Sensitivity, Specificity, and Cutoff Identifying Optic Atrophy by Macular Ganglion Cell Layer Volume in Syndromic Craniosynostosis.
Chang Yoon-Hee, Staffa Steven J, Yavuz Saricay Leyla, Zurakowski David, Gise Ryan, Dagi Linda R
AI Summary
This study found a GCL volume < 1.02 mm³ identifies optic atrophy in syndromic craniosynostosis children, with OSA and worse vision independently linked to lower GCL. This aids surveillance when other tests are difficult.
Abstract
Purpose
To determine the sensitivity, specificity, and cutoff of macular ganglion cell layer (GCL) volume consistent with optic atrophy in children with syndromic craniosynostosis and to investigate factors independently associated with reduction in GCL volume.
Design
Retrospective cross-sectional study.
Participants
Patients with syndromic craniosynostosis evaluated at Boston Children's Hospital (2010-2022) with reliable macular OCT scans.
Methods
The latest ophthalmic examination that included OCT macula scans was identified. Age at examination, sex, ethnicity, best-corrected logarithm of the minimum angle of resolution (logMAR) visual acuity, cycloplegic refraction, and funduscopic optic nerve appearance were recorded in addition to history of primary or recurrent elevation in intracranial pressure (ICP), Chiari malformation, and obstructive sleep apnea (OSA). Spectral-domain OCT software quantified segmentation of macula retinal layers and was checked manually.
Main outcome measures
The primary outcome was determining sensitivity, specificity, and optimal cutoff of GCL volume consistent with optic atrophy. The secondary outcome was determining whether previously elevated ICP, OSA, Chiari malformation, craniosynostosis diagnosis, logMAR visual acuity, age, or sex were independently associated with lower GCL volume.
Results
Median age at examination was 11.9 years (interquartile range, 8.5-14.8 years). Fifty-eight of 61 patients (112 eyes) had reliable macula scans, 74% were female, and syndromes represented were Apert (n = 14), Crouzon (n = 17), Muenke (n = 6), Pfeiffer (n = 6), and Saethre-Chotzen (n = 15). Optimal cutoff identifying optic atrophy was a GCL volume < 1.02 mm 3 with a sensitivity of 83% and specificity of 77%. Univariate analysis demonstrated that significantly lower macular GCL volume was associated with optic atrophy on fundus examination (P < 0.001), Apert syndrome (P < 0.001), history of elevated ICP (P = 0.015), Chiari malformation (P = 0.001), OSA (P < 0.001), male sex (P = 0.027), and worse logMAR visual acuity (P < 0.001). Multivariable median regression analysis confirmed that only OSA (P = 0.005), optic atrophy on fundus examination (P = 0.003), and worse logMAR visual acuity (P = 0.042) were independently associated with lower GCL volume.
Conclusions
Surveillance for optic atrophy by GCL volume may be useful in a population where cognitive skills can limit acquisition of other key ophthalmic measures. It is noteworthy that OSA is also associated with lower GLC volume in this population.
Financial disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
MeSH Terms
Shields Classification
Key Concepts3
In children with syndromic craniosynostosis, the optimal cutoff for identifying optic atrophy using macular ganglion cell layer (GCL) volume was < 1.02 mm³, demonstrating a sensitivity of 83% and a specificity of 77%.
Multivariable median regression analysis in children with syndromic craniosynostosis (58 patients, 112 eyes) confirmed that only obstructive sleep apnea (OSA) (P = 0.005), optic atrophy on fundus examination (P = 0.003), and worse logMAR visual acuity (P = 0.042) were independently associated with lower macular GCL volume.
Univariate analysis in children with syndromic craniosynostosis (58 patients, 112 eyes) revealed that significantly lower macular GCL volume was associated with optic atrophy on fundus examination (P < 0.001), Apert syndrome (P < 0.001), history of elevated intracranial pressure (P = 0.015), Chiari malformation (P = 0.001), obstructive sleep apnea (OSA) (P < 0.001), male sex (P = 0.027), and worse logMAR visual acuity (P < 0.001).
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