Lucire Yolande, Crotty Christopher
Edgecliff Centre, Edgecliff, NSW, Australia.
Pharmgenomics Pers Med. 2011;4:65-81. doi: 10.2147/PGPM.S17445. Epub 2011 Aug 1.
To examine the relation between variant alleles in 3 CYP450 genes (CYP2D6, CYP2C9 and CYP2C19), interacting drugs and akathisia in subjects referred to a forensic psychiatry practice in Sydney, Australia.
This paper concerns 10/129 subjects who had been referred to the first author's practice for expert opinion or treatment. More than 120 subjects were diagnosed with akathisia/serotonin toxicity after taking psychiatric medication that had been prescribed for psychosocial distress. They were tested for variant alleles in CYP450 genes, which play a major role in Phase I metabolism of all antidepressant and many other medications. Eight had committed homicide and many more became extremely violent while on antidepressants. Ten representative case histories involving serious violence are presented in detail.
Variant CYP450 allele frequencies were higher in akathisia subjects compared with random primary care patients tested at the same facility. Ten subjects described in detail had variant alleles for one or more of their tested CYP450 genes. All but two were also on interacting drugs, herbals or illicit substances, impairing metabolism further. All those described were able to stop taking antidepressants and return to their previously normal personalities.
THE PERSONAL, MEDICAL, AND LEGAL PROBLEMS ARISING FROM OVERUSE OF ANTIDEPRESSANT MEDICATIONS AND RESULTING TOXICITY RAISE THE QUESTION: how can such toxicity events be understood and prevented? The authors suggest that the key lies in understanding the interplay between the subject's CYP450 genotype, substrate drugs and doses, co-prescribed inhibitors and inducers and the age of the subject. The results presented here concerning a sample of persons given antidepressants for psychosocial distress demonstrate the extent to which the psychopharmacology industry has expanded its influence beyond its ability to cure. The roles of both regulatory agencies and drug safety "pharmacovigilantes" in ensuring quality and transparency of industry information is highlighted.
研究澳大利亚悉尼一家法医精神病学机构中,3种细胞色素P450基因(CYP2D6、CYP2C9和CYP2C19)的变异等位基因、相互作用药物与静坐不能之间的关系。
本文涉及10名/129名曾被转介至第一作者所在机构寻求专家意见或治疗的患者。120多名患者在服用因社会心理困扰而开具的精神科药物后被诊断为静坐不能/5-羟色胺毒性反应。他们接受了细胞色素P450基因变异等位基因检测,这些基因在所有抗抑郁药及许多其他药物的I期代谢中起主要作用。其中8人实施了杀人行为,还有更多人在服用抗抑郁药期间变得极其暴力。详细介绍了10个涉及严重暴力行为的代表性病例。
与在同一机构接受检测的随机初级保健患者相比,静坐不能患者中细胞色素P450变异等位基因频率更高。详细描述的10名患者中,其检测的一种或多种细胞色素P450基因存在变异等位基因。除两人外,其他人还同时服用相互作用的药物、草药或非法物质,进一步损害了代谢功能。所有被描述的患者都能够停止服用抗抑郁药,并恢复到以前的正常性格。
过度使用抗抑郁药物及其导致的毒性反应所引发的个人、医学和法律问题提出了一个问题:如何理解并预防此类毒性事件?作者认为关键在于了解受试者的细胞色素P450基因型、底物药物及其剂量、联合开具的抑制剂和诱导剂以及受试者的年龄之间的相互作用。此处呈现的关于因社会心理困扰而服用抗抑郁药的人群样本的结果表明,精神药理学行业的影响力已超出其治愈能力的范围。强调了监管机构和药物安全“药物警戒员”在确保行业信息质量和透明度方面的作用。