The Impact of Marijuana on Antidepressant Treatment in Adolescents: Clinical and Pharmacologic Considerations
Division of Child and Adolescent Psychiatry, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA; strawnjr@mail.uc.edu
Department of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45219, USA
Division of Clinical Pharmacology, Cincinnati Children’s Hospital Medical Center, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA; laura.ramsey@cchmc.org
Division of Biomedical Informatics, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA; poweleen@mail.uc.edu (E.A.P.); mayur.Sarangdhar@cchmc.org (M.S.)
Division of Research in Patient Services, Cincinnati Children’s Hospital Medical Center, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA
Department of Biomedical Informatics, College of Medicine, University of Cincinnati, Cincinnati, OH 45219, USA
Cancer and Blood Diseases Institute, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229, USA
Abstract
The neuropharmacology of marijuana, including its effects on selective serotonin reuptake inhibitor (SSRI)/antidepressant metabolism and the subsequent response and tolerability in youth, has received limited attention. We sought to (1) review clinically relevant pharmacokinetic (PK) and pharmacodynamic (PD) interactions between cannabinoids and selected SSRIs, (2) use PK models to examine the impact of cannabinoids on SSRI exposure (area under curve (AUC)) and maximum concentration (CMAX) in adolescents, and (3) examine the frequency of adverse events reported when SSRIs and cannabinoids are used concomitantly. Cannabinoid metabolism, interactions with SSRIs, impact on relevant PK/PD pathways and known drug–drug interactions were reviewed. Then, the impact of tetrahydrocannabinol (THC) and cannabidiol (CBD) on exposure (AUC24) and CMAX for escitalopram and sertraline was modeled using pediatric PK data. Using data from the Food and Drug Administration Adverse Events Reporting System (FAERS), the relationship between CBD and CYP2C19-metabolized SSRIs and side effects was examined. Cannabis and CBD inhibit cytochrome activity, alter serotonergic transmission, and modulate SSRI response. In PK models, CBD and/or THC increases sertraline and es/citalopram concentrations in adolescents, and coadministration of CBD and CYP2C19-metabolized SSRIs increases the risk of cough, diarrhea, dizziness, and fatigue. Given the significant SSRI–cannabinoid interactions, clinicians should discuss THC and CBD use in youth prescribed SSRIs and be aware of the impact of initiating, stopping, or decreasing cannabinoid use as this may significantly affect es/citalopram and sertraline exposure.
Untitled section
Keywords: selective serotonin reuptake inhibitors, marijuana, CYP2C19, drug–drug interaction, adverse reactions
Article notes
Untitled section
Received 2021 Jun 4; Accepted 2021 Jun 24; Collection date 2021 Jul.
1. Introduction
Anxiety and depressive disorders, the most common mental health conditions in children and adolescents [1], are frequently treated with selective serotonin reuptake inhibitors (SSRIs) [2,3,4]. However, treatment response varies considerably [5,6,7,8] and is often difficult to predict [9]. The considerable variation in SSRI response in adolescents with depressive and anxiety disorders is complex and is related to multiple factors, including comorbidity, pharmacogenetics, and substance use [10,11,12].
Youth with depression are twice as likely to report cannabis use and use amongst depressed teens has increased more rapidly over the past 15 years compared to their peers [13]. Further, an estimated one in three twelfth graders (17–18 years old) used marijuana in the past year and 6% of these adolescents used marijuana on a daily basis. Similarly, among eighth and tenth graders, daily use increased since 2018, with 1.3% of eighth graders (an 85.7% increase in 13–14-year-olds) and 4.8% of tenth graders (a 41.2% increase in 15–16-year-olds) reporting daily use (NIDA, NIH, NHHS).
Cannabinoids and several SSRIs are hepatically metabolized by CYP2C19 and CYP2D6. CYP2D6, and CYP2C19 metabolize many neuropsychiatric medications. CYP2D6 has over 100 known allelic variants and over 20 of these polymorphisms impact function. Broadly, these alleles are classified as normal function, decreased function, and no function [14]. As each individual patient inherits two alleles, phenotypes depend on the combination of inherited alleles. Four metabolic phenotypes have been predicted for CYP2D6: ultrarapid metabolizers inheriting duplications of functional alleles (1–20% of patients), normal (extensive) metabolizers inheriting at least one normal function allele (19–63%), intermediate metabolizers inheriting at least one decreased function or no function allele (14–72%), and poor metabolizers (0–6%) inheriting only no function alleles. Fluoxetine, fluvoxamine, and paroxetine are metabolized by CYP2D6 [15].
CYP2C19 is highly polymorphic, with over 30 identified allelic variants. These can be grouped in broad functional groups. There are five predicted phenotypes for CYP2C19: ultrarapid metabolizers carrying two increased function alleles (0–5% of patients), rapid metabolizers carrying an increased function allele paired with a normal function allele (1–27% of patients), normal (extensive) metabolizers carrying two normal function alleles (9–47%), intermediate metabolizers carrying one normal or increased function allele together with one decreased or no function allele (24–47%), and poor metabolizers carrying two decreased or no function alleles (2–46%). Citalopram, escitalopram, and sertraline are metabolized primarily by CYP2C19 [14,15,16] (Figure 1).
The predicted phenotypes are the focus of functional studies, which evaluate the impact of allelic variation on SSRI pharmacokinetics and clinical outcomes, including efficacy and tolerability. For example, we previously demonstrated that CYP2C19 metabolizer status impacts the outcomes with escitalopram/citalopram in youth with anxiety and depressive disorders [17,18]. Slower metabolizers were more likely to discontinue treatment compared to normal metabolizers, and were more likely to experience significant side effects, including weight gain and activation.
For citalopram and escitalopram, the Clinical Pharmacogenetics Implementation Consortium (CPIC) recommends that clinicians treating CYP2C19 rapid and ultrarapid metabolizers consider alternative medications that are not significantly metabolized by CYP2C19 [15]. For sertraline, the difference in CYP2C19 ultrarapid metabolizers appears to be less pronounced, so no dose adjustment is recommended [15]. In CYP2C19 poor metabolizers, CPIC recommends a dose reduction of 50% for citalopram, escitalopram, and sertraline because elevated medication concentrations have been observed (e.g., citalopram/escitalopram) or more side effects have been reported (e.g., sertraline). These recommendations are based on data from adults, but pediatric data are increasingly reported [17,19,20,21] and will be assessed in the update of the CPIC SSRI guideline, expected to be published in late 2021 or early 2022.
Variation in SSRI response may also relate to differences in SSRI exposure (e.g., blood concentration) among adolescents [12,22]. Importantly, marijuana use may also influence the pharmacology of SSRIs, including their pharmacokinetic profile. The pharmacology of cannabinoids may accentuate this variation in response in adolescents with these disorders. However, the neuropharmacology of marijuana use; interactions between marijuana and serotonergic transmission; and the effects of marijuana on an SSRI metabolism, response, and tolerability have received limited attention in the current literature. With this in mind, we sought to (1) describe the impact of marijuana on SSRI treatment in children and adolescents, (2) characterize and examine the effect of marijuana on enzymes that metabolize SSRIs with regard to variation in SSRI response in adolescents, and (3) examine the frequency of adverse events reported when SSRIs and cannabinoids are used concomitantly. Hereafter, we focus primarily on es/citalopram and sertraline as (1) these SSRIs are primarily metabolized by CYP2C19, (2) CPIC has issued genotype-specific dosing guidelines for these medications, and (3) CBD appears to have a greater interaction with CYP2C19 than CYP2D6.
2. Pharmacokinetic Interactions
2.1. Cannabis and Cannabidiol Impact Cytochrome Activity
Although cannabis contains hundreds of individual chemicals, we focus on cannabinoids in this review. The most abundant phytocannabinoids in cannabis are Δ9-tetrahydrocannabinol (THC) [23] and CBD [24,25]. Cannabinoids are metabolized in the liver predominantly by CYP2C9 and CYP3A4 [26], although CYP2D6 and CYP2C19 are also involved [27]. In addition to being metabolized by these enzymes, THC and CBD inhibit CYP2D6 [28] (Food and Drug Administration (FDA) Epidiolex, FDA news alert) and CYP2C19 [29] (FDA Epidiolex, FDA news alert, Sativex regulatory) in vitro (Table 1), as summarized in Zendulka, Dovrtelova [30]. Based on in vitro experiments and the estimated plasma drug levels, CBD was predicted to induce strong drug interactions with CYP2C19 and moderate interactions with CYP2D6 [31]. However, THC, taken orally or inhaled, was not predicted to induce drug interactions with CYP2C19 or CYP2D6 [31]. CBD also inhibits CYP2C19 in vivo [32,33,34]. Taken together, these data suggest that medications with a CYP2C19-dependent metabolism are likely to be susceptible to drug–drug interactions with cannabinoids [35].
| IC50µ (µM) 1 | ||
|---|---|---|
| CBD | THC | |
| CYP2C19 | 0.30 ± 0.03 | 0.57 ± 0.22 |
| CYP2D6 | 0.95 ± 0.50 | 1.28 ± 0.25 |
| CYP3A4 | 0.38 ± 0.11 | 1.30 ± 0.34 |
2.2. Cannabis and Cannabidiol Potentially Interact with SSRIs
To date, no studies have examined the impact of marijuana use on SSRI efficacy or tolerability in adolescents. However, extrapolating from in vivo studies of the impact of cannabidiols on medications metabolized in a manner similar to SSRIs can provide guidance. Clobazam, which is metabolized primarily by CYP3A4 and CYP2C19, is slowly metabolized in CYP2C19 poor metabolizers, leading to accumulation of the active metabolite n-clobazam and increased side effects [36]. Coadministering clobazam and CBD increases plasma clobazam concentrations by about 60% and increases n-clobazam concentrations five-fold [37]. Similarly, CBD also increases the concentrations of stiripentol, another antiepileptic medication metabolized by CYP2C19 [38].
2.3. Pharmacokinetics of Cannabinoids
One significant challenge to studying the drug–drug interaction between marijuana and SSRIs is the difficulty in estimating marijuana exposure. As marijuana is composed of numerous cannabinoids, which vary in their concentration, including cannabis strain differences, isolation of specific cannabinoids, such as those found in over-the-counter products such as CBD oil [39], to medicinal preparations of synthetic cannabinoids, such as dronabinol. Of relevance to pharmacokinetic effects of cannabinoids and SSRIs, the method of preparation and the administration route significantly impact cannabinoid pharmacokinetics, as do frequency and the amount of use (summarized in Grotenhermen [40]). For example, oral THC bioavailability ranges from 5–20% and its absorption is delayed by 1–3 h as it is slowly absorbed by the gastrointestinal tract. Further, oral THC absorption is also influenced by sex, weight, and the presence of food [41]. By contrast, the pharmacokinetics of inhaled THC are more variable, with up to 50% of inhaled smoke exhaled and some localized pulmonary metabolism. This results in a bioavailability of 10–25%, faster absorption (generally within minutes) [42], and inhaled THC exhibits first-order kinetics [43].
2.4. Preliminary Models Of SSRI–Cannabinoid Pharmacokinetic Interactions
We determined that the total body clearance of SSRIs may be reduced based on a recently reported pharmacokinetic interaction risk between oral THC or low-dose CBD and cytochrome enzymes [31]. Therefore, using previously estimated pharmacokinetic parameters and standard dosing regimens for an adolescent CYP2C19 normal metabolizer [12], we estimated the influence of concurrent THC or low-dose CBD (5–15 mg/day) use with escitalopram or sertraline (Figure 2).
In the pharmacokinetic model, the half-life of escitalopram with concurrent THC or low-dose over-the-counter CBD increased from 21.3 to 28.3 h. For escitalopram-treated adolescents receiving 20 mg/day, concurrent THC or low-dose over-the-counter CBD use increased the AUC and CMAX by 35% (34.1 vs. 46.1 days ng/mL) and 25% (45.3 vs. 56.9 ng/mL), respectively (Table 2). Similarly, in the pharmacokinetic model for sertraline, concurrent THC or low-dose over-the-counter CBD increased the half-life of sertraline from 22.1 to 29.5 h. For sertraline-treated adolescents receiving 150 mg/day, concurrent THC or low-dose over-the-counter CBD use increased the AUC and CMAX by 33% (54.2 vs. 72.1 days ng/mL) and 26% (66.0 vs. 83.2 ng/mL), respectively (Table 3). For both models, concurrent THC or low-dose CBD increased the time required for a patient to achieve a steady state.
| THC or Low-Dose CBD 1 | ||
|---|---|---|
| − | + | |
| t1/2 (h) | 21.3 | 28.3 |
| AUC24, 10 mg q.d. (days ng/mL) | 17.1 | 23.1 |
| Cmax, 10 mg q.d. (ng/mL) | 22.7 | 28.4 |
| AUC24, 20 mg q.d. (days ng/mL) | 34.1 | 46.1 |
| Cmax, 20 mg q.d. (ng/mL) | 45.4 | 56.9 |
| THC or Low-Dose CBD | ||
|---|---|---|
| − | + | |
| t1/2 (h) | 22.1 | 29.5 |
| AUC24, 50 mg q.d. (days ng/mL) | 18.0 | 23.7 |
| Cmax, 50 mg q.d. (ng/mL) | 21.9 | 27.4 |
| AUC24, 100 mg q.d. (days ng/mL) | 36.1 | 47.9 |
| Cmax, 100 mg q.d. (ng/mL) | 44.0 | 55.3 |
| AUC24, 150 mg q.d. (days ng/mL) | 54.2 | 72.1 |
| Cmax, 150 mg q.d. (ng/mL) | 66.0 | 83.2 |
| AUC24, 200mg q.d. (days ng/mL) | 72.3 | 98.45 |
| Cmax, 200 mg q.d. (ng/mL) | 88.0 | 111.7 |
We estimated the effects of concurrent THC or low-dose CBD use with sertraline or escitalopram using MwPharm (version 3.82, Mediware, Czech Republic [44]). MwPharm is a pharmacokinetic modeling program that enables users to approximate a patient’s clearance, volume of distribution, exposure, and concentration of individual medications (e.g., sertraline and escitalopram) based on previously published parameters. Model parameters of a medication are entered into the program, in addition to patient characteristics, including age, body size, sex, and medication/dosing history. Considering patient and medication information, the program simulates a time course of medication plasma concentrations for a patient, in addition to their estimated effects. For the escitalopram model, total body clearance was 25 L/h/70 kg, V1 was 12 L/kg lean body mass, and Ka was 0.8 h−1. For the sertraline model, total body clearance was 152 L/h/70 kg, V1 was 76 L/kg lean body mass, and Ka was 0.8 h−1. The effect of THC or low-dose CBD use was estimated based on recent clinical data [31] suggesting a reduction in escitalopram or sertraline clearance by 25% (to 18.75 and 114 L/h/70 kg, respectively). The area under the concentration–time curve (AUC) and the maximal concentration (CMAX) [45] were estimated from the final dose of each titration during steady state. Additional details of the pharmacokinetic modeling approach and specific pharmacokinetic parameters have been described (Strawn, Poweleit [12]).
2.5. Case Illustration of SSRI-Cannabinoid Pharmacokinetic Interactions
To illustrate the potential clinical impact of concurrent SSRI and cannabinoid use, we present the following.
A 15-year-old adolescent who met the DSM-5 criteria for generalized anxiety disorder with panic attacks and recurrent, moderate major depressive disorder was treated with escitalopram 5 mg beginning from the age of 15 years 8 months. She had no relevant past medical history, no history of trauma, and was not treated with any other CYP2C19-metabolized medications. Her depressive and anxiety symptoms were in remission while treated with escitalopram 10 mg each morning for 3 months, and titrated up to 15 mg/day when anxiety worsened, including increasing panic attacks. Unbeknownst to her clinician or parents, she began consuming CBD/THC in edible form. As CBD/THC use continued, her anxiety symptoms worsened, her panic attacks became more intense and more frequent, and her depressive symptoms intensified. Escitalopram was titrated to 20 mg each morning, with some initial improvement, but her anxiety symptoms recrudesced. Following disclosure of the CBD/THC use to her parents and clinician, CBD/THC use stopped. Nausea, abdominal pain, and headaches were also reported at this time. A time course of the patient’s treatment, clinical outcome scores, and simulated escitalopram levels is illustrated in Figure 3. Using the same escitalopram plasma drug level simulation strategy as described above and shown in Figure 2, we simulated the change in escitalopram plasma concentrations in this patient with concurrent CBD/THC use. The side effects reported at the first visit following disclosure of CBD/THC use may relate to the modeled elevation in escitalopram exposure.
2.6. Real-World Cannabinoid and SSRI Interactions
The increased use of cannabinoids both recreationally and in clinical practice leads to a greater chance for coadministration with SSRIs and possible adverse events. Foster et al. [47] examined the U.S. Food and Drug Administration (FDA)’s Adverse Event Reporting System (FAERS) and found a significant number of adverse event reports involving marijuana or a derivative thereof, suggesting that there is a risk of marijuana–drug interaction. Reports have increased over time compared to other drug–supplement interactions, possibly correlating with the increased availability of marijuana-derived products, including both prescription and OTC THC- and CBD-derived medical and recreational products. Data on direct clinical interactions are slowly emerging as evidenced by a recent case report of a cannabis hyperemesis syndrome that may have occurred at least in part due to concurrent SSRI use [48].
2.7. Data Mining of Large-Scale Clinical Effects and Hypothesis Generation Using U.S. Food and Drug Administration’s Adverse Event Reporting System (FAERS) Data
Adverse events data reported to FAERS and normalized within AERSMine [49] were used to identify differential rates of side effects typically associated with antidepressants. We analyzed ~15 million patient reports from the FDA for use of CYPC219-metabolized medications (sertraline, escitalopram, and citalopram, n = 427,932), cannabinoids (tetrahydrocannabinol, cannabidiol, and cannabinoids, n = 7008), and their combination (n = 421). The three mutually exclusive cohorts were analyzed for their frequencies of side effects. Side-effect frequencies in the CYP2C19 medication cohort were used as a baseline for comparison to the cannabinoid and combination cohorts. Drug label data were extracted from Lexicomp [50] and 23 side effects with >5% frequency on the sertraline or escitalopram label were used for benchmarking our comparative analysis. Standard pharmacovigilance metrics, relative risks, and safety signals [51,52], were used to identify drug and drug combination side effect associations. The Benjamini, Hochberg, and Yekutieli test [53] was used for false discovery rate (FDR) correction using a significance threshold of 0.05.
2.8. Combination Of CYP2C19-Metabolized Medications and Cannabinoids Presents Elevated Risk of Antidepressant-Related Side Effects
To understand the relative safety profile of sertraline and es/citalopram in combination with cannabinoids, we analyzed 23 side effects with >5% frequency on sertraline or es/citalopram labels. Comparative analysis of these 23 side effects in the FAERS data revealed that patients on a combination of CYP2C19-metabolized medications and cannabinoids showed a disproportionately higher risk of certain side effects. Compared to patients taking sertraline or es/citalopram alone, patients in the combination group presented a 4.97-fold increase in cough, 3.33-fold higher rate of diarrhea, 3.29-fold higher rate of fatigue, 2.87-fold increase in dizziness, and 2.54-fold increase in influenza (FDR correction at 0.05, Figure 4). Conversely, weight gain was not common in patients in the combination group, 0.24% vs. 2.53% in the sertraline or es/citalopram group (p < 0.005, Figure 4, See Supplementary Table S1 for side effect frequencies in the FAERS data).
3. Pharmacodynamic Interactions
In addition to the potential impact of cannabinoids on SSRI pharmacokinetics, studies also examined the impact of cannabinoids on serotonin pharmacodynamics. In preclinical studies, mice administered a CB1 antagonist together with an SSRI showed improved performance on a behavioral test compared to either agent alone, and at lower doses [54]. In another pre-clinical study, administration of citalopram together with a CB1 antagonist increased 5-HT release in both the prefrontal cortex and locus cereulus of awake rats [55]. However, neither study examined the impact of concurrent medications on cytochrome metabolism, so it is unclear if these results are due to direct action at CB1 or changes in medication exposure due to hepatic drug–drug interactions.
There is also a direct link between 5-HT signaling and the endocannabinoid system (Figure 5). Long-term cannabinoid administration alters the 5-HT receptor signaling, upregulating 5-HT2A activity and down-regulating 5-HT1A activity [56]. In addition, CB agonists upregulate the 5-HT2A receptor signaling [57]. This interaction appears to be bidirectional; serotonin-mediated 5-HT2 receptor activation increases endocannabinoid release and CB1 receptor activation [58]. Regarding exogenous cannabinoids, THC is an agonist at CB1 receptors, which may result in increased appetite, decreased working memory, and the euphoria associated with intoxication, whereas THC also agonizes CB2 [59] and 5-HT3, potentially conferring antiemetic properties (summarized in Pertwee [60]).
4. Discussion
Marijuana use is common in adolescents and its recreational and medicinal use has increased contemporaneously. The FDA has approved one cannabis-derived drug and three FDA-approved synthetic cannabis-related drugs. Further, OTC CBD products are increasingly marketed as treatments for anxiety and depression. As SSRIs are frequently prescribed in adolescents [61], we must better understand potential SSRI–cannabinoid interactions. Although there are limited studies of direct SSRI–cannabinoid interactions, accumulating data suggest the potential for PK and PD interactions.
As THC and CBD inhibit CYP2C19, and to a lesser degree CYP2D6, SSRIs metabolized by CYP2C19, including sertraline and es/citalopram, have a high likelihood of drug–drug interactions. This would be most likely observed in individuals with a poor metabolizer phenotype, who would already be likely to have increased drug concentrations (compared to normal metabolizers).
With the utility of cannabinoids as antiepileptic drugs, including recent FDA approval of the first cannabinoid-derived drug, Epidiolex® (cannabidiol), drug–drug interactions between cannabinoids and other antiepileptic drugs metabolized by cytochrome enzymes have been described. Drug–drug interactions between cannabinoids and two substrates of CYP2C19, stiripentol and clobazam, have been described, supporting the possibility that cannabinoids affect other CYP2C19 substrates, including sertraline and es/citalopram [62]. Herein, we focused on SSRIs metabolized primarily by CYP2C19. Thus, our conclusions may not generalize across SSRIs. The increased side effects from concurrent cannabinoid and SSRIs we identified were all amongst the most common identified in the FDA package insert, and may relate to SSRI dose or plasma concentrations [63].
Our model predicts a clinically significant increase in plasma drug concentration variation with concurrent use of marijuana or low-dose CBD and SSRIs. This increase in plasma concentration would be magnified if high-dose CBD and SSRIs were concomitantly prescribed. As increased SSRI plasma concentration is associated with increased activation [64], the implications include a decrease in tolerability secondary to activation. Because medication-related side effects and clinical symptoms of disease can overlap and monitoring SSRI plasma drug levels is uncommon in clinical practice, the correlation between drug levels and side effects is poorly understood. Multiple trials found that common SSRI side effects increase as the SSRI dose is increased [63]. However, as the psychological effects of cannabinoids include euphoria and relaxation [65], activation may be masked with active concurrent use. Interestingly, given the prolonged half-life of cannabinoids, cannabis cessation, especially in the short term, may lead to worsened symptoms, potentially unmasking any underlying activation as cannabis-induced pharmacokinetic changes are likely to linger compared to the immediate psychological effects, which will return to baseline relatively quickly. Alternatively, as SSRI plasma concentration decreases following cannabis cessation, efficacy would also likely decrease. Considering the delayed release of 5-HT following CB1 stimulation, serotonergic pharmacodynamics are likely to be disrupted, decreasing drug efficacy.
Although the existing literature suggests a direct interaction between cannabinoids and SSRIs, direct studies are lacking. Studies examining SSRIs coadministered with cannabinoids (either CBD or recreational marijuana) and tolerability/efficacy are needed. In addition, it will be vital to measure SSRI plasma concentrations to better characterize the potential drug–drug interactions.
5. Conclusions
Accumulating data suggest that CBD and THC affect concentrations of CYP2C19-metabolized SSRIs, including es/citalopram and sertraline. Using cannabidiol and or THC likely increases sertraline and es/citalopram concentrations in adolescents and may increase the risk of concentration-related SSRI side effects. Clinicians should consider inquiring as to the frequency and amount of THC and CBD use. Further, in sertraline- or es/citalopram-treated patients, stopping or decreasing marijuana or CBD use may decrease concentrations of sertraline or es/citalopram in stably treated patients.
Acknowledgments
Figures were created with Biorender.com.
Supplementary Materials
The following are available online at https://www.mdpi.com/article/10.3390/jpm11070615/s1, Table S1: Side effect frequencies in FAERS data.
Funding
This research was funded by Eunice Kennedy Shriver National Institute of Child Health and Human Development, grant numbers R01HD099775 (J.R.S. and L.B.R.) and R01HD098757 (J.R.S.)
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Adverse event data were obtained from the FDA Adverse Event Reporting System (https://fis.fda.gov/sense/app/d10be6bb-494e-4cd2-82e4-0135608ddc13/sheet/7a47a261-d58b-4203-a8aa-6d3021737452/state/analysis accessed on 14 March 2021).
Conflicts of Interest
Strawn has received research support from NIH (National Institute of Mental Health/National Institute of Environmental Health Sciences/NICHD), Allergan, Otsuka, and Neuronetics. He has received material support from and provided consultation to Myriad Genetics and has received royalties from the publication of two texts (Springer). He has served as an author for UpToDate, an Associate Editor for Current Psychiatry, and has received honoraria from CMEology and Neuroscience Educational Institute. He has provided consultation to the Food and Drug Administration. Ramsey has received research support from NIH (NICHD). She has received an educational grant and provided consultation to BTG Specialty Pharmaceuticals. The remaining authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
Footnotes
Footnote Group
References
Untitled section
References
- 1.Merikangas K.R., He J.-P., Burstein M., Swanson S.A., Avenevoli S., Cui L., Benjet C., Georgiades K., Swendsen J. Lifetime Prevalence of Mental Disorders in U.S. Adolescents: Results from the National Comorbidity Survey Replication—Adolescent Supplement (NCS-A) J. Am. Acad. Child. Adolesc. Psychiatry. 2010;49:980–989. doi: 10.1016/j.jaac.2010.05.017.
- 2.Strawn J.R., Lu L., Peris T.S., Levine A., Walkup J.T. Research Review: Pediatric anxiety disorders—What have we learnt in the last 10 years? J. Child. Psychol. Psychiatry. 2021;62:114–139. doi: 10.1111/jcpp.13262.
- 3.Mohatt J., Bennett S.M., Walkup J.T. Treatment of Separation, Generalized, and Social Anxiety Disorders in Youths. Am. J. Psychiatry. 2014;171:741–748. doi: 10.1176/appi.ajp.2014.13101337.
- 4.Wehry A.M., Beesdo-Baum K., Hennelly M.M., Connolly S.D., Strawn J.R. Assessment and Treatment of Anxiety Disorders in Children and Adolescents. Curr. Psychiatry Rep. 2015;17:1–11. doi: 10.1007/s11920-015-0591-z.
- 5.Brent D., Emslie G., Clarke G., Wagner K.D., Asarnow J.R., Keller M., Vitiello B., Ritz L., Iyengar S., Abebe K., et al. Switching to Another Ssri or to Venlafaxine with or without Cognitive Behavioral Therapy for Adolescents with Ssri-Resistant Depression: The Tordia Randomized Controlled Trial. JAMA. 2008;299:901–913. doi: 10.1001/jama.299.8.901.
- 6.March J.S., Vitiello B. Clinical Messages From the Treatment for Adolescents With Depression Study (TADS) Am. J. Psychiatry. 2009;166:1118–1123. doi: 10.1176/appi.ajp.2009.08101606.
- 7.Suresh V., Mills J.A., Croarkin P.E., Strawn J.R. What next? A Bayesian hierarchical modeling re-examination of treatments for adolescents with selective serotonin reuptake inhibitor-resistant depression. Depress. Anxiety. 2020;37:926–934. doi: 10.1002/da.23064.
- 8.Walkup J.T., Albano A.M., Piacentini J., Birmaher B., Compton S.N., Sherrill J.T., Ginsburg G.S., Rynn M.A., McCracken J., Waslick B., et al. Cognitive Behavioral Therapy, Sertraline, or a Combination in Childhood Anxiety. N. Engl. J. Med. 2008;359:2753–2766. doi: 10.1056/NEJMoa0804633.
- 9.Curry J., Rohde P., Simons A., Silva S., Vitiello B., Kratochvil C., Reinecke M., Feeny N., Wells K., Pathak S., et al. Predictors and Moderators of Acute Outcome in the Treatment for Adolescents With Depression Study (TADS) J. Am. Acad. Child. Adolesc. Psychiatry. 2006;45:1427–1439. doi: 10.1097/01.chi.0000240838.78984.e2.
- 10.Asselmann E., Wittchen H.-U., Lieb R., Beesdo-Baum K. Sociodemographic, clinical, and functional long-term outcomes in adolescents and young adults with mental disorders. Acta Psychiatr. Scand. 2017;137:6–17. doi: 10.1111/acps.12792.
- 11.Kaminer Y., Connor D.F., Curry J.F. Comorbid Adolescent Substance Use and Major Depressive Disorders: A Review. Psychiatry. 2007;4:32–43.
- 12.Strawn J.R., Poweleit E.A., Ramsey L.B. CYP2C19-Guided Escitalopram and Sertraline Dosing in Pediatric Patients: A Pharmacokinetic Modeling Study. J. Child. Adolesc. Psychopharmacol. 2019;29:340–347. doi: 10.1089/cap.2018.0160.
- 13.Weinberger A.H., Zhu J., Lee J., Anastasiou E., Copeland J., Goodwin R.D. Cannabis use among youth in the United States, 2004–2016: Faster rate of increase among youth with depression. Drug Alcohol Depend. 2020;209:107894. doi: 10.1016/j.drugalcdep.2020.107894.
- 14.Caudle K.E., Dunnenberger H.M., Freimuth R., Peterson J.F., Burlison J.D., Whirl-Carrillo M., Scott S.A., Rehm H.L., Williams M.S., Klein T.E., et al. Standardizing terms for clinical pharmacogenetic test results: Consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC) Genet. Med. 2017;19:215–223. doi: 10.1038/gim.2016.87.
- 15.Hicks J.K., Bishop J.R., Sangkuhl K., Müller D.J., Ji Y., Leckband S.G., Leeder J.S., Graham R.L., Chiulli D.L., Llerena A., et al. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline forCYP2D6andCYP2C19Genotypes and Dosing of Selective Serotonin Reuptake Inhibitors. Clin. Pharmacol. Ther. 2015;98:127–134. doi: 10.1002/cpt.147.
- 16.Strom C.M., Goos D., Crossley B., Zhang K., Buller-Burkle A., Jarvis M., Quan F., Peng M., Sun W. Testing for Variants in Cyp2c19: Population Frequencies and Testing Experience in a Clinical Laboratory. Genet. Med. 2012;14:95–100. doi: 10.1038/gim.0b013e3182329870.
- 17.Aldrich S.L., Poweleit E.A., Prows C.A., Martin L.J., Strawn J.R., Ramsey L.B. Influence of CYP2C19 Metabolizer Status on Escitalopram/Citalopram Tolerability and Response in Youth With Anxiety and Depressive Disorders. Front. Pharmacol. 2019;10:99. doi: 10.3389/fphar.2019.00099.
- 18.Strawn J.R., Mills J.A., Schroeder H., Mossman S.A., Varney S.T., Ramsey L.B., Poweleit E.A., Desta Z., Cecil K., DelBello M.P. Escitalopram in Adolescents with Generalized Anxiety Disorder: A Double-Blind, Randomized, Placebo-Controlled Study. J. Clin. Psychiatry. 2020;81 doi: 10.4088/JCP.20m13396.
- 19.Poweleit E.A., Aldrich S.L., Martin L.J., Hahn D., Strawn J.R., Ramsey L.B. Pharmacogenetics of Sertraline Tolerability and Response in Pediatric Anxiety and Depressive Disorders. J. Child. Adolesc. Psychopharmacol. 2019;29:348–361. doi: 10.1089/cap.2019.0017.
- 20.Strawn J.R., Mills J.A., Sauley B.A., Welge J.A. The Impact of Antidepressant Dose and Class on Treatment Response in Pediatric Anxiety Disorders: A Meta-Analysis. J. Am. Acad. Child. Adolesc. Psychiatry. 2018;57:235–244. doi: 10.1016/j.jaac.2018.01.015.
- 21.Rossow K.M., Aka I.T., Maxwell-Horn A.C., Roden D.M., Van Driest S.L. Pharmacogenetics to Predict Adverse Events Associated With Antidepressants. Pediatrics. 2020;146:e20200957. doi: 10.1542/peds.2020-0957.
- 22.Sakolsky D.J., Perel J.M., Emslie G.J., Clarke G.N., Wagner K.D., Vitiello B., Keller M.B., Birmaher B., Asarnow J.R., Ryan N.D., et al. Antidepressant Exposure as a Predictor of Clinical Outcomes in the Treatment of Resistant Depression in Adolescents (TORDIA) Study. J. Clin. Psychopharmacol. 2011;31:92–97. doi: 10.1097/JCP.0b013e318204b117.
- 23.Howlett A.C. The cannabinoid receptors. Prostaglandins Other Lipid Mediat. 2002;68:619–631. doi: 10.1016/S0090-6980(02)00060-6.
- 24.ElSohly M.A., Radwan M.M., Gul W., Chandra S., Galal A. Phytochemistry of Cannabis Sativa L. Prog. Chem. Org. Nat. Prod. 2017;103:1–36. doi: 10.1007/978-3-319-45541-9_1.
- 25.Fischedick J., Van Der Kooy F., Verpoorte R. Cannabinoid Receptor 1 Binding Activity and Quantitative Analysis of Cannabis sativa L. Smoke and Vapor. Chem. Pharm. Bull. 2010;58:201–207. doi: 10.1248/cpb.58.201.
- 26.Watanabe K., Yamaori S., Funahashi T., Kimura T., Yamamoto I. Cytochrome P450 enzymes involved in the metabolism of tetrahydrocannabinols and cannabinol by human hepatic microsomes. Life Sci. 2007;80:1415–1419. doi: 10.1016/j.lfs.2006.12.032.
- 27.Jiang R., Yamaori S., Takeda S., Yamamoto I., Watanabe K. Identification of cytochrome P450 enzymes responsible for metabolism of cannabidiol by human liver microsomes. Life Sci. 2011;89:165–170. doi: 10.1016/j.lfs.2011.05.018.
- 28.Yamaori S., Maeda C., Yamamoto I., Watanabe K. Differential inhibition of human cytochrome P450 2A6 and 2B6 by major phytocannabinoids. Forensic Toxicol. 2011;29:117–124. doi: 10.1007/s11419-011-0112-7.
- 29.Jiang R., Yamaori S., Okamoto Y., Yamamoto I., Watanabe K. Cannabidiol Is a Potent Inhibitor of the Catalytic Activity of Cytochrome P450 2C19. Drug Metab. Pharmacokinet. 2013;28:332–338. doi: 10.2133/dmpk.DMPK-12-RG-129.
- 30.Zendulka O., Dovrtělová G., Nosková K., Turjap M., Šulcová A., Hanuš L., Juřica J. Cannabinoids and Cytochrome P450 Interactions. Curr. Drug Metab. 2016;17:206–226. doi: 10.2174/1389200217666151210142051.
- 31.Bansal S., Maharao N., Paine M.F., Unadkat J.D. Predicting the Potential for Cannabinoids to Precipitate Pharmacokinetic Drug Interactions via Reversible Inhibition or Inactivation of Major Cytochromes P450. Drug Metab. Dispos. 2020;48:1008–1017. doi: 10.1124/dmd.120.000073.
- 32.Giraud C., Tran A., Rey E., Vincent J., Tréluyer J.-M., Pons G. In vitro characterization of clobazam metabolism by recombinant cytochrome P450 enzymes: Importance of CYP2C19. Drug Metab. Dispos. 2004;32:1279–1286. doi: 10.1124/dmd.32.11.1279.
- 33.Contin M., Sangiorgi S., Riva R., Parmeggiani A., Albani F., Baruzzi A. Evidence of Polymorphic CYP2C19 Involvement in the Human Metabolism of N-Desmethylclobazam. Ther. Drug Monit. 2002;24:737–741. doi: 10.1097/00007691-200212000-00009.
- 34.Kosaki K., Tamura K., Sato R., Samejima H., Tanigawara Y., Takahashi T. A Major Influence of Cyp2c19 Genotype on the Steady-State Concentration of N-Desmethylclobazam. Brain Dev. 2004;26:530–534. doi: 10.1016/j.braindev.2004.02.010.
- 35.Qian Y., Gurley B.J., Markowitz J.S. The Potential for Pharmacokinetic Interactions Between Cannabis Products and Conventional Medications. J. Clin. Psychopharmacol. 2019;39:462–471. doi: 10.1097/JCP.0000000000001089.
- 36.Seo T., Nagata R., Ishitsu T., Murata T., Takaishi C., Hori M., Nakagawa K. Impact ofCYP2C19polymorphisms on the efficacy of clobazam therapy. Pharmacogenomics. 2008;9:527–537. doi: 10.2217/14622416.9.5.527.
- 37.Geffrey A.L., Pollack S.F., Bruno P.L., Thiele E.A. Drug-drug interaction between clobazam and cannabidiol in children with refractory epilepsy. Epilepsia. 2015;56:1246–1251. doi: 10.1111/epi.13060.
- 38.Patsalos P.N., Szaflarski J.P., Gidal B., VanLandingham K., Critchley D., Morrison G. Clinical implications of trials investigating drug-drug interactions between cannabidiol and enzyme inducers or inhibitors or common antiseizure drugs. Epilepsia. 2020;61:1854–1868. doi: 10.1111/epi.16674.
- 39.Al Maruf A., Greenslade A., Arnold P.D., Bousman C. Antidepressant pharmacogenetics in children and young adults: A systematic review. J. Affect. Disord. 2019;254:98–108. doi: 10.1016/j.jad.2019.05.025.
- 40.Grotenhermen F. Pharmacokinetics and Pharmacodynamics of Cannabinoids. Clin. Pharmacokinet. 2003;42:327–360. doi: 10.2165/00003088-200342040-00003.
- 41.Agurell S., Halldin M., Lindgren J.E., Ohlsson A., Widman M., Gillespie H., Hollister L. Pharmacokinetics and metabolism of delta 1-tetrahydrocannabinol and other cannabinoids with emphasis on man. Pharmacol. Rev. 1986;38:21–43.
- 42.Strougo A., Zuurman L., Roy C., Pinquier J., Van Gerven J., Cohen A., Schoemaker R. Modelling of the concentration—Effect relationship of THC on central nervous system parameters and heart rate—Insight into its mechanisms of action and a tool for clinical research and development of cannabinoids. J. Psychopharmacol. 2008;22:717–726. doi: 10.1177/0269881108089870.
- 43.Sempio C., Huestis M.A., Mikulich-Gilbertson S.K., Klawitter J., Christians U., Henthorn T.K. Population Pharmacokinetic Modeling of Plasma Delta9-Tetrahydrocannabinol and an Active and Inactive Metabolite Following Controlled Smoked Cannabis Administration. Br. J. Clin. Pharmacol. 2020;86:611–619. doi: 10.1111/bcp.14170.
- 44.Proost J.H., Meijer D.K. MW/Pharm, an integrated software package for drug dosage regimen calculation and therapeutic drug monitoring. Comput. Biol. Med. 1992;22:155–163. doi: 10.1016/0010-4825(92)90011-B.
- 45.Morrison G., Crockett J., Blakey G., Sommerville K. A Phase 1, Open-Label, Pharmacokinetic Trial to Investigate Possible Drug-Drug Interactions Between Clobazam, Stiripentol, or Valproate and Cannabidiol in Healthy Subjects. Clin. Pharmacol. Drug Dev. 2019;8:1009–1031. doi: 10.1002/cpdd.665.
- 46.Hiemke C., Bergemann N., Clement H.W., Conca A., Deckert J., Domschke K., Eckermann G., Egberts K., Gerlach M., Greiner C., et al. Consensus Guidelines for Therapeutic Drug Monitoring in Neuropsychopharmacology: Update 2017. Pharmacopsychiatry. 2018;51:9–62. doi: 10.1055/s-0043-116492.
- 47.Foster B.C., Abramovici H., Harris C.S. Cannabis and Cannabinoids: Kinetics and Interactions. Am. J. Med. 2019;132:1266–1270. doi: 10.1016/j.amjmed.2019.05.017.
- 48.Iacopetti C.L., Packer C.D. Cannabinoid Hyperemesis Syndrome: A Case Report and Review of Pathophysiology. Clin. Med. Res. 2014;12:65–67. doi: 10.3121/cmr.2013.1179.
- 49.Sarangdhar M., Tabar S., Schmidt C., Kushwaha A., Shah K., Dahlquist J.E., Jegga A.G., Aronow B.J. Data mining differential clinical outcomes associated with drug regimens using adverse event reporting data. Nat. Biotechnol. 2016;34:697–700. doi: 10.1038/nbt.3623.
- 50.Lexicomp Online . Lexi-Drugs. Lexi-Comp, Inc.; Hudson, OH, USA: 2016. [(accessed on 8 April 2021)]. Available online: http://webstore.lexi.com/ONLINE.
- 51.Norén G.N., Hopstadius J., Bate A. Shrinkage observed-to-expected ratios for robust and transparent large-scale pattern discovery. Stat. Methods Med. Res. 2011;22:57–69. doi: 10.1177/0962280211403604.
- 52.Norén G.N., Sundberg R., Bate A., Edwards I.R. A statistical methodology for drug–drug interaction surveillance. Stat. Med. 2008;27:3057–3070. doi: 10.1002/sim.3247.
- 53.Benjamini Y., Yekutieli D. The control of the false discovery rate in multiple testing under dependency. Ann. Stat. 2001;29:1165–1188. doi: 10.1214/aos/1013699998.
- 54.Takahashi E., Katayama M., Niimi K., Itakura C. Additive subthreshold dose effects of cannabinoid CB1 receptor antagonist and selective serotonin reuptake inhibitor in antidepressant behavioral tests. Eur. J. Pharmacol. 2008;589:149–156. doi: 10.1016/j.ejphar.2008.05.020.
- 55.Ortega J.E., Gonzalez-Lira V., Horrillo I., Herrera-Marschitz M., Callado L.F., Meana J.J. Additive effect of rimonabant and citalopram on extracellular serotonin levels monitored with in vivo microdialysis in rat brain. Eur. J. Pharmacol. 2013;709:13–19. doi: 10.1016/j.ejphar.2013.03.043.
- 56.Hill M.N., Sun J.C., Tse M.T.L., Gorzalka B.B. Altered responsiveness of serotonin receptor subtypes following long-term cannabinoid treatment. Int. J. Neuropsychopharmacol. 2005;9:277–286. doi: 10.1017/S1461145705005651.
- 57.Franklin J.M., Carrasco G.A. Cannabinoid Receptor Agonists Upregulate and Enhance Serotonin 2a (5-Ht(2a)) Receptor Activity Via Erk1/2 Signaling. Synapse. 2013;67:145–159. doi: 10.1002/syn.21626.
- 58.Best A.R., Regehr W.G. Serotonin Evokes Endocannabinoid Release and Retrogradely Suppresses Excitatory Synapses. J. Neurosci. 2008;28:6508–6515. doi: 10.1523/JNEUROSCI.0678-08.2008.
- 59.Darmani N.A., Janoyan J.J., Crim J., Ramirez J. Receptor mechanism and antiemetic activity of structurally-diverse cannabinoids against radiation-induced emesis in the least shrew. Eur. J. Pharmacol. 2007;563:187–196. doi: 10.1016/j.ejphar.2007.01.093.
- 60.Pertwee R.G. The Diverse Cb1 and Cb2 Receptor Pharmacology of Three Plant Cannabinoids: Delta9-Tetrahydrocannabinol, Cannabidiol and Delta9-Tetrahydrocannabivarin. Br. J. Pharmacol. 2008;153:199–215. doi: 10.1038/sj.bjp.0707442.
- 61.Hales C.M., Kit B.K., Gu Q., Ogden C.L. Trends in Prescription Medication Use Among Children and Adolescents—United States, 1999–2014. JAMA. 2018;319:2009–2020. doi: 10.1001/jama.2018.5690.
- 62.Cox E.J., Maharao N., Patilea-Vrana G., Unadkat J.D., Rettie A.E., McCune J.S., Paine M.F. A marijuana-drug interaction primer: Precipitants, pharmacology, and pharmacokinetics. Pharmacol. Ther. 2019;201:25–38. doi: 10.1016/j.pharmthera.2019.05.001.
- 63.Luft M.J., Lamy M., DelBello M.P., McNamara R.K., Strawn J.R. Antidepressant-Induced Activation in Children and Adolescents: Risk, Recognition and Management. Curr. Probl. Pediatr. Adolesc. Heal. Care. 2018;48:50–62. doi: 10.1016/j.cppeds.2017.12.001.
- 64.Jakubovski E., Varigonda A.L., Freemantle N., Taylor M.J., Bloch M.H. Systematic Review and Meta-Analysis: Dose-Response Relationship of Selective Serotonin Reuptake Inhibitors in Major Depressive Disorder. Am. J. Psychiatry. 2016;173:174–183. doi: 10.1176/appi.ajp.2015.15030331.
- 65.Whiting P.F., Wolff R.F., Deshpande S., Di Nisio M., Duffy S., Hernandez A.V., Keurentjes J.C., Lang S., Misso K., Ryder S. Cannabinoids for Medical Use: A Systematic Review and Meta-Analysis. JAMA J. Am. Med. Assoc. 2015;313:2456–2473. doi: 10.1001/jama.2015.6358.
Associated Data
Supplementary Materials
Data Availability Statement
Adverse event data were obtained from the FDA Adverse Event Reporting System (https://fis.fda.gov/sense/app/d10be6bb-494e-4cd2-82e4-0135608ddc13/sheet/7a47a261-d58b-4203-a8aa-6d3021737452/state/analysis accessed on 14 March 2021).