Serological indication of chronic inflammatory demyelinating polyneuropathy as an extrahepatic manifestation of hepatitis E virus infection

Guillain-Barré syndrome and neuralgic amyotrophy have been associated with hepatitis E virus (HEV) genotype 3 infections, while myasthenia gravis (MG) has been associated with HEV genotype 4 infections. However, whether chronic inflammatory demyelinating polyneuropathy (CIDP) is associated with HEV infections has not been conclusively clarified yet. 102 CIDP patients, 102 age- and sex-matched blood donors, 61 peripheral neuropathy patients (non-CIDP patients), and 26 MG patients were tested for HEV and anti-HEV IgM and IgG. Sixty-five of the 102 (64%) CIDP patients tested positive for anti-HEV IgG and one (1%) for anti-HEV IgM. No other patient tested positive for ati-HEV IgM. In the subgroup of CIDP patients with initial diagnosis (without previous IVIG treatment), 30/54 (56%) tested positive for anti-HEV IgG. Anti-HEV rates were significantly lower in blood donors (28%), non-CIDP peripheral neuropathy patients (20%), and MG patients (12%). No subject tested positive for HEV viremia. CSF tested negative for in 61 CIDP patients (54 patients with primary diagnosis). The development of CIDP but not non-CIDP polyneuropathy may be triggered by HEV exposure in an HEV genotype 3 endemic region. The increased anti-HEV seroprevalence in CIDP patients is not a consequence of IVIG therapy.

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Publication Details

Journal
Scientific Reports
Published
2024-08-20
DOI
https://doi.org/10.1038/s41598-024-70104-3
Citations
1
Primary Topic
Peripheral Neuropathies and Disorders
Type
article
Field-Weighted Citation Impact
0.37

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article

Serological indication of chronic inflammatory demyelinating polyneuropathy as an extrahepatic manifestation of hepatitis E virus infection

Johannes H. Bannasch, Thomas Skripuletz, Tabea Seeliger, Stefan Gingele et al.
1 citations
Scientific Reports
Peripheral Neuropathies and Disorders
0.37
article

Serological indication of chronic inflammatory demyelinating polyneuropathy as an extrahepatic manifestation of hepatitis E virus infection

Johannes H. Bannasch, Thomas Skripuletz, Tabea Seeliger, Stefan Gingele, Thomas Horvatits, Jens Hiller, Julian Schulze zur Wiesch, Mathias Gelderblom, Franz Felix Konen, Amir Golsari, Sven Pischke, M. Mader, Christian Casar, Samuel Huber, Sven Peine, Andrzej Wolski, A. Kjasimov, G. Thayssen, Marc Lütgehetmann
article en
1 citations

Abstract

Guillain-Barré syndrome and neuralgic amyotrophy have been associated with hepatitis E virus (HEV) genotype 3 infections, while myasthenia gravis (MG) has been associated with HEV genotype 4 infections. However, whether chronic inflammatory demyelinating polyneuropathy (CIDP) is associated with HEV infections has not been conclusively clarified yet. 102 CIDP patients, 102 age- and sex-matched blood donors, 61 peripheral neuropathy patients (non-CIDP patients), and 26 MG patients were tested for HEV and anti-HEV IgM and IgG. Sixty-five of the 102 (64%) CIDP patients tested positive for anti-HEV IgG and one (1%) for anti-HEV IgM. No other patient tested positive for ati-HEV IgM. In the subgroup of CIDP patients with initial diagnosis (without previous IVIG treatment), 30/54 (56%) tested positive for anti-HEV IgG. Anti-HEV rates were significantly lower in blood donors (28%), non-CIDP peripheral neuropathy patients (20%), and MG patients (12%). No subject tested positive for HEV viremia. CSF tested negative for in 61 CIDP patients (54 patients with primary diagnosis). The development of CIDP but not non-CIDP polyneuropathy may be triggered by HEV exposure in an HEV genotype 3 endemic region. The increased anti-HEV seroprevalence in CIDP patients is not a consequence of IVIG therapy.

Scientific ReportsVol. 14(1)
Universität Hamburg (DE), Medizinische Hochschule Hannover (DE), University Medical Center Hamburg-Eppendorf (DE), German Center for Infection Research (DE)
Bristol-Myers Squibb Foundation, Bristol-Myers Squibb, Pfizer, Sanofi, Biogen, Teva Pharmaceutical Industries, Alexion Pharmaceuticals, Alnylam Pharmaceuticals, Celgene, CSL Behring, Deutsches Zentrum für Infektionsforschung, Argenx, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Else Kröner-Fresenius-Stiftung, Swedish Orphan Biovitrum, Sanofi Genzyme, Bayer Vital
Good health and well-being
Openalex Percentile: Top 37%
Peripheral Neuropathies and Disorders
0.37
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