Association of tumor necrosis factor alpha gene-G308A polymorphism with schizophrenia

作者：Schwab SG; Mondabon S; Knapp M; Albus M; Hallmayer J; Borrmann Hassenbach M; Trixler M; Gross M; Schulze TG; Rietschel M; Lerer B; Maier W; Wildenauer DB^*

来源：Schizophrenia Research, 2003, 65(1): 19-25.

DOI：10.1016/S0920-9964(02)00534-0

• cytokines
• TNF alpha
• LT alpha
• schizophrenia
• association
• linkage disequilibrium

Background: Tumor necrosis factor alpha (TNFalpha), a cytokine involved in inflammatory processes, has been implicated in the pathophysiology of schizophrenia. The chromosomal location in the major histocompatibility complex (MHC) region on 6p21.1-21.3, a region with evidence for linkage, suggests a role in susceptibility to schizophrenia. Association of the minor (A) allele of the -G308A TNFa gene polymorphism with schizophrenia has been reported [Mol. Psychiatry 6 (2001) 79]. Methods: Association of the -G308A TNFalpha gene and the lymphotoxin alpha (LTalpha) + A252G gene polymorphisms with schizophrenia was studied in 79 sib pair families with linkage in the MHC region and in 128 trio families using the transmission disequilibrium test (TDT). Results: Weak association of the common G allele was detected for TNFalpha -G308A in both samples independently with borderline significance in the sib pair families (0.064) and with a nominally significant value of P = 0.022 in the trio families. Combining both samples produced P = 0.003, while LTalpha + A252G, located approximately 2-3 kb distally, revealed P = 0.03 and the two locus haplotype yielded a P value of 0.001. Conclusion: Our data suggests association of the common G allele of the -G308A TNFalpha gene polymorphism with schizophrenia in a sample of 207 families. However, linkage disequilibrium with a different allele of the TNFa gene or another gene in the MHC region cannot be excluded.

• 出版日期2003-12-1