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. 2024 Aug 19;15:1431394. doi: 10.3389/fimmu.2024.1431394

Table 1.

Demographic, clinical, and visual characteristics of the multiple sclerosis (MS) patients and healthy control (HC) participants.

Characteristics MS patients HC participants
TOTAL
n = 54
HDHH
n = 20
(37%)
Non-HDHH
n = 34
(63%)
Total
n = 55
HDHH
n = 6
(11%)
Non-HDHH
n = 49
(89%)
Demographic
Age in years; mean (SD) 41.9 (± 11.8) 39.8 (± 13.4) 43.2 (± 10.9) 41.5 (± 13.2) 49.3 (± 8.7) 40.6 (± 13.4)
Female, n (%) 39 (72) 12 (60) 27 (79) 35 (64) 2 (33) 33 (67)
Visual
HCVA; LogMAR
mean (SD)
0.07 (± 0.32) 0.09 (± 0.23) 0.05 (± 0.36) -0.04 (± 0.1) -0.01 (± 0.1) -0.04 (± 0.1)
LCVA (2.5%); Letter
mean (SD)
25 (± 14) 21 (± 14) 27 (± 13) 40 (± 8) 38 (± 9) 40 (± 8)
Clinical
RRMS, n (%) 36 (67) 11 (55) 25 (73) N/A N/A N/A
SPMS, n (%) 13 (24) 7 (35) 6 (18) N/A N/A N/A
PPMS, n (%) 5 (9) 2 (10) 3 (9) N/A N/A N/A
Age at symptom onset, year; mean (SD) 29.5 (± 9.2) 26.1 (± 8.6) 32.1 (± 9.4) N/A N/A N/A
Age at diagnosis,
year; mean (SD)
32.5 (± 10.6) 28.6 (± 11.3) 34.8 (± 9.7) N/A N/A N/A
Disease duration in year; mean (SD) 11.9 (± 9.3) 12.5 (± 9.2) 11.4 (± 9.4) N/A N/A N/A
EDSS at orthoptic assessment, mean (SD) 3.4 (± 2.2) 4.2 (± 2.3) 3.0 (± 2.1) N/A N/A N/A
History of ON pat., n (%) 27 (50) 10 (50) 17 (50) N/A N/A N/A
History of diplopia, n (%) 30 (55.6) 16 (80) 14 (41) N/A N/A N/A
Therapy
None, n (%) 17 (32) 6 (30) 11 (33) N/A N/A N/A
Platform a , n (%) 12 (23) 3 (15) 9 (27) N/A N/A N/A
High efficacy b , n (%) 24 (45) 11 (55) 13 (40) N/A N/A N/A

EDSS, expanded disability status scale; ON, optic neuritis; SD, standard deviation; H/LCVA, high/low contrast visual acuity; RR/SP/PPMS, relapsing–remitting/secondary progressive/primary progressive multiple sclerosis, HDHH, high degree of horizontal heterophoria (outside the defined limits for horizontal heterophoria angles); non-HDHH, the part of the cohort inside of the defined limits for horizontal heterophoria.

a

Platform therapies were defined as Glatirameracetat, Dimethylfumarat, Teriflunomid, Interferon-ß-1b s.c., and Peginterferon.

b

High-efficacy therapies were defined as Fingolimod, Ocrelizumab, Natalizumab, Alemtuzumab, Rituximab, Mitoxantron, Cladribin, and Azathioprin.