de Leon J, Barnhill J, Rogers T, Boyle J, Chou W H, Wedlund P J
University of Kentucky Mental Health Research Center at Eastern State Hospital and the University of Kentucky College of Pharmacy, Lexington 40508, USA.
Am J Psychiatry. 1998 Sep;155(9):1278-80. doi: 10.1176/ajp.155.9.1278.
The authors conducted a pilot study to develop preliminary data on the frequency of cytochrome P450-2D6 (CYP2D6) genotypes in state psychiatric hospital patients and to establish population sizes needed to determine potential clinical relevance in therapeutic outcome.
One hundred consecutive inpatients at Eastern State Hospital in Kentucky who provided informed consent were genotyped at the CYP2D6 locus during their hospital stay.
Twelve of the patients were CYP2D6 deficient, and four carried the *1Xn or *2Xn allele associated with ultrarapid metabolism; all of these patients were Caucasian (N=87). The rate of deficiency in CYP2D6 expression in these Caucasian state psychiatric hospital patients (14%) was twice that of the U.S. population (7%). The patients with CYP2D6 deficiency also appeared more likely to experience side effects in response to CYP2D6 medications.
This study, limited by a small number of subjects, suggests that one-fifth of Caucasians admitted to a state hospital in Kentucky had genotypes associated with extremes in CYP2D6 activity that may have affected their response to CYP2D6 medications.
作者开展了一项初步研究,以获取州立精神病院患者细胞色素P450 - 2D6(CYP2D6)基因型频率的初步数据,并确定在治疗结果中确定潜在临床相关性所需的样本量。
肯塔基州东部州立医院100名连续住院且提供知情同意书的患者在住院期间进行了CYP2D6基因分型。
12名患者CYP2D6功能缺失,4名携带与超快代谢相关的1Xn或2Xn等位基因;所有这些患者均为白种人(n = 87)。这些白种人州立精神病院患者中CYP2D6表达缺失率(14%)是美国人群(7%)的两倍。CYP2D6功能缺失的患者似乎对CYP2D6药物产生副作用的可能性也更高。
本研究受样本量少的限制,表明肯塔基州一家州立医院五分之一的白种人患者具有与CYP2D6活性极端情况相关的基因型,这可能影响了他们对CYP2D6药物的反应。