliferative diabetic retinopathy (PDR) remains poorly understood.
Recent studies have implicated that monocyte chemoattractant protein-1 (MCP-1) is associated with diabetic microvascular or macrovascular complications.
However, the relationship between SNP polymorphism c.2518A/G in the MCP-1 gene with diabetic retinopathy remains controversial.
In the present study, we evaluated the association of a single nucleotide polymorphism (SNP) in the MCP-1 gene with diabetic retinopathy (DR) and diabetic macular edema (DME) in Chinese population from Southern China with type 2 diabetes.
Study Overview
Status
Completed
Conditions
Detailed Description
The association between polymorphism of MCP-1 c.2518A/G and DR had been reported in Japan and Korea, but their opinion were inconsistent.
However there is no report in China so far.
This study was designed to clarify the relationship of polymorphism of MCP-1 c.2518A/G with type 2 diabetes with or without DR.
The relationship between MCP-1 c.2518A/G and different stage of DR has also been studied.This article proved that the MCP-1 c.2518G/G genotype is a susceptibility gene for DR in Chinese type 2 diabetic patients, especially the High-risk PDR.
There is no association with DME and c.2518G/G.
Study Type
Observational
Enrollment (Actual)
1043
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Heilongjiang
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Harbin, Heilongjiang, China, 150001
- Harbin Medical University
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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
41 years to 68 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
residents of a certain province
Description
Inclusion Criteria:
- Type 2 diabetic retinopathy
- age at diagnosis ≥30 years and a known duration of diabetes of ≥5 years.
Exclusion Criteria:
- eyeball atrophy
- epimacular membrane
- age-related macular degeneration (ARMD)
- intravitreal injection medicine
- vitreous hemorrhage
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
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Genetic association
Time Frame: 1 year
|
age at diagnosis of diabetes ≥30 years and a known duration of diabetes of ≥5 years.
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1 year
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ping Liu, Doctor, First Affiliated Hospital of Harbin Medical University
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
September 1, 2011
Primary Completion (Actual)
February 1, 2013
Study Completion (Actual)
April 1, 2013
Study Registration Dates
First Submitted
June 10, 2013
First Submitted That Met QC Criteria
February 28, 2014
First Posted (Estimate)
March 4, 2014
Study Record Updates
Last Update Posted (Estimate)
March 5, 2014
Last Update Submitted That Met QC Criteria
March 3, 2014
Last Verified
March 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- dongli
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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