Actively Recruiting
Genetic Variants and Regulation of Specialized Pro-resolving Mediator
Led by Queen Mary University of London · Updated on 2026-02-05
200
Participants Needed
1
Research Sites
343 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Inflammation is the way that the body reacts against infection, injury or illness. An uncontrolled inflammatory response can lead to the development of inflammatory diseases, such as rheumatoid arthritis and cardiovascular conditions. Recent studies have shown that inflammation is a regulated process coordinated by a group of molecules known as specialized pro-resolving mediator (SPM). These molecules are produced by enzymes via the enzymatic conversion of essential fatty acids; whereas their biological actions are mediated by proteins expressed on the surface of cells known as receptors. Given the central role that pro-resolving mediators play in regulating the immune response, the aim of this study is to investigate whether there are genetic variants (mutations) in genes encoding for enzymes and receptors involved in the biology of these molecules and to determine how these mutations affect SPM's activity or function. Findings made as part of these studies will help shed light into mechanism influencing disease onset and/or progression and potentially enhance the discovery of new and more effective treatments.
CONDITIONS
Official Title
Genetic Variants and Regulation of Specialized Pro-resolving Mediator
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Current volunteer of the Genes & Health program with or without relevant genetic mutations
- Volunteer participates in Genes & Health program regions of East London and Bradford
- Volunteer has consented to be contacted for future research studies
- Volunteer is 18 years of age or older
You will not qualify if you...
- Volunteer has not had their genome sequenced after taking part in Genes & Health program Stage 1
- Volunteer has significant genetically inherited conditions
- Presence of any abnormality or pre-existing disease that may expose the subject to risk or affect results
- Volunteer is recovering from recent surgery
- Participation in a clinical study of new chemical entity, biological product, or prescription medicine, or loss of more than 400 mL blood within the previous 3 months
- History or presence of drug or alcohol abuse
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Queen Mary University of London
London, United Kingdom, EC1M 6BQ
Actively Recruiting
Research Team
E
Esteban A Gomez Cifuentes, PhD student
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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