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April 05, 2011; 76 (14) Articles

Neuromyelitis optica unique area postrema lesions

Nausea, vomiting, and pathogenic implications

B.F.Gh. Popescu, V.A. Lennon, J.E. Parisi, C.L. Howe, S.D. Weigand, J.A. Cabrera-Gómez, K. Newell, R.N. Mandler, S.J. Pittock, B.G. Weinshenker, C.F. Lucchinetti
First published March 2, 2011, DOI: https://doi.org/10.1212/WNL.0b013e318214332c
B.F.Gh. Popescu
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V.A. Lennon
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J.E. Parisi
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C.L. Howe
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S.D. Weigand
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J.A. Cabrera-Gómez
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K. Newell
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R.N. Mandler
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B.G. Weinshenker
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C.F. Lucchinetti
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Citation
Neuromyelitis optica unique area postrema lesions
Nausea, vomiting, and pathogenic implications
B.F.Gh. Popescu, V.A. Lennon, J.E. Parisi, C.L. Howe, S.D. Weigand, J.A. Cabrera-Gómez, K. Newell, R.N. Mandler, S.J. Pittock, B.G. Weinshenker, C.F. Lucchinetti
Neurology Apr 2011, 76 (14) 1229-1237; DOI: 10.1212/WNL.0b013e318214332c

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Abstract

Objective: To characterize the neuropathologic features of neuromyelitis optica (NMO) at the medullary floor of the fourth ventricle and area postrema. Aquaporin-4 (AQP4) autoimmunity targets this region, resulting in intractable nausea associated with vomiting or hiccups in NMO.

Methods: This neuropathologic study was performed on archival brainstem tissue from 15 patients with NMO, 5 patients with multiple sclerosis (MS), and 8 neurologically normal subjects. Logistic regression was used to evaluate whether the presence of lesions at this level increased the odds of a patient with NMO having an episode of nausea/vomiting.

Results: Six patients with NMO (40%), but no patients with MS or normal controls, exhibited unilateral or bilateral lesions involving the area postrema and the medullary floor of the fourth ventricle. These lesions were characterized by tissue rarefaction, blood vessel thickening, no obvious neuronal or axonal pathology, and preservation of myelin in the subependymal medullary tegmentum. AQP4 immunoreactivity was lost or markedly reduced in all 6 cases, with moderate to marked perivascular and parenchymal lymphocytic inflammatory infiltrates, prominent microglial activation, and in 3 cases, eosinophils. Complement deposition in astrocytes, macrophages, and/or perivascularly, and a prominent astroglial reaction were also present. The odds of nausea/vomiting being documented clinically was 16-fold greater in NMO cases with area postrema lesions (95% confidence interval 1.43–437, p = 0.02).

Conclusions: These neuropathologic findings suggest the area postrema may be a selective target of the disease process in NMO, and are compatible with clinical reports of nausea and vomiting preceding episodes of optic neuritis and transverse myelitis or being the heralding symptom of NMO.

Footnotes

  • Study funding: Supported by the NIH (RO1-NS049577-01-A2 to C.F.L.), the National Multiple Sclerosis Society (RG 3185-B-3 to C.F.L.), and the Guthy Jackson Foundation (to C.F.L.).

  • Editorial, page 1202

  • Supplemental data at www.neurology.org

  • AQP4
    aquaporin-4
    BBB
    blood–brain barrier
    CI
    confidence interval
    CVO
    circumventricular organs
    EAAT2
    excitatory amino acid transporter 2
    GFAP
    glial fibrillary acidic protein
    H&E
    hematoxylin & eosin
    IgG
    immunoglobulin G
    MS
    multiple sclerosis
    NMO
    neuromyelitis optica
    NMOSD
    neuromyelitis optica spectrum disorder
    OR
    odds ratio

  • Received September 30, 2010.
  • Accepted November 12, 2010.
  • Copyright © 2011 by AAN Enterprises, Inc.
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