Fluorescence lifetime imaging ophthalmoscopy and the influence of oral lutein/zeaxanthin supplementation on macular pigment (FLOS) - A pilot study.

Jaggi, Damian; Solberg, Yasmin; Dysli, Chantal; Lincke, Joel; Habra, Oussama; Wyss, Adrian; Wolf, Sebastian; Zinkernagel, Martin (2023). Fluorescence lifetime imaging ophthalmoscopy and the influence of oral lutein/zeaxanthin supplementation on macular pigment (FLOS) - A pilot study. Clinical Nutrition ESPEN, 56, pp. 127-134. Elsevier 10.1016/j.clnesp.2023.05.009

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BACKGROUND & AIMS

Oral lutein (L) and zeaxanthin (Z) supplementation enhances macular pigment optical density (MPOD) and plays a protective role in the development of age-related macular degeneration (AMD). Fluorescence lifetime imaging ophthalmoscopy (FLIO) is a novel in vivo retinal imaging method that has been shown to correlate to classical MPOD measurements and might contribute to a metabolic mapping of the retina in the future. Our aim was to show that oral supplementation of L and Z affects the FLIO signal in a positive way in patients with AMD.

METHODS

This was a prospective, single center, open label cohort study. Patients with early and intermediate AMD received oral L and Z supplementation during three months, and were observed for another three months after therapy termination. All visits included measurements of clinical parameters, serum L and Z concentration, MPOD measurements using heterochromatic flicker photometry, dual wavelength autofluorescence imaging, and FLIO. Correlation analysis between FLIO and MPOD were performed.

RESULTS

Twenty-one patients completed the follow up period. Serum L and Z concentrations significantly increased during supplementation (mean difference 244.8 ng/ml; 95% CI: 81.26-419.9, and 77.1 ng/ml; 95% CI: 5.3-52.0, respectively). Mean MPOD units significantly increased (mean difference 0.06; 95% CI: 0.02-0.09; at 0.5°, 202; 95% CI: 58-345; at 2°, 1033; 95% CI: 288-1668; at 9° of eccentricity, respectively) after three months of supplementation with macular xanthophylls, which included L and Z. Median FLIO lifetimes in the foveal center significantly decreased from 277.3 ps (interquartile range 230.2-339.1) to 261.0 ps (interquartile range 231.4-334.4, p = 0.027). All parameters returned to near-normal values after termination of the nutritional supplementation. A significant negative correlation was found between FLIO and MPOD (r2 = 0.57, p < 0.0001).

CONCLUSIONS

FLIO is able to detect subtle changes in MPOD after L and Z supplementation in patients with early and intermediate AMD. Our findings confirm the previous described negative correlation between FLIO and MPOD. Macular xanthophylls seem to contribute to short foveal lifetimes. This study is registered at ClinicalTrials.gov (identifier number NCT04761341).

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > Forschungsbereich Augenklinik > Forschungsgruppe Augenheilkunde
04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Ophthalmology

UniBE Contributor:

Jaggi, Damian, Solberg, Yasmin Samira, Dysli, Chantal-Simone, Lincke, Joel-Benjamin, Habra, Oussama, Wolf, Sebastian (B), Zinkernagel, Martin Sebastian

Subjects:

600 Technology > 610 Medicine & health

ISSN:

2405-4577

Publisher:

Elsevier

Language:

English

Submitter:

Pubmed Import

Date Deposited:

22 Jun 2023 09:13

Last Modified:

23 Jun 2023 06:57

Publisher DOI:

10.1016/j.clnesp.2023.05.009

PubMed ID:

37344061

Uncontrolled Keywords:

Age-related macular degeneration (AMD) Autofluorescence Carotenoids FLIO Fluorescence lifetime Macular pigment optical density (MPOD) Nutritional supplement Retinal imaging

BORIS DOI:

10.48350/183631

URI:

https://boris.unibe.ch/id/eprint/183631

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