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Br J Ophthalmol 2001;85:592-597 doi:10.1136/bjo.85.5.592
  • Original Article
    • Clinical science

Passive permeability and outward active transport of fluorescein across the blood-retinal barrier in early ARM

  1. Birgitte Moldow,
  2. Michael Larsen,
  3. Birgit Sander,
  4. Henrik Lund-Andersen
  1. Department of Ophthalmology, Herlev Hospital, University of Copenhagen, Denmark
  1. Birgitte Moldow, PhD, Soløsevej 39, DK- 2820 Gentofte, Denmark b.moldow{at}ofir.dk
  • Accepted 27 November 2000

Abstract

AIM To study the passive and active transport of fluorescein across the blood-retina barrier in early age related maculopathy (ARM) (soft drusen > 63 μm, hyperpigmentation and/or hypopigmentation in patients above 50 years of age).

METHODS 15 patients and 10 healthy subjects were included. Morphological changes were graded from 30 degrees fundus photographs using a simplified version of the epidemiological ARM study group classification system. Differential vitreous spectrofluorophotometry was used to assess the transport properties of the blood-retina barrier (that is, passive permeability and unidirectional permeability caused by outward active transport from the vitreous to the blood).

RESULTS The passive permeability of the patient group was not significantly different from that of the control group. Four patients with passive permeability more than 3 SD above the mean of the control group (mean 1.8 (SD 0.7) nm/s, range 1.0–3.0 nm/s, data normally distributed) all had centrally located drusen >500 μm and superjacent pigment clumps of 63–500 μm in diameter. There was no significant difference between the unidirectional permeabilities for the patient group and for the control group (mean 47.4 (29.3) nm/s, range 12.7–91.1 nm/s).

CONCLUSION There was no significant difference in the passive permeability and in the unidirectional permeability of fluorescein. However, the study may indicate that the combination of very large drusen and superjacent pigment clumps in ARM may be associated with a deterioration of the blood-retina barrier.

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