Université de Paris, INSERM UMR-S 1144, Optimisation Thérapeutique en Neuropsychopharmacologie OTeN, Paris F-75006, France; APHP, Hôpitaux Universitaires Henri Mondor, DMU IMPACT, Hôpital Emile ROUX, Service d'addictologie, Limeil Brévannes 94450, France.
Université de Paris, INSERM UMR-S 1144, Optimisation Thérapeutique en Neuropsychopharmacologie OTeN, Paris F-75006, France; EA 7537 BioSTM, Faculté de Pharmacie, Université Paris Descartes, USPC, Paris 75006, France.
Drug Alcohol Depend. 2022 Mar 1;232:109270. doi: 10.1016/j.drugalcdep.2022.109270. Epub 2022 Jan 11.
Cocaine-induced transient hallucinations (CIH) are a frequent complication following cocaine intake that is associated with addiction severity.
Two hundred and forty-two non-psychotic and Caucasian lifetime cocaine users were included in a French multicentric study. Clinical variables and dopamine pathway genotype data were extracted and tested with CIH scores using a zero-inflated binomial model, which allows for the exploration of factors associated with occurrence and severity separately.
Cocaine dependence (p= 6.18 × 10, p= 9.25 × 10), number of cocaine dependence DSM IV-Tr criteria (p= 1.22 × 10, p= 5.09 × 10), and frequency of intake during the worst period of misuse (p= 8.51 × 10, p= 0.04) were associated with greater occurrence and higher severity of CIH. The genetic associations did not yield significant results after correction for multiple tests. However, some nominal associations of SNPs mapped to the VMAT2, DBH, DRD1, and DRD2 genes were significant. In the multivariate model, the significant variables were the number of cocaine dependence criteria, lifetime alcohol dependence, and the nominally associated SNPs.
Our study shows that CIH occurrence and severity are two distinct phenotypes, with shared clinical risk factors; however, they likely do not share the same genetic background.
可卡因诱导的短暂幻觉(CIH)是可卡因摄入后的常见并发症,与成瘾严重程度有关。
我们纳入了 242 名非精神病和白种人终生可卡因使用者,进行了一项法国多中心研究。提取了临床变量和多巴胺通路基因型数据,并使用零膨胀二项式模型对 CIH 评分进行了测试,该模型允许分别探索与发生和严重程度相关的因素。
可卡因依赖(p=6.18×10,p=9.25×10)、可卡因依赖 DSM-IV-Tr 标准的数量(p=1.22×10,p=5.09×10)和滥用最严重期间的摄入频率(p=8.51×10,p=0.04)与 CIH 的发生和严重程度较高有关。在进行多重检验校正后,遗传关联没有产生显著结果。然而,一些映射到 VMAT2、DBH、DRD1 和 DRD2 基因的 SNP 的名义关联是显著的。在多变量模型中,显著的变量是可卡因依赖标准的数量、终生酒精依赖和名义相关的 SNPs。
我们的研究表明,CIH 的发生和严重程度是两种不同的表型,具有共同的临床危险因素;然而,它们可能没有相同的遗传背景。