Prata Diana P, Breen Gerome, Osborne Sarah, Munro Janet, St Clair David, Collier David A
Social Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, London, UK.
Psychiatr Genet. 2009 Jun;19(3):113-6. doi: 10.1097/YPG.0b013e32832a4f69.
As evidence of partial aetiological overlap between bipolar affective disorder and schizophrenia is accumulating, it is important to determine whether genes implicated in the aetiology of schizophrenia play a role in bipolar disorder, and vice versa. As the neuregulin 1 (NRG1) gene has been associated with schizophrenia, we set out to investigate whether it is also associated with bipolar affective disorder, using a sample from Scotland, UK.
We tested four single nucleotide polymorphisms (SNPs), SNP8NRG221533 (rs35753505), SNP8NRG241930, SNP8NRG243177 (rs6994992) and SNPNRG222662 (rs4623364) for allelic and haplotypic association with bipolar disorder and the presence of psychotic or mood-incongruent psychotic features.
We found nominal allele-wise significant association (P = 0.02) for SNP8NRG221533, with the T allele being overrepresented in cases. This is the opposite allelic association to the original association study where the C allele was associated with schizophrenia. Allele-wise significance increased when we tested for association with the subgroups of bipolar disorder with psychotic features (chi2 = 8.53; P = 0.003; odds ratio = 1.49) and, more specifically, with mood-incongruent psychotic features (chi2 = 7.13; P = 0.008; odds ratio = 1.57). Furthermore, both these subphenotypes were significantly associated with the SNP8NRG221533(T)-SNP8NRG241930(G) haplotype (chi2 = 11.94, global P = 0.027 and chi2 = 11.88, global P = 0.019, respectively) and with the SNP8NRG221533(T)-SNP8NRG222662(C)-SNP8NRG241930(G) haplotype (chi2 = 19.98, global P = 0.009) in case of the broader subphenotype of psychotic bipolar.
This study supports the hypothesis that NRG1 may play a role in the development of bipolar disorder, especially in psychotic subtypes, albeit with different alleles to previous association reports in schizophrenia and bipolar disorder.
鉴于双相情感障碍与精神分裂症之间部分病因重叠的证据不断积累,确定精神分裂症病因中涉及的基因是否在双相情感障碍中起作用,反之亦然,这一点很重要。由于神经调节蛋白1(NRG1)基因已与精神分裂症相关联,我们利用来自英国苏格兰的样本,着手研究它是否也与双相情感障碍相关联。
我们检测了四个单核苷酸多态性(SNP),即SNP8NRG221533(rs35753505)、SNP8NRG241930、SNP8NRG243177(rs6994992)和SNPNRG222662(rs4623364)与双相情感障碍以及精神病性或心境不一致的精神病性特征的等位基因和单倍型关联。
我们发现SNP8NRG221533存在名义上的等位基因水平显著关联(P = 0.02),病例组中T等位基因的比例过高。这与最初的关联研究中C等位基因与精神分裂症相关的等位基因关联相反。当我们检测与伴有精神病性特征的双相情感障碍亚组的关联时,等位基因水平的显著性增加(χ² = 8.53;P = 0.003;优势比 = 1.49),更具体地说,与心境不一致的精神病性特征的关联(χ² = 7.13;P = 0.008;优势比 = 1.57)。此外,这两种亚表型均与SNP8NRG221533(T)-SNP8NRG241930(G)单倍型(χ² = 11.94,全局P = 0.027;χ² = 11.88,全局P = 0.019)以及在更广泛的精神病性双相情感障碍亚表型情况下与SNP8NRG221533(T)-SNP8NRG222662(C)-SNP8NRG241930(G)单倍型(χ² = 19.98,全局P = 0.009)显著相关。
本研究支持以下假设,即NRG1可能在双相情感障碍的发病中起作用,尤其是在精神病性亚型中,尽管其等位基因与先前精神分裂症和双相情感障碍关联报告中的不同。