HLA-DRB1*15 association with multiple sclerosis is confirmed in a multigenerational Italian family.

Q2 Medicine Functional neurology Pub Date : 2017-04-01 DOI:10.11138/fneur/2017.32.2.083
L Mosca, V Mantero, S Penco, L La Mantia, S De Benedetti, M R Marazzi, C Spreafico, C Erminio, L Grassi, G Lando, M Zagaria, E Agostoni, A Protti
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引用次数: 7

Abstract

Environmental and genetic factors seem to play a pathogenetic role in multiple sclerosis (MS). The genetic component is partly suggested by familial aggregation of cases; however, MS families with affected subjects over different generations have rarely been described. The aim of this study was to report clinical and genetic features of a multigenerational MS family and to perform a review of the literature on this topic. We describe a multigenerational Italian family with six individuals affected by MS, showing different clinical and neuroradiological findings. HLA-DRB1* typing revealed the presence of the DRB1*15:01 allele in all the MS cases and in 4/5 non-affected subjects. Reports on six multigenerational MS families have previously been published, giving similar results. The HLA-DRB1*15:01 allele was confirmed to be linked to MS disease in this family; moreover, its presence in non-affected subjects suggests the involvement of other susceptibility factors in the development and expression of the disease, in accordance with the complex disease model now attributed to MS.

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HLA-DRB1*15与多发性硬化症的关联在一个多代意大利家庭中得到证实。
环境和遗传因素似乎在多发性硬化症(MS)中起发病作用。病例的家族聚集性部分说明了遗传因素;然而,不同世代的多发性硬化症家庭很少被描述。本研究的目的是报告一个多代多发性硬化症家族的临床和遗传特征,并对这一主题的文献进行回顾。我们描述了一个多代意大利家庭,有六个人受到MS的影响,表现出不同的临床和神经放射学结果。HLA-DRB1*分型显示,所有MS病例和4/5未受影响的受试者中均存在DRB1*15:01等位基因。先前发表的关于6个多代多发性硬化症家庭的报告也给出了类似的结果。HLA-DRB1*15:01等位基因被证实与该家族的MS疾病有关;此外,它在未受影响的受试者中的存在表明,根据目前归因于MS的复杂疾病模型,其他易感因素参与了疾病的发展和表达。
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来源期刊
Functional neurology
Functional neurology 医学-神经科学
CiteScore
3.90
自引率
0.00%
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0
审稿时长
>12 weeks
期刊介绍: Information not localized
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