TY - JOUR
T1 - Optical coherence tomography is highly sensitive in detecting prior optic neuritis
AU - Xu, Sarah Chaoying
AU - Kardon, Randy H.
AU - Leavitt, Jacqueline A.
AU - Flanagan, Eoin P.
AU - Pittock, Sean J.
AU - Chen, John J.
N1 - Funding Information:
Supported in part by an unrestricted grant to the Department of Ophthalmology by Research to Prevent Blindness, Inc., New York, NY.
Funding Information:
S. Xu reports no disclosures relevant to the manuscript. R. Kardon receives funding from the Department of Defense; W81XWH-16-1-0071, W81XWH-16-1-0211, Veterans Affairs Rehabilitation Research and Development; CENC0056P, I01 RX000889-01A1, C9251-C, 1 IO1 RX002101 VA-ORD, National Eye Institute; 1R01EY023279-01; and Novartis steering committee for Optical Coherence Tomography in Multiple Sclerosis (OCTiMS) multicenter study FTY720D2319, and is cofounder of MedFace and FaceX, which use facial features to assess light sensitivity and vision. J. Leavitt and E. Flanagan report no disclosures relevant to the manuscript. S. Pittock holds patents that relate to functional AQP4/NMO-IgG assays and NMO-IgG as a cancer marker; has a patent pending for GFAP as markers of neurologic autoimmunity and paraneo-plastic disorders; consulted for Alexion and Medimmune; and received research support from Grifols, Medimmune, and Alexion. All compensation for consulting activities is paid directly to Mayo Clinic. J. Chen reports no disclosures relevant to the manuscript. Go to Neurology.org/N for full disclosures.
Publisher Copyright:
© 2019 American Academy of Neurology.
PY - 2019/2/5
Y1 - 2019/2/5
N2 - Objective To explore sensitivity of optical coherence tomography (OCT) in detecting prior unilateral optic neuritis.MethodsThis is a retrospective, observational clinical study of all patients who presented from January 1, 2014, to January 6, 2017, with unilateral optic neuritis and OCT available at least 3 months after the attack. We compared OCT retinal nerve fiber layer (RNFL) and ganglion cell inner plexiform layer (GCIPL) thicknesses between affected and unaffected contralateral eyes. We excluded patients with concomitant glaucoma or other optic neuropathies. Based on analysis of normal controls, thinning was considered significant if RNFL was at least 9 μm or GCIPL was at least 6 μm less in the affected eye compared to the unaffected eye.ResultsFifty-one patients (18 male and 33 female) were included in the study. RNFL and GCIPL thicknesses were significantly lower in eyes with optic neuritis compared to unaffected eyes (p < 0.001). RNFL was thinner by ≥9 μm in 73% of optic neuritis eyes compared to the unaffected eye. GCIPL was thinner by ≥6 μm in 96% of optic neuritis eyes, which was more sensitive than using RNFL (p < 0.001). When using a threshold ≤1st percentile of age-matched controls, sensitivities were 37% for RNFL and 76% for GCIPL, each of which was lower than those calculated using the intereye difference as the threshold (p < 0.01).ConclusionsOCT, especially with GCIPL analysis, is a highly sensitive modality in detecting prior optic neuritis, which is made more robust by using intereye differences to approximate change.Classification of evidenceThis study provides Class III evidence that OCT accurately identifies patients with prior unilateral optic neuritis.
AB - Objective To explore sensitivity of optical coherence tomography (OCT) in detecting prior unilateral optic neuritis.MethodsThis is a retrospective, observational clinical study of all patients who presented from January 1, 2014, to January 6, 2017, with unilateral optic neuritis and OCT available at least 3 months after the attack. We compared OCT retinal nerve fiber layer (RNFL) and ganglion cell inner plexiform layer (GCIPL) thicknesses between affected and unaffected contralateral eyes. We excluded patients with concomitant glaucoma or other optic neuropathies. Based on analysis of normal controls, thinning was considered significant if RNFL was at least 9 μm or GCIPL was at least 6 μm less in the affected eye compared to the unaffected eye.ResultsFifty-one patients (18 male and 33 female) were included in the study. RNFL and GCIPL thicknesses were significantly lower in eyes with optic neuritis compared to unaffected eyes (p < 0.001). RNFL was thinner by ≥9 μm in 73% of optic neuritis eyes compared to the unaffected eye. GCIPL was thinner by ≥6 μm in 96% of optic neuritis eyes, which was more sensitive than using RNFL (p < 0.001). When using a threshold ≤1st percentile of age-matched controls, sensitivities were 37% for RNFL and 76% for GCIPL, each of which was lower than those calculated using the intereye difference as the threshold (p < 0.01).ConclusionsOCT, especially with GCIPL analysis, is a highly sensitive modality in detecting prior optic neuritis, which is made more robust by using intereye differences to approximate change.Classification of evidenceThis study provides Class III evidence that OCT accurately identifies patients with prior unilateral optic neuritis.
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U2 - 10.1212/WNL.0000000000006873
DO - 10.1212/WNL.0000000000006873
M3 - Article
C2 - 30674600
AN - SCOPUS:85061132788
SN - 0028-3878
VL - 92
SP - e527-e535
JO - Neurology
JF - Neurology
IS - 6
ER -