Hodges Laura M, Weissman Myrna M, Haghighi Fatemeh, Costa Ramiro, Bravo Oscar, Evgrafov Oleg, Knowles James A, Fyer Abby J, Hamilton Steven P
Department of Psychiatry, Institute for Human Genetics, University of California, San Francisco, 94143-0984, USA.
Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):65-73. doi: 10.1002/ajmg.b.30773.
Panic disorder (PD) is a debilitating anxiety disorder, characterized by recurrent episodes of intense fear that are accompanied by autonomic and psychological symptoms leading to behavioral impairment. Basic research implicates neuropeptide-signaling genes in the modulation of anxiety and stress. The genes encoding corticotropin releasing hormone receptor 1 (CRHR1), tachykinin receptor 1 (TACR1), gastrin releasing peptide (GRP), and gastrin releasing peptide receptor (GRPR) were selected as candidates for PD based on their biology. Linkage and association analysis in 120 multiplex U.S. PD pedigrees was performed using 21 single nucleotide polymorphisms (SNPs). Parametric and non-parametric linkage tests in pedigrees, for single point and multipoint analysis, revealed limited support for genetic linkage to TACR1 (parametric and non-parametric lod scores approximately 1). The family-based association test (FBAT) generated nominal support for allelic association in TACR1 (P = 0.02), and GRP (P = 0.02), findings which must be considered in the light of multiple comparisons. Further exploration of the GRP and TACR1 findings in large case-control PD samples may provide more definitive evidence implicating these loci in the genetic etiology of PD.
惊恐障碍(PD)是一种使人衰弱的焦虑症,其特征为反复发作的强烈恐惧,并伴有自主神经和心理症状,进而导致行为障碍。基础研究表明神经肽信号基因参与焦虑和应激的调节。基于其生物学特性,编码促肾上腺皮质激素释放激素受体1(CRHR1)、速激肽受体1(TACR1)、胃泌素释放肽(GRP)和胃泌素释放肽受体(GRPR)的基因被选为惊恐障碍的候选基因。利用21个单核苷酸多态性(SNP)对120个美国多重惊恐障碍家系进行连锁和关联分析。在家系中进行的单点位和多位点分析的参数和非参数连锁检验显示,对TACR1基因连锁的支持有限(参数和非参数连锁值约为1)。基于家系的关联检验(FBAT)对TACR1(P = 0.02)和GRP(P = 0.02)的等位基因关联产生了名义上的支持,鉴于多次比较,这些结果必须加以考虑。在大型病例对照惊恐障碍样本中对GRP和TACR1的研究结果进行进一步探索,可能会提供更确凿的证据,表明这些基因座与惊恐障碍的遗传病因有关。