Suicide is one of the leading causes of death amongst adolescents and decades of research have failed to curb suicide rates within this population. There is thus a need to better understand factors that correlate with adolescent suicidal thoughts and behaviors (STBs). MDMA/ecstasy and classic psychedelics represent two areas for exploration, as use of these substances has been associated with both increased and lowered odds of STBs. Thus, the goal of this study was to test the associations between MDMA/ecstasy and classic psychedelics (psilocybin, peyote, mescaline, LSD) and STBs in a nationally representative sample of U.S. adolescents. We tested these associations in a sample of adolescents aged 12–17 years old from the National Survey on Drug Use and Health (2004–2019) (N = 262,617) using survey-weighted multivariable logistic regression models. Lifetime psilocybin use was associated with lowered odds of lifetime suicidal thinking, planning, and attempts (aOR range 0.77–0.85). Conversely, LSD was associated with increased odds of these same outcomes (aOR range 1.20–1.35). MDMA/ecstasy, peyote, and mescaline did not share associations with STBs. Our study demonstrates that individual classic psychedelics share varying relationships to STBs among adolescents. Future cross-sectional and longitudinal studies are needed to further elucidate the link between classic psychedelic use and STBs in youth.
Suicide is the second leading cause of death among adolescents, and suicide rates in this population continue to rise despite years of research and medical advances1,2. Even with a nearly exponential increase in the number of RCTs studying suicidal thoughts and behaviors (STBs) in the last decades, existing treatments have continued to have limited efficacy3,4. Moreover, given that current research has not yielded improvements in treatment efficacy nor reductions in STBs among adolescents, there is a need for a wider range of research on factors that correlate with adolescent STBs.
Classic psychedelics (e.g., psilocybin, LSD, peyote, mescaline) and MDMA (3,4-methylenedioxymethamphetamine; also known as “ecstasy”) represent two frontiers for further exploration as use of these substances may share significant associations with STBs and related mental health conditions in adolescents.
Classic psychedelics are a group of naturally-occurring or naturally-derived psychoactive compounds that act as agonists of the serotonin 2A receptor and can give rise to mystical experiences that can in some cases improve one’s perceived quality of life5,6. Conversely, these substances also can have negative consequences such as increased anxiety, paranoia, and significant distress associated with acute administration. Some of the most commonly used classic psychedelics are psilocybin (the psychoactive agent in more than 200 species of fungi), lysergic acid diethylamide (LSD; derived from the hydrolysis of an ergot fungus), peyote (a small cactus), and mescaline (the main psychoactive compound in peyote). MDMA, on the other hand, is a synthetic amphetamine derivative that releases serotonin and is known to increase feelings of empathy and social connection; conversely, this substance can also give rise to adverse states of panic, anxiety, and fear as well.
Researchers in the last decade have begun to explore the potential of classic psychedelics as a treatment for a multitude of mental disorders, many of which confer risk for STBs7,8. Recent research has shown that classic psychedelics, most namely psilocybin and LSD, can alleviate anxiety and depression (two of the main risk factors of suicide9,10). In a 2011 pilot experiment, researchers found that a single session of psilocybin-assisted psychotherapy led to sustained decreases in both anxiety and depression among subjects with advanced-stage cancer11. In 2016, these findings were extended in a study that found that improvements in anxiety, depression, quality of life, and optimism due to psilocybin-assisted psychotherapy; furthermore, these improvements continued to be clinically significant at a 6-month follow-up12. Similarly, a pilot study in 2014 found that LSD can reduce anxiety when administered in a supervised psychotherapeutic environment13. Recent research has also found classic psychedelics to help treat substance use disorders, which are another significant risk factor for suicide14,15,16.
Recent research has also looked at the potential for MDMA to treat PTSD, one of the strongest anxiety-related predictors of suicidal ideation17. MDMA-assisted psychotherapy in particular has been found to be not only safe, but also more effective than traditional therapy in patients with treatment-resistant PTSD18,19,20,21,22. It is important to note, however, that all of the aforementioned treatment studies on MDMA and classic psychedelics have been conducted using adult samples, underscoring the need for examining the link between these substances and suicidality in adolescents.
Population-based survey studies, while not causal in nature, have helped further establish externally valid links between classic psychedelics and MDMA and STBs; these studies also invite further inquiry into the associations between psychedelics and suicidality in adolescents. Analyzing data from the National Survey on Drug Use and Health (NSDUH), Hendricks et al. (2015a) found that lifetime classic psychedelic use was associated with reduced odds of past-year suicidal thinking, planning, and attempts in a sample of U.S. adults, while the lifetime use of other illicit drugs was associated with increased odds of these same outcomes23. A follow-up study by Hendricks et al. (2015b) extended the previous findings to psilocybin specifically and found that it is especially protective with regard to STBs24. Additionally, Sexton et al. (2020) found that lifetime classic tryptamine use (e.g. psilocybin and DMT, another classic psychedelic) was associated with decreased odds of psychological distress and suicidal thinking in a sample of U.S. adults as well25.
More recently, research by this team has extended previous work by analyzing data from the NSDUH spanning from 2008 to 2019 and found that lifetime MDMA use was associated with reduced odds of past-year suicidal thinking and planning while lifetime psilocybin use was associated with reduced odds of past month psychological distress and past year suicidal thinking in adults26. Importantly, this study also found that LSD was associated with increased odds of past-year suicidal thinking, indicating that in some cases classic psychedelics can confer increased risk for STBs.
Although previous research has established an association between classic psychedelics and MDMA and STBs, few studies have examined the effects of these substances, let alone their link with STBs, among adolescents. Given that classic psychedelic use among adolescents has been rising27 and MDMA is one of the most commonly used illicit substances by adolescents28, there is a need to assess the link between these substances and STBs in adolescents.
The aim of this paper is to test the associations between MDMA and four individual classic psychedelics (psilocybin, peyote, mescaline, and LSD) and STBs in adolescents in a nationally representative sample (NSDUH). More specifically, this paper aimed to compare the associations among these substances to those reported in Jones and Nock (2022a)26, which found MDMA/ecstasy and psilocybin to confer lowered odds of STBs and LSD to confer increased odds of STBs.
This study used data from the National Survey on Drug Use and Health (NSDUH; 2004–2019), an annual survey that collects information on substance use and mental health outcomes in a nationally representative sample of the U.S. population aged 12 years and older. We included adolescents aged 12–17 years old from the NSDUH in our analyses (N = 262,617). The study was exempt from review from the Harvard IRB as the NSDUH data are publicly available at the following web address (https://www.datafiles.samhsa.gov/). Furthermore, we carried out all methods in this project in accordance with the relevant guidelines and procedures.
In our study, lifetime use of MDMA/ecstasy and four commonly used classic psychedelics (psilocybin, peyote, mescaline, LSD) served as independent variables. These independent variables were selected as this study aimed to extend findings from Jones and Nock (2022a), which assessed the relationships of these substances to STBs in a sample of U.S. adults.
In line with Jones and Nock (2022a), our study included the following demographic factors and substance use variables as a priori covariates in our analyses: sex, age, income, race, education, self-reported engagement in risky behavior, and lifetime use of the following substances (cocaine, heroin, PCP, inhalants, pain relievers, tranquilizers, stimulants, sedatives, marijuana). Furthermore, these covariates also match those from numerous population-based psychedelic studies as well23,25,29,30,31,32,33,34.
We used three binary suicide-related variables (yes/no) as outcomes in our study: lifetime suicidal thinking, lifetime suicidal planning, and a lifetime suicide attempt. Our time horizons for the dependent variables in this study deviate from Jones and Nock (2022a), which examined the associations between psychedelic use and past year STB outcomes for adults; however, all adolescent suicidality variables in the NSDUH assess lifetime STBs, thus explaining our approach for the current study.
We used survey-weighted multivariable logistic regression to estimate the associations between our independent variables and our STB outcomes in this study. For all analyses, we used the ‘Survey’ package in R version 4.1.2 as this software allowed us to incorporate the complex design and survey-weighting from the NSDUH into our analyses.
The demographics of our sample are presented in Table 1, stratified by those who have versus have not tried classic psychedelics. Adolescents who have tried classic psychedelics were significantly more likely to fall into the following demographic categories: older, male, White, and more likely to engage in risky behavior. There were no significant differences in the income levels of those who had versus had not tried psychedelics.
The results of our main models testing the associations between MDMA/ecstasy and classic psychedelics and STBs are presented in Table 2, along with the frequency and prevalence of lifetime use for each substance. Psilocybin conferred significant lowered odds of all three outcome measures: lifetime suicidal thinking (aOR 0.85), planning (aOR 0.78), and attempt (aOR 0.77). On the other hand, LSD conferred increased odds of all three outcomes: lifetime suicidal thinking (aOR 1.20), planning (aOR 1.35), and attempt (aOR 1.23). MDMA/ecstasy, peyote, and mescaline did not share significant associations with any of these outcomes.
In Supplemental Table 1, we report the results from robustness analyses that assess whether our associations for psilocybin and LSD remain consistent while additionally controlling for a lifetime major depressive episode (MDE), a major risk factor for suicide. We reconducted our original survey-weighted multivariable logistic regression models while including all of our original independent variables and covariates but also added a lifetime MDE in all models as a covariate as well. When we controlled for a lifetime MDE, psilocybin no longer shared a significant association with lifetime suicidal thinking (aOR changed from 0.84 to 0.86). However, aside from this one difference, our pattern of results remained unchanged (i.e., psilocybin was significantly associated with lower odds of suicidal planning and attempt), demonstrating that our findings for psilocybin and LSD remain stable even when one accounts for a major contributing factor to suicidality.
This study tested the non-causal associations between four commonly used lifetime classic psychedelics (psilocybin, LSD, peyote, LSD) and MDMA with STBs in a large representative sample of U.S adolescents. This study was an extension of Jones and Nock (2022a), which tested the associations of the aforementioned substances to STBs in U.S. adults. Although MDMA/ecstasy was not associated with STBs in this study, lifetime use of psilocybin was associated with significantly lower odds of all three STB outcomes whereas LSD was associated with increased odds of all three outcomes. Importantly, this study yielded a similar pattern of results to Jones and Nock (2022a), which found lifetime psilocybin use to be associated with reduced odds of past month psychological distress and past year suicidal thinking, and LSD to be associated with increased odds of past-year suicidal thinking in adults.
The main limitation to this study is the findings cannot be used to establish a causal relationship between psychedelic use and STBs in adolescents. More specifically, this study cannot establish a causal relationship between psilocybin use and lowered odds of STBs nor between LSD use and increased odds STBs. Future longitudinal research will be needed to more rigorously assess the associations that these substances share with STBs in adolescents. Additionally, because we used binary lifetime use outcomes to measure substance use, we cannot establish the recency nor the frequency of psychedelic use in the study. Future studies that can employ more granular measures of substance use can shed further light on the associations between MDMA/ecstasy, classic psychedelics, and STBs in young people.
Relatedly, the operationalization of the variables in the NSDUH does not allow us to establish temporal precedence between psychedelic use and STBs as well. Since STB outcomes are also assessed as binary variables over participants’ lifetimes, we cannot establish that substance use occurred prior to the onset of STBs. Follow-up work that employs more granular assessments of STBs can support a greater understanding of the impact of psychedelics on STBs in adolescents as well. Next, although we conducted robustness analyses to control for MDEs in our analyses, it nevertheless remains possible that psilocybin lowers odds of STBs by way of alleviating harmful and severe mental health conditions that give rise to STBs. Future studies that can control for a wider range of mental disorders and can assess the clinical severity of participants can overcome this limitation.
Finally, multicollinearity—high levels of intercorrelation between independent variables in a given model—represents a possible limitation to our findings as well. Our models featured multiple psychedelic use variables (MDMA/ecstasy, psilocybin, peyote, mescaline, LSD) and demographic factors that are likely correlated with each other, meaning that multicollinearity was likely present in this study. However, the impact of multicollinearity on our results is likely minimal. The main effect of multicollinearity is to increase the standard errors within a given model, widening confidence intervals and making it less likely for statistical tests to reach significance; however, such an effect is mitigated in large sample sizes like the one included in this study35. Thus, although our independent variables may correlate with one another, one can remain confident in the observed findings, particularly given that they align with prior work in this research area26.
Given the association between LSD use and increased odds of STBs in our study, LSD and other classic psychedelics may have caused harm at the individual or group level within our sample. Additionally, since these associations follow a pattern of results from other populations based research on classic psychedelics26, future research should be aimed at better understanding the link between naturalistic psychedelic use and adverse outcomes in both adolescents and adults. The need to study the potential harm of psychedelics is especially relevant as these substances are increasingly explored as potential treatments within clinical research. Although future research is needed, there are known risks associated with psychedelic use that may lead to increased odds of STBs.
First, a risk associated with psychedelic use is that adolescent substance use is linked to the onset of substance use disorders, a key risk factor for suicide. For instance, epidemiological research has illustrated that individuals who start drinking at 11–12 years of age have nearly double the rate of problematic alcohol use than do individuals who begin drinking at age 2136. Generally, young people have higher rates of substance abuse than those who are older as well37. Hence, adolescent psychedelic users may be at increased risk for problematic use of these substances and ultimately may be at higher risk for STBs. Future research should examine whether earlier psychedelic use is associated with increased risk of substance use disorders and STBs.
Second, another risk associated with acute classic psychedelic use is a “bad trip” which is characterized by intense fear, anxiety, and/or paranoia while using these substances38. The distress experienced in “bad trips” may increase the odds of STBs given how anxiety and paranoia are both well-known risk factors for STBs9,39. Furthermore, adolescents might be less equipped to manage the distress engendered from bad trips, as research has demonstrated that younger individuals may be less successful at regulating their emotions40. Thus, adolescents may be at particular risk for STBs as a result of adverse psychedelic experiences. Additional investigations that explore the effects of ”bad trips” on adolescent mental health can facilitate greater understanding of our observed findings.
Psychedelic use is also reported to increase the risk of psychosis, although evidence on this link is equivocal38. Some historical studies have suggested that psychedelics engender an earlier onset of a psychotic break in individuals with premorbid mental illness41. Given that episodes of psychosis are a risk factor for STBs42, classic psychedelics could thereby also increase the odds of STBs in adolescents by increasing the risk of an early psychotic episode43.
Our study also presents non-causal associations between psilocybin and lowered odds of STBs in adolescents that builds on previous work by Jones and Nock (2022a) linking psilocybin use with reduced odds of past year suicidal thinking in adults. Several mechanisms may underlie our findings linking psilocybin use to lowered odds of STBs in adolescents, although the below mechanisms remain speculative.
Third variable factors
For one, psilocybin use could have been associated with lowered odds of STBs in our sample because of demographic differences between adolescents who have versus have not used psilocybin. Our analysis controlled for confounding demographic variables such as age, sex, race/ethnicity, and yearly household income, but it is plausible that demographic factors not measured in the data might have driven the association between psilocybin use and lowered odds of STBs. Future studies that examine the associations between demographics, LSD use, and STBs can shed light on these potential mechanisms.
Additionally, there may be pre-drug differences between individuals who have versus have not used classic psychedelics, as previous work has found personality differences between psychedelic-using and psychedelic-naive adults that could extend to adolescent populations. Erritzoe et al.44 found that psychedelic users score higher on openness ratings and Johnstad45 found that psychedelic users score higher on each of the Big Five personality traits except for extraversion (agreeableness, openness, conscientiousness, and neuroticism). Thus, future work should further examine pre-drug differences associated with those who have versus have not used psychedelics, as investigations such as these may further explain our observed associations between psychedelics and STBs.
Finally, there may be clinically-relevant third variable factors that also underlie these findings as well. For instance, there is robust evidence indicating that perceived social support from peers and school teachers is associated with STBs in adolescents, with greater support being linked to lowered odds of STBs46,47. If such differences exist within adolescent populations who have used psilocybin—such that adolescents who have used psilocybin spend more time with supportive peers or go to school in more supportive environments—these clinically relevant third variable factors may also underlie our observed findings. Better understanding the relationship between such factors and psilocybin use may further clarify the link between psilocybin and lowered odds of adolescent STBs.
There are potential pharmacological explanations for our observed findings, although these mechanisms remain purely speculative. For instance, psilocybin may lower odds of STBs via interacting with and downregulating serotoninergic 5-HT2A receptors48,49. Suicidal behavior has been linked to alterations in the serotonergic system50,51 and the activation of 5-HT2A receptors has been found to reduce markers of inflammation in adults that are linked to STBs and related mental health disorders52. Additionally, many mainline antidepressants and antipsychotics potentiate their effects through 5-HT2A receptors as well53,54. Thus, it is plausible that psilocybin could have lowered odds of STBs among our sample population through interactions with 5-HT2A receptors50,55. However, as none of the pharmacological mechanisms of psilocybin have been explored in adolescents, future pharmacological work is needed to better understand the link between psychedelic use and STBs in young people. These investigations can also further elucidate the mechanisms underlying any potential harm that may be associated with adolescent psychedelic use as well.
Although classic psychedelic use among adolescents has been rising, and more attention has been given to the therapeutic and clinical potential of classic psychedelics in adults, we still know very little about how these drugs affect adolescent mental health. Extending Jones and Nock’s (2022) study on adults, this study similarly found psilocybin to confer with lowered odds of STBs and LSD to confer increased odds of STBs. This study represents an important step forward to better understanding the relationship of psychedelic use to STBs in adolescents and highlights the importance of future cross-sectional, longitudinal, and clinical investigations within this research area.
The data from this project are publicly available at the Substance Abuse & Mental Health Data Archive (SAMHDA) at the following address: https://www.datafiles.samhsa.gov/.
Curtin, S (2020) State suicide rates among adolescents and young adults aged 10–24 : United States, 2000–2018. In: CDC. https://stacks.cdc.gov/view/cdc/93667. Accessed 5 Jan 2022.
Hawton, K., Saunders, K. E. & O’Connor, R. C. Self-harm and suicide in adolescents. Lancet 379, 2373–2382 (2012).
Fox, K. R. et al. Interventions for suicide and self-injury: A meta-analysis of randomized controlled trials across nearly 50 years of research. Psychol. Bull. 146, 1117–1145 (2020).
Kothgassner, O. D., Robinson, K., Goreis, A., Ougrin, D. & Plener, P. L. Does treatment method matter? A meta-analysis of the past 20 years of research on therapeutic interventions for self-harm and suicidal ideation in adolescents. Bord. Personal. Disord. Emot. Dysregul. 7, 9 (2020).
Griffiths, R. R., Richards, W. A., McCann, U. & Jesse, R. Psilocybin can occasion mystical-type experiences having substantial and sustained personal meaning and spiritual significance. Psychopharmacology 187, 268–283 (2006).
Johnson, M. W., Hendricks, P. S., Barrett, F. S. & Griffiths, R. R. Classic psychedelics: An integrative review of epidemiology, therapeutics, mystical experience, and brain network function. Pharmacol. Ther. 197, 83–102 (2019).
Müller, F., Johnson, M. W. & Borgwardt, S. Editorial: Hallucinogens and entactogens: Establishing a new class of psychotherapeutic drugs?. Front. Psychiatry 11, 497 (2020).
Nutt, D. et al. Effects of schedule I drug laws on neuroscience research and treatment innovation. Nat. Rev. Neurosci. 14, 577–585. https://doi.org/10.1038/nrn3530 (2013).
Gaynes, B. N. et al. Screening for suicide risk in adults: A summary of the evidence for the U.S. preventive services task force. Ann. Intern. Med. 140, 822–835 (2004).
Hirschfeld, R. M. A. & Russell, J. M. Assessment and treatment of suicidal patients. N. Engl. J. Med. 337, 910–915 (1997).
Grob, C. S. et al. Pilot study of psilocybin treatment for anxiety in patients with advanced-stage cancer. Arch. Gen. Psychiatry 68, 71–78 (2011).
Griffiths, R. R. et al. Psilocybin produces substantial and sustained decreases in depression and anxiety in patients with life-threatening cancer: A randomized double-blind trial. J. Psychopharmacol. 30, 1181–1197 (2016).
Gasser, P. et al. Safety and efficacy of lysergic acid diethylamide-assisted psychotherapy for anxiety associated with life-threatening diseases. J. Nerv. Ment. Dis. 202, 513–520 (2014).
Bohnert, K. M., Ilgen, M. A., Louzon, S., McCarthy, J. F. & Katz, I. R. Substance use disorders and the risk of suicide mortality among men and women in the U.S. Veterans health administration. Addiction 112, 1193–1201 (2017).
Bogenschutz, M. P. et al. Psilocybin-assisted treatment for alcohol dependence: A proof-of-concept study. J. Psychopharmacol. Oxf. Engl. 29, 289–299 (2015).
Johnson, M. W., Garcia-Romeu, A., Cosimano, M. P. & Griffiths, R. R. Pilot study of the 5-HT2AR agonist psilocybin in the treatment of tobacco addiction. J. Psychopharmacol. Oxf. Engl. 28, 983–992 (2014).
Bentley, K. H. et al. Anxiety and its disorders as risk factors for suicidal thoughts and behaviors: A meta-analytic review. Clin. Psychol. Rev. 43, 30–46 (2016).
Mitchell, J. M. et al. MDMA-assisted therapy for severe PTSD: A randomized, double-blind, placebo-controlled phase 3 study. Nat. Med. 27, 1025–1033 (2021).
Ot’alora, G. M. et al. 3,4-Methylenedioxymethamphetamine-assisted psychotherapy for treatment of chronic posttraumatic stress disorder: A randomized phase 2 controlled trial. J. Psychopharmacol. 32, 1295–1307 (2018).
Mithoefer, M. C., Wagner, M. T., Mithoefer, A. T., Jerome, L. & Doblin, R. The safety and efficacy of ±3, 4-methylenedioxymethamphetamine-assisted psychotherapy in subjects with chronic, treatment-resistant posttraumatic stress disorder: The first randomized controlled pilot study. J. Psychopharmacol. 25, 439–452 (2011).
Mithoefer, M. C. et al. Durability of improvement in post-traumatic stress disorder symptoms and absence of harmful effects or drug dependency after 3,4-methylenedioxymethamphetamine-assisted psychotherapy: A prospective long-term follow-up study. J. Psychopharmacol. 27, 28–39 (2013).
Mithoefer, M. C. et al. MDMA-assisted psychotherapy for treatment of PTSD: Study design and rationale for phase 3 trials based on pooled analysis of six phase 2 randomized controlled trials. Psychopharmacology 236, 2735–2745 (2019).
Hendricks, P. S., Thorne, C. B., Clark, C. B., Coombs, D. W. & Johnson, M. W. Classic psychedelic use is associated with reduced psychological distress and suicidality in the United States adult population. J. Psychopharmacol. 29, 280–288 (2015).
Hendricks, P. S., Johnson, M. W. & Griffiths, R. R. Psilocybin, psychological distress, and suicidality. J. Psychopharmacol. 29, 1041–1043 (2015).
Sexton, J. D., Nichols, C. D. & Hendricks, P. S. Population survey data informing the therapeutic potential of classic and novel phenethylamine, tryptamine, and lysergamide psychedelics. Front. Psychiatry 10, 896 (2020).
Jones, G. M. & Nock, M. K. MDMA/ecstasy use and psilocybin use are associated with lowered odds of psychological distress and suicidal thoughts in a sample of US adults. J. Psychopharmacol. Oxf. Engl. 36, 46–56 (2022).
Miech, R. A. et al. Monitoring the Future National Survey Results on Drug Use, 1975–2019 Vol. I (Institute for Social Research, 2020).
Bates, M. L. S. & Trujillo, K. A. Use and abuse of dissociative and psychedelic drugs in adolescence. Pharmacol. Biochem. Behav. 203, 173129 (2021).
Hendricks, P. et al. The relationships of classic psychedelic use with criminal behavior in the United States adult population. J. Psychopharmacol. 32, 026988111773568 (2017).
Jones, G., Lipson, J. & Nock, M. K. Associations between classic psychedelics and nicotine dependence in a nationally representative sample. Sci. Rep. 12, 10578 (2022).
Jones, G., Ricard, J. A., Lipson, J. & Nock, M. K. Associations between classic psychedelics and opioid use disorder in a nationally-representative U.S. adult sample. Sci. Rep. 12, 4099 (2022).
Jones, G. M. & Nock, M. K. Lifetime use of MDMA/ecstasy and psilocybin is associated with reduced odds of major depressive episodes. J. Psychopharmacol. Oxf. Engl. 36, 57–65 (2022).
Jones, G. M. & Nock, M. K. Psilocybin use is associated with lowered odds of crime arrests in U.S. adults: A replication and extension. J. Psychopharmacol. Oxf. Engl. 36, 66–73 (2022).
Jones, G. M. & Nock, M. K. Exploring protective associations between the use of classic psychedelics and cocaine use disorder: A population-based survey study. Sci. Rep. 12, 2574 (2022).
Gujarati, D. N. Basic Econometrics 4th edn. (McGraw Hill, 2003).
Winters, K. C. & Lee, C.-Y.S. Likelihood of developing an alcohol and cannabis use disorder during youth: Association with recent use and age. Drug Alcohol Depend 92, 239–247 (2008).
Grant, B. F. et al. The 12-month prevalence and trends in DSM-IV alcohol abuse and dependence: United States, 1991–1992 and 2001–2002. Drug Alcohol Depend. 74, 223–234 (2004).
Johnson, M. W., Richards, W. A. & Griffiths, R. R. Human hallucinogen research: Guidelines for safety. J. Psychopharmacol. Oxf. Engl. 22, 603–620 (2008).
Carrillo de Albornoz, C. M., Gutierrez, B., Ibanez-Casas, I. & Cervilla, J. A. Paranoia and suicidality: A cross sectional study in the general population. Arch Suicide Res. 0, 1–13 (2021).
Silvers, J. A. et al. Age-related differences in emotional reactivity, regulation, and rejection sensitivity in adolescence. Emotion Washington DC 12, 1235–1247 (2012).
Strassman, R. J. Adverse reactions to psychedelic drugs. A review of the literature. J. Nerv. Ment. Dis. 172, 577–595 (1984).
Girgis, R. R. The neurobiology of suicide in psychosis: A systematic review. J. Psychopharmacol. Oxf. Engl. 34, 811–819 (2020).
Pompili, M. et al. Suicide risk in first episode psychosis: A selective review of the current literature. Schizophr. Res. 129, 1–11 (2011).
Erritzoe, D. et al. Recreational use of psychedelics is associated with elevated personality trait openness: Exploration of associations with brain serotonin markers. J. Psychopharmacol. Oxf. Engl. 33, 1068–1075 (2019).
Johnstad, P. G. The psychedelic personality: Personality structure and associations in a sample of psychedelics users. J. Psychoact. Drugs 53, 97–103 (2021).
Miller, A. B., Esposito-Smythers, C. & Leichtweis, R. N. Role of social support in adolescent suicidal ideation and suicide attempts. J. Adolesc. Health 56, 286–292 (2015).
Forster, M., Grigsby, T. J., Gower, A. L., Mehus, C. J. & McMorris, B. J. The role of social support in the association between childhood adversity and adolescent self-injury and suicide: Findings from a statewide sample of high school students. J. Youth Adolesc. 49, 1195–1208 (2020).
Ling, S. et al. Molecular mechanisms of psilocybin and implications for the treatment of depression. CNS Drugs 36, 17–30 (2022).
Vollenweider, F. X. The neurobiology of psychedelic drugs: Implications for the treatment of mood disorders. Nat. Rev. Neurosci. 11, 642–651 (2010).
Sudol, K. & Mann, J. J. Biomarkers of suicide attempt behavior: Towards a biological model of risk. Curr. Psychiatry Rep. 19, 31 (2017).
Underwood, M. D. et al. Serotonin receptors and suicide, major depression, alcohol use disorder and reported early life adversity. Transl. Psychiatry 8, 1–15 (2018).
Flanagan, T. W. & Nichols, C. D. Psychedelics as anti-inflammatory agents. Int. Rev. Psychiatry Abingdon Engl. 30, 363–375 (2018).
Feighner, J. P. Mechanism of action of antidepressant medications. J. Clin. Psychiatry 60(Suppl 4), 4–11 (1999).
Schmidt, C. J., Sorensen, S. M., Kenne, J. H., Carr, A. A. & Palfreyman, M. G. The role of 5-HT2A receptors in antipsychotic activity. Life Sci. 56, 2209–2222 (1995).
Lengvenyte, A., Conejero, I., Courtet, P. & Olie, E. Biological bases of suicidal behaviours: A narrative review. Eur. J. Neurosci. https://doi.org/10.1111/ejn.14635 (2019).
Dr. Nock receives publication royalties from Macmillan, Pearson, and UpToDate. He has been a paid consultant in the past year for Microsoft Corporation, the Veterans Health Administration, Cerebral, and for legal cases regarding deaths by suicide. He is an unpaid scientific advisor for Empatica, Koko, and TalkLife.
The authors declare no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Jones, G., Arias, D. & Nock, M. Associations between MDMA/ecstasy, classic psychedelics, and suicidal thoughts and behaviors in a sample of U.S. adolescents. Sci Rep 12, 21927 (2022). https://doi.org/10.1038/s41598-022-25658-5
This article is cited by
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.