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Lens factor as an underlying mechanism in primary angle closure with gonioscopically-visualized ciliary body
Hatice Tekcan1, Mehmet Serhat Mangan2, Gökhan Celik3
1Ophthalmology Department, University of Health Sciences, Haydarpasa Numune Research and Training Hospital, Tıbbiye Street, No: 40, Uskudar, Istanbul, Turkey.
Visible ciliary body processes in primary angle closure (PAC) eyes correlate with smaller axial length and anterior chamber depth, but greater lens thickness. This suggests lens crowding is a key factor in PAC pathophysiology.
Area of Science:
- Ophthalmology
- Anterior Segment Imaging
- Glaucoma Research
Background:
- Primary angle closure (PAC) is a significant cause of irreversible blindness.
- Understanding the anatomical factors contributing to PAC is crucial for effective management.
- Ciliary body processes (CBP) visualization during gonioscopy may offer insights into PAC mechanisms.
Purpose of the Study:
- To compare anterior segment parameters in primary angle closure (PAC) eyes with and without gonioscopically visualized ciliary body processes (CBP).
- To identify anatomical differences associated with visible CBP in PAC patients.
Main Methods:
- Prospective, observational, comparative clinical study involving 89 PAC patients.
- Detailed ocular examinations including gonioscopy and ultrasound biomicroscopy.
- Measurement of anterior chamber depth (ACD), anterior chamber width, lens thickness (LT), lens vault (LV), pupil diameter, lens-axial length factor (LAF), and relative lens position (RLP).
Main Results:
- Eyes with visible CBP (PAC+CBP group) had significantly smaller axial length and ACD compared to the PAC-CBP group.
- The PAC+CBP group exhibited significantly greater LT, LV, and LAF.
- LAF showed the strongest association with visible CBP (Odds ratio = 141.70, p = 0.002).
Conclusions:
- Gonioscopic visualization of CBP in PAC eyes suggests anterior segment crowding, particularly lens-related factors, as a primary underlying mechanism.
- Visible CBP may serve as a practical gonioscopic marker for predicting PAC pathophysiology.
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