Intravenous immunoglobulin treatment for acute attacks in myelin oligodendrocyte glycoprotein antibody disease.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
08 2023
Historique:
medline: 10 8 2023
pubmed: 11 7 2023
entrez: 11 7 2023
Statut: ppublish

Résumé

The potential therapeutic benefit of intravenous immunoglobulins (IVIGs) for acute attacks of myelin oligodendrocyte glycoprotein antibody disease (MOGAD) is unknown. The objective was to describe the outcomes of IVIG treatment for acute MOGAD attacks. A retrospective observational study involving seven tertiary neuroimmunology centers. Data collection included patients' demographics, Expanded Disability Status Scale (EDSS), and visual acuity (VA) before the attack, at the nadir of the attack before IVIG treatment, and at follow-up visits ⩾3 months after treatment. Thirty-nine patients were included, of which 21 (53.8%) were female. The median age was 23 years (range 5-74 years), and the median disease duration was 4 months (range 0-93 months). The most common type of attack treated with IVIG was isolated optic neuritis (ON) (unilateral IVIG may be an effective treatment option for acute MOGAD attacks. Further prospective studies are warranted to validate our results.

Sections du résumé

BACKGROUND
The potential therapeutic benefit of intravenous immunoglobulins (IVIGs) for acute attacks of myelin oligodendrocyte glycoprotein antibody disease (MOGAD) is unknown.
OBJECTIVE
The objective was to describe the outcomes of IVIG treatment for acute MOGAD attacks.
METHODS
A retrospective observational study involving seven tertiary neuroimmunology centers. Data collection included patients' demographics, Expanded Disability Status Scale (EDSS), and visual acuity (VA) before the attack, at the nadir of the attack before IVIG treatment, and at follow-up visits ⩾3 months after treatment.
RESULTS
Thirty-nine patients were included, of which 21 (53.8%) were female. The median age was 23 years (range 5-74 years), and the median disease duration was 4 months (range 0-93 months). The most common type of attack treated with IVIG was isolated optic neuritis (ON) (unilateral
CONCLUSION
IVIG may be an effective treatment option for acute MOGAD attacks. Further prospective studies are warranted to validate our results.

Identifiants

pubmed: 37431144
doi: 10.1177/13524585231184738
doi:

Substances chimiques

Immunoglobulins, Intravenous 0
Myelin-Oligodendrocyte Glycoprotein 0
Autoantibodies 0

Types de publication

Observational Study Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1080-1089

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS113828
Pays : United States

Auteurs

Itay Lotan (I)

Neuroimmunology Clinic and Research Laboratory, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Rabin Medical Center and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

John J Chen (JJ)

Department of Ophthalmology and Neurology, Mayo Clinic, Rochester, MN, USA.
Center for MS and Autoimmune Neurology, Mayo Clinic, Rochester, MN, USA.

Yael Hacohen (Y)

Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Department of Neurology, Great Ormond Street Hospital for Children, London, UK.

Omar Abdel-Mannan (O)

Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Department of Neurology, Great Ormond Street Hospital for Children, London, UK.

Sara Mariotto (S)

Neurology Unit, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

Saif Huda (S)

Department of Neurology, Walton Centre NHS Foundation Trust, Liverpool, UK.

Emily Gibbons (E)

Department of Neurology, Walton Centre NHS Foundation Trust, Liverpool, UK.

Adi Wilf-Yarkoni (A)

Rabin Medical Center and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Mark A Hellmann (MA)

Rabin Medical Center and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Hadas Stiebel-Kalish (H)

Rabin Medical Center and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Sean J Pittock (SJ)

Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Center for MS and Autoimmune Neurology, Mayo Clinic, Rochester, MN, USA.

Eoin P Flanagan (EP)

Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Center for MS and Autoimmune Neurology, Mayo Clinic, Rochester, MN, USA.

Negar Molazadeh (N)

Neuroimmunology Clinic and Research Laboratory, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Monique Anderson (M)

Neuroimmunology Clinic and Research Laboratory, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Rebecca Salky (R)

Neuroimmunology Clinic and Research Laboratory, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Gabriela Romanow (G)

Neuroimmunology Clinic and Research Laboratory, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Patrick Schindler (P)

Experimental and Clinical Research Center, A Cooperation Between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and the Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Neurology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.

Ankelien Solveig Duchow (AS)

Experimental and Clinical Research Center, A Cooperation Between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and the Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Neurology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.

Friedemann Paul (F)

Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, NeuroCure Clinical Research Center, Berlin, Germany.
Max Delbrueck Center for Molecular Medicine, Experimental and Clinical Research Center, Berlin, Germany.

Michael Levy (M)

Neuroimmunology Clinic and Research Laboratory, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

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