4.4 Article

Occurrence and severity of cocaine-induced hallucinations: Two distinct phenotypes with shared clinical factors but specific genetic risk factors

期刊

DRUG AND ALCOHOL DEPENDENCE
卷 232, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.drugalcdep.2022.109270

关键词

Cocaine; Substance induced psychotic symptoms; Mixture model; Hallucinations

资金

  1. Ministere Francais des Solidarites et de la Sante, Programme Hospitalier de Recherche Clinique (PHRC National 2010) [AOM10165]

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This study finds that the occurrence and severity of cocaine-induced transient hallucinations (CIH) are two distinct phenotypes in cocaine users. Cocaine dependence, number of dependence criteria, and frequency of use during the worst period of misuse are significantly associated with the occurrence and severity of CIH.
Cocaine-induced transient hallucinations (CIH) are a frequent complication following cocaine intake that is associated with addiction severity. Methods: 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. Results: Cocaine dependence (p(occurrence) = 6.18 x 10(-5), p(severity) = 9.25 x 10(-8)), number of cocaine dependence DSM IV-Tr criteria (p(occurrence) = 1.22 x 10(-7), p(severity) = 5.09 x 10(-6)), and frequency of intake during the worst period of misuse (p(occurrence) = 8.51 x 10(-04), p(severity) = 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. Conclusion: 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.

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