Pseudoexfoliation syndrome (PEX) has been suggested to represent a blood-aq
ueous barrier impairment leading to a higher protein content in aqueous hum
our of eyes with PEX. However, the nature of a prospective PEX protein has
not yet been described. We set out to reevaluate protein content and examin
e protein composition for prospective PEX protein candidates in aqueous hum
our of eyes with PEX syndrome. Aqueous humour of 52 patients with PEX and 3
8 without PEX signs was sampled during cataract or glaucoma surgery. Total
aqueous protein concentration in the samples was analysed in 43 PEX specime
ns and 32 non-PEX specimens according to Bradford. Aqueous protein composit
ion of all samples was determined by sodium dodecylsulphate polyacrylamide
gel electrophoresis (SDS PAGE) and silver staining. Screening for amyloids
was performed in nine PEX samples and six non-PEX samples by Congo Red stai
ning and polarised light microscopy. Aqueous protein concentration was not
significantly increased in PEX eyes in comparison with non-PEX eyes. Furthe
rmore, we could not detect any characteristic difference in protein band si
zes of the two groups after SDS PAGE. However, we were able to show the pre
sence of amyloid exclusively in aqueous humour of PEX patients. Conclusion:
our results do not confirm a generally higher protein concentration in pse
udoexfoliation syndrome eyes. This does not necessarily contradict a blood-
aqueous barrier impairment but illustrates the variance in protein concentr
ation between and within the two groups. No characteristic protein band all
ocatable to pseudoexfoliation syndrome proteins could be detected in any of
the samples. However, our findings support the theory that the pseudoexfol
iation syndrome is associated with an amyloid of a serum protein.