Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Nov;29(11):3466-3472.
doi: 10.1111/ene.15479. Epub 2022 Jul 10.

Investigating paraneoplastic aquaporin-4-IgG-seropositive neuromyelitis optica spectrum disorder through a data-driven approach

Affiliations

Investigating paraneoplastic aquaporin-4-IgG-seropositive neuromyelitis optica spectrum disorder through a data-driven approach

Alessandro Dinoto et al. Eur J Neurol. 2022 Nov.

Abstract

Background: Aquaporin-4 IgG seropositive neuromyelitis optica spectrum disorder (AQP4-IgG NMOSD) might occur in association with cancer. According to diagnostic criteria, a probable paraneoplastic NMOSD can be diagnosed only in patients with isolated myelitis and adenocarcinoma or tumors expressing AQP4. The aim of this study was to explore the features of paraneoplastic NMOSD through a data-driven approach.

Methods: A systematic literature review was performed. Patients with AQP4-IgG positivity in association with tumor in the absence of history of checkpoint inhibitors administration/central nervous system metastases were included. Demographic, clinical, and oncological data were collected. A hierarchical cluster analysis (HCA) was performed and data were compared between resulting clusters.

Results: A total of 1333 records were screened; 46 studies (72 patients) fulfilled inclusion criteria. Median age was 54 (14-87) years; adenocarcinoma occurred in 41.7% of patients, and 44% of cases had multifocal index events. Cancer and NMOSD usually co-occurred. HCA classified patients in three clusters that differed in terms of isolated/multifocal attacks, optic neuritis, pediatric onset, and type of underlying tumor. Age, time from neoplasm to NMOSD onset, and tumor AQP4 staining did not differ between clusters.

Conclusions: Our data-driven approach reveals that paraneoplastic NMOSD does not present a homogeneous phenotype nor peculiar features. Accordingly, cancer screening may be useful in AQP4-IgG NMOSD regardless of age and clinical presentation.

Keywords: AQP4; NMOSD; cancer; paraneoplastic; tumor.

PubMed Disclaimer

Conflict of interest statement

The authors have nothing to disclose.

Figures

FIGURE 1
FIGURE 1
PRISMA flow chart of the study selection process [Colour figure can be viewed at wileyonlinelibrary.com]
FIGURE 2
FIGURE 2
Dendrogram, heatmap, and peculiar features of each cluster. In the upper part of the figure the dendrogram obtained through a hierarchical cluster analysis is represented. Each number at the bottom of the dendrogram represents the identity (ID) of an individual patient (refer to the [Table S1] for references and extracted data [Appendix S1])) and each column under ID represents the most relevant clinical and oncological accompaniments of each included patient (middle part of the figure). The heatmap summarizes the presence (yellow) or absence (light blue) of each clinical and oncological feature. Finally, in the lower part of the figure, the boundaries of each cluster and their peculiar features are summarized [Colour figure can be viewed at wileyonlinelibrary.com]

References

    1. Wingerchuk DM, Banwell B, Bennett JL, et al. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders. Neurology. 2015;85(2):177‐189. doi:10.1212/WNL.0000000000001729 - DOI - PMC - PubMed
    1. Sepúlveda M, Sola‐Valls N, Escudero D, et al. Clinical profile of patients with paraneoplastic neuromyelitis optica spectrum disorder and aquaporin‐4 antibodies. Mult Scler J. 2018;24(13):1753‐1759. doi:10.1177/1352458517731914 - DOI - PMC - PubMed
    1. Dinoto A, Bosco A, Sartori A, et al. Hiccups, severe vomiting and longitudinally extensive transverse myelitis in a patient with prostatic adenocarcinoma and aquaporin‐4 antibodies. J Neuroimmunol. 2021;352:577488. doi:10.1016/j.jneuroim.2021.577488 - DOI - PubMed
    1. Graus F, Delattre JY, Antoine JC, et al. Recommended diagnostic criteria for paraneoplastic neurological syndromes. J Neurol Neurosurg Psychiatry. 2004;75(8):1135‐1140. doi:10.1136/jnnp.2003.034447 - DOI - PMC - PubMed
    1. Graus F, Vogrig A, Muñiz‐Castrillo S, et al. Updated diagnostic criteria for paraneoplastic neurologic syndromes. Neurol Neuroimmunol Neuroinflamm. 2021;8(4):e1014. doi:10.1212/NXI.0000000000001014 - DOI - PMC - PubMed

Publication types