Neuropediatrics 2013; 44(04): 187-190
DOI: 10.1055/s-0033-1338134
Original Article
Georg Thieme Verlag KG Stuttgart · New York

PD-1 Gene Polymorphism in Children with Subacute Sclerosing Panencephalitis

Ibrahim Etem Piskin
1   Department of Pediatrics, Bülent Ecevit University Faculty of Medicine, Zonguldak, Turkey
,
Mustafa Calık
2   Department of Pediatric Neurology, Harran University School of Medicine, Sanlıurfa, Turkey
,
Mahmut Abuhandan
3   Department of Pediatrics, Harran University School of Medicine, Sanlıurfa, Turkey
,
Ebru Kolsal
4   Department of Pediatric Neurology, Bakirkoy Dr Mazhar Osman Psychiatric and Neurological Diseases Research and Education Hospital, Istanbul, Turkey
,
Sevim Karakas Celik
5   Department of Genetic, Bülent Ecevit University Faculty of Medicine, Zonguldak, Turkey
,
Akın İscan
6   Department of Pediatric Neurology, Bezmialem Vakif University, Faculty of Medicine, Istanbul, Turkey
› Institutsangaben
Weitere Informationen

Publikationsverlauf

01. Oktober 2012

30. Januar 2013

Publikationsdatum:
16. März 2013 (online)

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Abstract

Subacute sclerosing panencephalitis (SSPE) is a progressive inflammatory and degenerative disorder of the central nervous system. Several factors influence the risk of chronic brain infection with the mutant measles virus. However, to date, no pathogenic mechanism that may predispose to SSPE has been determined. Studies have indicated that specific polymorphisms in certain host genes are probably involved in impairing the ability of host immune cells to eradicate the measles virus in SSPE patients. Programmed cell death protein 1 (PD-1), a member of the CD28 family, is a negative regulator of the immune system. The purpose of our study was to investigate whether PD-1 gene polymorphisms affect susceptibility to the development of SSPE in Turkish children. In total, 109 subjects (54 SSPE patients and 55 healthy controls) were genotyped for the PD-1.9 C/T (rs2227982) single-nucleotide polymorphism (SNP). The distributions of T alleles in the PD-1.9 polymorphism in SSPE patients and healthy controls were 2.8 and 10.9%, respectively. There was a statistically significant difference between the groups; the 95% confidence interval (CI) was 0.06 to 0.85 and the odds ratio (OR) was 0.23 (χ2 test). Thus, we identified an association between SSPE and the PD-1 rs2227982 gene polymorphism; the frequency of T alleles was higher in controls than in SSPE patients.