FLOS: FLIO and the Influence of Oral Lutein Supplementation on Macular Pigment

Sponsor
University Hospital Inselspital, Berne (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04761341
Collaborator
(none)
80
1
2
38
2.1

Study Details

Study Description

Brief Summary

To investigate the effects of lutein supplementation on macular pigment density using FLIO and MPOD measurements in patients with age-related macular degeneration and healthy subjects over a course of 6 months.

Condition or Disease Intervention/Treatment Phase
  • Drug: NUTROF TOTAL
Phase 4

Detailed Description

The human macula is a small area of the retina responsible for central vision. The yellow macular pigment contains three carotenoids, lutein ((3R,3'R,6'R)-lutein), zeaxanthin ((3R,3'R)-zeaxanthin), and meso-zeaxanthin ((3R,3'S;meso)-zeaxanthin). The human body is unable to synthesize lutein and zeaxanthin, thus needs to be obtained from dietary sources such as green leafy vegetables and supplements. The function of the macular pigment is to act as a filter by absorbing blue light that may attenuate photochemical damage of the retina. Furthermore, it protects against light induced oxidative damage by functioning as an antioxidant; scavenging free radicals. A growing body of evidence has established a link between the concentrations of the macular pigment carotenoids, the macular pigment optical density (MPOD) levels, visual performance and the risk of macular degeneration.

The ability of the macular pigment to absorb or filter blue light can be measured as macular pigment optical density (MPOD), which is directly related to the quantity of lutein and zeaxanthin in the macula. Furthermore, preliminary data showed that macular pigment can be evaluated using Fluorescence lifetime imaging ophthalmoscopy (FLIO). In a previous study the investigators have shown that FLIO provides contrast for macular pigment in patients with AMD and healthy subjects.

The purpose of this study is to investigate the effects of oral lutein supplementation on macular pigment density using FLIO and MPOD measurements in healthy subjects and patients with age-related macular degeneration (AMD) over a course of 6 months. Furthermore, the investigators will assess whether compositional and functional alterations of the gut metagenome may be related to age-related macular degeneration, and the effects of lutein supplementation on the gut. In addition, to blood samples, stool samples will be analysed accordingly to the currently running study on "The role of the gut metagenome on the development of ophthalmic diseases" ClinicalTrials.gov Identifier: NCT02438111. Faecal analyses will provide insight to how oral lutein supplementation effects the gut microbiota and how it is influenced by serum lutein Levels.

Objective is to investigate the effects of lutein supplementation on macular pigment density using FLIO and MPOD measurements in patients with age-related macular degeneration and healthy subjects over a course of 6 months.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
FLIO and the Influence of Oral Lutein Supplementation on Macular Pigment
Actual Study Start Date :
Jun 1, 2018
Actual Primary Completion Date :
Oct 22, 2019
Anticipated Study Completion Date :
Aug 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: AMD

Drug: NUTROF TOTAL
1 per day over a course of 3 months

Active Comparator: healthy control

Drug: NUTROF TOTAL
1 per day over a course of 3 months

Outcome Measures

Primary Outcome Measures

  1. MPOD (macular pigment optical Density) [6 Months]

    Method to detect changes in macular pigment optic Density using dual wavelength autofluorescence

  2. Fluorescence Lifetime Imaging Ophthalmoscopy (FLIO) [6 Months]

    Retinal Autofluorescence lifetimes

  3. Macular pigment screener (MPS) II [6 Months]

    Screening Method to detect changes in macular pigment optic Density using heterochromatic flicker photometry

Secondary Outcome Measures

  1. Contrast sensitivity [6 Months]

    Using Pelli-Robson charts

  2. Visual acuity [6 Months]

    Visual acuity using ETDRS charts

  3. Serum Lutein concentration [6 Months]

  4. Stool Analysis namely taxonomic and functional characterization of gut microbiota [6 Months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Subject must be willing to give written informed consent

  • Probands 18 years of age or greater

  • Both eyes will be assessed in the study

Exclusion Criteria:
  • Opacities of ocular media excluding detailed observation of the retina

  • Gastrointestinal diseases that could cause disturbance of dietary absorption

  • History of lutein supplementation

  • Allergy to lutein and zeaxanthin

  • Missing compliance

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Ophthalmology, Inselspital, Bern University Hostpital, University of Bern, Bern, Switzerland Bern Switzerland 3010

Sponsors and Collaborators

  • University Hospital Inselspital, Berne

Investigators

  • Study Chair: Martin Zinkernagel, MD, PHD, Department of Ophthalmology, Inselspital, Bern University Hostpital, University of Bern, Bern, Switzerland

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital Inselspital, Berne
ClinicalTrials.gov Identifier:
NCT04761341
Other Study ID Numbers:
  • FLOS Study
First Posted:
Feb 18, 2021
Last Update Posted:
Feb 18, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 18, 2021