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Association of primary central nervous system vasculitis with the presence of specific human leucocyte antigen gene variant.
Kraemer, Markus; Becker, Jana; Horn, Peter A; Schwitalla, Jan Claudius; Keyvani, Kathy; Metz, Imke; Wegner, Christiane; Brück, Wolfgang; Schlamann, Marc; Heinemann, Falko M; Berlit, Peter.
Afiliação
  • Kraemer M; Department of Neurology, Alfried-Krupp-von Bohlen und Halbach Hospital, Alfried-Krupp-Straße 21, 45130 Essen, Germany. Electronic address: markus.kraemer@krupp-krankenhaus.de.
  • Becker J; Department of Neurology, Alfried-Krupp-von Bohlen und Halbach Hospital, Alfried-Krupp-Straße 21, 45130 Essen, Germany.
  • Horn PA; Institute for Transfusion Medicine, University of Duisburg-Essen, Virchowstraße 179, 45147 Essen, Germany.
  • Schwitalla JC; Department of Neurology, Alfried-Krupp-von Bohlen und Halbach Hospital, Alfried-Krupp-Straße 21, 45130 Essen, Germany.
  • Keyvani K; Institute of Neuropathology, University of Duisburg-Essen, Hufelandstrasse 55, 45147 Essen, Germany.
  • Metz I; Department of Neuropathology, University Medical Center Göttingen, Robert-Koch-Str. 40, 37099 Göttingen, Germany.
  • Wegner C; Department of Neuropathology, University Medical Center Göttingen, Robert-Koch-Str. 40, 37099 Göttingen, Germany.
  • Brück W; Department of Neuropathology, University Medical Center Göttingen, Robert-Koch-Str. 40, 37099 Göttingen, Germany.
  • Schlamann M; Department of Neuroradiology, University Hospital Giessen, 35385 Giessen, Germany.
  • Heinemann FM; Institute for Transfusion Medicine, University of Duisburg-Essen, Virchowstraße 179, 45147 Essen, Germany.
  • Berlit P; Department of Neurology, Alfried-Krupp-von Bohlen und Halbach Hospital, Alfried-Krupp-Straße 21, 45130 Essen, Germany.
Clin Neurol Neurosurg ; 160: 137-141, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28734234
ABSTRACT

OBJECTIVES:

The etiology and genetic susceptibility of primary central nervous system vasculitis (PCNSV) are still unclear. PATIENTS AND

METHODS:

We analyzed the DNA of 25 Caucasian patients with PCNSV for human leucocyte antigen genes HLA-A, HLA-B, HLA-DRB1, and HLA-DQB1, respectively. HLA-frequencies of the 25 patients with PCNSV were compared with HLA-frequencies of matched Caucasian controls.

RESULTS:

No statistically significant associations were found for HLA-B, HLA-DR1 and HLA-DQB1 variant. In the PCNSV group, only the HLA-A*69 variant was found more often than expected statistically.

CONCLUSION:

The results of this study indicate a potential association of HLA marker with PCNSV in Caucasian patients. Further studies are needed to elucidate the role of genes within the human major histocompatibility complex in the pathogenesis of this angiopathy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos de Histocompatibilidade Classe I / Antígenos HLA-A / Vasculite do Sistema Nervoso Central Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos de Histocompatibilidade Classe I / Antígenos HLA-A / Vasculite do Sistema Nervoso Central Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article