Deep brain stimulation removal after successful treatment for heroin addiction

Chencheng Zhang, Jun Li, Dianyou Li, Bomin Sun
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引用次数: 7

Abstract

Australian & New Zealand Journal of Psychiatry, 54(5) the normal range, and lenograstim increased to 250 μg on 29 June. On 5 July, 11 days after CIA occurrence, the patient’s ANC increased to 9560 cells/ mm3. After that, his ANC returned to a stable range. Examination of HLA alleles revealed the following: HLAA*11:01/24:02, HLA-B*54:01/55:02, HLA-Cw*01:02/03:03, HLA-RB1*04:05/ 08:03, HLA-DQB1*04:01/06:01. Several pharmacogenetic studies found that HLA alleles that differ between ethnics are implicated in the development of CIA (Numata et al., 2018). Because agranulocytosis is a rare adverse drug reaction, only 22 patients with CIA were included for detection of the responsible alleles in a study of Japanese (Saito et al., 2016). We suspected that HLA-DRB1*04:05 is in linkage disequilibrium and HLA-DRB1*04:05 might be an independent risk factor for CIA in Japanese. Further pharmacogenetic studies are needed to clarify the HLA alleles associated with CIA.
成功治疗海洛因成瘾后进行深部脑刺激去除
澳大利亚和新西兰精神病学杂志,54(5),正常范围,lenograstim在6月29日增加到250 μg。7月5日,CIA发生11天后,患者ANC升高至9560个细胞/ mm3。在那之后,他的ANC回到了稳定的范围。HLA等位基因检测结果如下:HLA- a *11:01/24:02, HLA- b *54:01/55:02, HLA- cw *01:02/03:03, HLA- rb1 *04:05/ 08:03, HLA- dqb1 *04:01/06:01。几项药物遗传学研究发现,不同种族的HLA等位基因与CIA的发展有关(Numata等人,2018)。由于粒细胞缺乏症是一种罕见的药物不良反应,日本的一项研究只纳入了22例CIA患者进行相关等位基因检测(Saito et al., 2016)。我们推测HLA-DRB1*04:05存在连锁不平衡,HLA-DRB1*04:05可能是日本人CIA的独立危险因素。需要进一步的药物遗传学研究来阐明与CIA相关的HLA等位基因。
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