Background: To evaluate the quantity of oxidative stress (OS), immune activation (IA) and exfoliation
material before and after four months daily ingestion of Strix® Forte in exfoliation
syndrome (XFS) and exfoliative glaucoma (XFG). Methods: 15 XFS, 15 XFG and 15 control patients ingested one Strix® Forte tablet twice daily
during four months containing 74mg bilberry (Vaccinium myrtillus L.) anthocyanosides, 6mg lutein, 15mg zinc sulphate, 10mg dl-α-tocopheryl acetate, 800µg
retinyl acetate and 50µg selenomethionine. Exfoliation material quantity (EmQ), scale
0–3, was also examined. Plasma concentrations of isoprostanes, malondialdehyde, carbonyl
proteins and oxidized albumin were measured as markers for OS. Neopterin and kynurenine/tryptophan
ratio were measured as markers for IA. Wilcoxon Signed Ranks Tests were used for statistical
analyses. Results: EmQ was significantly reduced after four months in both XFS and XFG group (XFS: P=0.007 for right and 0.003 for left eyes, XFG: P=014 for right and 0.005 for left
eyes. Isoprostanes were reduced in XFS group (P=0.001) and in controls (P=0.009), but not in XFG group (P=0.191). Malondialdehyde levels were not diminished in any groups. Carbonyl proteins
were reduced in all groups: [XFS (P=0.002), XFG (P=0.001), controls (P=0.015)]. Oxidized albumin diminished in all groups [XFS (P=0.003), XFG (P=0.005), controls (P=0.001)]. Neopterin levels were slightly increased in the XFG group (P=0.020) and tryptophan levels were slightly elevated in the XFS group (P=0.047). Kynurenine levels decreased in the XFG group (P=0.012) and in controls (P=0.008). Kynurenine/tryptophan levels decreased in all three groups [XFS (P=0.006), XFG (P=0.003), controls (P=0.006)]. Conclusion: Regular Strix® Forte ingestion reduced besides OS and IA also EmQ in XFS and XFG
patients which may be explained by the observed beneficial alterations in the OS and
IA markers.
Acknowledgements: Research supported by Ferrosan A/S, Sjøborg, Denmark
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