No association between the G308A polymorphism of the tumor necrosis factor-alpha gene and schizophrenia

被引:36
作者
Riedel, M
Krönig, H
Schwarz, MJ
Engel, RR
Kühn, KU
Sikorski, C
Sokullu, S
Ackenheil, M
Möller, HJ
Müller, N
机构
[1] Univ Munich, Hosp Psychiat, D-80336 Munich, Germany
[2] Univ Bonn, Hosp Psychiat, D-5300 Bonn, Germany
关键词
tumor necrosis factor-alpha; G308A polymorphism; schizophrenia; ethnic differences; chromosome; 6;
D O I
10.1007/s00406-002-0386-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several linkage analyses in schizophrenia research point to a locus on chromosome 6p22, where the gene coding for tumor necrosis factor-alpha. (TNF-alpha) is located. A marked influence of antipsychotic medication on TNF-a has been described. As the involvement of an immune process in the pathophysiology of schizophrenia has been discussed, a functional TNF-alpha polymorphism appears to be a candidate in genetic schizophrenia research. The G308A polymorphism of the TNF-a gene was described to be associated with increased TNF-alpha production. Boin and colleagues have already described a significant association between the polymorphic allele and schizophrenia, investigating 84 schizophrenic patients (21% polymorphic allele) and 138 healthy volunteers (11% polymorphic allele), recruited in Northern Italy. We carried out a replication study including 157 schizophrenic patients and 186 healthy persons, who were recruited in Southern Germany. Psychopathology was additionally monitored by PANSS. We were not able to replicate the findings of Boin et al., as we did not find any difference in allele frequency or genotype distribution between our schizophrenic patients (13.7% polymorphic allele) and healthy controls (16.9% polymorphic allele). Moreover, we did not find any association between genotype and psychopathology, as measured by PANSS. The different results between these two studies may be due to ethnic differences.
引用
收藏
页码:232 / 234
页数:3
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