Gillespie Nathan A, Aggen Steven H, Gentry Amanda E, Neale Michael C, Knudsen Gun P, Krueger Robert F, South Susan C, Czajkowski Nikolai, Nesvåg Ragnar, Ystrom Eivind, Rosenström Tom H, Torvik Fartein A, Reichborn-Kjennerud Ted, Kendler Kenneth S
Department of Psychiatry,Virginia Institute for Psychiatric and Behavioral Genetics,Virginia Commonwealth University,Richmond,VA,USA.
Department of Biostatistics,Virginia Commonwealth University,Richmond,VA,USA.
Twin Res Hum Genet. 2018 Feb;21(1):24-32. doi: 10.1017/thg.2017.73.
Until now, data have not been available to elucidate the genetic and environmental sources of comorbidity between all 10 DSM-IV personality disorders (PDs) and cocaine use. Our aim was to determine which PD traits are linked phenotypically and genetically to cocaine use. Cross-sectional data were obtained in a face-to-face interview between 1999 and 2004. Subjects were 1,419 twins (µage = 28.2 years, range = 19-36) from the Norwegian Institute of Public Health Twin Panel, with complete lifetime cocaine use and criteria for all 10 DSM-IV PDs. Stepwise multiple and Least Absolute Shrinkage and Selection Operator (LASSO) regressions were used to identify PDs related to cocaine use. Twin models were fitted to estimate genetic and environmental associations between the PD traits and cocaine use. In the multiple regression, antisocial (OR = 4.24, 95% CI [2.66, 6.86]) and borderline (OR = 2.19, 95% CI [1.35, 3.57]) PD traits were significant predictors of cocaine use. In the LASSO regression, antisocial, borderline, and histrionic were significant predictors of cocaine use. Antisocial and borderline PD traits each explained 72% and 25% of the total genetic risks in cocaine use, respectively. Genetic risks in histrionic PD were not significantly related to cocaine use. Importantly, after removing criteria referencing substance use, antisocial PD explained 65% of the total genetic variance in cocaine use, whereas borderline explained only 4%. Among PD traits, antisocial is the strongest correlate of cocaine use, for which the association is driven largely by common genetic risks.
到目前为止,尚无数据能够阐明所有10种《精神疾病诊断与统计手册》第四版(DSM-IV)人格障碍(PDs)与可卡因使用之间共病的遗传和环境来源。我们的目的是确定哪些PD特质在表型和遗传上与可卡因使用有关。1999年至2004年期间通过面对面访谈获得横断面数据。研究对象是来自挪威公共卫生研究所双胞胎小组的1419对双胞胎(平均年龄 = 28.2岁,范围 = 19 - 36岁),他们有完整的可卡因使用史且符合所有10种DSM-IV PDs的标准。采用逐步多元回归和最小绝对收缩和选择算子(LASSO)回归来识别与可卡因使用相关的PDs。拟合双胞胎模型以估计PD特质与可卡因使用之间的遗传和环境关联。在多元回归中,反社会型(比值比[OR] = 4.24,95%置信区间[CI][2.66, 6.86])和边缘型(OR = 2.19,95% CI[1.35, 3.57])PD特质是可卡因使用的显著预测因素。在LASSO回归中,反社会型、边缘型和表演型是可卡因使用的显著预测因素。反社会型和边缘型PD特质分别解释了可卡因使用中总遗传风险的72%和25%。表演型PD的遗传风险与可卡因使用无显著相关性。重要的是,去除参考物质使用的标准后,反社会型PD解释了可卡因使用中总遗传变异的65%,而边缘型仅解释了4%。在PD特质中,反社会型是与可卡因使用最强的关联因素,其关联在很大程度上由共同的遗传风险驱动。