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Optic chiasm involvement in multiple sclerosis, aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein-associated disease.
Bianchi, Alessia; Cortese, Rosa; Prados, Ferran; Tur, Carmen; Kanber, Baris; Yiannakas, Marios C; Samson, Rebecca; De Angelis, Floriana; Magnollay, Lise; Jacob, Anu; Brownlee, Wallace; Trip, Anand; Nicholas, Richard; Hacohen, Yael; Barkhof, Frederik; Ciccarelli, Olga; Toosy, Ahmed T.
Afiliação
  • Bianchi A; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Cortese R; Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.
  • Prados F; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Tur C; Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.
  • Kanber B; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Yiannakas MC; Centre for Medical Image Computing, Medical Physics and Biomedical Engineering, University College London, London, UK.
  • Samson R; eHealth Centre, Universitat Oberta de Catalunya, Barcelona, Spain.
  • De Angelis F; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Magnollay L; MS Centre of Catalonia (Cemcat), Vall d'Hebron Institute of Research, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
  • Jacob A; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Brownlee W; Centre for Medical Image Computing, Medical Physics and Biomedical Engineering, University College London, London, UK.
  • Trip A; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Nicholas R; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Hacohen Y; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Barkhof F; Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
  • Ciccarelli O; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK.
  • Toosy AT; Department of Neurology, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
Mult Scler ; 30(6): 674-686, 2024 May.
Article em En | MEDLINE | ID: mdl-38646958
ABSTRACT

BACKGROUND:

Optic neuritis (ON) is a common feature of inflammatory demyelinating diseases (IDDs) such as multiple sclerosis (MS), aquaporin 4-antibody neuromyelitis optica spectrum disorder (AQP4 + NMOSD) and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). However, the involvement of the optic chiasm (OC) in IDD has not been fully investigated.

AIMS:

To examine OC differences in non-acute IDD patients with (ON+) and without ON (ON-) using magnetisation transfer ratio (MTR), to compare differences between MS, AQP4 + NMOSD and MOGAD and understand their associations with other neuro-ophthalmological markers.

METHODS:

Twenty-eight relapsing-remitting multiple sclerosis (RRMS), 24 AQP4 + NMOSD, 28 MOGAD patients and 32 healthy controls (HCs) underwent clinical evaluation, MRI and optical coherence tomography (OCT) scan. Multivariable linear regression models were applied.

RESULTS:

ON + IDD patients showed lower OC MTR than HCs (28.87 ± 4.58 vs 31.65 ± 4.93; p = 0.004). When compared with HCs, lower OC MTR was found in ON + AQP4 + NMOSD (28.55 ± 4.18 vs 31.65 ± 4.93; p = 0.020) and MOGAD (28.73 ± 4.99 vs 31.65 ± 4.93; p = 0.007) and in ON- AQP4 + NMOSD (28.37 ± 7.27 vs 31.65 ± 4.93; p = 0.035). ON+ RRMS had lower MTR than ON- RRMS (28.87 ± 4.58 vs 30.99 ± 4.76; p = 0.038). Lower OC MTR was associated with higher number of ON (regression coefficient (RC) = -1.15, 95% confidence interval (CI) = -1.819 to -0.490, p = 0.001), worse visual acuity (RC = -0.026, 95% CI = -0.041 to -0.011, p = 0.001) and lower peripapillary retinal nerve fibre layer (pRNFL) thickness (RC = 1.129, 95% CI = 0.199 to 2.059, p = 0.018) when considering the whole IDD group.

CONCLUSION:

OC microstructural damage indicates prior ON in IDD and is linked to reduced vision and thinner pRNFL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quiasma Óptico / Autoanticorpos / Neuromielite Óptica / Esclerose Múltipla Recidivante-Remitente / Tomografia de Coerência Óptica / Aquaporina 4 / Glicoproteína Mielina-Oligodendrócito Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quiasma Óptico / Autoanticorpos / Neuromielite Óptica / Esclerose Múltipla Recidivante-Remitente / Tomografia de Coerência Óptica / Aquaporina 4 / Glicoproteína Mielina-Oligodendrócito Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article