Frequency of cannabis use and symptoms of anxiety and depression: a cross-sectional analysis of the Colorado cannabis users health cohort

Article type: Research Article

Keywords: Cannabis use, Anxiety, Depression, Urinary cannabinoids, Adults

Authors: Christine M. Steeger, Poojashree Tandukar, Karin F. Hoth, Mark Aloia, Fred Wamboldt, Peter Castaldi, Sunita Sharma, Nancy Lorenzon, Laura E. Crotty Alexander, Jost Klawitter, Cristina Sempio, Gregory L. Kinney, Meghan D. Althoff, Gina R. Kruse, Russell P. Bowler

Affiliations: https://ror.org/02ttsq026grid.266190.a0000 0000 9621 4564University of Colorado Boulder, Boulder, Colorado USA; https://ror.org/02gn3zg65grid.254551.20000 0001 2286 2232Colorado State University Pueblo, Aurora, Colorado USA; https://ror.org/036jqmy94grid.214572.70000 0004 1936 8294University of Iowa, Iowa Iowa City, USA; https://ror.org/016z2bp30grid.240341.00000 0004 0396 0728National Jewish Health, Denver, Colorado USA; https://ror.org/03vek6s52grid.38142.3c0000 0004 1936 754XChanning Laboratory of Network Medicine, Harvard University, Cambridge, Massachusetts USA; https://ror.org/04w7skc03grid.266239.a0000 0001 2165 7675University of Denver, Denver, Colorado USA; https://ror.org/0168r3w48grid.266100.30000 0001 2107 4242University of California San Diego and VA San Diego Healthcare System, San Diego, California USA; https://ror.org/02hh7en24grid.241116.10000 0001 0790 3411University of Colorado Denver, Denver, Colorado USA; https://ror.org/03xjacd83grid.239578.20000 0001 0675 4725Cleveland Clinic, Cleveland, Ohio USA

License: © The Author(s) 2025 CC BY 4.0 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/.

Article links: DOI: 10.1186/s42238-025-00327-2  |  PubMed: 41107903  |  PMC: PMC12535088

Relevance: Relevant: mentioned in keywords or abstract

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Background

Mild to moderate anxiety and depressive symptoms are common in adults, with annual prevalence of anxiety disorders affecting 19% and major depressive episode affecting 8% of adults in the U.S., respectively (NIMH, ref. 2017). Δ⁹-tetrahydrocannabinol (THC) has long been recognized as having potential anxiolytic effects, possibly directly through cannabinoid receptors (CB1R) or indirectly through benzodiazepine receptors (Berrendero and Maldonado ref. 2002; García-Gutiérrez and Manzanares ref. 2010; Witkin et al. ref. 2005). Though evidence is mixed, recent reviews and meta-analyses generally show positive associations between greater cannabis use and higher frequencies of mental health conditions, with chronic cannabis users reporting the highest levels of mood and anxiety disorders, and psychosis symptomology (Martinotti and Di Forti ref. 2025; Onaemo et al. ref. 2021; Polkosnik et al. ref. 2021; Sorkhou et al. ref. 2021, ref. 2024). Some studies show a dose-dependent relationship between cannabis use and mental health symptoms, with low doses of Δ⁹-THC producing anxiolytic effects and high doses producing anxiogenic responses (Petrilli et al. ref. 2022; Sorkhou et al. ref. 2021; Turna et al. ref. 2017). Further, in the current cannabis legalization environment, THC potency has increased substantially over the past two decades (e.g., average ranges of 20% to above 90% THC, depending on the cannabis form and U.S. state dispensary regulations) (Chandra et al. ref. 2019; Orens ref. 2018). Although THC can show anxiolytic effects at low doses in laboratory settings, more research is needed to understand its associations with mood and anxiety symptoms at the higher concentrations now common in cannabis products.

One of the major side effects of anxiety and depressive symptoms is disturbed sleep, particularly insomnia (Staner ref. 2003). Insomnia and difficulty sleeping are common reasons for cannabis use, as shown by decreases in over-the-counter sleep medication after introduction of dispensaries (Doremus et al. ref. 2019). Studies have documented subjective improvements in sleep with cannabis use, however research to date has not observed improvements in sleep architecture among those using and not using cannabis, including our own work (Althoff et al. ref. 2024; Lavender et al. ref. 2022; Pacek et al. ref. 2017; Velzeboer et al. ref. 2022). The relationship between anxiety and depression and sleep disturbance may be explained by chronic stress leading to activation of the corticosteroid axis, resulting in chronic alertness (Hirotsu et al. ref. 2015). Population studies suggest that anxiety disorders are present in roughly one quarter to one third of those with insomnia (Breslau et al. ref. 1996). Further complicating the sleep-mental health disorder interactions are the adverse effects of cannabis withdrawal on mood, which may potentiate continued cannabis use (Bonnet and Preuss ref. 2017). While legalization of medical and recreational cannabis has become more common, there are few studies examining the prevalence of anxiety and depression in those taking cannabis for sleep.

Cannabis is still a Schedule I drug in the U.S. (i.e., cannot be prescribed by physicians using a Drug Enforcement Administration [DEA] license), though it might become Schedule III and is more likely to be used outside of the medical establishment. Patients who use cannabis to treat medical disorders are more likely to seek homeopathic solutions to their medical problems and forsake U.S. Food and Drug Administration (FDA) approved medications (Wallis et al. ref. 2022). Moreover, there is evidence that the legalization of cannabis has resulted in a 10–15% reduction in prescriptions for anxiolytic and antidepressant medications in states that have legalized cannabis (Bradford and Bradford ref. 2016), despite the lack of clear evidence that recreational doses of THC have a beneficial impact on anxiety and depressive symptoms.

Purpose of study

While existing studies have linked greater self-reported cannabis use frequency to more severe mental health symptoms (e.g., Leadbeater et al. ref. 2019; Rup et al. ref. 2021; Steeger et al. ref. 2021), few have incorporated biological measures of THC to validate cannabis exposure or examined use of FDA-approved pharmacotherapy among individuals with elevated anxiety and depressive symptoms. To our knowledge, this is one of the first community-based studies to integrate multiple validated mental health scales, urinary THC biomarkers, and prescription medication data. This approach aims to clarify anxiety and depressive symptom burden among individuals who frequently self-administer cannabis, and how this cannabis use relates to use of pharmacotherapy for anxiety or depression. The findings will offer important insight into symptom burden and self-medication behavior, informing efforts to improve screening and treatment for adult cannabis users.

We conducted a secondary analysis of anxiety and depressive symptoms in a cohort of cannabis users and comparison participant non-users (controls) who were recruited for a study examining the impact of cannabis use on sleep. We hypothesized that participants who self-dosed cannabis frequently, as measured by self-report and urinary cannabinoids, will have more symptoms of anxiety and depression than those who infrequently self-dosed cannabis or cannabis users who have not used in the past 30 days. We further hypothesized that frequent cannabis users with high anxiety and depression scores would infrequently use traditional FDA-approved anxiolytic and antidepressant medications such as benzodiazepines, selective serotonin reuptake inhibitors (SSRIs), serotonin and norepinephrine inhibitors (SNRIs), tricyclic antidepressants (TCAs), monoamine oxidase inhibitors (MAOIs), etc.

Methods

Participants and procedures

The National Jewish Health Institutional Review Board approved this research. All participants consented to the study and were adults (aged 21–80 years) with less than 30 pack-year tobacco smoking history and were willing to complete a Home Sleep Test (HST). The age range was selected to encompass a broad adult demographic for comprehensive assessment. The exclusion of individuals with 30 pack-year or more of tobacco smoking history aimed to minimize the confounding effects of significant pulmonary comorbidities on sleep and other physiological measures relevant to the broader study aims, as this is a common criterion in respiratory and sleep research. Participants were recruited through local dispensaries, research bulletin boards, and word of mouth with flyers that included keywords such as cannabis and sleep.

Cases were defined as those who typically used cannabis > 3 days per week for at least one year and were further subdivided into infrequent (< 15 days in the past month) versus frequent (≥ 15 days in the past month). Further details on frequency cutoffs are described below in the measures section. Controls (non-cannabis users) were recruited from similar sources who had not used cannabis in the past 30 days.

Participants enrolled in the study completed two study visits and underwent a HST over an ~ 18-hour period, described elsewhere in a parent study (Althoff et al. ref. 2024). First, a baseline visit was conducted in the clinic in the evening. During this visit, participants completed questionnaires including demographic information and medical history, sleep quality, mental health, and cannabis use. They were also provided with sleep diaries and fitted for a HST (Althoff et al. ref. 2024). Participants completed one night of diary tracking and HST recording and returned for the second and final follow-up visit the next morning to provide a blood and urine sample. A total of 218 participants were enrolled in the study from 2016 to 2019; 23 participants were excluded from the analysis due to incomplete or missing data for cannabis use or missing anxiety or depression measures (Fig. 1). Thus, 195 participants were included for analysis.

Measures

Participants completed a medical history form regarding current and past medical conditions diagnosed by a medical provider (Supplemental Materials Table 1), substance use history, sleep quality (Pittsburgh Sleep Quality Index; PSQI; Buysse et al. ref. 1989), and current medication use (Supplemental Materials Table 2).

Self-reported cannabis use

The cannabis use questionnaire included a detailed history of recent cannabis use. Participants were categorized into three groups based on the number of days they used cannabis in the past 30 days: non-users (0 days), infrequent users (1–14 days), and frequent users (15 or more days). The frequency of cannabis use cutoff scores used in this study divided the distribution of past 30-day use in our sample (see Supplemental Materials Table 3 for frequency of use information) and aligns with published thresholds indicating semi-frequent (10–19 days/month) and frequent (≥ 20 days/month) use (Caulkins et al., ref. 2020; Lorenzetti et al., ref. 2021; Sofis et al., ref. 2020; Walsh et al., ref. 2025). Thus, our 15 day cutoff captures use patterns of individuals who use cannabis on most days, reflecting elevated exposure.

Quantitation of cannabis in urine

Urine and blood assay methods are described elsewhere and included a panel of 11 total cannabinoids (Althoff et al. ref. 2024; Klawitter et al. ref. 2017). 11-nor-Δ9-tetrahydrocannabinol-9-carboxylic acid glucuronide (THC-COOH-gluc) (Althoff et al. ref. 2024) is reported in the current study because most other cannabinoids, including cannabidiol (CBD), were below the limit of quantitation in most participants.

Self-reported anxiety and depressive symptoms

At enrollment, participants completed the 14-question Hospital Anxiety and Depression Scale (HADS), 21-question Beck Anxiety Inventory (BAI), and the 21-question Beck Depression Inventory-II (BDI-II). Moderate to severe (or clinically significant) anxiety and depression cutoffs for the HADS-Anxiety Subscale (HADS-A) and HADS-Depression Subscale (HADS-D) were both ≥ 8 (Bjelland et al. ref. 2002; Zigmond and Snaith ref. 1983). BDI-II cutoffs were: 0–13 minimal depression, 14–19 mild depression, 20–28 moderate depression, and 29–63 severe depression (Beck et al. ref. 1996). BAI cutoffs were: 0–7 minimal anxiety, 8–15 mild anxiety, 16–25 moderate anxiety, and 26–63 severe anxiety (Julian ref. 2011).

Statistical analysis

All analyses were performed in SAS 9.4 or R 3.6.1. ANOVA was used to assess differences in demographic variables across the three cannabis use groups. Proportions were compared using NPAR1WAY Chi-square test. Multivariable logistic regression was used to examine the associations between the frequency of cannabis use (days of cannabis use per month, continuous variable) and elevated anxiety and depressive symptoms (HADS-A ≥ 8, BAI ≥ 16, HADS-D ≥ 8 and BDI-II ≥ 20). Regression analyses adjusted for age (years), sex (male/female), education (bachelor’s or more/less than bachelor’s), sleep quality (PSQI score), and anxiolytic-hypnotic use or antidepressant use (any use/no use). Linear regression was used to assess the relationship between HADS-A, BAI, HADS-D, and BDI-II scores and urinary cannabinoids. Variance inflation factors (VIF) were checked for model multicollinearity, and values were not elevated (VIF > 5) (see Supplemental Materials Table 4).

Results

Participant characteristics and cannabis use group comparisons

Participant demographic and substance use characteristics are shown in Table 1. Non-users of cannabis were more likely to report as female, have a bachelor’s degree or higher, earn more money, and have never used tobacco cigarettes, but were otherwise similar in age, race, employment status, and alcohol use compared to current (frequent or infrequent) cannabis users. Frequent cannabis users were more likely to be unmarried and used cigarettes compared to non-users or infrequent cannabis users.

In current cannabis users, the reason for using cannabis at night was: to initiate sleep (78%) and/or to maintain sleep (48%). The major conditions that participants listed as the reason for taking cannabis at night were stress (57%), anxiety (52%), pain (46%), post-traumatic stress disorder (PTSD, 12%), and nightmares (9%). The prevalence of other medical conditions by cannabis frequency group were not significantly different among groups (Supplemental Materials Table 1).

Anxiety and depression

Elevated anxiety was more frequent in cannabis users measured using both the HADS (HADS-A ≥ 8: 33% among frequent users, 18% among infrequent users, and 8% among non-users; p = 0.002) and the BAI instruments (BAI score ≥ 16: 30% among frequent users, 14% among infrequent users, and 0% among non-users, p < 0.001; Table 2). Despite much higher report of anxiety symptoms among frequent cannabis users, there was no significant difference in the use of FDA-approved anxiolytic-hypnotics between groups (21% among frequent users, 18% among infrequent users, and 20% among non-users), p > 0.05 (Table 2). Multivariable logistic regression models indicated that frequent cannabis use (days per month) was associated with higher likelihood of elevated anxiety, AOR = 1.06 (95% CI 1.01, 1.12), p < 0.01 for the BAI and AOR = 1.05 (95% CI 1.01, 1.09), p < 0.05 for the HADS-A (Table 3).

Clinically-elevated symptoms of depression (HADS-D score ≥ 8) were not significantly different across groups (11% among frequent users, 5% among infrequent users, and 4% among non-users), p > 0.05. However, using the BDI-II, frequent cannabis users were more likely to have moderate or severe symptoms of depression compared to infrequent users or never users (BDI-II ≥ 20: 12% vs. 10% vs. 2%, p = 0.011) (Table 2). Among frequent cannabis users, there were more participants with moderate or severe anxiety symptoms (30%) than moderate or severe depressive symptoms (12%). There was not a significant difference in use of antidepressants among cannabis use types (11% among frequent users, 9% among infrequent users, and 14% among non-users), p > 0.05 (Table 2). Finally, in multivariable regression models, the frequency of cannabis use was not associated with elevated depressive symptoms for either the BDI-II, AOR = 0.98 (95% CI 0.92, 1.04) or HADS-D, AOR = 0.99 (95% CI 0.94, 1.05), ps > 0.05 (Table 3).

Urinary cannabinoids and anxiety and depressive symptoms

Although infrequent cannabis users had significantly less urinary cannabinoids compared to frequent users (1.46 ± 3.09 ng/ml versus 9.58 ± 26.2 ng/ml; p = 0.013; Supplemental Materials Fig. 1), there were no significant associations between urinary cannabinoids and the severity of anxiety symptoms or depressive symptoms, ps > 0.05 (Fig. 2).

Discussion

This study found that frequent cannabis use in the past month was associated with elevated symptoms of anxiety but not depression, even after adjusting for key covariates. Though anxiety scores were higher among frequent cannabis users, there was no significant difference in the use of anxiolytic-hypnotic medications among frequent users, infrequent users, and non-users, which suggests that frequent users are not using FDA-approved medications as a primary method to treat their anxiety. Contrary to expectation, we also found no relationship between urinary THC-COOH-gluc (i.e., the highest detectable cannabinoid in this sample) and either elevated anxiety or depressive symptoms, suggesting that participants may not be fully self-titrating with cannabis to attenuate symptoms. It is also likely that at high levels of anxiety and depression, cannabis use is ineffective in fully controlling symptoms (Feingold et al. ref. 2015). Although anxiety symptoms were higher in frequent cannabis users for both anxiety measures, there was a significant difference in BDI-II depression scores but not HADS-D scores. Additionally, the use of antidepressant medications was similar across groups.

Although the HADS-D did not indicate significant group differences in depression, the BDI-II found higher levels of moderate to severe depression for frequent cannabis users. This discrepancy may reflect differences in how the two depression measures assess symptoms. The BDI-II includes somatic symptoms (e.g., sleep disturbance, fatigue), which may be relevant to frequent users in this community-based sample, in addition to affective and cognitive symptoms.

Though it is difficult to speculate about the reasons for null findings, there are several possible explanations for why there could have been significant associations between cannabis use and anxiety symptoms but not depressive symptoms. Results may be due to differences in the acute self-medicating potential of cannabis for anxiety (particularly with CBD-dominant strains; Bidwell et al. ref. 2024; Kosiba et al. ref. 2019; Sharpe et al. ref. 2020). There is also some evidence for a stronger neurobiological overlap between cannabinoids and anxiety-related circuits (e.g., CB1R) (Lutz et al. ref. 2015) than depression pathways. Finally, in the current study, participants’ most prevalent reasons for cannabis use were for sleep, anxiety, stress, and pain reduction rather than depressive symptoms. Prospective studies and randomized controlled trials (RCTs) are needed to differentiate symptom-specific motivations and neurobiological pathways linking cannabis use and mental health (Hasbi et al. ref. 2023).

Anxiety disorders are among the most prevalent mental health conditions worldwide (Kessler et al. ref. 2010); yet nearly half of sufferers do not achieve complete relief with pharmacologic treatment (Bandelow et al. ref. 2008). Endocannabinoids such as anandamide (AEA), metabolizing enzymes such as fatty acid amide hydrolase (FAAH), and CB1R have all been shown experimentally to play an important role in anxiety (Patel et al. ref. 2017; Scherma et al. ref. 2018). CB1R is found extensively throughout the brain in regions such as the amygdala, hippocampus, and prefrontal cortex and are likely to mediate most of the anxiolytic effects of cannabinoids such as THC, although there is still uncertainty about the role other cannabinoids (such as CBD) play in these pathways (Patel et al. ref. 2017). Further evidence to support a role for cannabinoids in treating mental health includes a cross-over RCT of 10 participants in which the synthetic cannabinoid nabilone reduced PTSD-associated nightmares (Jetly et al. ref. 2015). Additionally, a meta-analysis of 14 clinical studies of anxiety disorders (including six RCTs) showed a -1.85 standardized mean difference in subjects who received cannabinoids without significant adverse effect (Bahji et al. ref. 2020). Thus, it is not surprising that cannabis is currently being used as a self-remedy by many participants.

The current study shows that frequent cannabis users had higher BAI and HADS-A scores than non-frequent users or non-users. This is consistent with recent reports indicating that individuals with anxiety disorders or depression who self-medicate with cannabis have a more severe course and worse symptoms (Bahorik et al. ref. 2017; Beletsky et al. ref. 2024; Wilkinson et al. ref. 2015). In our study, frequent cannabis use was still associated with elevated anxiety symptoms after controlling for confounders. One explanation may be self-titration, a concept supported by studies showing that use of cannabinoids can have anxiolytic effects at low doses but may provoke anxiety at higher doses (Turna et al. ref. 2017; Viveros et al. ref. 2005). However, we did not collect longitudinal measurements on changes in anxiety after cannabis use and cannot comment on the impact of cannabis on anxiety symptoms. Although cessation of cannabis was not part of this study, the short half-life of cannabinoids combined with self-medication behavior may lead cannabis users to rely on cannabis for short-term relief, unaware that frequent use could perpetuate a long-term usage because of anxiety induced by withdrawal.

A major challenge for cannabis research is assessing dose. To our knowledge, our study is among the first to include quantitative urinary cannabinoid measurements to objectively assess the relationship between dose and severity of anxiety and depressive symptoms. While there was a strong association between self-reported frequency of dosing and urinary cannabinoids, there was no association between urinary cannabinoids and severity of depression. This result confirms the lack of association between self-reported frequency of use and severity of depressive symptoms and suggests accuracy in self-reported use data for the current sample. Interestingly, while using cannabis more days per month was associated with elevated anxiety, the urinary cannabinoid levels were not associated with severity of anxiety scores, suggesting that daily use may be more important than high doses of cannabis.

Our observation of a low prevalence of anxiolytics in participants who have elevated levels of anxiety supports the idea that participants may be self-treating with cannabis instead of using FDA-approved medications, though we cannot exclude barriers to seeking medical care for anxiety and depression in medication differences between groups. Differences between the Bradford and Bradford (ref. 2016) study and the current study were primarily that the authors included only Medicare patients, who are older, and represent only 21% of medical cannabis users in Colorado (CDPHE, ref. 2020). Additionally, Bradford & Bradford did not account for the legalization of recreational cannabis use, which occurred in 2012 in Colorado. Furthermore, pain is by far the most reported therapeutic target of medical cannabis use and anxiety and depression are not listed as conditions for medical use in Colorado. The observed infrequent use of FDA-approved anxiolytic medications in participants with high anxiety scores who frequently use cannabis suggests potential for both medication substitution and self-management of symptoms.

The finding that frequent cannabis users with elevated anxiety and depression scores were not more likely to use FDA-approved treatments is consistent with prior evidence on self-medication and under-treatment in this population. Past research shows that individuals may substitute cannabis for anxiolytics or antidepressants (Corroon et al., ref. 2017; Kvamme et al., ref. 2021; Lucas & Walsh, ref. 2017), and many people with mood or anxiety symptoms are undertreated (Lamoureux-Lamarche, Berbiche, & Vasiliadis, ref. 2022; Weisberg et al., ref. 2014). The current study adds to the cannabis use and mental health literature by demonstrating this pattern using both validated anxiety and depressive symptom scales and biomarker-confirmed cannabis use.

Limitations and future directions

While this study is among the largest to investigate the relationship between anxiety and depression and biologic measurements of cannabinoids, there are several limitations. First, the study was cross-sectional, and we were not able investigate the relationship between cannabis use and mental health over time to determine whether frequent cannabis use causes future mood and anxiety symptoms, mood and anxiety symptoms lead to more frequent cannabis use, or whether associations are bidirectional. In an Australian cohort study of adolescents, daily cannabis use was associated with a higher prevalence of depression and anxiety six years later; however, anxiety or depression in adolescence were not associated with more frequent cannabis use over time (Patton et al. ref. 2002). The Patton et al. study contrasts results from the current research, which only includes adults. Mixed findings in this area underscore the need for prospective research to investigate the direction of associations between cannabis use and mental health symptoms, and how associations may vary across adolescent, young adult, and adult age groups (Gobbi et al. ref. 2019; Lowe et al. ref. 2024; Sorkhou et al. ref. 2021, ref. 2024).

Second, while the strongest determinant of urinary cannabinoids was frequency of use and not type of use, we were not statistically powered to assess whether method of cannabis use (e.g., smoking, vaping, edibles, dabbing, etc.) was associated with severity of anxiety and depression. Additionally, this community-based sample recruited for a study on sleep and cannabis use had complex patterns of use, including various methods of use, products, and dosage particularly for daily users, which made it difficult to determine predominant cannabis use methods and products. Third, the current study did not systematically assess cannabis potency (% THC and CBD concentration) or quantity, which are important considerations when examining frequency of use and mental health symptoms given the range of cannabis strains and products currently available in the legal market (Prince and Conner ref. 2019; Steeger et al. ref. 2021). Though some recent reviews on cannabis potency and mental health show that THC is the primary cannabinoid responsible for the health effects of cannabis use (Petrilli et al. ref. 2022), there is mixed evidence of the therapeutic role of CBD in reducing mental health symptoms (Khan et al. ref. 2020). Well-designed clinical trials and longitudinal research are needed to further understand how CBD and other cannabinoids may moderate the effects of THC on anxiety and depressive symptoms (Bhuller et al. ref. 2024; Bidwell et al. ref. 2024; Khan et al. ref. 2020).

Fourth, this study was not funded to quantitate nicotine in addition to THC. Future studies should examine whether tobacco smoking may be a confounding factor of associations among nicotine use, anxiety, and sleep disturbances. Fifth, this research was designed as an observational study of frequent users, primarily recruited from cannabis dispensaries, which can introduce selection bias including study participants who may not generalize to broader or clinical populations with diagnosed mental health conditions. Medical cannabis vs. recreational cannabis use status was not available for this sample and should be measured in future studies given some evidence of different cannabis use patterns for medically- vs. recreationally-motivated cannabis user types, including different product preferences and cannabinoid profiles (Sznitman ref. 2017; Turna et al. ref. 2020). However, in the current study, participants had zero to low detectable levels of CBD in biological specimens, which suggests that regardless of medical or recreational user status, this sample of cannabis users largely used THC-dominant products. Sixth, participants did not endorse depression as a common reason for cannabis use. Thus, the lack of association between frequent cannabis use and depression may be sample-specific. Finally, while we did not specifically recruit those with sleep disorders, the primary study objective of understanding cannabis and sleep using a HST may have led to increased participation among those with sleep problems, impacting generalizability of our findings.

Conclusions

We found that elevated anxiety is common in frequent cannabis users, but those with elevated anxiety were not more likely to be taking FDA-approved anxiolytic medications. These findings support the concept that cannabis users may be self-treating their anxiety with cannabis. Our findings suggest that anxiety symptom screening among adults who use cannabis may present opportunities to connect individuals with FDA-approved anxiolytic/hypnotic treatment. There is also a clear need for prospective studies and randomized trials to determine causal associations between cannabis use and anxiety or depressive symptoms, including any interactions between cannabis use and anxiolytics or antidepressants on mental health symptoms.

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