Diagnostic value of aquaporin-4-IgG live cell based assay in neuromyelitis optica spectrum disorders
Objective Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD). Methods We included Mayo Clinic patients (1/1/2018-12/31/2019) tested for serum AQP4-IgG by live cell-based flow-cytometric assay. Medical records were r...
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Published in | Multiple sclerosis journal - experimental, translational and clinical Vol. 7; no. 4; p. 20552173211052656 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London, England
SAGE Publications
01.10.2021
Sage Publications Ltd |
Subjects | |
Online Access | Get full text |
ISSN | 2055-2173 2055-2173 |
DOI | 10.1177/20552173211052656 |
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Abstract | Objective
Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD).
Methods
We included Mayo Clinic patients (1/1/2018-12/31/2019) tested for serum AQP4-IgG by live cell-based flow-cytometric assay. Medical records were reviewed to assess if patients fulfilled 2015 NMOSD criteria.
Results
Of 1371 patients tested, 41 were positive (3%) and all fulfilled NMOSD criteria with AQP4-IgG (specificity = 100%). Only 10/1330 testing negative met NMOSD criteria without AQP4-IgG (sensitivity = 80%) and seven of these 10 were MOG-IgG positive.
Conclusions
AQP4-IgG by live cell-based assay was highly specific and without false positives in a high throughput setting. |
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AbstractList | Objective Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD). Methods We included Mayo Clinic patients (1/1/2018-12/31/2019) tested for serum AQP4-IgG by live cell-based flow-cytometric assay. Medical records were reviewed to assess if patients fulfilled 2015 NMOSD criteria. Results Of 1371 patients tested, 41 were positive (3%) and all fulfilled NMOSD criteria with AQP4-IgG (specificity = 100%). Only 10/1330 testing negative met NMOSD criteria without AQP4-IgG (sensitivity = 80%) and seven of these 10 were MOG-IgG positive. Conclusions AQP4-IgG by live cell-based assay was highly specific and without false positives in a high throughput setting. Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD). We included Mayo Clinic patients (1/1/2018-12/31/2019) tested for serum AQP4-IgG by live cell-based flow-cytometric assay. Medical records were reviewed to assess if patients fulfilled 2015 NMOSD criteria. Of 1371 patients tested, 41 were positive (3%) and all fulfilled NMOSD criteria with AQP4-IgG (specificity = 100%). Only 10/1330 testing negative met NMOSD criteria without AQP4-IgG (sensitivity = 80%) and seven of these 10 were MOG-IgG positive. AQP4-IgG by live cell-based assay was highly specific and without false positives in a high throughput setting. Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD).OBJECTIVEDetermine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD).We included Mayo Clinic patients (1/1/2018-12/31/2019) tested for serum AQP4-IgG by live cell-based flow-cytometric assay. Medical records were reviewed to assess if patients fulfilled 2015 NMOSD criteria.METHODSWe included Mayo Clinic patients (1/1/2018-12/31/2019) tested for serum AQP4-IgG by live cell-based flow-cytometric assay. Medical records were reviewed to assess if patients fulfilled 2015 NMOSD criteria.Of 1371 patients tested, 41 were positive (3%) and all fulfilled NMOSD criteria with AQP4-IgG (specificity = 100%). Only 10/1330 testing negative met NMOSD criteria without AQP4-IgG (sensitivity = 80%) and seven of these 10 were MOG-IgG positive.RESULTSOf 1371 patients tested, 41 were positive (3%) and all fulfilled NMOSD criteria with AQP4-IgG (specificity = 100%). Only 10/1330 testing negative met NMOSD criteria without AQP4-IgG (sensitivity = 80%) and seven of these 10 were MOG-IgG positive.AQP4-IgG by live cell-based assay was highly specific and without false positives in a high throughput setting.CONCLUSIONSAQP4-IgG by live cell-based assay was highly specific and without false positives in a high throughput setting. Objective Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD). Methods We included Mayo Clinic patients (1/1/2018-12/31/2019) tested for serum AQP4-IgG by live cell-based flow-cytometric assay. Medical records were reviewed to assess if patients fulfilled 2015 NMOSD criteria. Results Of 1371 patients tested, 41 were positive (3%) and all fulfilled NMOSD criteria with AQP4-IgG (specificity = 100%). Only 10/1330 testing negative met NMOSD criteria without AQP4-IgG (sensitivity = 80%) and seven of these 10 were MOG-IgG positive. Conclusions AQP4-IgG by live cell-based assay was highly specific and without false positives in a high throughput setting. |
Author | Weinshenker, Brian G. Tariq Bhatti, M. Flanagan, Eoin P. Montalvo, Mayra Fryer, James P. Lennon, Vanda A. Mills, John R. Wingerchuk, Dean M. Redenbaugh, Vyanka McKeon, Andrew Lopez Chiriboga, A. Sebastian Sechi, Elia Buciuc, Marina Chen, John J. Pittock, Sean J. |
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CitedBy_id | crossref_primary_10_1002_ana_26722 crossref_primary_10_3389_fneur_2022_866824 crossref_primary_10_1001_jamaneurol_2023_2974 crossref_primary_10_1111_ene_15983 crossref_primary_10_1080_14728222_2023_2240017 crossref_primary_10_1002_glia_24675 crossref_primary_10_1177_13524585251313744 crossref_primary_10_3389_fneur_2022_885218 crossref_primary_10_17816_ACEN_1124 crossref_primary_10_3389_fneur_2022_912050 crossref_primary_10_3389_fneur_2024_1326867 crossref_primary_10_1212_NXI_0000000000200329 crossref_primary_10_1212_WNL_0000000000206820 |
Cites_doi | 10.1016/j.msard.2021.103030 10.1111/bpa.12084 10.1001/jamaneurol.2020.2743 10.1136/jnnp-2015-312601 10.3389/fneur.2019.01028 10.1212/WNL.0000000000001729 10.1212/NXI.0000000000000231 10.1001/jamaneurol.2021.0912 10.1212/WNL.0b013e3182a6cb5c 10.1212/NXI.0000000000000011 |
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References | Waters, Reindl, Saiz 2016; 87 Jarius, Wildemann 2013; 23 Fryer, Lennon, Pittock 2014; 1(1):e11 Jiao, Fryer, Lennon 2013; 81 Prain, Woodhall, Vincent 2019; 10 Wingerchuk, Banwell, Bennett 2015; 85 Kunchok, Chen, Saadeh 2020; 77 Majed, Fryer, McKeon 2016; 3 Li, Zhang, Jia 2021; 53 bibr9-20552173211052656 bibr10-20552173211052656 bibr1-20552173211052656 bibr7-20552173211052656 bibr4-20552173211052656 bibr3-20552173211052656 bibr5-20552173211052656 bibr8-20552173211052656 bibr6-20552173211052656 bibr2-20552173211052656 |
References_xml | – volume: 77 start-page: 1572 year: 2020 end-page: 1575 article-title: Application of 2015 seronegative neuromyelitis Optica Spectrum disorder diagnostic criteria for patients With myelin oligodendrocyte glycoprotein IgG–associated disorders publication-title: JAMA Neurol – volume: 87 start-page: 1005 year: 2016 end-page: 1015 article-title: Multicentre comparison of a diagnostic assay: aquaporin-4 antibodies in neuromyelitis optica publication-title: J Neurol Neurosurg Psychiatry – volume: 53 start-page: 103030 year: 2021 article-title: The occurrence of myelin oligodendrocyte glycoprotein antibodies in aquaporin-4-antibody seronegative neuromyelitis Optica Spectrum disorder: a systematic review and meta-analysis publication-title: Mult Scler Relat Disord – volume: 81 start-page: 1197 year: 2013 end-page: 1204 article-title: Updated estimate of AQP4-IgG serostatus and disability outcome in neuromyelitis optica publication-title: Neurology – volume: 3 year: 2016 article-title: Clinical utility of testing AQP4-IgG in CSF: guidance for physicians publication-title: Neurology-Neuroimmunology Neuroinflammation – volume: 1(1):e11 year: 2014 article-title: AQP4 Autoantibody assay performance in clinical laboratory service publication-title: Neurology-Neuroimmunology Neuroinflammation – volume: 85 start-page: 177 year: 2015 end-page: 189 article-title: International consensus diagnostic criteria for neuromyelitis optica spectrum disorders publication-title: Neurology – volume: 10 start-page: 1028 year: 2019 article-title: AQP4 Antibody assay sensitivity comparison in the Era of the 2015 diagnostic criteria for NMOSD publication-title: Front Neurol – volume: 23 start-page: 661 year: 2013 end-page: 683 article-title: Aquaporin-4 antibodies (NMO-IgG) as a serological marker of neuromyelitis optica: a critical review of the literature publication-title: Brain Pathol – ident: bibr7-20552173211052656 doi: 10.1016/j.msard.2021.103030 – ident: bibr4-20552173211052656 doi: 10.1111/bpa.12084 – ident: bibr8-20552173211052656 doi: 10.1001/jamaneurol.2020.2743 – ident: bibr2-20552173211052656 doi: 10.1136/jnnp-2015-312601 – ident: bibr3-20552173211052656 doi: 10.3389/fneur.2019.01028 – ident: bibr6-20552173211052656 doi: 10.1212/WNL.0000000000001729 – ident: bibr10-20552173211052656 doi: 10.1212/NXI.0000000000000231 – ident: bibr5-20552173211052656 doi: 10.1001/jamaneurol.2021.0912 – ident: bibr9-20552173211052656 doi: 10.1212/WNL.0b013e3182a6cb5c – ident: bibr1-20552173211052656 doi: 10.1212/NXI.0000000000000011 |
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Snippet | Objective
Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD).
Methods
We... Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD). We included Mayo... Objective Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD). Methods We... Determine the utility of aquaporin 4 IgG (AQP4-IgG) testing (live cell-based assay) for Neuromyelitis Optica Spectrum Disorders (NMOSD).OBJECTIVEDetermine the... |
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Title | Diagnostic value of aquaporin-4-IgG live cell based assay in neuromyelitis optica spectrum disorders |
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