Finn C T, Smoller J W
Department of Psychiatry, Massachusetts General Hospital, 15 Parkman Street, WACC-812, Boston, MA 02114, USA.
Curr Psychiatry Rep. 2001 Apr;3(2):131-7. doi: 10.1007/s11920-001-0010-5.
Of the anxiety disorders, panic disorder (PD) has been the most extensively studied from a genetic standpoint. Results of family studies have consistently demonstrated that PD runs in families, and twin studies indicate that genes contribute to this familiality. However, phenotypic and genetic complexity has made finding the specific genes involved in PD a challenge. There is still uncertainty about how best to define the phenotype for genetic studies and whether it is the clinical phenotype of PD or more latent psychologic and biologic traits that are inherited. To date, molecular genetic studies have suggested some chromosomal regions and genes that may contribute to risk, but none of these have been established. We review the genetic epidemiology of PD as well as recent molecular genetic studies of the disorder, and conclude with a discussion of promising strategies that attempt to uncover specific genetic loci involved in the etiology of PD.
在焦虑症中,惊恐障碍(PD)从遗传学角度受到了最广泛的研究。家族研究结果一致表明,惊恐障碍具有家族聚集性,而双生子研究表明基因导致了这种家族聚集性。然而,表型和遗传复杂性使得找到与惊恐障碍相关的特定基因成为一项挑战。关于如何最好地定义用于遗传研究的表型,以及遗传的是惊恐障碍的临床表型还是更潜在的心理和生物学特征,仍然存在不确定性。迄今为止,分子遗传学研究已经提出了一些可能与风险相关的染色体区域和基因,但这些都尚未得到证实。我们回顾了惊恐障碍的遗传流行病学以及该疾病最近的分子遗传学研究,并以对一些有前景的策略的讨论作为结尾,这些策略试图揭示参与惊恐障碍病因的特定基因位点。