Abstract
Background: The demographic associations among patients presenting with myasthenia gravis with only ocular manifestations (OMG) is not clear. Methods: In this 5-center case series, we collected the race, gender, and age at diagnosis of patients diagnosed with myasthenia gravis who had no signs or symptoms of generalized myasthenia gravis (GMG). An a priori sample size calculation determined that 140 patients were required to accept that there was a ≤10-year difference in mean age (equivalence testing: power 90%, α = 0.05). Robust Bayesian analysis and linear regression were applied to evaluate whether age differed by gender or race. Results: Of 433 patients included, 258 (60%) were men. Mean age among men was 57 years (SD = 19) and 52 years (SD = 21) among women. The 95% credible interval (CI) (Bayesian equivalent of confidence interval) was 0.8-8.7 years for mean age, and there was a 99.6% probability that the mean difference in age between sexes was <10 years. Race was documented in 376 (68 [18%] non-Caucasian). Caucasians were 17.3 years older than non-Caucasians at diagnosis (95% CI, 12.2-22.3 y; P < 0.001) controlling for gender. There was no additive interaction of gender and race (P = 0.74). There was a bimodal distribution for women peaking around 30 and 60 years. Men had a left skewed unimodal age distribution peaking at age 70. Conclusions: The distribution of age at presentation in patients with OMG is different between men and women, similar to GMG. Non-Caucasian patients tend to develop OMG at a younger age.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 29-32 |
| Number of pages | 4 |
| Journal | Journal of Neuro-Ophthalmology |
| Volume | 36 |
| Issue number | 1 |
| DOIs | |
| State | Published - 2016 |
Bibliographical note
Funding Information:J. H. Peragallo is supported by a departmental grant from Research to Prevent Blindness. E. Bitrian is supported by a grant from the Vitreoretinal Surgery Foundation. M. J. Kupersmith is supported by grants U10 EY017281-01A1, Kriser Foundation, Empire Clinical Research Investigator Program (ERIP), and U10EY017281-06S2. M. S. Lee is supported by an unrestricted grant from Research to Prevent Blindness. B. B. Bruce is supported by an NIH/NEI grant K23EY019341, Research to Prevent Blindness, and is a consultant for Bayer and MedImmune. This study was not industry supported. The other authors report no conflicts of interest.
Publisher Copyright:
Copyright © 2016 North American Neuro-Ophthalmology Society.