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Seasonal distribution of attacks in aquaporin-4 antibody disease and myelin-oligodendrocyte antibody disease.
Dos Passos, Giordani Rodrigues; Elsone, Liene; Luppe, Sebastian; Kitley, Joanna; Messina, Silvia; Rodríguez Cruz, Pedro María; Harding, Katharine; Mutch, Kerry; Leite, Maria Isabel; Robertson, Neil; Jacob, Anu; Palace, Jacqueline.
Affiliation
  • Dos Passos GR; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
  • Elsone L; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom.
  • Luppe S; Department of Neurology, University Hospital of Wales, Cardiff University, Cardiff, United Kingdom.
  • Kitley J; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
  • Messina S; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
  • Rodríguez Cruz PM; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
  • Harding K; Department of Neurology, University Hospital of Wales, Cardiff University, Cardiff, United Kingdom.
  • Mutch K; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom.
  • Leite MI; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
  • Robertson N; Department of Neurology, University Hospital of Wales, Cardiff University, Cardiff, United Kingdom.
  • Jacob A; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, United Kingdom.
  • Palace J; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom. Electronic address: jacqueline.palace@ndcn.ox.ac.uk.
J Neurol Sci ; 415: 116881, 2020 Aug 15.
Article de En | MEDLINE | ID: mdl-32428758
ABSTRACT

BACKGROUND:

Seasonal variation in incidence and exacerbations has been reported for neuroinflammatory conditions such as multiple sclerosis and acute disseminated encephalomyelitis (ADEM). It is unknown whether seasonality also influences aquaporin-4 antibody (AQP4-Ab) disease and myelin-oligodendrocyte antibody (MOG-Ab) disease.

OBJECTIVE:

We examined the seasonal distribution of attacks in AQP4-Ab disease and MOG-Ab disease.

METHODS:

Observational study using data prospectively recorded from three cohorts in the United Kingdom.

RESULTS:

There was no clear seasonal variation in AQP4-Ab or MOG-Ab attacks for either the onset attack nor subsequent relapses. In both groups, the proportion of attacks manifesting with each of the main phenotypes (optic neuritis, transverse myelitis, ADEM/ADEM-like) appeared stable across the year. This study is the first to examine seasonal distribution of MOG-Ab attacks and the largest in AQP4-Ab disease so far.

CONCLUSION:

Lack of seasonal distribution in AQP4-Ab and MOG-Ab disease may argue against environment factors playing a role in the aetiopathogenesis of these conditions.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Aquaporines / Gaine de myéline Pays/Région comme sujet: Europa Langue: En Journal: J Neurol Sci Année: 2020 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Aquaporines / Gaine de myéline Pays/Région comme sujet: Europa Langue: En Journal: J Neurol Sci Année: 2020 Type de document: Article Pays d'affiliation: Royaume-Uni