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  Vol. 123 No. 2, February 2005 TABLE OF CONTENTS
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Plasminogen Activator Inhibitor-1 in the Aqueous Humor of Patients With and Without Glaucoma

Jacob Dan, MD, PhD; David Belyea, MD; Gregory Gertner, MD; Israel Leshem, MD; Moshe Lusky, MD; Ruth Miskin, PhD

Arch Ophthalmol. 2005;123:220-224.

Objective  To determine the levels of plasminogen activator inhibitor-1 (PAI-1) and total protein in the aqueous humor of patients with glaucoma vs those without glaucoma.

Methods  A total of 125 aqueous humor samples (50-150 µL each) were collected at 3 institutions from patients with glaucoma and a control group of patients with cataract. Fifteen samples were excluded, and the levels of PAI-1 antigen were determined by enzyme-linked immunosorbent assay in 110 samples (36 glaucoma and 74 control). Total protein levels were determined by the Bradford method in 81 samples (28 glaucoma and 53 control), in which the aqueous humor collected was sufficient. Statistical analysis of the results was conducted using the Mann-Whitney U test. The correlation between PAI-1 and protein levels was calculated using the Spearman rank correlation coefficient.

Results  The mean ± SD PAI-1 levels detected in aqueous humor samples of the control and glaucoma groups were 0.44 ± 0.61 and 1.45 ± 1.91 ng/mL, respectively. The mean ± SD levels of total protein were 64.91 ± 89.75 and 86.64 ± 44.16 µg/mL, respectively. For both parameters, the difference between the 2 groups was significant (P< .001). The correlation between PAI-1 and total protein levels was moderate in the glaucoma group (r = 0.43; P = .01) and low in the control group (r = 0.23; P = .04).

Conclusions  The glaucoma group showed in the aqueous humor a 3.3-fold increase in the mean level of PAI-1 compared with the control group, whereas the increase in total protein level was only 1.3-fold. These data are consistent with the possibility that intraocularly produced PAI-1 may contribute to glaucoma pathogenesis.

Clinical Relevance  Reducing the production or activity of PAI-1 in the eye could constitute a new target for the design of drugs to treat glaucoma.


Author Affiliations: Department of Biological Chemistry, The Weizmann Institute of Science, Rehovot, Israel (Drs Dan and Miskin); Department of Ophthalmology, The George Washington University, Washington, DC (Drs Dan, Belyea, and Gertner); Maccabi Ophthalmic Surgical Center, Tel-Aviv, Israel (Dr Leshem); and Department of Ophthalmology, Beilinson Campus, Rabin Medical Center, Tel-Aviv University (Dr Lusky), Tel-Aviv.



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