Measurement of retinal nerve fiber layer (RNFL) thickness in multiple sclerosis (MS)
is gaining increasing attention.
To explore the relationship between RNFL thickness as measured by optical coherence
tomography (OCT) and scanning laser polarimetry with variable corneal compensation
(GDx), and conventional and non-conventional optic nerve and brain MRI measures.
Twelve relapsing-remitting (RR) MS patients (12 affected and 12 unaffected eyes) and
4 age- and sex-matched normal controls (NC) (8 unaffected eyes) were enrolled. Four
MS patients had a history of bilateral optic neuritis (ON), four had a history of
unilateral ON, and 4 had no history of ON. Optic nerve MRI measurements included the
length of T2 lesions, measurement of optic nerve atrophy, magnetization transfer ratio
(MTR) and diffusion tensor imaging (DTI) measures. Optic nerve atrophy was measured
by a novel method with high reproducibility. Brain MRI measurements included T1 and
T2 lesion volumes (LVs) and their relative MTRs, and tissue class specific atrophy,
MTR and DTI measures. Measures of RNFL were evaluated with OCT and GDx. We also evaluated
both high and low contrast letter acuities (LCLA) in order to determine the relationship
between vision, MRI metrics, and retinal structural architecture.
LCLA, RNFL-OCT and optic nerve radius measures showed more robust differences between
NC and MS patients, and between MS patients with affected and unaffected eyes. T2-LV
and T1-LV, as well as gray matter atrophy, DTI and MTR measures were related to LCLA
and RNFL thickness. Unique additive variance regression models showed that both brain
and optic nerve MRI measures independently accounted for about 50% of the variance
in LCLA and RNFL thickness. In reverse models, about 20% of the additional independent
variance was explained by optic nerve or brain MRI metrics.
Measurement of RNFL thickness and radius of the optic nerve should be preferred to
the other optic nerve MRI measures in clinical studies. Whole brain lesion and GM
measures are predictive of impaired visual function with corresponding structural
concomitants.