Pharmacogenomic Study of Clozapine-Induced Agranulocytosis/Granulocytopenia in a Japanese Population

نویسندگان

  • Takeo Saito
  • Masashi Ikeda
  • Taisei Mushiroda
  • Takeshi Ozeki
  • Kenji Kondo
  • Ayu Shimasaki
  • Kohei Kawase
  • Shuji Hashimoto
  • Hidenaga Yamamori
  • Yuka Yasuda
  • Michiko Fujimoto
  • Kazutaka Ohi
  • Masatoshi Takeda
  • Yoichiro Kamatani
  • Shusuke Numata
  • Tetsuro Ohmori
  • Shu-ichi Ueno
  • Manabu Makinodan
  • Yosuke Nishihata
  • Masaharu Kubota
  • Takemi Kimura
  • Nobuhisa Kanahara
  • Naoki Hashimoto
  • Kiyoshi Fujita
  • Kiyotaka Nemoto
  • Taku Fukao
  • Taro Suwa
  • Tetsuro Noda
  • Yuji Yada
  • Manabu Takaki
  • Naoya Kida
  • Taku Otsuru
  • Masaru Murakami
  • Atsushi Takahashi
  • Michiaki Kubo
  • Ryota Hashimoto
  • Nakao Iwata
چکیده

BACKGROUND Clozapine-induced agranulocytosis (CIA)/clozapine-induced granulocytopenia (CIG) (CIAG) is a life-threatening event for schizophrenic subjects treated with clozapine. METHODS To examine the genetic factor for CIAG, a genome-wide pharmacogenomic analysis was conducted using 50 subjects with CIAG and 2905 control subjects. RESULTS We identified a significant association in the human leukocyte antigen (HLA) region (rs1800625, p = 3.46 × 10(-9), odds ratio [OR] = 3.8); therefore, subsequent HLA typing was performed. We detected a significant association of HLA-B*59:01 with CIAG (p = 3.81 × 10(-8), OR = 10.7) and confirmed this association by comparing with an independent clozapine-tolerant control group (n = 380, p = 2.97 × 10(-5), OR = 6.3). As we observed that the OR of CIA (OR: 9.3~15.8) was approximately double that in CIG (OR: 4.4~7.4), we hypothesized that the CIG subjects were a mixed population of those who potentially would develop CIA and those who would not develop CIA (non-CIA). This hypothesis allowed the proportion of the CIG who were non-CIA to be calculated, enabling us to estimate the positive predictive value of the nonrisk allele on non-CIA in CIG subjects. Assuming this model, we estimated that 1) ~50% of CIG subjects would be non-CIA; and 2) ~60% of the CIG subjects without the risk allele would be non-CIA and therefore not expected to develop CIA. CONCLUSIONS Our results suggest that HLA-B*59:01 is a risk factor for CIAG in the Japanese population. Furthermore, if our model is true, the results suggest that rechallenging certain CIG subjects with clozapine may not be always contraindicated.

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عنوان ژورنال:
  • Biological Psychiatry

دوره 80  شماره 

صفحات  -

تاریخ انتشار 2016