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. 2021 Sep 29;7(10):e08069. doi: 10.1016/j.heliyon.2021.e08069

Table 2.

Epidemiological and clinical characteristics.

CIS (n:12) RRMS (n:71) SPMS (n:15) PPMS (n:23) TOTAL p
Age at diagnosis Mean (SD) 32 (14.1) 28 (9.8) 37 (12.9) 40 (9.9) 31.24 (11.19) 0.0002∗
Gender Female (70) 7 (58.33 %) 38 (53.52 %) 12 (80.00 %) 13 (56.52 %) 70 (57.85 %) 0.324∗∗
Male (51) 5 (41.67 %) 33 (46.48 %) 3 (20.00 %) 10 (43.48 %) 51 (42.15 %) Reference group
Onset syndrome Optic neuritis 6 (50%) 13 (18.31%) 3 (20.00%) --- 22 (18.18) 0.005∗∗
Brainstem syndrome 4 (33.33%) 18 (25.35%) 2 (13.33%) 3 (13.04%) 27 (22.31) 0.059∗∗
Myelitis --- 25 (35.21%) 4 (26.67%) 8 (34.78%) 37 (30.58) 0.130∗∗
Other syndromes 2 (16.67%) 15 (21.13%) 6 (40.00%) 12 (52.17%) 35 (28.93) Reference group
Relapses at diagnosis Median (IR) 1 (1–1) 2 (1–3) 2 (2–3) 0 (0–0) 2 (1–3) 0.0001
Time to Diagnosis (months)
Median (IR)
Optic neuritis 2.5 (2–5) 12 (1–24) 73 (24–859) --- 7 (2–24) 0.059∗
Brainstem syndrome 1.5 (1–37.5) 7 (2–13) 48 (24–73) 31 (14–61) 8 (2–24) 0.068∗
Myelitis --- 23 (3–49) 43 (25–85) 41 (16–55) 28 (4–49) 0.297∗
Other syndromes 67 (24–110) 24 (1–52) 79 (24–122) 18 (10–40) 24 (11–61) 0.128∗

(∗) Kruskal-Wallis test; (∗∗) Chi2 test. p-value represents the comparison between different phenotypes for baseline variables. p values <0.05, statistically significant.