Table 4.
Better prognosis | Poorer prognosis |
---|---|
White | African American or nonwhite |
Female | Male |
Younger age | Older age |
Monofocal onset | Multifocal onset |
Minimal cortical pathology | Early cortical involvement |
Onset with optic neuritis or isolated sensory symptoms | Onset with motor, cerebellar, or bladder/bowel symptoms |
Low relapse rate first 2–5 years | High relapse rate first 2–5 years |
High degree of remission after first relapse | Short interattack latency |
Long interval to second relapse | Short interval to second relapse |
Mild relapse | Severe relapse ≥1 moderate or severe attack Steroids/hospitalization required Severe effect on activities of daily living >1 functional system affected Severe motor/cerebellar brainstem involvement |
No or low disability at 5 years | Disability at 2 or 5 years |
Low lesion load on MRI | Abnormal MRI ≥2 Gd+/new or newly enlarging T2 hyperintense lesions or ≥ 2 T1 hypointense lesions ≥2 spinal cord lesions Baseline brain atrophy |
NEDA at 2 years | Disease activity at 2 years |
Early treatment | Late treatment |
Low (≤386 ng/L) neurofilament light levels | Elevated (>386 ng/L) neurofilament light levels |
Absence of oligoclonal IgG bands | Presence of oligoclonal IgG bands and ≥10 brain T2 lesions |
Absence of IgM bands | Presence of IgM bands |
Gd + gadolinium-enhancing, Ig immunoglobulin, MRI magnetic resonance imaging, MS multiple sclerosis, NEDA no evidence of disease activity