Clinical Characteristics, MRI Findings, Disease Progression, and Management of Neuro-Behçet’s Disease: A Retrospective Study in Lebanon

<b>Background</b>: Behçet's Disease (BD) is a complex vasculitis affecting multiple organ systems, with Neuro-Behçet's Disease (NBD) representing a rare yet severe manifestation. Data on NBD are limited, particularly in Middle Eastern populations. <b>Methods</b>: This retrospective observational study, spanning from 2000 to 2021, involved 262 BD patients at a tertiary medical center in Lebanon. NBD was diagnosed based on International Consensus Recommendation diagnostic criteria. Clinical data, including demographics, manifestations, inflammatory blood markers, genetics, and treatments, were collected. The modified Rankin Scale (mRS) was used to assess disease severity. <b>Results</b>: Among the cohort, 27 (10.3%) had NBD, with headaches, weakness, and dizziness as the most common presenting symptoms. The prevalence of NBD was similar across genders, which differs from some regional studies. HLA-B51 positivity was found in 50 out of 60 (83.3%) tested BD patients. Parenchymal NBD cases exhibited greater disease severity than non-parenchymal cases, with female patients experiencing a more severe course compared to males. Elevated inflammatory markers (CRP and ESR) were more common in patients with severe NBD. Corticosteroids and colchicine were the most commonly used therapies overall, while patients with better disease severity were more frequently prescribed methotrexate, mycophenolate, cyclophosphamide, adalimumab, and rituximab. An analysis of disease progression showed that at presentation, 57.1% (<i>n</i> = 12) of NBD patients had mild to moderate disability, which increased to 76.2% (<i>n</i> = 16) at the last follow-up, including 10 patients who showed an improvement in their mRS score. <b>Conclusions</b>: This study provides valuable insights into the prevalence and clinical characteristics of NBD in a Middle Eastern population. These findings enhance our understanding of NBD in the Middle East, highlighting the need for further research to improve diagnosis and management.

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Journal
Journal of Clinical Medicine
Published
2025-04-08
DOI
https://doi.org/10.3390/jcm14082543
Primary Topic
Ocular Diseases and Behçet’s Syndrome
Type
article
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article

Clinical Characteristics, MRI Findings, Disease Progression, and Management of Neuro-Behçet’s Disease: A Retrospective Study in Lebanon

Dana Hazimeh, Mira Merashli, Nadia Chamoun, Martine Elbejjani et al.
Journal of Clinical Medicine
Ocular Diseases and Behçet’s Syndrome
article

Clinical Characteristics, MRI Findings, Disease Progression, and Management of Neuro-Behçet’s Disease: A Retrospective Study in Lebanon

Dana Hazimeh, Mira Merashli, Nadia Chamoun, Martine Elbejjani, Michael Ibrahim, Taha Hatab, Nabil El Ayoubi
article en

Abstract

<b>Background</b>: Behçet's Disease (BD) is a complex vasculitis affecting multiple organ systems, with Neuro-Behçet's Disease (NBD) representing a rare yet severe manifestation. Data on NBD are limited, particularly in Middle Eastern populations. <b>Methods</b>: This retrospective observational study, spanning from 2000 to 2021, involved 262 BD patients at a tertiary medical center in Lebanon. NBD was diagnosed based on International Consensus Recommendation diagnostic criteria. Clinical data, including demographics, manifestations, inflammatory blood markers, genetics, and treatments, were collected. The modified Rankin Scale (mRS) was used to assess disease severity. <b>Results</b>: Among the cohort, 27 (10.3%) had NBD, with headaches, weakness, and dizziness as the most common presenting symptoms. The prevalence of NBD was similar across genders, which differs from some regional studies. HLA-B51 positivity was found in 50 out of 60 (83.3%) tested BD patients. Parenchymal NBD cases exhibited greater disease severity than non-parenchymal cases, with female patients experiencing a more severe course compared to males. Elevated inflammatory markers (CRP and ESR) were more common in patients with severe NBD. Corticosteroids and colchicine were the most commonly used therapies overall, while patients with better disease severity were more frequently prescribed methotrexate, mycophenolate, cyclophosphamide, adalimumab, and rituximab. An analysis of disease progression showed that at presentation, 57.1% (<i>n</i> = 12) of NBD patients had mild to moderate disability, which increased to 76.2% (<i>n</i> = 16) at the last follow-up, including 10 patients who showed an improvement in their mRS score. <b>Conclusions</b>: This study provides valuable insights into the prevalence and clinical characteristics of NBD in a Middle Eastern population. These findings enhance our understanding of NBD in the Middle East, highlighting the need for further research to improve diagnosis and management.

Journal of Clinical MedicineVol. 14(8)
American University of Beirut Medical Center (LB)
Openalex Percentile: Top 88%
Ocular Diseases and Behçet’s Syndrome
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