AI Article Synopsis

  • The study identifies different categories of drug use based on substance type and frequency over time, highlighting five main groups: low/no use, desistant cannabis and party drug users, and two types of persistent drug misuse.
  • It uses a twin design to understand genetic influences on these categories, finding twin concordance rates higher in identical twins compared to fraternal twins, especially for persistent polydrug use, which is shown to be highly heritable.
  • The research also links various mental health issues, like conduct disorder and depression, as significant risk factors for persistent drug misuse, emphasizing the complex interplay between genetics and behavioral health in substance use.

Article Abstract

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  = 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  = 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882637PMC
http://dx.doi.org/10.1111/add.15225DOI Listing

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