Population-based head-to-head comparison of the clinical characteristics and epidemiology of AQP4 antibody-positive NMOSD between two European countries

被引:5
|
作者
Viktoria, Papp [1 ]
Trones, Kim D. P. [2 ]
Magyari, Melinda [3 ,4 ]
Koch-Henriksen, Nils [4 ,5 ]
Iljicsov, Anna [6 ]
Rajda, Cecilia [7 ]
Nielsen, Helle H. [1 ,8 ,9 ]
Lovas, Gabor [10 ]
Rozsa, Csilla [10 ]
Kristiansen, Bjorn H. [2 ]
Stenager, Egon [11 ,12 ]
Frederiksen, Jette L. [13 ]
Komoly, Samuel [14 ]
Sellebjerg, Finn [3 ,4 ]
Petersen, Thor [15 ]
Illes, Zsolt [1 ,8 ]
机构
[1] Odense Univ Hosp, Dept Neurol, JB Winslow Vej 4, DK-5000 Odense, Denmark
[2] Univ Southern Denmark, Odense, Denmark
[3] Univ Copenhagen, Rigshosp, Danish Multiple Sclerosis Ctr, Dept Neurol, Glostrup, Denmark
[4] Copenhagen Univ Hosp, Rigshosp, Dept Neurol, Danish Multiple Sclerosis Registry, Glostrup, Denmark
[5] Aarhus Univ Hosp, Dept Clin Epidemiol, Aarhus, Denmark
[6] Semmelweis Univ, Dept Neurol, Budapest, Hungary
[7] Univ Szeged, Dept Neurol, Szeged, Hungary
[8] Univ Southern Denmark, Inst Clin Res, Odense, Denmark
[9] Univ Southern Denmark, Inst Mol Biol, Odense, Denmark
[10] Jahn Ferenc Hosp, Dept Neurol, Budapest, Hungary
[11] Hosp Southern Jutland, Dept Neurol, MS Clin Southern Jutland Sonderborg Esbjerg Koldi, Sonderborg, Denmark
[12] Univ Southern Denmark, Fac Hlth Sci, Dept Reg Hlth Res, Odense, Denmark
[13] Univ Copenhagen, Rigshosp Glostrup, Fac Hlth & Med Sci, Dept Neurol, Glostrup, Denmark
[14] Univ Pecs, Dept Neurol, Pecs, Hungary
[15] Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark
关键词
Neuromyelitis optica; NMOSD; Population-based; AQP4-antibody; Incidence; Prevalence; OPTICA SPECTRUM DISORDER; NEUROMYELITIS-OPTICA; DIAGNOSTIC-CRITERIA; PREVALENCE;
D O I
10.1016/j.msard.2021.102879
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Population-based clinical studies in neuromyelitis optica spectrum disorder (NMOSD) and epidemiological and clinical comparisons of White ethnicities are missing. In a large population-based international cohort, we extensively characterized aquaporin-4 antibody seropositive (AQP4-Ab+) NMOSD, and also compared the clinical, radiological and epidemiological features between two European populations residing in different areas. Methods: Between self-reported Danish and Hungarian ethnicities, we compared the population-based clinical features, disability outcomes, and death of 134 AQP4-Ab+ NMOSD cases fulfilling the 2015 International Panel for NMO Diagnosis (IPND) criteria. For precise comparison of epidemiology, we conducted a population-based head-to-head comparative study of the age-standardized prevalence (January 1, 2014) and incidence (2007-2013) of AQP4-Ab+ NMO/NMOSD among adults (>= 16 years) in Denmark (4.6 million) and Hungary (6.4 million) by applying 2015 IPND (NMOSD) criteria and 2006 Wingerchuk (NMO). Results: Danes were more likely to present with transverse myelitis and were more affected by spinal cord damage on long-term disability. Hungarians presented most often with optic neuritis, although visual outcome was similar in the groups. No differences were observed in sex, disease course, relapse rate, autoimmune comorbidity, mortality, brain MRI, and treatment strategies. The age-standardized prevalence estimates of AQP4-Ab+ NMOSD (2015 IPND criteria) in Denmark vs. Hungary were 0.66 vs. 1.43 (/100,000) while incidence rates were 0.04 vs. 0.11 (/100,000 person-years); similar differences were found based on the 2006 NMO criteria. Conclusions: This head-to-head comparative study indicates different disease characteristics and epidemiology among White populations in Europe, and substantiates the need for population-based genetic and environmental studies in NMOSD.
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页数:9
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