Polymorphism of Toll-like receptor 4 gene in bipolar disorder

被引:56
作者
Oliveira, Jose [1 ,2 ,6 ]
Busson, Marc [1 ]
Etain, Bruno [2 ,4 ,5 ,6 ]
Jamain, Stephane [2 ,4 ,5 ,6 ]
Hamdani, Nora [2 ,4 ,5 ,6 ]
Boukouaci, Wahid [1 ]
Amokrane, Kahina [1 ,3 ]
Bennabi, Meriem [1 ,6 ]
Le Guen, Emmanuel [1 ,2 ,6 ]
Dargel, Aroldo Ayub [1 ,2 ,6 ,7 ]
Houenou, Josselin [2 ,4 ,5 ,6 ]
Ivanova, Rayna [3 ]
Bellivier, Frank [2 ,4 ,5 ,6 ]
Henry, Chantal [2 ,4 ,5 ,6 ]
Kahn, Jean-Pierre [6 ,8 ]
Charron, Dominique [1 ,3 ,6 ,9 ]
Krishnamoorthy, Rajagopal [1 ,10 ]
Vervoitte, Laetitia [11 ,12 ]
Leboyer, Marion [2 ,4 ,5 ,6 ]
Tamouza, Ryad [1 ,3 ,6 ,9 ]
机构
[1] Hop St Louis, INSERM, UMRS 940, F-75010 Paris, France
[2] IMRB, INSERM, U955, F-94000 Creteil, France
[3] Hop St Louis, Lab Jean Dausset, F-75010 Paris, France
[4] Univ Paris Est Creteil, UMR S955, F-94000 Creteil, France
[5] Grp Hosp Henri Mondor, AP HP, F-94000 Creteil, France
[6] Fdn Cooperat Sci, Fdn FondaMental, Creteil, France
[7] Univ Fed Rio Grande do Sul, CNPq Conselho Nacl Desenvolvimento Cient & Tecnol, Ctr Pesquisas Expt,Hosp Clin Porto Alegre, Programa Posgrad Med Psiquiatria,Lab Psiquiatria, BR-90046900 Porto Alegre, RS, Brazil
[8] Hop Brabois, CHU Nancy, Serv Psychiat & Psychol Clin, F-54500 Vandoeuvre Les Nancy, France
[9] Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
[10] Robert Debre Hosp, INSERM, U763, F-75019 Paris, France
[11] Ctr Invest Clin 006, INSERM, U955, F-94000 Creteil, France
[12] Hop Henri Mondor, F-94000 Creteil, France
关键词
Bipolar disorders; Innate immunity; TLR-4; Polymorphism; PARVOVIRUS B19 INFECTION; SIMPLEX-VIRUS TYPE-1; AUTOIMMUNE-THYROIDITIS; PATHOGEN RECOGNITION; IMMUNE ACTIVATION; ONSET; TLR4; AGE; RISK; INFLAMMATION;
D O I
10.1016/j.jad.2013.09.043
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Bipolar disorder (BD) is considered as a multifactorial disorder involving complex interactions between genetic and environmental factors, where immune dysfunction is thought to play a key etiopathogenic role. In particular, excess of winter births associated with early-life infections raise the possibility of the implication of innate immunity. Given the pivotal role of Toll-like receptor 4 (TLR-4), a major innate immune sensor molecule, we hypothesized that genetic variations of TLR-4 may be associated to BD. Methods: Genomic DNAs from 572 BD patients and 202 healthy controls (HC) were analyzed for the distribution of six single nucleotides polymorphisms (SINPs) scattered along the TLR-4 locus (rs1927914, rs10759932, rs4986790, rs4986791, rs11536889 and rs11536891). Associations between BD and these polymorphisms were examined using the Chi-square test. Results: We found that rs1927914 AA and r.s11536891 TT genotype are more frequent in BD patients than in controls (corrected p; pc=.02 and .02 respectively) particularly in early onset BD patients (pc=.004 and .006) born during the summer season (pc=.02 and .002 respectively). We also found that rs4986790 AG and rs4986791 CT genotypes were significantly associated with presence of autoimmune thyroiditis (pc=.002). Limitations: Our results are to be confirmed by replication in independent BD cohorts. Conclusions: We report for the first time a genetic association between BD and TLR-4 a major player of innate immunity. Possible mechanisms underlying bipolar disorders linking altered TLR-4 expression and increased susceptibility to infections and/or autoimmunity are discussed. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:395 / 402
页数:8
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