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ORIGINAL RESEARCH article
Front. Neurol.
Sec. Neuro-Ophthalmology
Volume 16 - 2025 | doi: 10.3389/fneur.2025.1503956
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We aimed to explore the clinical features and predictive factors for the visual prognosis of neurosyphilis-associated optic atrophy (NSAOA). This retrospective observational study included 17 patients (33 eyes) with NSAOA who received standard anti-ocular syphilis treatment. LogMAR (logarithm of the minimum angle of resolution) best-corrected visual acuity (BCVA), visual field, and optical coherence tomography, were recorded at baseline, short-term (within one month after treatment), and long-term (> 6 months) follow-up. Patients with at least one eye with LogMAR BCVA of ≥1.3 at the last follow-up visit were categorized as the blind group. A change ≥ 0.2 on the LogMAR BCVA indicated improvement or deterioration. The mean age was 58.5 years, and 15 patients were males. The mean time between the onset and treatment was 10.1 months. Thirteen patients had Argyll-Robertson pupils. The unblinded group had younger age, shorter disease duration, better baseline visual acuity, higher baseline cerebrospinal fluid (CSF) venereal disease research laboratory (VDRL) titer and CSF total protein counts than the blind group. BCVA of most eyes improved after treatment but experienced deterioration during the follow-up. The deteriorated group of eyes had lower baseline visual field parameters, thinner inferior peripapillary retinal nerve fiber layer (RNFL) thickness. The long-term LogMAR BCVA moderately negatively correlated with CSF VDRL titers before and after treatment. The diagnosis is often delayed in NSAOA, and the overall visual prognosis is poor. Older age, longer symptom duration, worse baseline vision, thinner RNFL thickness, and lower CSF VDRL titer and total protein counts are significantly associated with worse long-term visual prognosis. The correlation between syphilis serologic tests and visual prognosis is poor. It is recommended to reexamine CSF in the follow-up.
Keywords: Cerebral spinal fluid (CSF), Neurosyphilis, Optic Atrophy, Visual Acuity, Visual Field
Received: 30 Sep 2024; Accepted: 13 Feb 2025.
Copyright: © 2025 Zhu, Gu, Zhou and Yan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Yan Yan, Eye and Ent Hospital, Fudan University, Shanghai, China
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
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