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A Reproducible Computerized Method for Quantitation of Capillary Density using Nailfold Capillaroscopy
Published on: October 27, 2015
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Nailfold capillary morphology and platelet function in patients with exfoliative glaucoma
Vesna Maric1,2, Anita Grgurevic3, Andja Cirkovic4
1Clinic for Eye Diseases, Clinical Center of Serbia, Belgrade, Serbia.
Plos One
|July 10, 2019
Summary
Exfoliative glaucoma (XFG) patients show distinct nailfold capillary changes and altered platelet parameters compared to primary open-angle glaucoma (POAG) and normal controls. This study highlights microvascular abnormalities in XFG.
Area of Science:
- Ophthalmology
- Microcirculation Research
- Hematology
Background:
- Exfoliative glaucoma (XFG) is a significant cause of vision loss.
- Nailfold capillaroscopy is a non-invasive method to assess microvascular changes.
- Platelet parameters may offer insights into glaucoma pathophysiology.
Purpose of the Study:
- To evaluate nailfold capillary morphology in XFG patients.
- To compare these features with primary open-angle glaucoma (POAG), exfoliation syndrome (XFS), and normal controls (NC).
- To investigate platelet count (PLT), mean platelet volume (MPV), platelet distribution width (PDW), and plateletcrit (PCT) in XFG patients.
Main Methods:
- A case-control study involving 152 glaucoma patients.
- Nailfold capillaroscopy was performed to assess capillary morphology.
- Hemogram parameters including platelet indices were analyzed and compared across groups.
Main Results:
- Significant differences in capillary diameter, tortuosity, loop distribution, and avascular zones were observed between XFG and POAG/NC groups.
- XFG patients exhibited lower PLT values compared to POAG patients.
- XFG patients showed lower PLT and higher MPV compared to NC and POAG.
Conclusions:
- This study is the first to examine capillary morphology and comprehensive platelet parameters in newly diagnosed XFG.
- Findings indicate nailfold capillary morphological vascular changes in XFG patients.
- Further research is needed to understand the clinical implications of these microvascular abnormalities in XFG.
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