Abstract
ABSTRACTObjectiveTo measure the active remodeling of the lamina cribrosa (LC) years after IOP lowering by suturelysis.DesignCohort study.ParticipantsGlaucoma patients were imaged 20 minutes after laser suturelysis following trabeculectomy surgery and at their follow-up appointment 1-4 years later (16 image pairs; 15 persons).InterventionNon-invasive optical coherence tomography (OCT) imaging of the eye.Main OutcomesDeformation calculated by correlating OCT scans of the LC immediately after IOP lowering by suturelysis and those acquired years later (defined asfollow-upstrain).ResultsMean LC follow-up strain in the anteroposterior direction (Ezz) was 14.0 ± 21.3% (mean, standard deviation, p=0.03), while the LC anterior border moved 60.9 ± 54.6 μm into the eye (p=0.0006) on long-term, maintained IOP lowering.Ezzat follow-up was 14 times larger than the directEzzresponse to IOP lowering by suturelysis. There was a significant association between larger LC anterior movement and greaterEzz(p=0.004) at follow-up. Thinner retinal nerve fiber layer (RNFL) at suturelysis was associated with greater follow-upEzz(p=0.04). Worsening visual field indexes during follow-up were associated with greater LC widening (positive remodelingEθθ, p=0.02). Eyes with a greater counterclockwise twist (positiveEθz) at suturelysis had greater reversal clockwise twist at follow-up (negative remodelingEθz, p=0.007).ConclusionFollow-up strains and LC border position changes measured years after IOP lowering are far larger than the immediate strain response and LC border movement response to IOP lowering and indicate dramatic remodeling of the LC anatomical structure caused by IOP lowering and glaucoma progression. The remodeling includes a substantial increase in LC thickness and movement into the eye. Eyes with greater direct strain response to IOP-lowering strains, greater glaucoma damage at suturelysis, and greater worsening of visual field at follow-up experienced greater remodelingTrial RegistrationClinicalTrials.govIdentifier:NCT03267849
Publisher
Cold Spring Harbor Laboratory
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