Study of the Discriminating Power of a Blood Biomarker for Omega-3 Polyunsaturated Fatty Acid Content of the Retina for Age-related Macular Degeneration (AMD)

NCT ID: NCT04278300

Last Updated: 2020-11-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

205 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-02-11

Study Completion Date

2020-09-09

Brief Summary

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Age-related macular degeneration is a chronic degenerative retinal disease, which can lead to a progressive loss of visual acuity without affecting peripheral vision. It is a public health problem as it remains the leading cause of visual impairment in people over 50 years of age in industrialized countries.

Age-related macular degeneration has two clinical forms:

* Atrophic or dry form: progressive disappearance of photoreceptors, alteration of the pigmentary epithelium leading to a thinning of the macula.
* Exudative or humid form: development of immature choroidal neo-vessels, leading to the formation of edema or intra or sub-retinal hemorrhage at the origin of the symptoms.

There are still many questions about the pathogenesis of age-related macular degeneration, and there is currently no etiological treatment. The disorder is thought to have a multifactorial, genetic and environmental origin.

Among the environmental risk factors, dietary intake of omega-3 polyunsaturated acids and its effect on the retina are factors that influence both the incidence and progression of the disease. However, intervention studies have not been able to demonstrate the preventive value of omega-3 polyunsaturated fatty acids. It is likely that the precise identification of patients who could benefit from this supplementation is necessary. Currently, the estimation of dietary intake of omega-3 polyunsaturated fatty acids is based on dietary surveys, which implies a number of limits. A blood biomarker of omega-3 polyunsaturated fatty acid content in the retina has been previously identified, which if lowered may be a risk factor for age-related macular degeneration. A low level could also help to identify patients who would best respond to supplementation. A publication has been submitted and a patent has been filed for this biomarker. The objective of this project is to confirm the relationship between this biomarker and the presence of age-related macular degeneration. The analysis will be refined by correlating the discriminating character of the biomarker with factors that may influence the intestinal metabolism of dietary lipids and their bioavailability in the blood. For this purpose, the status of the subjects with regard to their intestinal flora (microbiota) will be evaluated. The relationship between lipid metabolism, microbiota and age-related macular degeneration should also provide a better understanding of the pathophysiological mechanisms that link diet, lipid metabolism and age-related macular degeneration.

Detailed Description

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Conditions

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Age-related Macular Degeneration

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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case

patient with age-related exudative macular degeneration

blood sampling

Intervention Type BIOLOGICAL

dosage of omega 3 polyunsaturated fatty acids, search for age-related macular degeneration susceptibility genese

faecal sampling (optional)

Intervention Type BIOLOGICAL

analysis of the microbiota by DNA sequencing

control

Patient with no macular disorder and in need of cataract surgery

blood sampling

Intervention Type BIOLOGICAL

dosage of omega 3 polyunsaturated fatty acids, search for age-related macular degeneration susceptibility genese

faecal sampling (optional)

Intervention Type BIOLOGICAL

analysis of the microbiota by DNA sequencing

Interventions

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blood sampling

dosage of omega 3 polyunsaturated fatty acids, search for age-related macular degeneration susceptibility genese

Intervention Type BIOLOGICAL

faecal sampling (optional)

analysis of the microbiota by DNA sequencing

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Subject who has provided written informed consent for participation in the study and genetic analyses
* Subject aged 50 years or older
* Subject with exudative AMD or
* Subject with macular disorder requiring cataract surgery

Exclusion Criteria

* Person not affiliated to the national health insurance system
* Protected adults (curatorship, guardianship)
* Persons deprived of their liberty by judicial or administrative decision
* Adult unable to express consent
* Subject who has already participated in the study
* Subject with pre-existing maculopathy not labelled AMD
* Subject refusing blood sample
* Subject with diabetes
* Subject on antibiotics or having had an antibiotic treatment in the last 3 months
* Subject with a BMI \< 18.5 or \> 30 kg/m2
* Subject with extreme eating habits (veganism, bulimia, anorexia)
* Subject currently on a diet with avoidance of certain types of food or a low-calorie diet
* Subject with an inflammatory disease (especially digestive disease)
* Subject having undergone bariatric surgery
* Subject having digestive tract malformations
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire Dijon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU dijon Bourgogne

Dijon, , France

Site Status

Countries

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France

Other Identifiers

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CREUZOT 2019

Identifier Type: -

Identifier Source: org_study_id