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. 2023 Apr 19;94(9):726–737. doi: 10.1136/jnnp-2022-330796

Table 5.

Comparison of validity measures of biomarker composites and aAQP4 testing to differentiate between acute NMOSD and acute RRMS

Time included
in ROC model
N AUC† Sensitivity† Specificity
Composite 1§
nEla, MPO, NGAL, MMP-8
No 57 90 (79 to 100) 87 (62 to 96)‡ 81
Yes 55 96 (90 to 100) 100 (77 to 100)‡ 76
Composite 2§
nEla, MPO, NGAL, MMP-8, TIMP-1
No 57 94 (84 to 100) 87 (62 to 96)‡ 100
Yes 55 98 (94 to 100) 92 (67 to 99)‡ 100
aAQP4 test performance* T-IIF 79 (69 to 87) 100
ELISA 60 (44 to 73) 97
EI-M1/M23 90 (78 to 96) 95
Fixed cell-based assay 94 (82 to 98) 98
Live cell-based assay 92 (78 to 97) 100

*Prain et al.27

†Values are 95% CI.

‡Sensitivity values were calculated by Wilson method.

§Data based on modelling of combined cohorts, with patients without corticosteroid pretreatment.

aAQP4, anti-aquaporin-4 antibody; AUC, area under the curve; EI-M1/M23, Neuroimmune M1/M23 biochip slide; MMP, matrix metalloproteinase; MPO, myeloperoxidase; nEla, neutrophil elastase; NGAL, neutrophil gelatinase-associated lipocalin; NMOSD, neuromyelitis optica spectrum disorder; ROC, receiver operating characteristics; RRMS, relapsing-remitting multiple sclerosis; T-IIF, tissue-based indirect immunofluorescence; TIMP-1, tissue inhibitor of metalloproteinase-1.