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Volume

Læknablaðið - 15.06.1997, Page 75

Læknablaðið - 15.06.1997, Page 75
LÆKNABLAÐIÐ 1997; 83 427 cataract extraction and generally to surgery of the anterior segment. A-4. Linkeage of Macular Corneal Dys- trophy (MCD) to chromosome 16q: evi- dence that MCD types I and II are due to the same locus Friðberl Jónasson*, Vance JM**, Lennon F**, Sarrica J**, Damji K**, Pericak-Vance MA**, Klintworth GK** From The *Department of Ophthalmology, Uni- versity of Iceland, Reykjavík, Iceland, **Duke University, Durham, NC, USA Introduction: MCD is an autosomal recessive disorder leading to opacity of the cornea and visual loss. The proposed defect is in the bio- synthesis of keratan sulfated (KS) corneal pro- teins. MCD has been divided into two types. Type I lacks an immune response to KS derived antibodies while type II demonstrates a positive reaction in serum and corneas. Material and methods: Seventeen USA and Icelandic MCD families (13 type I and four type II) were initially genotyped with 208 genomic markers. Subsequent genealogy analysis revealed that four of the Icelandic families could be con- nected into a single, highly consanguineous fam- ily. These families can be traced back 15 gener- ations to a single individual, suggesting a founder effect in this population. Results: Significant linkage was found for a series of markers on chromosome (chr) 16q. The peak LOD score was with D 16S518 (z(theta) =8.11@theta=0.05). Significant heterogeneity (p<0.05) was observed with one American MCD type I family excluding linkage to this chr 16 re- gion. The remaining American and Icelandic families demonstrated linkage to chr 16. Haplo- type analysis localizes MCD to a Ð15 cM region flanked by cent-D16S512 and D16S507-tel. Conclusion: Both MCD type I and type II fam- ilies showed evidence for linkage to the same chromosomal region, suggesting they are due to a mutation at the same primary locus. Therefore, the division of MCD into types I and II based on their KS antibody response appears due to a yet unknown secondary effect. This hypothesis is fur- ther supported by the large Icelandic family which includes nuclear families of both MCD types. To date, common haplotypes have not been ovserved, indicating the potential for fur- ther refinement of the MCD region by developing additional markers in this area. A-5. Topical acetazolamide in 2-hydrox- ypropyl-I5-cyclodextrin (HPBCD) eye drops lowers intraocular pressure in hu- mans Einar Stefánsson, Sigríður Þórisdóttir, Hafrún Friðriksdóttir, Þorsteinn Loftsson, Jóhannes Kári Kristinsson, Guðrún J. Guðmundsdóttir From The Departments of Ophthalmology and Pharmacy, University of Iceland, Reykjavík, Ice- land Purpose: The purpose of this study is to create an effective topical preparation for use in glauco- ma. HP6CD increases the solubility of lipophilic drugs in aqueous solutions, such as eye drops and may also enhance the availability of the drug to the ocular surface. We have prepared eye drops containing 18% HPBCD and 1% Acetazolamide in aqueous solution. We measured the intraocular pressure (IOP) lowering effect of the eye drops in rabbits and human patients with ocular hyperten- sion. Material and methods: Resting IOP level in ten English brown rabbits was determined with pneu- matonometry before application. A single drop was administered to one eye and IOP measured every 30 minutes up to five hours after instillation of the drop. Nine patients with ocular hyperten- sion used the eye drops in one eye and IOP was measured with applanation tonometry at three timepoints on days 0, 3, 7,14 and 28. Results: In both species, statistically significant lowering of IOP was found. In the rabbits, maxi- mum decline was 2.7+/-0.95 torr (mean+/- S.E.M., n=10, p<.001) 2.5 hours after instilla- tion. In comparison, Timolol maleate (Bloca- dren®) and 0.3% Ethoxyzolamide showed maxi- mum decline of 5.6+/-1.1 torr and 2.6+/-0.7 torr 1.5 hours after instillation respectively (mean+/- S.E.M., n=10, p<.001). In patients with ocular hypertension acetazolamide lowered IOP by 3.6+/-0.4 torr or 16.7+/-2.0% (mean+/-S.E.M., n=7, p<.001) on day 14. No toxic effects were observed. Conclusion: 1% Acetazolamide-HPBCD is a non-toxic and effective IOP lowering eye drop. It may be a useful glaucoma medication, alone or in combination with other drugs. A-6. Mitomycin trabeculectomy for glaucoma with poor surgical prognosis compared with standard trabeculectomy with good prognosis Neelakantan A, Stewart JFJ, Jay JL From The Tennent Institute of Ophthalmology,
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