Division of Clinical Psychology, Institute of Allied Health Sciences, Tainan, Taiwan; Department of Psychiatry, National Cheng Kung University, Tainan, Taiwan.
J Affect Disord. 2013 Dec;151(3):967-72. doi: 10.1016/j.jad.2013.08.017. Epub 2013 Aug 27.
The high comorbidity rate between bipolar disorder (BP) and anxiety disorder (AD) has been studied in depth. This comorbidity is not as high in Han Chinese in Taiwan. Therefore, we explored the genetic effects BP comorbid with AD.
We recruited 1316 participants: 286 with BP-I, 681 with BP-II, and 349 healthy Controls. Genotypes of the BDNF Val66Met and DRD3 Ser9Gly polymorphisms were determined using polymerase chain reactions plus restriction fragment length polymorphism analysis.
The DRD3 Ser9Gly polymorphism was associated with BP-II comorbid with AD (BPII(+AD)), and the BDNF Val66Met polymorphism was associated with BP-I comorbid with AD (BPI(+AD)). An interaction between the Val/Val genotype of the BDNF Val66Met and Gly/Gly polymorphism of the DRD3 Ser9Gly was found in BPII(+AD), but not in BP-II not comorbid with AD (BPI(-AD)) compared with healthy Controls.
The low comorbidity rate of AD in both BP subtypes, especially BP-I, limit generalizing our findings.
The involvement of the dopaminergic pathway in AD was confirmed, particularly with BP-II rather than BP-I. Because the Val/Val genotype of the BDNF Val66Met polymorphism, rather than the other two polymorphisms, has been associated with anxiety, it seems to affect BP-I comorbid with AD without the involvement of the DRD3 Seg9Gly polymorphism, but may modify the involvement of DRD3 Gly/Gly in BP-II comorbid with AD.
双相障碍(BP)和焦虑障碍(AD)的高共病率已得到深入研究。这种共病在台湾的汉族人群中并不高。因此,我们探讨了 BP 伴发 AD 的遗传效应。
我们招募了 1316 名参与者:286 名 BP-I 患者,681 名 BP-II 患者和 349 名健康对照者。使用聚合酶链反应加限制性片段长度多态性分析确定 BDNF Val66Met 和 DRD3 Ser9Gly 多态性的基因型。
DRD3 Ser9Gly 多态性与 BP-II 伴发 AD(BPII(+AD))相关,BDNF Val66Met 多态性与 BP-I 伴发 AD(BPI(+AD))相关。在 BPII(+AD)中发现 BDNF Val66Met 的 Val/Val 基因型与 DRD3 Ser9Gly 的 Gly/Gly 多态性之间存在相互作用,但在 BP-II 不伴发 AD(BPI(-AD))中与健康对照者相比则没有。
两种 BP 亚型,尤其是 BP-I,AD 的共病率较低,限制了我们研究结果的推广。
多巴胺能通路在 AD 中的作用得到了证实,特别是在 BP-II 而不是 BP-I 中。由于 BDNF Val66Met 多态性的 Val/Val 基因型而非其他两种多态性与焦虑相关,因此它似乎影响了没有 DRD3 Ser9Gly 多态性参与的 BP-I 伴发 AD,但可能会改变 DRD3 Gly/Gly 参与 BP-II 伴发 AD 的情况。