Abstract
Aims
Failure to complete high school predicts substantial economic and social disadvantage in adult life. The aim was to determine the longitudinal association of mid-adolescent polydrug use and high school non-completion, relative to other drug use profiles.
Design
A longitudinal analysis of the relationship between polydrug use in three cohorts at Grade 9 (age 14–15) and school non-completion (reported post high school).
Setting
A State-representative sample of students across Victoria, Australia.
Participants
2287 secondary school students from 152 high schools. The retention rate was 85%.
Measurements
The primary outcome was noncompletion of Grade 12 (assessed at age 19–23 years). At Grade 9, predictors included 30 day use of eight drugs, school commitment, academic failure, and peer drug use. Other controls included socioeconomic status, family relationship quality, depressive symptoms, gender, age, and cohort.
Findings
Three distinct classes of drug use were identified - no drug use (31.7%), mainly alcohol use (61.8%), and polydrug use (6.5%). Polydrug users were characterised by high rates of alcohol, tobacco, and cannabis use. In the full model, mainly alcohol users and polydrug users were less likely to complete school than nondrug users [OR = 1.54 (95% CIs 1.17–2.03), and OR = 2.51 (95% CIs 1.45–4.33), respectively, ps < .001]. These effects were independent of school commitment, academic failure, peer drug use, and other controls.
Conclusions
Mid-adolescent polydrug use in Australia predicts subsequent school non-completion after accounting for a range of potential confounding factors. Adolescents who mainly consume alcohol are also at elevated risk of school non-completion.
Keywords: adolescent, polydrug use, alcohol use, tobacco use, school non-completion, longitudinal, education level
International research consistently shows that high school non-completion is related to lower subsequent participation in paid work, fewer employment opportunities, and lower engagement in further education1–4. Average rates of high school non-completion in Western countries vary from 9% to 27%2,5,6. It is important to identify modifiable determinants of school non-completion to prevent poor educational, health, and occupational outcomes. This study focuses on the association between patterns of adolescent substance use and school non-completion.
To date, research has focused primarily on cannabis and alcohol use which, along with tobacco, are the drugs most often used by adolescents7. Research shows a consistent association between adolescent cannabis use and school non-completion8–13. Larger effects are found in young people from socio-economically disadvantaged backgrounds compared to those from advantaged backgrounds12,14. The association between alcohol use and school non-completion is less clear15. Alcohol use also predicts subsequent disconnection from school and poorer academic performance16,17, but the strength of these associations varies with peer alcohol use18 and these associations often become statistically nonsignificant after controlling for family background17. Alcohol use12 and frequent intoxication19 do not predict school non-completion, after controlling for cannabis use, tobacco use, and demographic variables. Tobacco use is also associated with school noncompletion12,17,20,21, with effect sizes smaller than those for cannabis. Other illicit drug use has been found to reduce grade level attainment by one year22.
Mechanisms linking drug use and school performance probably vary by drug type. In the case of cannabis, poor educational outcomes may reflect its negative effects on neuropsychological/cognitive functioning23–25, as well as a social component, in which users affiliate with deviant and drug using peers26 who foster ‘anticonventional’ attitudes and behaviors, including the devaluation of education21. In the case of alcohol, ‘hangovers’ result in poorer school attendance and classroom performance27,28, and increased connection with antisocial peers29. The effects of tobacco use relate to health rather than educational outcomes, but peer influences are well established30. Drug use may be a marker of engagement with high risk groups31 and of school disengagement32,33 that undermines school outcomes.
There is little longitudinal research on the extent to which polydrug use (defined as the consumption of more than one type of drug during a specific time period34) is related to school noncompletion. Available research has focused on communalities in drug use profiles across individuals, with findings indicating that polydrug use is not significantly related to school outcomes20. However, more recent studies indicate that adolescents vary in the extent and nature of polydrug use, and school non-completion may be more related to certain drug use profiles than others. Nationally representative studies show that between about 18% and 34% of adolescents (<16 years of age) report limited polydrug use (alcohol, tobacco and cannabis) and about 2% engage in more extended polydrug use (using these drugs plus other illicit drugs)35–37. Adolescent polydrug use may be more closely associated with school non-completion than individual drug use for at least two reasons. First, given legislative, educational policy, and normative constraints on adolescent substance use, adolescent polydrug use may be an indicator of stronger anticonventional attitudes and behavior than any single type of drug use. Second, large scale cross-sectional research shows that adolescent polydrug users report more drug use among peers and more depressed mood than nonpolydrug users36. These factors are likely to be related to poorer school performance.
This study examined whether adolescent polydrug use predicted school non-completion, after accounting for known confounding factors. Adolescents in middle high school (Grade 9, age 14) were the focus because in Australia, cannabis use is comparatively rare before this age and cannabis use around this age is more predictive of school non-completion than use at older ages12. Tobacco use38–40 and heavy alcohol41 use also increase in prevalence at this age. The study was conducted in two phases. In the first phase, latent class analysis (LCA) was used to classify individuals according to unobserved communalities in patterns of substance use42. LCA is a ‘person-centred’ analytic approach42 that avoids the well-documented statistical challenges of distinguishing specific drug effects, given high collinearities in the use of different drugs21. In the second phase, we used the results of the LCA to examine the association between polydrug use and subsequent school non-completion in three longitudinal cohorts, and the extent to which socio-educational disengagement accounted for this association. Control factors included: depressed mood, family relationship quality29,36,43–50, gender1, age36, family socioeconomic status12,14,51,52, and cohort differences.
METHOD
Sample
The participants were from the International Youth Development Study (Australia), a longitudinal study of adolescent health and problem behaviours. The study consisted of three cohorts (see Table 1). The youngest cohort (n = 804 at Grade 9) participated in a seven-wave study from Grade 5 (approximately aged 10) through to post high school (including Grade 9 but excluding Grade 8). The middle cohort (n = 955 at Grade 9) participated in four waves (Grade 7–9 and post high school). The oldest cohort (n = 973 at Grade 9) participated in 3 waves (Grade 9/10/post high school). The sample recruited was found to be representative of the school aged population of Victoria (McMorris et al., 2007).
Table 1.
Year | Cohort
|
|||
---|---|---|---|---|
Youngest | Middle | Oldest | ||
Wave 1 | 2002 | Grade 5 | Grade 7 | Grade 9 |
Wave 2 | 2003 | Grade 6 | Grade 8 | Grade 10 |
Wave 3 | 2004 | Grade 7 | Grade 9 | |
Wave 4 | 2006 | Grade 9 | ||
Wave 5 | 2007 | Grade 10 | ||
Wave 6 | 2008 | Grade 11 | ||
Wave 7 | 2010 | Age 19 | Age 21 | Age 23 |
| ||||
N at Grade 9 | 804 | 955 | 973 | |
N at Wave 7 | 727 | 814 | 788 | |
Retention rate (from Grade 9 to Wave 7)a | 90.4% | 85.2% | 81.0% | |
| ||||
Demographic at Grade 9b | ||||
Age | 15.15 | 14.99 | 14.89 | |
% of female | 51.5% | 51.1% | 52.2% | |
% of students from | ||||
Government schools | 61.4% | 62.1% | 22.4% | |
Independent schools | 16.2% | 16.3% | 21.6% | |
Catholic schools | 22.4% | 14.1% | 22.7% |
Notes. Bold text shows the wave used in the present study.
Measures
Students completed a modified version of the Communities That Care Youth Survey, an epidemiological assessment of adolescent health and social problems used in the US53. Minor language adaptations were made to fit it to Australian youth54. Psychometric analyses confirmed the reliability and longitudinal correlations confirmed the validity of these measures in Australian samples55.
The key outcome variable was noncompletion of Grade 12 (assessed in the final wave). This was assessed with the item “What was the highest Grade level at secondary school you completed?” Responses were coded as 0 “Completed Grade 12” or 1 “Not completed Grade 12”.
The following predictors were measured at Grade 9. Drug use was measured via questions on past month use of tobacco (“not at all” to “40+ per day”), alcohol, cannabis, stimulants, ecstasy, glue/inhalants, LSD/other psychedelics, and cocaine/crack (“never” to “40+ times”). Response categories were recoded because of the low frequencies in the heaviest categories of use. Tobacco use was recoded to four categories from “not at all” to “6+ per day”. Alcohol and cannabis use were recoded to four categories from “never” to “6+ times” (past month). Use of other drugs was recoded to “No” and “1+ times” (past month).
Academic failure was measured by two items “Putting them all together, what were your grades/ marks like last year?” (1 ‘Very good’ to 4 ‘Very poor’) and “Are your school grades better than the grades/ marks of most students in your class?” (1 ‘Definitely yes’ to 4 ‘Definitely no’) (r = 0.59).
School commitment was measured with seven items (1 ‘Never’ to 5 ‘Always’, α = 0.78) (e.g., “During the last four weeks, how often do you feel the school work you are assigned is meaningful and important?”).
Peer drug use was assessed with “In the past year, how many of your best friends have used (alcohol/tobacco/marijuana/other illegal drugs)?” (5-point scale, α = 0.75)56.
Depressive symptoms were measured using the 13-item Short Mood and Feelings Questionnaire57 (α = 0.91).
Family conflict, attachment and family management were measured using separate four-point scales with established validity58–60 (e.g., “We argue about the same things in my family over and over”, “Do you feel very close to your mother?”, “My parents ask if I’ve gotten my homework done”) (α > 0.70 for all three scales).
Family socioeconomic status (SES) was based on an algorithm of mother/father education and income with known validity/reliability, based on parent telephone interviews conducted in the first year of the study (2002)61,62.
A measure of honesty was calculated based on student responses to three survey items including use of a fictional drug, as described previously63.
Procedure
Approval for the research was obtained from the Ethics Committees of the Royal Children’s Hospital and the University of Melbourne. The study used a two-stage cluster sampling design. In the first stage, public and private schools in Victoria, Australia were randomly selected via probability proportional to size sampling. A total of 234 schools were approached and 152 agreed to participate54. In the second stage, a single classroom was randomly selected. The three cohorts all participated in Wave 1 in 2002, and the final assessment (post high school) was conducted in 2010. Grade 9 surveys were administered by project staff in the classroom54 and post high school surveys were completed online. Active parental consent was required for participation.
Analysis
Latent class analysis (LCA) was used to determine classes of drug use64. Based on existing research on adolescent polydrug use, a non-user class was specified a priori65. There is no single approach that is generally accepted for determining the number of classes for LCA66, so criteria included the Sample Size Adjusted Bayesian Information Criteria (SSABIC)67 and the Lo-Mendell-Rubin likelihood ratio test (LMR-LRT)68. A lower value in SSABIC indicates a better balance between model fit and model parsimony. A significant LMR-LRT p-value indicates better model fit than a model with one fewer classes. Because the robustness and utility of a given class is likely to be low when the size of a class is small, the solution was required to have a minimum class size of 1%50,69. Average posterior probabilities and entropy were used to evaluate classification quality70. Model fitting began with a two-class solution and was successively increased to five classes. Mplus Version 6.0170 was used for the LCA.
Once the optimal number of classes was determined, class memberships were imputed based on the posterior probabilities71,72. Fifty datasets were imputed to take into account the probabilistic assignment of class membership and to replace missing values on controls73. School non-completion was regressed onto membership of drug classes and controls using logistic regression.
RESULTS
Forty-two participants were excluded because responses suggested dishonest reporting (e.g. reporting use of a bogus drug) at Grade 9. A further 15 participants were excluded because of missing data on drug use, and 393 participants were excluded from the logistic regression analysis because of missing data on school completion. The sample for the LCA was 2675 and the sample for logistic regression modeling was 2287 participants (84% of the initial sample). Excluded participants were more likely to be male, to be from the middle/oldest cohorts, to be of low SES, to have more drug using peers, lower school commitment, and lower academic achievement (p < .05). They did not differ on age, depressive symptoms, and family factors.
Prior to the main analyses, attrition rates and associated variations on key sociodemographic variables at Grade 9 were assessed. The attrition rates for the three cohorts were consistently low (15%). Retention rates dropped somewhat across the youngest/middle/oldest cohorts respectively (90.4%, 85.2%, 81.0%), which was likely due to the progressively larger lapses between the final school assessment and the post high school assessment (Table 1). There was a small variation in age across the cohorts, reflecting the fact that school assessments occurred at different times of the year. Cohort differences in gender were statistically nonsignificant.
LCA model fit statistics and minimum group sizes are shown in Table 2. There was a large drop in the SSABIC from the two-class model to the three-class model, and there was a further small drop in the SSABIC for the four-class model. The LMR-LRT indicated that the fit of the three-class model was significantly better than the two-class model, and the fit of the four-class solution did not significantly improve on the three-class solution. In the three-class and four-class solutions, the smallest class sizes were 6.37% and 0.9% (n = 24) respectively. The three-class solution had very good classification quality (average posterior assignment probability 0.92, entropy 0.77) (see Tables 2/3). Overall, the three-class solution showed the best overall fit, parsimony, and robustness/utility.
Table 2.
Class | SSABIC | LMR-LRT (p value) | Minimum class size (% of N) | Entropy |
---|---|---|---|---|
Two | 13195.25 | < .001 | 35.4 | 0.81 |
Three | 12694.56 | 0.0028 | 6.37 | 0.769 |
Four | 12641.68 | 0.76 | 0.90 | 0.754 |
Five | 12680.87 | 0.807 | 0.90 | 0.753 |
Note. Three-class solution chosen as the optimal solution based on SSABIC, LMR-LRT, and minimum class size.
Table 3.
Past (30 day) use | Class 1: No drug use (31.7%) | Class 2: Mainly alcohol use (61.8%) | Class 3: Polydrug use (6.5%) | |
---|---|---|---|---|
Alcohol | Never | 1 | 0.17 | 0.02 |
1 – 2 times | 0 | 0.48 | 0.20 | |
3 – 5 times | 0 | 0.2 | 0.25 | |
6 or more times | 0 | 0.14 | 0.54 | |
|
||||
Tobacco | Not at all | 1 | 0.80 | 0.10 |
Less than 1 per day | 0 | 0.12 | 0.21 | |
1–5 per day | 0 | 0.04 | 0.24 | |
6 or more per day | 0 | 0.04 | 0.45 | |
|
||||
Cannabis | Never | 1 | 0.98 | 0.27 |
1 – 2 times | 0 | 0.02 | 0.38 | |
3 – 5 times | 0 | 0 | 0.08 | |
6 or more times | 0 | 0 | 0.27 | |
|
||||
LSD | No | 1 | 1 | 0.94 |
1 or more times | 0 | 0 | 0.06 | |
|
||||
Cocaine | No | 1 | 1 | 0.96 |
1 or more times | 0 | 0 | 0.04 | |
|
||||
Inhalants | No | 1 | 0.95 | 0.83 |
1 or more times | 0 | 0.05 | 0.17 | |
|
||||
Stimulants | No | 1 | 1 | 0.88 |
1 or more times | 0 | 0 | 0.12 | |
|
||||
Ecstasy | No | 1 | 1 | 0.89 |
1 or more times | 0 | 0 | 0.11 |
Class 1: This was an a priori specified class in which participants reported no drug use in Grade 9 (n = 847, 31.7%).
Class 2: Participants in this class reported high probabilities of alcohol use, low but significant probabilities of any tobacco use (0.20), and negligible probabilities of using cannabis and other drugs and inhalants. The modal frequency of tobacco use was less than one cigarette/day. The class was labeled Mainly alcohol use (n = 1653, 61.8%).
Class 3: There were elevated probabilities of alcohol (0.98), tobacco (0.90), and cannabis use (0.73), and low probabilities of other illicit drug use. This class was labeled polydrug use (n = 175, 6.5%). Approximately half of the participants in this class used tobacco 6+ times/day and used alcohol 6+ times in the last month. 73% used cannabis one or more times in the last month.
We modeled drug class membership and high school non-completion in two steps (Table 4). In Model 1, school non-completion was regressed onto drug classes with controls included (gender, age, socioeconomic status, family variables, depressed mood, cohort). There were significant effects for mainly alcohol use and polydrug use on school non-completion (ORs = 1.93 and 5.42 respectively, p < .001) compared to the no drug use class, and participants in the polydrug use class were at significantly higher risk of school non-completion than those in the mainly alcohol class (OR = 2.81, p < .001). In Model 2, after other predictors of high school non-completion were added (peer drug use, low school connectedness and academic failure), peer drug use and academic failure were significant (p < .01). Participants in the mainly alcohol class and the polydrug use class were at higher risk of school non-completion than the no drug use class (OR = 1.54 and 2.51 respectively, p < .001). Participants in the polydrug use class were at higher risk of school non-completion than those in the mainly alcohol class (OR = 1.62, p < .05). Both models were adjusted for gender, age, cohort, family variables, depressed mood and socioeconomic status (see Table 4). Sensitivity analyses were conducted to assess any effects of relationships between missing data and class membership. The adjusted ORs for the mainly alcohol use and the polydrug use classes remained statistically significant and changed marginally to 1.38 and 2.24 respectively after missing school completion data were imputed based on class membership and variables that discriminated between excluded and included cases. This indicates the robustness of findings to missing data.
Table 4.
Model 1ˆ | 95% CIs | Model 2ˆ | 95% CIs | |
---|---|---|---|---|
Drug use class (Ref: Class 1 – no drug use) | ||||
Class 2 – Mainly alcohol use | 1.93*** | (1.42, 2.63) | 1.54*** | (1.17, 2.03) |
Class 3 - Polydrug use | 5.42*** | (3.31, 8.89) | 2.51*** | (1.45, 4.33) |
School variables | ||||
Peer’s drug use | 1.25** | (1.08, 1.43) | ||
Low school connectedness | 1.14 | (0.91, 1.43) | ||
Academic failure | 2.37*** | (1.93, 2.90) |
Notes.
Estimates for Models 1 and 2 were adjusted for gender, age, socioeconomic status, depressed mood, family conflict/attachment/management, and cohort (youngest/middle/oldest). Model 1 (the partially adjusted model) does not adjust for school variables (peer drug use, school connectedness and academc failure). In Model 1, the following controls were significant: gender, p < .001; age, p < .01; SES, p < .001; cohort, p < .01; family management, p < .05; depressed mood, p < .001. Model 2 is the fully adjusted model (including the above listed controls as well as the three school variables). In Model 2, the controls showed the same significance levels except for family management and depressed mood, which were nonsignificant.
p < .05,
p < .01,
p < .001.
In supplementary analyses, we used a more traditional “variable-centred” approach to examine whether the effect of polydrug use on school completion was primarily related to specific drugs within this class (i.e., alcohol, tobacco, cannabis use entered as independent variables in a 2×2×2 design, with prevalence (yes/no) used to maximize cell sizes) using logistic regression analyses. There were major statistical obstacles associated with this type of analysis applied to this data set. Cell sizes were heavily imbalanced (greater than 900 for 2 cells) and some cells had inadequate ns (1 or 2 participants for 2 cells, between 30 and 40 for 2 cells). This meant that modelling of the effects of individual drugs on school completion was likely to produce distorted and/or unreliable estimates. We therefore do not report these results.
DISCUSSION
A small but notable proportion of mid-adolescents (6.5%) reported concurrent and frequent use of alcohol, tobacco, and cannabis. Relative to nonusers and mainly alcohol users, polydrug users were at significantly greater odds of school non-completion. Compared to nonusers, those adolescents who mainly used alcohol (61.8% of the sample) also had higher odds of school non-completion. These relationships persisted after controlling for the effects of plausible confounding factors, including established correlates of substance use and school completion. Prior research has pointed to the prognostic importance of engagement with anticonventional subgroups, indicated by variables such as low school commitment, low academic achievement, peer drug use, and polydrug use. For the present sample, the results were only partially consistent with this mechanism. Low school commitment was not a predictor of school non-completion, and there was a large effect for polydrug use that was independent of academic achievement. The results suggested that peer drug use partially accounted for the association of polydrug use and school non-completion, but the effect for polydrug use remained statistically significant after accounting for peer drug use.
Despite a longitudinal design, causal inferences are precluded. It remains possible that early vulnerabilities such as child conduct problems, environmental, and/or genetic predispositions drive subsequent problems, including low school performance and polydrug use. The present study goes some way towards ruling out earlier-proposed environmental drivers such as family dysfunction and socio-economic disadvantage74 because these were controlled at Grade 9. Family variables that were controlled included relationship quality (conflict/closeness), and it remains possible that poor parental supervision/ monitoring may be important drivers of polydrug use and poor school performance29,75. Polydrug users may also be more likely than their peers to be subject to school disciplinary processes (such as suspension and expulsion) which may have long-term negative effects on school outcomes and peer networks63,76. Cannabis use was almost exclusively a characteristic of the polydrug use class, so it remains possible that cannabis use was the key agent in the effect for polydrug use. However, most polydrug users reported relatively low frequencies of cannabis use (1–2 times/month), and recent cross-sectional research has found that early cannabis use was not related to school non-completion74. For the present dataset, regression models examining specific drug effects were severely unbalanced and/or contained inadequate sizes for some drug combinations, so estimates of individual drug effects were considered to be unstable.
We raise some possible implications for prevention cautiously, given that causal directions cannot be established, and that effective prevention may not necessarily depend on addressing original drivers. There was a stepped increase in the risk of school non-completion for adolescents engaging mainly in alcohol use, and those engaging in polydrug use, relative to no drug use. If alcohol use and polydrug use increases the risk of school non-completion, universal prevention programs addressing alcohol and polydrug use may improve school outcomes77. While beyond the scope of these data, alcohol use may increase the probability that vulnerable students transit to polydrug use. Given that the majority of the sample were mainly alcohol users, and the likelihood that alcohol acts as a ‘gateway’ to other drug use in adolescent populations78, a universal prevention focus on alcohol use may be an important way of improving school completion rates, as well as limiting transitions to polydrug use where the risk of school non-completion is exacerbated. Targeted prevention programs for mid-adolescent polydrug users may also improve outcomes.
The study capitalizes on three cohorts from a large prospective study, and its ‘person-centred’ analytic method better accounts for the strong inter-relatedness of drug use patterns in adolescent subgroups than prior variable-centred approaches79. The study could not investigate factors occurring before or after age 14 that may account for the core findings, and the study is limited by its reliance on self-report.
CONCLUSION
Polydrug use in mid-adolescence longitudinally predicted school non-completion, and this effect was significant after accounting for known strong confounds. The results pointed to the importance of universal prevention programs for alcohol use and targeted interventions for polydrug use.
Acknowledgments
ABK had the primary role in manuscript writing. TJEW provided substantial contributions to the design and development of the manuscript. RS contributed to conceptualization and analysis. JWT, GCP, SAH guided the theoretical contribution and the analytic method, and were lead investigators on the study on which this manuscript is based. GCKC conducted the analysis and assisted with writing the results section. WDH had significant input into the manuscript draft. RFC provided critical review and feedback on the manuscript and was a chief investigator on the project on which the manuscript is based. ABK and GCKC had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. ABK and GCKC are affiliated with the Centre for Youth Substance Abuse Research, The University of Queensland. There are no potential conflicts of interest to declare.
The authors are grateful for the financial support of the National Institute on Drug Abuse (R01-DA012140-05) for the International Youth Development Study and the National Institute on Alcoholism and Alcohol Abuse (R01AA017188-01) for analysis of the alcohol data. Continued data collection in Victoria has been supported by funding from Australian Research Council (ARC) Discovery Projects (DPO663371, DPO877359, DP1095744) and the Australian National Health and Medical Research Council (NHMRC) (Project 594793). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute On Drug Abuse, National Institute on Alcoholism and Alcohol Abuse, the National Institutes of Health, ARC or NHMRC. Data analysis was supported by ARC Discovery Project DP130102015 to A. B. Kelly (chief investigator). Gary Chan is a postdoctoral researcher under the supervision of A. B. Kelly.
Footnotes
DECLARATION: The authors declare that the material has not been published in whole or in part elsewhere, the paper is not currently being considered for publication elsewhere, all authors have been personally and actively involved in substantive work leading to the report and will hold themselves jointly and individually responsible for its content, and all relevant ethical safeguards have been met in relation to patient or subject protection. The authors declare that there are no potential conflicts of interest in relation to this study.
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