7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Alterations in Aquaporin‐4‐IgG Serostatus in 986 Patients: A Laboratory‐Based Longitudinal Analysis

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Objective

          This study was undertaken to investigate factors associated with aquaporin‐4 (AQP4)‐IgG serostatus change using a large serological database.

          Methods

          This retrospective study utilizes Mayo Clinic Neuroimmunology Laboratory data from 2007 to 2021. We included all patients with ≥2 AQP4‐IgG tests (by cell‐based assay). The frequency and clinical factors associated with serostatus change were evaluated. Multivariable logistic regression analysis examined whether age, sex, or initial titer was associated with serostatus change.

          Results

          There were 933 patients who had ≥2 AQP4‐IgG tests with an initial positive result. Of those, 830 (89%) remained seropositive and 103 (11%) seroreverted to negative. Median interval to seroreversion was 1.2 years (interquartile range [IQR] = 0.4–3.5). Of those with sustained seropositivity, titers were stable in 92%. Seroreversion was associated with age ≤ 20 years (odds ratio [OR] = 2.25; 95% confidence interval [CI] = 1.09–4.63; p = 0.028) and low initial titer of ≤1:100 (OR = 11.44, 95% CI = 3.17–41.26, p < 0.001), and 5 had clinical attacks despite seroreversion. Among 62 retested after seroreversion, 50% returned to seropositive (median = 224 days, IQR = 160–371). An initial negative AQP4‐IgG test occurred in 9,308 patients. Of those, 99% remained seronegative and 53 (0.3%) seroconverted at a median interval of 0.76 years (IQR = 0.37–1.68).

          Interpretation

          AQP4‐IgG seropositivity usually persists over time with little change in titer. Seroreversion to negative is uncommon (11%) and associated with lower titers and younger age. Seroreversion was often transient, and attacks occasionally occurred despite prior seroreversion, suggesting it may not reliably reflect disease activity. Seroconversion to positive is rare (<1%), limiting the utility of repeat testing in seronegative patients unless clinical suspicion is high. ANN NEUROL 2023

          Related collections

          Most cited references30

          • Record: found
          • Abstract: not found
          • Article: not found

          Eculizumab in Aquaporin-4–Positive Neuromyelitis Optica Spectrum Disorder

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel

            Neuromyelitis optica (NMO) is an inflammatory demyelinating disease that selectively affects optic nerves and spinal cord. It is considered a severe variant of multiple sclerosis (MS), and frequently is misdiagnosed as MS, but prognosis and optimal treatments differ. A serum immunoglobulin G autoantibody (NMO-IgG) serves as a specific marker for NMO. Here we show that NMO-IgG binds selectively to the aquaporin-4 water channel, a component of the dystroglycan protein complex located in astrocytic foot processes at the blood-brain barrier. NMO may represent the first example of a novel class of autoimmune channelopathy.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Inebilizumab for the treatment of neuromyelitis optica spectrum disorder (N-MOmentum): a double-blind, randomised placebo-controlled phase 2/3 trial

              No approved therapies exist for neuromyelitis optica spectrum disorder (NMOSD), a rare, relapsing, autoimmune, inflammatory disease of the CNS that causes blindness and paralysis. We aimed to assess the efficacy and safety of inebilizumab, an anti-CD19, B cell-depleting antibody, in reducing the risk of attacks and disability in NMOSD.
                Bookmark

                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Annals of Neurology
                Annals of Neurology
                Wiley
                0364-5134
                1531-8249
                July 05 2023
                Affiliations
                [1 ] Department of Neurology Mayo Clinic Rochester MN USA
                [2 ] Department of Neurology Mayo Clinic Scottsdale AZ USA
                [3 ] Departments of Neurology and Ophthalmology Programs in Neuroscience and Immunology, University of Colorado Anschutz Medical Campus Aurora CO USA
                [4 ] Department of Laboratory Medicine and Pathology Mayo Clinic Rochester MN USA
                [5 ] Center for Multiple Sclerosis and Autoimmune Neurology Mayo Clinic Rochester MN USA
                [6 ] Department of Immunology Mayo Clinic Rochester MN USA
                [7 ] Department of Neurology University of Virginia Charlottesville VA USA
                [8 ] Department of Ophthalmology Mayo Clinic Rochester MN USA
                [9 ] Department of Neurology Cleveland Clinic Cleveland OH USA
                [10 ] Mellen Center for Multiple Sclerosis Cleveland Clinic Cleveland OH USA
                Article
                10.1002/ana.26722
                37314750
                c084c922-ee95-47ec-be71-16bf2e95282b
                © 2023

                http://creativecommons.org/licenses/by-nc-nd/4.0/

                History

                Comments

                Comment on this article