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G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study
被引:43
作者:
Sacchetti, Emilio
Bocchio-Chiavetto, Luisella
Valsecchi, Paolo
Scassellati, Catia
Pasqualetti, Patrizio
Bonvicini, Cristian
Corsini, Paola
Rossi, Giuseppe
Cesana, Bruno Mario
Barlati, Sergio
Gennarelli, Massimo
[1
]
机构:
[1] IRCCS San Giovanni di Dio, Genet Unit, Brescia, Italy
[2] Univ Brescia, Sch Med, Dept Psychiat, I-25121 Brescia, Italy
[3] Univ Brescia, Psychiat Unit, I-25121 Brescia, Italy
[4] Spedali Civil Brescia, Dept Mental Hlth, I-25125 Brescia, Italy
[5] Univ Brescia, Ctr Behav & Neurodegenerat Disorders, I-25121 Brescia, Italy
[6] Fatebenefratelli Hosp, AFaR, Ctr Med Stat, Dept Neurosci, Rome, Italy
[7] IRCCS San Giovanni di Dio, Psychiat Rehabil Ctr, Brescia, Italy
[8] Univ Brescia, Sch Med, Dept Biomed Sci & Biotechnol, Sect Med Stat & Biometry, I-25121 Brescia, Italy
[9] Univ Brescia, Sch Med, Dept Biomed Sci & Biotechnol, Biol & Genet Div, I-25121 Brescia, Italy
关键词:
TNF alpha;
gene;
schizophrenia;
association;
meta-analysis;
polymorphism;
paranoid;
age at onset;
gender;
diagnostic subtypes;
D O I:
10.1016/j.bbi.2006.11.009
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Research on -G308A functional polymorphism in the tumor necrosis factor alpha (TNF alpha) gene as a susceptibility factor for schizophrenia has provided contrasting results in different populations. Therefore we conducted a meta-analysis of the published case-control association studies and a replication study in a large sample. Meta-analyses (total sample: 2512 cases versus 3223 controls) showed that the AA genotype was weakly associated with schizophrenia susceptibility in Caucasoids (Odd Ratio OR= 1.65, 95% CI = 1.00-2.71 Z = 1.98 p = 0.05). The replication case-cantrol association study (323 DSM-IV-TR schizophrenia patients and 346 controls) showed that the A allele conferred an increased susceptibility for schizophrenia only in males (OR = 1.73, 95% CI = 1.07-2.79,p = 0.025), and the association became more specige when only patients of the paranoid subtype were compared to the controls (relative risk ratio = 3.09, 95% CI = 1.287.47, p=0.012). The presence of the A allele was also, associated with a later age at onset of schizophrenia in the whole sample (F-1,F-291 = 7.094, p = 0.008). Our results confirm that TNF alpha A allele could have an effect on vulnerability to schizophrenia but further studies revaluating the role of gender and diagnostic subtypes are necessary to confirm these findings. (c) 2006 Elsevier Inc. All rights reserved.
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页码:450 / 457
页数:8
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