Typologies of illicit drug use in mid-adulthood: a quasi-longitudinal latent class analysis in a community-based sample of twins

被引:5
|
作者
Dash, Genevieve F. [1 ]
Martin, Nicholas G. [2 ]
Agrawal, Arpana [3 ]
Lynskey, Michael T. [4 ]
Slutske, Wendy S. [1 ]
机构
[1] Univ Missouri, Dept Psychol Sci, 210 McAlester Hall, Columbia, MO 65211 USA
[2] QIMR Berghofer, Brisbane, Qld, Australia
[3] Washington Univ, Sch Med, St Louis, MO USA
[4] Kings Coll London, Inst Psychiat, London, England
关键词
Illicit drugs; latent class analysis; persistent drug use; polydrug use; quasi-longitudinal; twin study; PRESCRIPTION-OPIOID USE; SUBSTANCE USE; ECSTASY USE; ANTISOCIAL PERSONALITY; AUSTRALIAN TWIN; NATIONAL-SURVEY; UNITED-STATES; USE DISORDERS; PATTERNS; DEPENDENCE;
D O I
10.1111/add.15225
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Aims To identify drug use typologies based on substances used and persistence of use over two time points, use a genetically informed design to explore twin concordance of and genetic influence on the use typologies and compare patterns of declined/discontinued ("desistant") and persistent drug use on drug use correlates. Design Latent class analysis was applied to data from a cross-sectional self-report survey on current and past drug use. Use characteristics, use disorder, and psychiatric problems were compared across classes. Setting Computer-assisted telephone interview in respondents' homes. Participants A total of 3785 individual twins and siblings (1365 men, 2420 women; M-age = 32) from the Australian Twin Registry Cohort III. Measurements A comprehensive interview assessed prior to past year and past year use of cannabis, stimulants, cocaine/crack, hallucinogens, opioids, sedatives, inhalants, dissociatives, and solvents; age of first use; opportunity to use; peer drug use; attention deficit/hyperactivity, conduct, antisocial personality, depressive, and substance use disorders; and suicidality. Findings A five-class solution emerged: no/low use (50%), desistant cannabis use (23%), desistant party drug use (18%), persistent prescription drug misuse (4%), and persistent polydrug use (5%). Twin concordances were higher among monozygotic (k = 0.30-0.35) than dizygotic pairs (same-sex k = 0.19-0.20; opposite sex k = 0.07), and biometric modeling suggested that the persistent polydrug use class, in particular, was highly heritable (a(2) = 0.94). Conduct disorder (OR = 2.40), antisocial personality disorder (OR = 3.27), and suicidal ideation (OR = 1.98) increased persistent polydrug use risk; depression (OR = 2.38) and lifetime suicide attempt (OR = 2.31) increased persistent prescription misuse risk. Relative to persistent prescription drug misuse, persistent polydrug use was associated with higher rates of cannabis and stimulant use disorder (OR = 6.14-28.01), younger first substance use (OR = 0.82-0.83), more drug use opportunity (OR = 10.66-66.06), and more drug-using peers (OR = 4.66-9.20). Conclusions Unique patterns of declined/discontinued ("desistant") and persistent drug use are differentially heritable and differentially associated with risk factors, psychiatric symptoms, and substance use disorder outcomes.
引用
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页码:1101 / 1112
页数:12
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