Promoter Polymorphisms of TNF-α Gene as a Risk Factor for Schizophrenia
The latest data showed a link between mental disorders and altered immune function. Schizophrenia is a multifactorial disease with numerous changes in the immunological system. The TNF-α gene is a strong candidate for schizophrenia susceptibility. The focus of this paper were the −1031 T/C, −863 C/A...
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Published in: | Archives of medical research Vol. 49; no. 4; pp. 248 - 254 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Elsevier Inc
01-05-2018
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Subjects: | |
Online Access: | Get full text |
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Summary: | The latest data showed a link between mental disorders and altered immune function. Schizophrenia is a multifactorial disease with numerous changes in the immunological system. The TNF-α gene is a strong candidate for schizophrenia susceptibility. The focus of this paper were the −1031 T/C, −863 C/A, −857 C/T, −308 G/A single nucleotide polymorphisms (SNPs) of the TNF-α gene.
We conducted a case-control study of 401 patients with schizophrenia and 606 healthy subjects. The connections between tested SNPs and clinical variables (PANSS, age of onset, a family history, and suicide attempts) were also examined.
The presence of genotypes: the C/C at −1031 T/C; the C/C at −863 C/A; the G/G at −308 G/A in the TNF-α gene was associated with a higher risk of schizophrenia in men. The presence of A allele at −308 G/A increased a risk of schizophrenia in women. Three haplotypes were associated with a higher risk of schizophrenia in men but not women. We did not reveal any associated tested SNPs with intensity of schizophrenia symptoms.
Our results indicate that in addition to −308 G/A, other promoter polymorphisms of TNF-α gene are associated with schizophrenia susceptibility depending on the sex. Tested SNPs are not associated with the psychopathology of schizophrenia. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0188-4409 1873-5487 |
DOI: | 10.1016/j.arcmed.2018.09.007 |