Boston University School of Medicine, Massachusetts, USA.
Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1139-46. doi: 10.1002/ajmg.b.30939.
There is comorbidity and a possible genetic connection between Bipolar disease (BP) and panic disorder (PD). Genes may exist that increase risk to both PD and BP. We explored this possibility using data from a linkage study of PD (120 multiplex families; 37 had > or =1 BP member). We calculated 2-point lodscores maximized over male and female recombination fractions by classifying individuals with PD and/or BP as affected (PD + BP). Additionally, to shed light on possible heterogeneity, we examine the pedigrees containing a bipolar member (BP+) separately from those that do not (BP-), using a Predivided-Sample Test (PST). Linkage evidence for common genes for PD + BP was obtained on chromosomes 2 (lodscore = 4.6) and chromosome 12 (lodscore = 3.6). These locations had already been implicated using a PD-only diagnosis, although at both locations this was larger when a joint PD + BP diagnosis was used. Examining the BP+ families and BP- families separately indicates that both BP+ and BP- pedigrees are contributing to the peaks on chromosomes 2 and 12. However, the PST indicates different evidence of linkage is obtained from BP+ and BP- pedigrees on chromosome 13. Our findings are consistent with risk loci for the combined PD + BP phenotype on chromosomes 2 and 12. We also obtained evidence of heterogeneity on chromosome 13. The regions on chromosomes 12 and 13 identified here have previously been implicated as regions of interest for multiple psychiatric disorders, including BP.
双相情感障碍(BP)和恐慌症(PD)之间存在共病和可能的遗传联系。可能存在增加 PD 和 BP 风险的基因。我们使用 PD 连锁研究的数据(120 个多态性家族;37 个家族中有>或=1 个 BP 成员)探索了这种可能性。我们通过将 PD 和/或 BP 患者分类为受影响者(PD+BP),计算了男性和女性重组分数的 2 点 lodscore。此外,为了阐明可能的异质性,我们使用预先划分样本检验(PST)分别检查包含双相成员(BP+)的家系和不包含双相成员(BP-)的家系。在 PD+BP 中常见基因的连锁证据获得了染色体 2(lodscore=4.6)和染色体 12(lodscore=3.6)。虽然在使用联合 PD+BP 诊断时,这两个位置的 lodscore 更大,但以前已经使用 PD 单一诊断暗示了这两个位置。分别检查 BP+家族和 BP-家族表明,BP+和 BP-家系都对染色体 2 和 12 上的峰有贡献。然而,PST 表明,从 BP+和 BP-家系获得的染色体 13 的连锁证据不同。我们的研究结果与染色体 2 和 12 上联合 PD+BP 表型的风险基因座一致。我们还在染色体 13 上获得了异质性的证据。以前,染色体 12 和 13 上的这些区域已被确定为多个精神障碍(包括 BP)的感兴趣区域。