Literature DB >> 9744376

Quantification of aqueous melanin granules in primary pigment dispersion syndrome.

M Küchle1, C Y Mardin, N X Nguyen, P Martus, G O Naumann.   

Abstract

PURPOSE: Aqueous melanin granules are essential in the pathogenesis of pigment dispersion syndrome and pigmentary glaucoma. We quantified aqueous melanin granules with the laser flare-cell meter in patients with pigment dispersion syndrome, assessed the measurement reproducibility, and correlated the numbers with clinical findings.
METHODS: Aqueous melanin granules were counted by means of the cell count mode of the laser flare-cell meter (KOWA FC-1000; Kowa, Tokyo, Japan) in 42 eyes of 21 patients with primary pigment dispersion syndrome under three conditions (undilated pupils, dilated pupils, after exercise). The reproducibility of the measurements was determined with the intraclass correlation coefficient. A control group of 40 age- and sex-matched eyes was also examined after pupillary dilation. The results were correlated with biomicroscopic findings in eyes with pigment dispersion syndrome (retrocorneal Krukenberg spindle, iris transillumination, pigmentation of trabecular meshwork).
RESULTS: Numerous aqueous melanin granules were detected in eyes with pigment dispersion syndrome (mean, 2.9 +/- 3.7 granules/0.075 mm3) but only small numbers were counted in normal eyes (0.2 +/- 0.3, P < .001). Medical pupil dilation caused an additional increase of aqueous melanin granules in pigment dispersion syndrome (6.3 +/- 5.3, P < .001), but not undilated exercise (climbing stairs) (2.9 +/- 3.7, P > .5). The reproducibility of the measurements was very high (intraclass coefficient >0.92). The number of melanin granules correlated with the degree of Krukenberg spindle (r = .61, P = .004) and with iris transillumination (r = .69, P = .001).
CONCLUSIONS: Quantification of aqueous melanin granules yields reproducible results and shows increased numbers in pigment dispersion syndrome, especially after pupillary dilation. Aqueous melanin granule quantification may be useful for evaluating eyes with pigment dispersion syndrome and for assessing treatment effects.

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Year:  1998        PMID: 9744376     DOI: 10.1016/s0002-9394(98)00098-1

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  5 in total

Review 1.  Focus on molecular events in the anterior chamber leading to glaucoma.

Authors:  Sergio Claudio Saccà; Alberto Izzotti
Journal:  Cell Mol Life Sci       Date:  2013-10-19       Impact factor: 9.261

2.  [Is prophylactic YAG iridotomy useful in pigment dispersion syndrome?].

Authors:  A Rosentreter; O Schwenn; J Funk; T Dietlein
Journal:  Ophthalmologe       Date:  2013-04       Impact factor: 1.059

3.  [Pigment dispersion syndrome and pigmentary glaucoma. Morphometric analysis of the anterior chamber segment with SL-OCT].

Authors:  B Birner; T Tourtas; J M Wessel; A G Jünemann; C Y Mardin; F E Kruse; R Laemmer
Journal:  Ophthalmologe       Date:  2014       Impact factor: 1.059

4.  Longitudinal stability of the diurnal rhythm of intraocular pressure in subjects with healthy eyes, ocular hypertension and pigment dispersion syndrome.

Authors:  Cord Huchzermeyer; Udo Reulbach; Folkert Horn; Robert Lämmer; Christian Y Mardin; Anselm G M Jünemann
Journal:  BMC Ophthalmol       Date:  2014-10-15       Impact factor: 2.209

5.  Near-infrared transillumination imaging combined with aperture photometry for the quantification of melanin in the iris pigment epithelium.

Authors:  Maciej Czepita
Journal:  PLoS One       Date:  2020-03-06       Impact factor: 3.240

  5 in total

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