Antidepressant-induced akathisia-related homicides associated with diminishing mutations in metabolizing genes of the CYP450 family

被引:17
作者
Lucire, Yolande [1 ]
Crotty, Christopher [1 ]
机构
[1] Edgecliff Ctr, 203-233 New South Head Rd, Edgecliff, NSW 2027, Australia
来源
PHARMACOGENOMICS & PERSONALIZED MEDICINE | 2011年 / 4卷
关键词
adverse drug reaction; drug therapy; safety pharmacogenetics; CYP1A2; CYP3A4; CYP2D6; CYP2C9; CYP2C19; drug metabolism; public health; suicide; violence; human rights;
D O I
10.2147/PGPM.S17445
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: 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. Patients and methods: 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. Results: 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. Conclusion: 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.
引用
收藏
页码:65 / 81
页数:17
相关论文
共 116 条
  • [1] Alexander J, 2011, AUS NZJ PSYCHIAT
  • [2] *AM PSYCH ASS, 1994, DIAGN STAT MAN MENT, P273
  • [3] [Anonymous], 2008, HUM CYT P450
  • [4] Six patterns of drug-drug interactions
    Armstrong, SC
    Cozza, KL
    Sandson, NB
    [J]. PSYCHOSOMATICS, 2003, 44 (03) : 255 - 258
  • [5] Atbasoglu EC, 2001, J NEUROPSYCH CLIN N, V13, P336
  • [6] Australian Bureau of Statistics, 2001, NAT HLTH SURV MENT H
  • [7] The AGNP-TDM expert group consensus guidelines:: Therapeutic Drug Monitoring in psychiatry
    Baumann, P
    Hiemke, C
    Ulrich, S
    Eckermann, G
    Gaertner, I
    Gerlach, M
    Kuss, HJ
    Laux, G
    Müller-Oerlinghausen, B
    Rao, ML
    Riederer, P
    Zernig, G
    [J]. PHARMACOPSYCHIATRY, 2004, 37 (06) : 243 - 265
  • [8] DRUG-INTERACTION BETWEEN RIFAMPIN AND NORTRIPTYLINE - A CASE-REPORT
    BEBCHUK, JM
    STEWART, DE
    [J]. INTERNATIONAL JOURNAL OF PSYCHIATRY IN MEDICINE, 1991, 21 (02) : 183 - 187
  • [9] Bertilsson L, 1997, ACTA PSYCHIAT SCAND, V96, P14
  • [10] NORTRIPTYLINE AND ANTIPYRINE CLEARANCE IN RELATION TO DEBRISOQUINE HYDROXYLATION IN MAN
    BERTILSSON, L
    EICHELBAUM, M
    MELLSTROM, B
    SAWE, J
    SCHULZ, HU
    SJOQVIST, F
    [J]. LIFE SCIENCES, 1980, 27 (18) : 1673 - 1677